<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0">
    <channel>
        <title>Genetics and Molecular Research via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'Genetics and Molecular Research' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Genetics+and+Molecular+Research&t=Genetics+and+Molecular+Research&s=Search&f=source]]></link>
        <lastBuildDate>Thu, 09 Feb 2012 09:43:37 +0100</lastBuildDate>
        <item>
            <title>Combined analysis of the MspI and XbaI  polymorphisms in intron 22 of the factor VIII gene for  detection of hemophilia A in a Korean population.</title>
            <link>http://www.medworm.com/index.php?rid=5653993&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22290460%26dopt%3DAbstract</link>
            <description>Combined analysis of the MspI and XbaI polymorphisms in intron 22 of the factor VIII gene for detection of hemophilia A in a Korean population.
    Genet Mol Res. 2012;11(1):1-9
    Authors: Park SH, Chung N, Lee MR, Yoo SK, Choi YM
    Abstract
    To determine the usefulness of MspI/int22h-1 (intron 22 homologous region-1) polymorphism of the factor VIII gene for molecular genetic diagnosis of hemophilia A in the Korean population, MspI/intron 22 and XbaI/intron 22 polymorphisms were analyzed in 101 unrelated Korean families with severe hemophilia A. The expected heterozygosity rates of MspI/int22h-1 and XbaI/int22h-1 polymorphisms were 49.5 and 43.6%, respectively; these polymorphisms were not in complete linkage disequilibrium. Combined analysis using both polymorphisms provided an inf...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5653993</comments>
            <pubDate>Fri, 03 Feb 2012 11:24:05 +0100</pubDate>
            <guid isPermaLink="false">5653993</guid>        </item>
        <item>
            <title>Genetic  diversity of Metrodorea nigra (Rutaceae) from a small forest remnant in  Brazil assessed with microsatellite markers.</title>
            <link>http://www.medworm.com/index.php?rid=5653992&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22290461%26dopt%3DAbstract</link>
            <description>Genetic diversity of Metrodorea nigra (Rutaceae) from a small forest remnant in Brazil assessed with microsatellite markers.
    Genet Mol Res. 2012;11(1):10-6
    Authors: Guidugli MC, Ferreira-Ramos R, de Sousa AC, Cidade FW, Marconi TG, Mestriner MA, Groppo M, Alzate-Marin AL
    Abstract
    Metrodorea nigra (Rutaceae) is an endemic Brazilian tree of great ecological importance, frequently found in the submontane regions of ombrophilous dense and semideciduous forests. This tree is useful for reforesting degraded areas and the wood can be employed in construction. We developed 12 microsatellite markers from a genomic library enriched for GA/CA repeats, for this species. Polymorphisms were assessed in 40 trees of a highly fragmented population found in Cravinhos, State of São Paulo, in...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5653992</comments>
            <pubDate>Fri, 03 Feb 2012 11:24:05 +0100</pubDate>
            <guid isPermaLink="false">5653992</guid>        </item>
        <item>
            <title>Bayesian  inference to study genetic control of resistance to gray leaf spot in maize.</title>
            <link>http://www.medworm.com/index.php?rid=5653991&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22290462%26dopt%3DAbstract</link>
            <description>Bayesian inference to study genetic control of resistance to gray leaf spot in maize.
    Genet Mol Res. 2012;11(1):17-29
    Authors: Balestre M, Von Pinho RG, Brito AH
    Abstract
    Gray leaf spot (GLS) is a major maize disease in Brazil that significantly affects grain production. We used Bayesian inference to investigate the nature and magnitude of gene effects related to GLS resistance by evaluation of contrasting lines and segregating populations. The experiment was arranged in a randomized block design with three replications and the mean values were analyzed using a Bayesian shrinkage approach. Additive-dominant and epistatic effects and their variances were adjusted in an over-parametrized model. Bayesian shrinkage analysis showed to be an excellent approach to handle complex m...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5653991</comments>
            <pubDate>Fri, 03 Feb 2012 11:24:05 +0100</pubDate>
            <guid isPermaLink="false">5653991</guid>        </item>
        <item>
            <title>Food assimilated by two  sympatric populations of the brown planthopper Nilaparvata lugens (Delphacidae)  feeding on different host plants contaminates insect DNA detected by RAPD-PCR  analysis.</title>
            <link>http://www.medworm.com/index.php?rid=5653990&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22290463%26dopt%3DAbstract</link>
            <description>Food assimilated by two sympatric populations of the brown planthopper Nilaparvata lugens (Delphacidae) feeding on different host plants contaminates insect DNA detected by RAPD-PCR analysis.
    Genet Mol Res. 2012;11(1):30-41
    Authors: Latif MA, Omar MY, Tan SG, Siraj SS, Ali ME, Rafii MY
    Abstract
    Contamination of insect DNA for RAPD-PCR analysis can be a problem because many primers are non-specific and DNA from parasites or gut contents may be simultaneously extracted along with that of the insect. We measured the quantity of food ingested and assimilated by two sympatric populations of brown planthopper (BPH), Nilaparvata lugens, one from rice and the other from Leersia hexandra (Poaceae), a wetland forage grass, and we also investigated whether host plant DNA contaminates ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5653990</comments>
            <pubDate>Fri, 03 Feb 2012 11:24:05 +0100</pubDate>
            <guid isPermaLink="false">5653990</guid>        </item>
        <item>
            <title>Molecular  characteristics and expression of calmodulin cDNA from the freshwater pearl  mussel, Hyriopsis schlegelii.</title>
            <link>http://www.medworm.com/index.php?rid=5653989&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22290464%26dopt%3DAbstract</link>
            <description>Molecular characteristics and expression of calmodulin cDNA from the freshwater pearl mussel, Hyriopsis schlegelii.
    Genet Mol Res. 2012;11(1):42-52
    Authors: Zeng LG, Wang JH, Li YJ, Sheng JQ, Gu Q, Hong YJ
    Abstract
    Calmodulin (CaM) is a multifunctional intracellular calcium ion receptor protein that participates in a range of cellular processes, including calcium metabolism in mussels. To investigate the role of CaM in freshwater mollusk shell calcium metabolism, the full-length CaM cDNA was isolated from the freshwater pearl mussel, Hyriopsis schlegelii (referred to as hsCaM) using SMART RACE technology. The full-length hsCaM was 855 bp in size, containing a 70-bp 5ꞌ-untranslated sequence, a 447-bp open reading frame, a 309-bp 3ꞌ-untranslated sequence, and a 26-nucleot...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5653989</comments>
            <pubDate>Fri, 03 Feb 2012 11:24:05 +0100</pubDate>
            <guid isPermaLink="false">5653989</guid>        </item>
        <item>
            <title>An improved reverse dot hybridization for simple and rapid  detection of adefovir dipivoxil-resistant  hepatitis B virus.</title>
            <link>http://www.medworm.com/index.php?rid=5653988&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22290465%26dopt%3DAbstract</link>
            <description>An improved reverse dot hybridization for simple and rapid detection of adefovir dipivoxil-resistant hepatitis B virus.
    Genet Mol Res. 2012;11(1):53-60
    Authors: Hu Y, Zhang WL, Xie SL, Zhao Y, Hu JL, Cai XF, Lai GQ, Huang AL
    Abstract
    Early detection of adefovir dipivoxil-resistant mutants during long-term treatment of chronic hepatitis B virus (HBV) infection with this drug is of great clinical importance. We developed an improved reverse dot hybridization test for simple and rapid detection of the rtA181V/T and rtN236T mutations associated with adefovir dipivoxil resistance in chronic hepatitis B patients. Probes were designed for genotypes B, C, and D of this resistance characteristic; a total of 70 clinical samples were analyzed with this improved reverse dot hybridizati...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5653988</comments>
            <pubDate>Fri, 03 Feb 2012 11:24:05 +0100</pubDate>
            <guid isPermaLink="false">5653988</guid>        </item>
        <item>
            <title>Polymorphisms of the TIM-1  gene are associated with rheumatoid arthritis in the Chinese Hui minority  ethnic population.</title>
            <link>http://www.medworm.com/index.php?rid=5653987&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22290466%26dopt%3DAbstract</link>
            <description>Polymorphisms of the TIM-1 gene are associated with rheumatoid arthritis in the Chinese Hui minority ethnic population.
    Genet Mol Res. 2012;11(1):61-9
    Authors: Xu JR, Yang Y, Liu XM, Sun JY, Wang YJ
    Abstract
    The T-cell immunoglobulin and mucin domain 1 (TIM-1) is known to be associated with susceptibility to rheumatoid arthritis (RA). We investigated the association of four single-nucleotide polymorphisms (SNPs) in the promoter region of the TIM-1 gene with susceptibility to RA in a Chinese Hui ethnic minority group. Using RFLP or sequence specific primer-PCR, 118 RA patients and 118 non-arthritis control individuals were analyzed for the -1637A&amp;gt;G, -1454G&amp;gt;A, -416G&amp;gt;C, and -232A&amp;gt;G SNPs in the TIM-1 gene. The polymorphisms -232A&amp;gt;G and -1637A&amp;gt;G in the promoter...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5653987</comments>
            <pubDate>Fri, 03 Feb 2012 11:24:05 +0100</pubDate>
            <guid isPermaLink="false">5653987</guid>        </item>
        <item>
            <title>Prevalence  of CYP2C9 and VKORC1 alleles in the Argentine population and implications for  prescribing dosages of anticoagulants.</title>
            <link>http://www.medworm.com/index.php?rid=5653986&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22290467%26dopt%3DAbstract</link>
            <description>We examined the frequency of the most relevant variants encoding CYP2C9 (alleles *1, *2 and *3) and VKORC1 (SNP -1639A&amp;gt;G) in the Argentinian population. Molecular typing was performed by PCR-RFLP on a randomly selected sample of 101 healthy volunteers from the Hospital Italiano de Buenos Aires gene bank. Fifty-seven subjects were identified as homozygous for CYP2C9*1 and 14 for *2, while 24 and 5 were heterozygous for *2 and *3 alleles; one individual was a composite heterozygote (*2/*3). When we examined VKORC1, 21 subjects were AA homozygous, 60 were AG heterozygotes and 20 were GG homozygotes. This is the first analysis of genotypic frequencies for CYP2C9 and VKORC1 performed in an Argentinian population. These allele prevalences are similar to what is known for Caucasian population,...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5653986</comments>
            <pubDate>Fri, 03 Feb 2012 11:24:05 +0100</pubDate>
            <guid isPermaLink="false">5653986</guid>        </item>
        <item>
            <title>Sodium valproate inhibits  MDA-MB-231 breast cancer cell migration by upregulating NM23H1 expression.</title>
            <link>http://www.medworm.com/index.php?rid=5653985&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22290468%26dopt%3DAbstract</link>
            <description>Sodium valproate inhibits MDA-MB-231 breast cancer cell migration by upregulating NM23H1 expression.
    Genet Mol Res. 2012;11(1):77-86
    Authors: Li GF, Qian TL, Li GS, Yang CX, Qin M, Huang J, Sun M, Han YQ
    Abstract
    Breast cancer is a common cancer in women, with a highly variable course, from inoffensive to lethal. To find a more effective strategy for its treatment, sodium valproate has been tested as an anti-cancer drug; it is the only clinically available histone deacetylase inhibitor. However, data about the effects of sodium valproate on breast cancer are insufficient in both animals and humans; studies have yielded conflicting conclusions. In particular, little is known about the association between expression of the metastasis suppressor Nm23H1 gene and breast cancer. ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5653985</comments>
            <pubDate>Fri, 03 Feb 2012 11:24:05 +0100</pubDate>
            <guid isPermaLink="false">5653985</guid>        </item>
        <item>
            <title>Association of T869C gene  polymorphism  of transforming growth factor-β1 with low protein  levels and anthropometric indices in osteopenia/osteoporosis postmenopausal Thai women.</title>
            <link>http://www.medworm.com/index.php?rid=5653984&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22290469%26dopt%3DAbstract</link>
            <description>Association of T869C gene polymorphism of transforming growth factor-β1 with low protein levels and anthropometric indices in osteopenia/osteoporosis postmenopausal Thai women.
    Genet Mol Res. 2012;11(1):87-99
    Authors: Utennam D, Tungtrongchitr A, Phonrat B, Tungtrongchitr R, Preutthipan S
    Abstract
    Osteoporosis is the most common metabolic bone disease; it is an important health problem among postmenopausal women. We evaluated the association of three polymorphisms, T869C, C-509T and G915C, of the TGF-β1 gene with bone mineral density (BMD) serum TGF-β1 levels in 278 postmenopausal female osteopenia/osteoporosis subjects and 95 postmenopausal female control subjects. Serum TGF-β1 levels were significantly lower in osteopenia/osteoporosis subjects than in control subjects...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5653984</comments>
            <pubDate>Fri, 03 Feb 2012 11:24:05 +0100</pubDate>
            <guid isPermaLink="false">5653984</guid>        </item>
        <item>
            <title>Genotoxicity, cytotoxicity and  toxicological evaluation of whole plant extracts of the medicinal plant Phyllanthus niruri  (Phyllanthaceae).</title>
            <link>http://www.medworm.com/index.php?rid=5653983&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22290470%26dopt%3DAbstract</link>
            <description>We examined the geno-, cyto- and overall toxicity of P. niruri whole plant ethanolic extract. The extract was administered as a single dose of 30 or 300 mg/kg to laboratory rats by gavage, accompanied by negative (0.9% saline) and positive (10 mg/mL N-ethyl-N-nitrosourea) controls that were injected intramuscularly 48 h after extract administration. The ratio of polychromatic (PCE)/normochromatic erythrocytes (NCE) from femur bone marrow was scored for genotoxicity. Cytotoxicity was determined using descending concentrations (0.2-0.0125 g/mL) of the extract incubated with peripheral blood mononuclear cells. Lactate dehydrogenase release from damaged cells was determined and the CC(50) calculated. Subchronic administration of the extract at 30 or 300 mg/kg was done for 90 days to determine ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5653983</comments>
            <pubDate>Fri, 03 Feb 2012 11:24:05 +0100</pubDate>
            <guid isPermaLink="false">5653983</guid>        </item>
        <item>
            <title>Abnormal male meiosis explains  pollen sterility in the polyploid medicinal plant Pinellia ternata (Araceae).</title>
            <link>http://www.medworm.com/index.php?rid=5653982&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22290471%26dopt%3DAbstract</link>
            <description>Abnormal male meiosis explains pollen sterility in the polyploid medicinal plant Pinellia ternata (Araceae).
    Genet Mol Res. 2012;11(1):112-20
    Authors: Liu Y, Hui RK, Deng RN, Wang JJ, Wang M, Li ZY
    Abstract
    Pinellia ternata is an important traditional Chinese medicinal plant. Its different populations in China have various ploidy levels, based on x = 13, as well as extensive aneuploid series. The microsporogenesis process was observed in specimens from three populations from three regions of Hubei Province; they were characterized by normal and abnormal meiotic divisions in pollen mother cells (PMCs) at all stages simultaneously. Meiotic abnormalities including univalents/multivalents, chromosomal laggards/bridges and micronuclei appeared in about 50% of the PMCs, together ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5653982</comments>
            <pubDate>Fri, 03 Feb 2012 11:24:05 +0100</pubDate>
            <guid isPermaLink="false">5653982</guid>        </item>
        <item>
            <title>Cytomixis and meiotic  abnormalities during microsporogenesis are responsible for male sterility and  chromosome variations in Houttuynia cordata.</title>
            <link>http://www.medworm.com/index.php?rid=5653981&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22290472%26dopt%3DAbstract</link>
            <description>Cytomixis and meiotic abnormalities during microsporogenesis are responsible for male sterility and chromosome variations in Houttuynia cordata.
    Genet Mol Res. 2012;11(1):121-30
    Authors: Guan JZ, Wang JJ, Cheng ZH, Liu Y, Li ZY
    Abstract
    Houttuynia cordata (Saururaceae) is a leaf vegetable and a medicinal herb througout much of Asia. Cytomixis and meiotic abnormalities during microsporogenesis were found in two populations of H. cordata with different ploidy levels (2n = 38, 96). Cytomixis occurred in pollen mother cells during meiosis at high frequencies and with variable degrees of chromatin/chromosome transfer. Meiotic abnormalities, such as chromosome laggards, asymmetric segregation and polyads, also prevailed in pollen mother cells at metaphase of the first division an...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5653981</comments>
            <pubDate>Fri, 03 Feb 2012 11:24:05 +0100</pubDate>
            <guid isPermaLink="false">5653981</guid>        </item>
        <item>
            <title>Karyotype analysis of mithun (Bos  frontalis) and mithun bull x Brahman cow hybrids.</title>
            <link>http://www.medworm.com/index.php?rid=5653980&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22290473%26dopt%3DAbstract</link>
            <description>We examined the cytogenetics of mithun (Bos frontalis), a domesticated version of the Asian gaur, and hybrids (F(1) generation) produced by artificial insemination of Brahman cows (Bos indicus) with mithun semen. Reproductive potential was also examined in the F(1) generation and a backcrossed heifer for utilization of heterosis. Metaphase chromosome spreads were examined by conventional staining and fluorescence in situ hybridization hybridized with the entire chromosome 1 of mithun as a specific probe. Chromosome 1 of mithun was found to be equivalent to Bos taurus chromosomes 2 and 28. The karyotype of the female mithun (N = 4) comprised 58 chromosomes, including 54 acrocentric and four large submetacentric chromosomes, without the four acrocentric chromosomes found in the domesticated ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5653980</comments>
            <pubDate>Fri, 03 Feb 2012 11:24:05 +0100</pubDate>
            <guid isPermaLink="false">5653980</guid>        </item>
        <item>
            <title>Back fat thickness and meat  tenderness are associated with a 526 T→A mutation in the exon 1 promoter region  of the MyF-5 gene  in Chinese Bos taurus.</title>
            <link>http://www.medworm.com/index.php?rid=5544091&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194162%26dopt%3DAbstract</link>
            <description>Back fat thickness and meat tenderness are associated with a 526 T→A mutation in the exon 1 promoter region of the MyF-5 gene in Chinese Bos taurus.
    Genet Mol Res. 2011;10(4):3070-9
    Authors: Ujan JA, Zan LS, Ujan SA, Adoligbe C, Wang HB
    Abstract
    Qualitative trait loci (QTL) for growth and meat quality traits in cattle (Bos taurus) have been previously mapped to three chromosome regions, 0 to 30, 55 to 70, and 70 to 80 cM on chromosome 5. We evaluated the allele frequencies and gene-specific single nucleotide polymorphisms (SNPs) of bovine myogenic factor 5 (MyF-5) in the QTL regions and their associations with live weight and meat characteristics in indigenous Chinese cattle breeds. PCR-SSCP methodology showed a T&amp;gt;A mutation at 526 bp. Least square analysis revealed a ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544091</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544091</guid>        </item>
        <item>
            <title>RAPD analysis of the genetic  diversity of mango (Mangifera indica) germplasm in Brazil.</title>
            <link>http://www.medworm.com/index.php?rid=5544090&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194163%26dopt%3DAbstract</link>
            <description>RAPD analysis of the genetic diversity of mango (Mangifera indica) germplasm in Brazil.
    Genet Mol Res. 2011;10(4):3080-9
    Authors: Souza IG, Valente SE, Britto FB, de Souza VA, Lima PS
    Abstract
    We evaluated genetic variability of mango (Mangifera indica) accessions maintained in the Active Germplasm Bank of Embrapa Meio-Norte in Teresina, Piauí, Brazil, using RAPDs. Among these accessions, 35 originated from plantings in Brazil, six from the USA and one from India. Genomic DNA, extracted from leaf material using a commercial purification kit, was subjected to PCR with the primers A01, A09, G03, G10, N05, and M16. Fifty-five polymorphic loci were identified, with mean of 9.16 ± 3.31 bands per primer and 100% polymorphism. Application of unweighted pair group method using ar...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544090</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544090</guid>        </item>
        <item>
            <title>Detection of novel SNPs and mapping of the fatness QTL  on pig chromosome 7q1.1-1.4 region.</title>
            <link>http://www.medworm.com/index.php?rid=5544089&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194164%26dopt%3DAbstract</link>
            <description>Detection of novel SNPs and mapping of the fatness QTL on pig chromosome 7q1.1-1.4 region.
    Genet Mol Res. 2011;10(4):3090-7
    Authors: Huang WH, Ma ZX, Xu ZY, Xiong YZ, Zuo B
    Abstract
    Many QTLs for fatness traits have been mapped on pig chromosome 7q1.1-1.4 in various pig resource populations. Eight novel markers, including seven SNPs and one insertion or deletion within BTNL1, COL21A1, PPARD, GLP1R, MDFI, GNMT, ABCC10, and PLA2G7 genes, as well as two previously reported SNPs in SLC39A7 and HMGA1 genes, were genotyped in Large White and Meishan pig breeds. Except for two SNPs in HMGA1 and ABCC10 genes, allele frequencies of the other eight markers are highly significant different between Chinese indigenous Meishan breeds and Large White pig breeds. Eight polymorphic sites we...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544089</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544089</guid>        </item>
        <item>
            <title>Isolation and characterization of  nucleotide-binding site and C-terminal leucine-rich repeat-resistance gene candidates in bananas.</title>
            <link>http://www.medworm.com/index.php?rid=5544088&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194165%26dopt%3DAbstract</link>
            <description>Isolation and characterization of nucleotide-binding site and C-terminal leucine-rich repeat-resistance gene candidates in bananas.
    Genet Mol Res. 2011;10(4):3098-108
    Authors: Lu Y, Xu WH, Xie YX, Zhang X, Pu JJ, Qi YX, Li HP
    Abstract
    Commercial banana varieties are highly susceptible to fungal pathogens, as well as bacterial pathogens, nematodes, viruses, and insect pests. The largest known family of plant resistance genes encodes proteins with nucleotide-binding site (NBS) and C-terminal leucine-rich repeat (LRR) domains. Conserved motifs in such genes in diverse plant species offer a means for the isolation of candidate genes in banana that may be involved in plant defense. Six degenerate PCR primers were designed to target NBS and additional domains were tested on comme...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544088</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544088</guid>        </item>
        <item>
            <title>Association between HLA-Cw*0602 polymorphism and psoriasis risk: a meta-analysis.</title>
            <link>http://www.medworm.com/index.php?rid=5544087&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194166%26dopt%3DAbstract</link>
            <description>In conclusion, the positive allele of HLA-Cw*0602 polymorphism appears to be a risk factor for psoriasis.
    PMID: 22194166 [PubMed - in process] (Source: Genetics and Molecular Research)</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544087</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544087</guid>        </item>
        <item>
            <title>A study on the relationship  between TCTA tetranucleotide polymorphism of the HPRT gene and primary  hyperuricemia.</title>
            <link>http://www.medworm.com/index.php?rid=5544086&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194167%26dopt%3DAbstract</link>
            <description>We examined polymorphism of the TCTA tetranucleotide sequence in the 3rd intron of the hypoxanthine-guanine phosphoribosyltransferase (HPRT) gene in the Han population of Ningxia Province in China. We also looked for a possible relationship between STR polymorphism in the 3rd intron of the HPRT gene and primary hyperuricemia. We used Chelex-100 to extract DNA, then PCR, PAGE and silver staining for allele genotyping and DNA sequencing to obtain the distribution of the alleles. We found, for the first time, that there is high STR polymorphism in the 3rd intron of the HPRT gene. We detected 5 STR alleles in this intron in the Han population of Ningxia Province, with 15 genotypes in females; significant differences were observed in the distribution of alleles and genotypes between control and...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544086</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544086</guid>        </item>
        <item>
            <title>Genetic parameter estimates  and response to selection for weight and testicular traits in Nelore cattle.</title>
            <link>http://www.medworm.com/index.php?rid=5544085&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194168%26dopt%3DAbstract</link>
            <description>Genetic parameter estimates and response to selection for weight and testicular traits in Nelore cattle.
    Genet Mol Res. 2011;10(4):3127-40
    Authors: Araujo Neto FR, Lôbo RB, Mota MD, Oliveira HN
    Abstract
    We estimated genetic parameters for various phases of body and testicular growth until 550 days of age in Nelore cattle, using Bayesian inference, including correlation values and error estimates. Weight and scrotal records of 54,182 Nelore animals originating from 18 farms participating in the Brazilian Nelore Breeding Program (PMGRN) were included. The following traits were measured: weight at standard ages of 120 (W120), 210 (W210), 365 (W365), 450 (W450), and 550 (W550) days; weight gain between 120/210 (WG1), 210/365 (WG2), 365/450 (WG3), 450/550 (WG4), 120/365 (WG5), ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544085</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544085</guid>        </item>
        <item>
            <title>Polymorphic microsatellite  loci for the genetic analysis of Lycoris radiata (Amaryllidaceae) and  cross-amplification in other congeneric species.</title>
            <link>http://www.medworm.com/index.php?rid=5544084&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194169%26dopt%3DAbstract</link>
            <description>Polymorphic microsatellite loci for the genetic analysis of Lycoris radiata (Amaryllidaceae) and cross-amplification in other congeneric species.
    Genet Mol Res. 2011;10(4):3141-5
    Authors: Xuan SQ, Zheng JY, Wang H, Gao P, Zhou SB, Liu K, Zhu GP
    Abstract
    Lycoris radiata is a perennial herb that has been used in traditional Chinese medicine for a long time and has two main medicinal components in its bulb, lycorine and galanthamine. However, the original microsatellite loci have not been developed for any species of Lycoris. Total genomic DNA was extracted from fresh bulbs using a modified CTAB protocol. We isolated 10 microsatellite loci from 21 L. radiata individuals of a natural population from Yellow Mountain in Anhui Province, China. The number of alleles ranged from two...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544084</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544084</guid>        </item>
        <item>
            <title>Genetic markers of body  composition and carcass quality in grazing Brangus steers.</title>
            <link>http://www.medworm.com/index.php?rid=5544083&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194170%26dopt%3DAbstract</link>
            <description>Genetic markers of body composition and carcass quality in grazing Brangus steers.
    Genet Mol Res. 2011;10(4):3146-56
    Authors: Baeza MC, Corva PM, Soria LA, Rincon G, Medrano JF, Pavan E, Villarreal EL, Schor A, Melucci L, Mezzadra C, Miquel MC
    Abstract
    The somatotropic axis is a major regulatory pathway of energy metabolism during postnatal growth in mammals. Genes involved in this pathway influence many economically important traits. The association of selected SNPs in these genes with carcass traits was examined in grazing Brangus steers. These traits included final live weight, ultrasound backfat thickness (UBFT), rib-eye area, kidney fat weight, hot carcass weight, and intramuscular fat percentage (%IMF). Genomic DNA (N = 246) was genotyped for a panel of 15 tag SNPs lo...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544083</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544083</guid>        </item>
        <item>
            <title>XPD and hOGG1 gene  polymorphisms in reperfusion oxidative stress.</title>
            <link>http://www.medworm.com/index.php?rid=5544082&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194171%26dopt%3DAbstract</link>
            <description>XPD and hOGG1 gene polymorphisms in reperfusion oxidative stress.
    Genet Mol Res. 2011;10(4):3157-62
    Authors: Isbir O, Görmüş U, Ergen HA, Cakmakoğlu B, Kahraman OT, Baykan N
    Abstract
    Knee replacement surgery is an ischemia/reperfusion model, as it uses tourniquet applied to the knee area to stop the blood flow during the operation. Fifty patients that were undergoing elective arthroscopic knee surgery were included in our study. Human 8-oxoguanine glycosylase 1 (hOGG1) is an enzyme to repair specific DNA lesions and a good marker of hydroxyl radical damage to DNA. XPD is another DNA repair gene. We investigated the effect of hOGG1 (Ser326Cys) and XPD (Lys751Gln) polymorphisms on the oxidative stress level after reperfusion. To evaluate oxidative stress conditions, we me...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544082</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544082</guid>        </item>
        <item>
            <title>Sulcus  vocalis: evidence for autosomal dominant inheritance.</title>
            <link>http://www.medworm.com/index.php?rid=5544081&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194172%26dopt%3DAbstract</link>
            <description>Sulcus vocalis: evidence for autosomal dominant inheritance.
    Genet Mol Res. 2011;10(4):3163-8
    Authors: Martins RH, Gonçalves TM, Neves DS, Fracalossi TA, Tavares EL, Moretti-Ferreira D
    Abstract
    We found evidence of autosomal dominant hereditary transmission of sulcus vocalis. Four dysphonic patients from three generations of the same family were submitted to videolaryngoscopic examination (three patients) and to direct laryngoscopy (one patient) to diagnose the hoarseness. Sulcus vocalis was diagnosed in all four patients. The finding of four affected individuals in three generations, with vertical transmission affecting man and women, is more consistent with autosomal dominant inheritance pattern; it is an etiological model that we propose for the sulcus vocalis in this p...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544081</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544081</guid>        </item>
        <item>
            <title>In vitro antioxidant  activities of endophytic fungi isolated from the liverwort Scapania verrucosa.</title>
            <link>http://www.medworm.com/index.php?rid=5544080&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194173%26dopt%3DAbstract</link>
            <description>In vitro antioxidant activities of endophytic fungi isolated from the liverwort Scapania verrucosa.
    Genet Mol Res. 2011;10(4):3169-79
    Authors: Zeng PY, Wu JG, Liao LM, Chen TQ, Wu JZ, Wong KH
    Abstract
    We investigated in vitro antioxidant activities of 49 endophytic fungi isolated from the liverwort Scapania verrucosa. Based on morphological and molecular identification, the endophytic fungi isolated were classified into seven genera (Hypocrea, Penicillium, Tolypocladium, Chaetomium, Xylaria, Nemania, and Creosphaeria), all belonging to one family (Xylariaceae). By screening with the 2,2'-azino-di(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) decolorization assay, the ethyl acetate extracts of five endophytic fungi (T7, T21, T24, T32, and T38 strains), which exhibited remark...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544080</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544080</guid>        </item>
        <item>
            <title>Methodology Adaptation of a low-cost  medium-throughput genotyping system for ovine prion protein gene polymorphims  associated with scrapie.</title>
            <link>http://www.medworm.com/index.php?rid=5544079&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194174%26dopt%3DAbstract</link>
            <description>Methodology Adaptation of a low-cost medium-throughput genotyping system for ovine prion protein gene polymorphims associated with scrapie.
    Genet Mol Res. 2011;10(4):3180-5
    Authors: Ianella P, McManus CM, Paiva SR, Caetano AR
    Abstract
    Resistance and susceptibility to scrapie in sheep have been associated with SNPs located at codons 136, 154 and 171 of the prion protein (PRNP) gene. Many countries have sheep breeding programs selecting for resistance to scrapie based on the genotyping of these SNPs. We adapted a fast and robust method for genotyping sheep flocks for these polymorphisms, with reduced costs. Ninety-six samples were genotyped using an adapted SNaPshot PRNP assay, and the results were checked by resequencing. The results showed 100% concordance, using a method t...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544079</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544079</guid>        </item>
        <item>
            <title>Population genetic structure  of the tropical tree species Aegiphila sellowiana (Lamiaceae).</title>
            <link>http://www.medworm.com/index.php?rid=5544078&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194175%26dopt%3DAbstract</link>
            <description>Population genetic structure of the tropical tree species Aegiphila sellowiana (Lamiaceae).
    Genet Mol Res. 2011;10(4):3186-98
    Authors: Medri C, Ruas EA, Ruas CF, Medri PS, Medri ME, Ruas PM
    Abstract
    The Tibagi River, located in southern Brazil, is associated with a significant degree of environmental heterogeneity, along its 550 km extension. There is concern about the integrity of this river's ecosystem, as human interference has been increasing. Aegiphila sellowiana (Lamiaceae) is an important pioneer tree species, commonly found near rivers; the fruit is consumed by avifauna. We studied this species along three ecological gradients, comprising the upper, middle, and lower regions of the Tibagi River basin. The genetic structure of nine subpopulations of A. sellowiana dis...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544078</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544078</guid>        </item>
        <item>
            <title>Two splice variants of the bovine  lactoferrin gene identified in Staphylococcus aureus  isolated from mastitis in dairy cattle.</title>
            <link>http://www.medworm.com/index.php?rid=5544077&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194176%26dopt%3DAbstract</link>
            <description>Two splice variants of the bovine lactoferrin gene identified in Staphylococcus aureus isolated from mastitis in dairy cattle.
    Genet Mol Res. 2011;10(4):3199-203
    Authors: Huang JM, Wang ZY, Ju ZH, Wang CF, Li QL, Sun T, Hou QL, Hang SQ, Hou MH, Zhong JF
    Abstract
    Bovine lactoferrin (bLF) is a member of the transferrin family; it plays an important role in the innate immune response. We identified novel splice variants of the bLF gene in mastitis-infected and healthy cows. Reverse transcription-polymerase chain reaction (RT-PCR) and clone sequencing analysis were used to screen the splice variants of the bLF gene in the mammary gland, spleen and liver tissues. One main transcript corresponding to the bLF reference sequence was found in three tissues in both healthy and mastit...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544077</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544077</guid>        </item>
        <item>
            <title>Methodology Molecular cloning and characterization of gene coding  for γ-tocopherol  methyltransferase from lettuce (Lactuca sativa).</title>
            <link>http://www.medworm.com/index.php?rid=5544076&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194177%26dopt%3DAbstract</link>
            <description>Methodology Molecular cloning and characterization of gene coding for γ-tocopherol methyltransferase from lettuce (Lactuca sativa).
    Genet Mol Res. 2011;10(4):3204-12
    Authors: Tang YL, Ren WW, Zhang L, Tang KX
    Abstract
    γ-tocopherol methyltransferase is an important rate-limiting enzyme involved in tocopherol biosynthesis. The full-length cDNA encoding γ-tocopherol methyltransferase (designated as LsTMT) was cloned from Lactuca sativa for the first time by rapid amplification of cDNA ends and characterized by means of quantitative RT-PCR. The full-length cDNA of LsTMT was 1131 bp, with an open reading frame of 897 bp encoding a γ-tocopherol methyltransferase protein of 298 amino acids, with a calculated molecular mass of 33.06 kDa and an isoelectric point of 5.86. Compara...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544076</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544076</guid>        </item>
        <item>
            <title>Evaluation of HPFH and δβ-thalassemia  mutations in a Brazilian group with high Hb F levels.</title>
            <link>http://www.medworm.com/index.php?rid=5544075&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194178%26dopt%3DAbstract</link>
            <description>Evaluation of HPFH and δβ-thalassemia mutations in a Brazilian group with high Hb F levels.
    Genet Mol Res. 2011;10(4):3213-9
    Authors: Carrocini GC, Ondei LS, Zamaro PJ, Bonini-Domingos CR
    Abstract
    Fetal hemoglobin (Hb F) is characteristic of the fetal development period. However, in some genetic conditions, such as hereditary persistence of fetal hemoglobin (HPFH) and delta-beta thalassemia (δβ-thalassemia), Hb F continues to be produced in adulthood. We evaluated the frequency of two mutations of HPFH, HPFH-1 and HPFH-2 African, and two mutations in δβ-thalassemia, Sicilian and Spanish, in a Brazilian population. Peripheral blood samples were collected from adults from hospitals and blood centers in southeast and northeast Brazil. These individuals were healthy and w...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544075</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544075</guid>        </item>
        <item>
            <title>Age-related pyrethroid resistance is not a function of  P450 gene expression in the major African malaria vector, Anopheles funestus (Diptera: Culicidae).</title>
            <link>http://www.medworm.com/index.php?rid=5544074&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194179%26dopt%3DAbstract</link>
            <description>We examined the relationship between pyrethroid resistance and gene transcription levels of two closely related genes, CYP6P9 and CYP6P13, in FUMOZ-R. Levels of resistance to 0.75% permethrin were determined based on standard WHO insecticide susceptibility assays using females and males of different ages, ranging from 3 to 30 days old. The transcription levels of the two genes were quantified using qPCR for each age cohort. In the WHO insecticide susceptibility assays, survival of both males and females significantly decreased as age increased. Quantitative analysis of the two genes CYP6P9 and CYP6P13 showed the highest levels of expression at 10 days of age. There was no correlation between expression of these two genes and pyrethroid survival by age. We conclude that the resistance of th...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544074</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544074</guid>        </item>
        <item>
            <title>Eight polymorphic  microsatellite markers for the spotted babylon, Babylonia areolata (Buccinidae).</title>
            <link>http://www.medworm.com/index.php?rid=5544073&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194180%26dopt%3DAbstract</link>
            <description>Eight polymorphic microsatellite markers for the spotted babylon, Babylonia areolata (Buccinidae).
    Genet Mol Res. 2011;10(4):3230-5
    Authors: Wang Y, Lu H, Zheng J, Long K, Shi YH, Gu ZF, Wang AM
    Abstract
    The spotted babylon, Babylonia areolata, is one of the most extensively cultured marine mollusks in southeast Asia. Eight polymorphic microsatellite markers were developed for this species, from a microsatellite-enriched library. These markers, characterized in 32 individuals from a hatchery population, were polymorphic, with allele numbers ranging from 6 to 18 per locus, expected and observed heterozygosities ranging from 0.68 to 0.94 and 0.56 to 0.81, respectively. One locus (HUBA09) showed significant deviation from Hardy-Weinberg equilibrium, probably due to the presenc...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544073</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544073</guid>        </item>
        <item>
            <title>Lapachol as an epithelial  tumor inhibitor agent in Drosophila melanogaster heterozygote for tumor  suppressor gene wts.</title>
            <link>http://www.medworm.com/index.php?rid=5544072&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194187%26dopt%3DAbstract</link>
            <description>Lapachol as an epithelial tumor inhibitor agent in Drosophila melanogaster heterozygote for tumor suppressor gene wts.
    Genet Mol Res. 2011;10(4):3236-45
    Authors: Costa WF, Oliveira AB, Nepomuceno JC
    Abstract
    The search for new and effective antitumor agents with fewer cytotoxic side effects on normal tissue has increasingly become important. Lapachol, a natural organic compound isolated from the lapacho tree (Tabebuia avellandedae), is chemically identified as belonging to the naphthoquinone group and is known for its anti-inflammatory, analgesic and antibiotic properties, although there are questions about its effectiveness for treating neoplasic cells. We evaluated the antitumoral effects of lapachol by testing for clones of epithelial tumors in Drosophila melanogaster. S...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544072</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544072</guid>        </item>
        <item>
            <title>Characterization of 12  microsatellite loci for the Pacific lamprey, Entosphenus tridentatus (Petromyzontidae),  and cross-amplification in five other lamprey species.</title>
            <link>http://www.medworm.com/index.php?rid=5544071&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194188%26dopt%3DAbstract</link>
            <description>Characterization of 12 microsatellite loci for the Pacific lamprey, Entosphenus tridentatus (Petromyzontidae), and cross-amplification in five other lamprey species.
    Genet Mol Res. 2011;10(4):3246-50
    Authors: Spice EK, Whitesel TA, McFarlane CT, Docker MF
    Abstract
    The Pacific lamprey (Entosphenus tridentatus) is an anadromous fish that is of conservation concern in North America and Asia. Data on Pacific lamprey population structure are scarce and conflicting, impeding conservation efforts. We optimized 12 polymorphic microsatellite loci for the Pacific lamprey. Three to 13 alleles per locus were observed in a sample of 51 fish collected from the West Fork Illinois River, Oregon. Observed heterozygosity ranged from 0.235 to 0.902 and expected heterozygosity ranged from 0.21...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544071</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544071</guid>        </item>
        <item>
            <title>A rapid protocol for  purification of total RNA for tissues collected from pigs at a slaughterhouse.</title>
            <link>http://www.medworm.com/index.php?rid=5544070&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194189%26dopt%3DAbstract</link>
            <description>A rapid protocol for purification of total RNA for tissues collected from pigs at a slaughterhouse.
    Genet Mol Res. 2011;10(4):3251-5
    Authors: Méndez V, Avelar E, Morales A, Cervantes M, Araiza A, González D
    Abstract
    Since RNA extraction is a crucial step in many molecular techniques, the protocols for sample collection and RNA purification need to be adapted to optimize their performance when samples are collected from animals at commercial facilities. Here we provide an RNA purification protocol for animal tissues collected from slaughterhouses. This protocol, modified from other techniques, uses TRIzol Reagent. Sample collection was performed wearing sterile gloves and facemasks, using sterile surgical instruments, and no longer than 8 min spent for each sample. A 0.9% ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544070</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544070</guid>        </item>
        <item>
            <title>S323I  polymorphism of the C5L2 gene was not identified in a Chinese population with familial combined  hyperlipidemia or with type 2 diabetes.</title>
            <link>http://www.medworm.com/index.php?rid=5544069&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194190%26dopt%3DAbstract</link>
            <description>S323I polymorphism of the C5L2 gene was not identified in a Chinese population with familial combined hyperlipidemia or with type 2 diabetes.
    Genet Mol Res. 2011;10(4):3256-66
    Authors: Zheng YY, Xie X, Ma YT, Yang YN, Fu ZY, Li XM, Liu F, Yang SJ, Ma X, Chen BD
    Abstract
    C5L2, a G protein-coupled receptor, is known to be a functional receptor of acylation-stimulating protein, which is a stimulator of triglyceride synthesis and glucose transport. A novel C5L2 variant (S323I) was identified and its association with familial combined hyperlipidemia (FCH) was recently reported. We looked for this SNP in three Chinese ethnic groups, including Han, Uygur, and Kazakh controls and patients with FCH and type 2 diabetes. One hundred and eighty-two unrelated subjects (77 of Han, 57 of ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544069</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544069</guid>        </item>
        <item>
            <title>Genetic loci mapping associated  with maize kernel number per ear based on a recombinant inbred line population  grown under different nitrogen regimes.</title>
            <link>http://www.medworm.com/index.php?rid=5544068&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22194191%26dopt%3DAbstract</link>
            <description>Genetic loci mapping associated with maize kernel number per ear based on a recombinant inbred line population grown under different nitrogen regimes.
    Genet Mol Res. 2011;10(4):3267-74
    Authors: Liu XH, He SL, Zheng ZP, Tan ZB, Li Z, He C
    Abstract
    Kernel number per ear (KNE) is one of the most important yield-related agronomic traits in maize (Zea mays). To clarify its genetic basis, we made a quantitative trait locus (QTL) analysis of KNE in a recombinant inbred line population derived from lines Mo17 and Huangzao4, under two nitrogen (N) regimes. Seven QTLs, on chromosomes 4, 6 and 9, were mapped under the high N regime, which explained phenotypic variation ranging from 5.03 to 15.49%. Under the low N regime, three QTLs were located on chromosomes 6 and 9, which accounted ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544068</comments>
            <pubDate>Wed, 28 Dec 2011 02:00:11 +0100</pubDate>
            <guid isPermaLink="false">5544068</guid>        </item>
        <item>
            <title>Molecular characterization and  tissue-specific expression of invariant chain in the muscovy duck (Cairina  moschata).</title>
            <link>http://www.medworm.com/index.php?rid=5524578&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22179959%26dopt%3DAbstract</link>
            <description>Molecular characterization and tissue-specific expression of invariant chain in the muscovy duck (Cairina moschata).
    Genet Mol Res. 2011;10(4):2867-80
    Authors: Liu SJ, Chen FF, Dai Y, Wu C, Ni QS, Yu WY
    Abstract
    The invariant chain (Ii) plays an important role as a chaperone for MHC II maturation and facilitates antigen presentation in vertebrates. We cloned, characterized and made a homology analysis of healthy adult muscovy duck Ii (MDIi), from a poultry farm in the suburban district of Hefei city in China, by rapid amplification of cDNA ends (RACE)-PCR and by measuring expression of the MDIi gene in various tissues by real-time quantitative PCR. A full-length cDNA sequence of MDIi was obtained, 1188-bp long, encoding a 222-amino acid protein. A comparison of the amino ac...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524578</comments>
            <pubDate>Thu, 22 Dec 2011 03:54:02 +0100</pubDate>
            <guid isPermaLink="false">5524578</guid>        </item>
        <item>
            <title>Detection of two  morphologically cryptic species from the cursor complex (Akodon spp;  Rodentia, Cricetidae) through the use of RAPD markers.</title>
            <link>http://www.medworm.com/index.php?rid=5524577&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22179960%26dopt%3DAbstract</link>
            <description>Detection of two morphologically cryptic species from the cursor complex (Akodon spp; Rodentia, Cricetidae) through the use of RAPD markers.
    Genet Mol Res. 2011;10(4):2881-92
    Authors: Yazbeck GM, Brandão RL, Cunha HM, Paglia AP
    Abstract
    The cursor complex is a group within the Akodon genus of South American rodents, formed by Akodon cursor and A. montensis. Correct distinction between these two species is of great importance since they can harbor different Hantavirus strains. These species are only distinguishable by means of karyotypic or internal anatomic features, requiring dissection; recently, some other genetic methods have become available. We developed RAPD markers capable of distinguishing between A. cursor and A. montensis. Samples included 42 individuals of A. c...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524577</comments>
            <pubDate>Thu, 22 Dec 2011 03:54:02 +0100</pubDate>
            <guid isPermaLink="false">5524577</guid>        </item>
        <item>
            <title>Molecular characterization of  cajá, Spondias mombin (Anacardiaceae), by RAPD markers.</title>
            <link>http://www.medworm.com/index.php?rid=5524576&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22179961%26dopt%3DAbstract</link>
            <description>Molecular characterization of cajá, Spondias mombin (Anacardiaceae), by RAPD markers.
    Genet Mol Res. 2011;10(4):2893-904
    Authors: Lima AT, de Souza VA, Gomes RL, Lima PS
    Abstract
    The arboreal species Spondias mombin L. (Anacardiaceae) is widely distributed in Brazil, where the fruits, known by the common name of cajá, are an important commercial commodity. We evaluated genetic variability among 32 cajá accessions of the Germplasm Collection of Embrapa Meio-Norte using RAPD technique. Reaction conditions for efficient RAPD amplifications were optimized in preliminary tests, and primers were selected from a set designed by the University of British Columbia on the basis of high levels of polymorphism and adequate band resolution. The 21 primers employed in the final analys...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524576</comments>
            <pubDate>Thu, 22 Dec 2011 03:54:02 +0100</pubDate>
            <guid isPermaLink="false">5524576</guid>        </item>
        <item>
            <title>Novel NKX2-5 mutations  responsible for congenital heart disease.</title>
            <link>http://www.medworm.com/index.php?rid=5524575&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22179962%26dopt%3DAbstract</link>
            <description>Novel NKX2-5 mutations responsible for congenital heart disease.
    Genet Mol Res. 2011;10(4):2905-15
    Authors: Wang J, Liu XY, Yang YQ
    Abstract
    Congenital heart disease (CHD) is the most common birth defect and is the leading cause of infant morbidity and mortality resulting from birth defects. Increasing evidence demonstrates that genetic variation in the NKX2-5 gene, which encodes a homeobox-containing transcription factor crucial to cardiogenesis, is an important molecular determinant for CHD. Nevertheless, the genetic components underlying CHD remain largely unknown. We screened NKX2-5 for potential molecular defects in patients with CHD. The entire coding region of NKX2-5 was initially sequenced in a cohort of 268 unrelated patients with CHD. The relatives of the patients...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524575</comments>
            <pubDate>Thu, 22 Dec 2011 03:54:02 +0100</pubDate>
            <guid isPermaLink="false">5524575</guid>        </item>
        <item>
            <title>Transferability and utility of  white oat (Avena sativa) microsatellite markers for genetic studies in black oat (Avena strigosa).</title>
            <link>http://www.medworm.com/index.php?rid=5524574&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22179963%26dopt%3DAbstract</link>
            <description>Transferability and utility of white oat (Avena sativa) microsatellite markers for genetic studies in black oat (Avena strigosa).
    Genet Mol Res. 2011;10(4):2916-23
    Authors: Da-Silva PR, Milach SC, Tisian LM
    Abstract
    Preservation and use of wild oat species germplasm are essential for further improvement of cultivated oats. We analyzed the transferability and utility of cultivated (white) oat Avena sativa (AACCDD genome) microsatellite markers for genetic studies of black oat A. strigosa (AsAs genome) genotypes. The DNA of each black oat genotype was extracted from young leaves and amplified by PCR using 24 microsatellite primers developed from white oat. The PCR products were separated on 3% agarose gel. Eighteen microsatellite primer pairs amplified consistent products and...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524574</comments>
            <pubDate>Thu, 22 Dec 2011 03:54:02 +0100</pubDate>
            <guid isPermaLink="false">5524574</guid>        </item>
        <item>
            <title>Meta-analysis demonstrates no association between p53  codon 72 polymorphism and prostate cancer risk.</title>
            <link>http://www.medworm.com/index.php?rid=5524573&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22179964%26dopt%3DAbstract</link>
            <description>We examined whether p53 codon 72 polymorphism confers prostate cancer risk by conducting a meta-analysis. Two investigators independently searched the Pubmed, Embase and CBM databases. This meta-analysis was made of seven case-control studies, that included 892 prostate cancer cases and 1020 healthy controls. Meta-analysis results based on all the studies showed no significant association between p53 codon 72 polymorphism and prostate cancer risk in the comparisons of Pro allele vs Arg allele; Pro/Pro + Pro/Arg vs Arg/Arg; Pro/Pro vs Pro/Arg + Arg/Arg; Pro/Pro vs Arg/Arg, and Pro/Arg vs Arg/Arg [odds ratio (OR) = 1.09, 95% confidence interval (CI) = 0.87-1.36, P = 0.47; OR = 1.22, 95%CI = 0.86-1.73, P = 0.27; OR = 1.03, 95%CI = 0.62-1.72, P = 0.91; OR = 1.22, 95%CI = 0.66-2.26, P = 0.52; O...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524573</comments>
            <pubDate>Thu, 22 Dec 2011 03:54:02 +0100</pubDate>
            <guid isPermaLink="false">5524573</guid>        </item>
        <item>
            <title>Evaluation of genetic diversity in Piper spp  using RAPD and SRAP markers.</title>
            <link>http://www.medworm.com/index.php?rid=5524572&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22179965%26dopt%3DAbstract</link>
            <description>Evaluation of genetic diversity in Piper spp using RAPD and SRAP markers.
    Genet Mol Res. 2011;10(4):2934-43
    Authors: Jiang Y, Liu JP
    Abstract
    Random amplified polymorphic DNA (RAPD) and sequence-related amplified polymorphism (SRAP) analysis were applied to 74 individual plants of Piper spp in Hainan Island. The results showed that the SRAP technique may be more informative and more efficient and effective for studying genetic diversity of Piper spp than the RAPD technique. The overall level of genetic diversity among Piper spp in Hainan was relatively high, with the mean Shannon diversity index being 0.2822 and 0.2909, and the mean Nei's genetic diversity being 0.1880 and 0.1947, calculated with RAPD and SRAP data, respectively. The ranges of the genetic similarity coeffic...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524572</comments>
            <pubDate>Thu, 22 Dec 2011 03:54:02 +0100</pubDate>
            <guid isPermaLink="false">5524572</guid>        </item>
        <item>
            <title>Phenotypic and genetic  parameters compared during repeated measures of longissimus muscle area and  subcutaneous fat thickness in Nelore cattle.</title>
            <link>http://www.medworm.com/index.php?rid=5524571&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22179966%26dopt%3DAbstract</link>
            <description>Phenotypic and genetic parameters compared during repeated measures of longissimus muscle area and subcutaneous fat thickness in Nelore cattle.
    Genet Mol Res. 2011;10(4):2944-52
    Authors: Pinheiro TR, Mercadante ME, Albuquerque LG, Cyrillo JN, Branco RH
    Abstract
    Real-time ultrasound is currently used for in vivo carcass evaluation of beef cattle. We estimated heritability and repeatability coefficients for ultrasound-measured carcass traits in Nelore cattle. We measured longissimus muscle area, backfat thickness, and rump fat thickness in male and female animals ranging in age from 10 to 26 months. The variance components were estimated by single-trait analysis using the derivative-free restricted maximum likelihood method, under an animal model. The complete data file inclu...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524571</comments>
            <pubDate>Thu, 22 Dec 2011 03:54:02 +0100</pubDate>
            <guid isPermaLink="false">5524571</guid>        </item>
        <item>
            <title>Molecular cytogenetic  characterization of a new leaf rolling triticale.</title>
            <link>http://www.medworm.com/index.php?rid=5524570&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22179967%26dopt%3DAbstract</link>
            <description>Molecular cytogenetic characterization of a new leaf rolling triticale.
    Genet Mol Res. 2011;10(4):2953-61
    Authors: Yang EN, Yang ZJ, Zhang JF, Zou YC, Ren ZL
    Abstract
    Leaf rolling occurs in some cereal genotypes in response to drought. We identified and made a phenotypic, cytological and physiological analysis of a leaf-rolling genotype (CMH83) of hexaploid triticale (X Triticosecale Wittmack) that exhibited reduced plant height, rolled and narrow leaves. Gliadin electrophoresis of seed protein showed that CMH83 was genetically stable. Sequential Giemsa-C-banding and genomic in situ hybridization showed that CMH83 contains 12 rye chromosomes; two pairs of these chromosomes have reduced telomeric heterochromatin bands. Tests of relative water content and water loss rate of l...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524570</comments>
            <pubDate>Thu, 22 Dec 2011 03:54:02 +0100</pubDate>
            <guid isPermaLink="false">5524570</guid>        </item>
        <item>
            <title>The effects of resveratrol on  cyclooxygenase-1 and -2, nuclear factor kappa beta, matrix metalloproteinase-9, and sirtuin 1 mRNA  expression in hearts of streptozotocin-induced  diabetic rats.</title>
            <link>http://www.medworm.com/index.php?rid=5524569&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22179968%26dopt%3DAbstract</link>
            <description>The effects of resveratrol on cyclooxygenase-1 and -2, nuclear factor kappa beta, matrix metalloproteinase-9, and sirtuin 1 mRNA expression in hearts of streptozotocin-induced diabetic rats.
    Genet Mol Res. 2011;10(4):2962-75
    Authors: Yar AS, Menevse S, Alp E
    Abstract
    Resveratrol (RSV) has a beneficial role in the prevention of diabetes and alleviates some diabetic complications, such as cardiomyopathy. We investigated cyclooxygenase-1 (COX-1), COX-2, nuclear factor κB (NF-κB), matrix metalloproteinase-9 (MMP-9), and sirtuin 1 (SIRT1) mRNA expression levels in heart tissue after RSV treatment in streptozotocin (STZ)-induced diabetic rats. After induction of chronic diabetes with STZ, 10 mg RSV/kg per day was administered to DM and DM+RSV groups for four weeks. At the end o...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524569</comments>
            <pubDate>Thu, 22 Dec 2011 03:54:02 +0100</pubDate>
            <guid isPermaLink="false">5524569</guid>        </item>
        <item>
            <title>Genetic diversity in  tetraploid switchgrass revealed by AFLP marker polymorphisms.</title>
            <link>http://www.medworm.com/index.php?rid=5524568&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22180031%26dopt%3DAbstract</link>
            <description>Genetic diversity in tetraploid switchgrass revealed by AFLP marker polymorphisms.
    Genet Mol Res. 2011;10(4):2976-86
    Authors: Todd J, Wu YQ, Wang Z, Samuels T
    Abstract
    Switchgrass (Panicum virgatum) is a perennial warm-season grass native to North America that has been identified as a dedicated cellulosic biofuel crop. We quantified genetic diversity in tetraploid switchgrass germplasm collected at Oklahoma State University and characterized genetic relatedness among the collections from distinct regions. Fifty-six tetraploid accessions, including seven upland and 49 lowland genotypes from throughout the US, were examined. The amplified fragment length polymorphism (AFLP) procedure was utilized to generate DNA profiling patterns that were scored visually. Sixteen selective ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524568</comments>
            <pubDate>Thu, 22 Dec 2011 03:54:02 +0100</pubDate>
            <guid isPermaLink="false">5524568</guid>        </item>
        <item>
            <title>Neuroprotective effects of  NEP1-40 and fasudil on Nogo-A expression in neonatal rats with hypoxic-ischemic  brain damage.</title>
            <link>http://www.medworm.com/index.php?rid=5524567&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22180032%26dopt%3DAbstract</link>
            <description>Neuroprotective effects of NEP1-40 and fasudil on Nogo-A expression in neonatal rats with hypoxic-ischemic brain damage.
    Genet Mol Res. 2011;10(4):2987-95
    Authors: Zhu WW, Ma XL, Guo AL, Zhao HY, Luo HH
    Abstract
    The hypoxic-ischemic encephalopathy caused by peripartum asphyxia is a serious disease in newborn infants, and effective therapies need to be developed to reduce injury-related disorders. We evaluated the effects of NEP1-40 and fasudil on Nogo-A expression in neonatal hypoxic-ischemic brain damage (HIBD) rats. Seven-day-old Wistar rats were randomly divided into control, HIBD, NEP1-40, and fasudil groups. NEP1-40 and fasudil groups were injected intraperitoneally with these compounds. Rat brains at 6, 24, 72 h, and 7 days after HIBD were collected to determine histo...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524567</comments>
            <pubDate>Thu, 22 Dec 2011 03:54:02 +0100</pubDate>
            <guid isPermaLink="false">5524567</guid>        </item>
        <item>
            <title>Analysis of glutathione peroxidase  1 gene polymorphism and Keshan disease in Heilongjiang Province, China.</title>
            <link>http://www.medworm.com/index.php?rid=5524566&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22180033%26dopt%3DAbstract</link>
            <description>Analysis of glutathione peroxidase 1 gene polymorphism and Keshan disease in Heilongjiang Province, China.
    Genet Mol Res. 2011;10(4):2996-3001
    Authors: Wei HL, Pei JR, Jiang CX, Zhou LW, Lan T, Liu M, Wang T
    Abstract
    Keshan disease (KD) is an endemic cardiomyopathy associated with selenium deficiency. Recent studies indicate that glutathione peroxidase 1 (GPx1) mutation decreases GPx activity in myocardial cells and increases the risk of KD. To further clarify the correlation between GPx1 polymorphism and KD, we analyzed GPx1 polymorphism, blood selenium levels and GPx activity in KD patients and healthy controls in Heilongjiang Province. Four and 24 new mutation loci in the promoter and the exon region, respectively, of the GPx1 gene were found in the subjects, in contrast...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524566</comments>
            <pubDate>Thu, 22 Dec 2011 03:54:02 +0100</pubDate>
            <guid isPermaLink="false">5524566</guid>        </item>
        <item>
            <title>Carnitine and carnitine orotate  affect the expression of the prolactin-releasing  peptide gene.</title>
            <link>http://www.medworm.com/index.php?rid=5524565&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22180034%26dopt%3DAbstract</link>
            <description>Carnitine and carnitine orotate affect the expression of the prolactin-releasing peptide gene.
    Genet Mol Res. 2011;10(4):3013-9
    Authors: Zhu HS, Wang YY, Lin MW, Du JX, Hang LQ, Chen Y, Wang LF
    Abstract
    Carnitine is involved in fatty acid metabolism in mammals and is widely used as a nutritional supplement; carnitine orotate is a more absorbable form of carnitine. We investigated the effects of carnitine and carnitine orotate on mouse prolactin-releasing peptide (PrRP) mRNA expression. Twenty-four female mice were randomly divided into four groups of six; control mice were orally drenched with physiological saline solution (250 mg/kg body weight) and treatment mice were orally drenched with carnitine (250 mg/kg) or carnitine orotate (250 or 750 mg/kg), once a day, for 20 da...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524565</comments>
            <pubDate>Thu, 22 Dec 2011 03:54:02 +0100</pubDate>
            <guid isPermaLink="false">5524565</guid>        </item>
        <item>
            <title>Simple method for culture of  peripheral blood lymphocytes of Testudinidae.</title>
            <link>http://www.medworm.com/index.php?rid=5524564&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22180035%26dopt%3DAbstract</link>
            <description>Simple method for culture of peripheral blood lymphocytes of Testudinidae.
    Genet Mol Res. 2011;10(4):3020-5
    Authors: Silva TL, Silva MI, Venancio LP, Zago CE, Moscheta VA, Lima AV, Vizotto LD, Santos JR, Bonini-Domingos CR, Azeredo-Oliveira MT
    Abstract
    We developed and optimized a simple, efficient and inexpensive method for in vitro culture of peripheral blood lymphocytes from the Brazilian tortoise Chelonoidis carbonaria (Testudinidae), testing various parameters, including culture medium, mitogen concentration, mitotic index, culture volume, incubation time, and mitotic arrest. Peripheral blood samples were obtained from the costal vein of four couples. The conditions that gave a good mitotic index were lymphocytes cultured at 37°C in minimum essential medium (7.5 mL), ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524564</comments>
            <pubDate>Thu, 22 Dec 2011 03:54:02 +0100</pubDate>
            <guid isPermaLink="false">5524564</guid>        </item>
        <item>
            <title>Transposable elements in Phyllostachys  pubescens (Poaceae) genome survey sequences and the full-length cDNA sequences, and their association with  simple-sequence repeats.</title>
            <link>http://www.medworm.com/index.php?rid=5524563&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22180036%26dopt%3DAbstract</link>
            <description>Transposable elements in Phyllostachys pubescens (Poaceae) genome survey sequences and the full-length cDNA sequences, and their association with simple-sequence repeats.
    Genet Mol Res. 2011;10(4):3026-37
    Authors: Zhou MB, Liu XM, Tang DQ
    Abstract
    Phyllostachys pubescens is a woody bamboo with the highest ecological, economic, and cultural values of all bamboos in Asia. There is more genomic data available for P. pubescens than for any other bamboo species, including 2.12-Mb genome survey sequences (GSS) and 11.4-Mb full-length cDNA sequences (FL-cDNAs) currently deposited in GenBank. Analysis of these sequences revealed that transposable elements (TEs) are abundant, diverse and polyphyletic in the P. pubescens genome, of which Ty3-gypsy and Ty1-copia are the two most abund...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524563</comments>
            <pubDate>Thu, 22 Dec 2011 03:54:02 +0100</pubDate>
            <guid isPermaLink="false">5524563</guid>        </item>
        <item>
            <title>Genetic polymorphism of the  glutathione-S-transferase P1 gene (GSTP1) and susceptibility to prostate cancer  in the Kashmiri population.</title>
            <link>http://www.medworm.com/index.php?rid=5524562&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22180037%26dopt%3DAbstract</link>
            <description>Genetic polymorphism of the glutathione-S-transferase P1 gene (GSTP1) and susceptibility to prostate cancer in the Kashmiri population.
    Genet Mol Res. 2011;10(4):3038-45
    Authors: Qadri Q, Sameer AS, Shah ZA, Hamid A, Alam S, Manzoor S, Siddiqi MA
    Abstract
    Glutathione-S-transferase P1 (GSTP1) is a critical enzyme of the phase II detoxification pathway. One of the common functional polymorphisms of GSTP1 is A→G at nucleotide 313, which results in an amino acid substitution (Ile105Val) at the substrate binding site of GSTP1 and reduces catalytic activity of GSTP1. To investigate the GSTP1 Ile105Val genotype frequency in prostate cancer cases in the Kashmiri population, we designed a case-control study, in which 50 prostate cancer cases and 45 benign prostate hyperplasia case...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524562</comments>
            <pubDate>Thu, 22 Dec 2011 03:54:02 +0100</pubDate>
            <guid isPermaLink="false">5524562</guid>        </item>
        <item>
            <title>Generation of transgenic chicks  using an oviduct-specific expression system.</title>
            <link>http://www.medworm.com/index.php?rid=5524561&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22180038%26dopt%3DAbstract</link>
            <description>Generation of transgenic chicks using an oviduct-specific expression system.
    Genet Mol Res. 2011;10(4):3046-55
    Authors: Kaleri HA, Xu SY, Lin HL
    Abstract
    We successfully replaced the ovalbumin gene of a magnum region in chickens with a human plasminogen activator. We constructed pL-eGFP, pL-tPAGFP and pL-2.8OVtPAGFP vectors and cultured 293FT chicken embryo fibroblasts, chicken primordial germ cells, Hela C127 cells, and oviduct epithelial cells. All vectors were expressed in the transfected cells, except pL-2.8OVtPAGFP vector, which was only expressed in oviduct epithelial cells. A lentivirus with pL-2.8OVtPAGFP was injected in fertilized eggs; 11 chicks hatched in the G(0) generation, four of them carried the tPAGFP. Two cockerels from the G(0) generation were crossed wit...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524561</comments>
            <pubDate>Thu, 22 Dec 2011 03:54:02 +0100</pubDate>
            <guid isPermaLink="false">5524561</guid>        </item>
        <item>
            <title>An overview of odorant-binding protein functions in  insect peripheral olfactory reception.</title>
            <link>http://www.medworm.com/index.php?rid=5524560&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22180039%26dopt%3DAbstract</link>
            <description>An overview of odorant-binding protein functions in insect peripheral olfactory reception.
    Genet Mol Res. 2011;10(4):3056-69
    Authors: Fan J, Francis F, Liu Y, Chen JL, Cheng DF
    Abstract
    Insect olfactory perception involves many aspects of insect life, and can directly or indirectly evoke either individual or group behaviors. Insect olfactory receptors and odorant-binding proteins (OBPs) are considered to be crucial to insect-specific and -sensitive olfaction. Although the mechanisms of interaction between OBPs or OBP/ligand complex with olfactory receptors are still not well understood, it has been shown that many OBPs contribute to insect olfactory perception at various levels. Some of these are numerous and divergent members in OBP family; expression in the olfactory orga...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524560</comments>
            <pubDate>Thu, 22 Dec 2011 03:54:02 +0100</pubDate>
            <guid isPermaLink="false">5524560</guid>        </item>
        <item>
            <title>Comparison of oxidative stress and  the frequency of polymorphisms in the HFE  gene between hemoglobin S trait blood donors and sickle cell disease patients.</title>
            <link>http://www.medworm.com/index.php?rid=5524546&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22183944%26dopt%3DAbstract</link>
            <description>Comparison of oxidative stress and the frequency of polymorphisms in the HFE gene between hemoglobin S trait blood donors and sickle cell disease patients.
    Genet Mol Res. 2011 Dec 8;10(4)
    Authors: Viana-Baracioli LM, Tukamoto Junior NC, Ricci Júnior O, Mattos LC, Angulo IL, Bonini-Domingos CR
    Abstract
    It is well documented that Hb S and iron affect blood cells, and trigger oxidative processes and generation of free radicals with potential for lipid peroxidation. We evaluated the frequency of polymorphisms in the HFE gene in Hb AS blood donors and how these polymorphisms influenced lipid peroxidation and antioxidant capacity. Blood samples were collected from 211 Hb AS blood donors, 119 Hb AA blood donors as a control group, and 28 sickle cell disease patients (Hb SS). The ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524546</comments>
            <pubDate>Thu, 08 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5524546</guid>        </item>
        <item>
            <title>Genetic diversity of  sea-island cotton (Gossypium barbadense) revealed by mapped SSRs.</title>
            <link>http://www.medworm.com/index.php?rid=5524545&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22183945%26dopt%3DAbstract</link>
            <description>Genetic diversity of sea-island cotton (Gossypium barbadense) revealed by mapped SSRs.
    Genet Mol Res. 2011 Dec 8;10(4)
    Authors: Wang XQ, Feng CH, Lin ZX, Zhang XL
    Abstract
    In order to evaluate the genetic diversity of sea-island cotton (Gossypium barbadense), 237 commonly mapped SSR markers covering the cotton genome were used to genotype 56 sea-island cotton accessions. A total of 218 polymorphic primer pairs (94.75%) amplified 361 loci, with a mean of 1.66 loci. Polymorphism information content values of the SSR primers ranged from 0.035 to 0.862, with a mean of 0.320. The highest mean polymorphism information content value for the SSR motifs was from a compound motif (0.402), and for the chromosomes it was Chr10 (0.589); the highest ratio of polymorphic primers in Xinjia...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524545</comments>
            <pubDate>Thu, 08 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5524545</guid>        </item>
        <item>
            <title>Resistance to  lipopolysaccharide-induced  endotoxic shock in heterozygous Zfp191  gene-knockout mice.</title>
            <link>http://www.medworm.com/index.php?rid=5524544&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22183946%26dopt%3DAbstract</link>
            <description>Resistance to lipopolysaccharide-induced endotoxic shock in heterozygous Zfp191 gene-knockout mice.
    Genet Mol Res. 2011 Dec 8;10(4)
    Authors: Sun RL, Wang HY, Yang XY, Sheng ZJ, Li LM, Wang L, Wang ZG, Fei J
    Abstract
    Zinc finger protein 191, ZNF24 and Zfp191 in both humans and mice belong to the SCAN domain subfamily of Krüppel-like zinc finger transcription factors. Previous studies have suggested that Zfp191 is a pleiotropic factor involved in embryonic development, hematopoiesis and tumorigenesis. However, little is known about its target genes or its role in other physiological and pathological processes. We have identified the putative target genes of Zfp191, using an in silico genome-wide scan. Three hundred and fifty-five putative target genes were identified, which ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524544</comments>
            <pubDate>Thu, 08 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5524544</guid>        </item>
        <item>
            <title>Methylation status and  chromatin structure of the myostatin gene promoter region in the sea perch Lateolabrax  japonicus (Perciformes).</title>
            <link>http://www.medworm.com/index.php?rid=5524543&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22183947%26dopt%3DAbstract</link>
            <description>Methylation status and chromatin structure of the myostatin gene promoter region in the sea perch Lateolabrax japonicus (Perciformes).
    Genet Mol Res. 2011 Dec 8;10(4)
    Authors: Abbas EM, Takayanagi A, Shimizu N, Kato M
    Abstract
    Myostatin is a negative regulator of the growth and development of skeletal muscle mass. In fish, myostatin is expressed in several organs in addition to skeletal muscle. To understand the mechanisms regulating myostatin gene expression in the sea perch, Lateolabrax japonicus, we examined the methylation status of the myostatin gene promoter region in several tissues (liver, eye, kidney, brain, and heart) isolated from adult specimens. The frequency of methylated cytosines was very low in all tissues, regardless of the level of myostatin expression, s...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524543</comments>
            <pubDate>Thu, 08 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5524543</guid>        </item>
        <item>
            <title>Comparison of bacterial  communities in the Solimões and Negro River tributaries of the Amazon River  based on small subunit rRNA gene sequences.</title>
            <link>http://www.medworm.com/index.php?rid=5524542&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22183948%26dopt%3DAbstract</link>
            <description>Comparison of bacterial communities in the Solimões and Negro River tributaries of the Amazon River based on small subunit rRNA gene sequences.
    Genet Mol Res. 2011 Dec 8;10(4)
    Authors: Peixoto JC, Leomil L, Souza JV, Peixoto FB, Astolfi-Filho S
    Abstract
    The microbiota of the Amazon River basin has been little studied. We compared the structure of bacterial communities of the Solimões and Negro Rivers, the main Amazon River tributaries, based on analysis of 16S rRNA gene sequences. Water was sampled with a 3-L Van Dorn collection bottle; samples were collected at nine different points/depths totaling 27 L of water from each river. Total DNA was extracted from biomass retained by a 0.22-μm filter after sequential filtration of the water through 0.8- and 0.22-μm filters. T...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524542</comments>
            <pubDate>Thu, 08 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5524542</guid>        </item>
        <item>
            <title>Elimination of breast tumor-associated chondroitin  sulfate promotes metastasis.</title>
            <link>http://www.medworm.com/index.php?rid=5524541&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22183949%26dopt%3DAbstract</link>
            <description>We examined the role of tumor-associated chondroitin sulfate in breast cancer progression. Enzymatic elimination of endogenous chondroitin sulfate by intra-tumor injections of chondroitinase ABC leads to the development of secondary tumors and increased lung metastases, while primary orthotopic tumor growth was not affected. These results establish a metastasis-inhibiting effect of primary breast tumor-associated chondroitin sulfate, which may open novel carbohydrate-based therapeutic strategies to combat breast cancer.
    PMID: 22183949 [PubMed - as supplied by publisher] (Source: Genetics and Molecular Research)</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524541</comments>
            <pubDate>Thu, 08 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5524541</guid>        </item>
        <item>
            <title>Genetic diversity analysis of an  indigenous Chinese buffalo breed and hybrids based  on microsatellite data.</title>
            <link>http://www.medworm.com/index.php?rid=5524555&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22180069%26dopt%3DAbstract</link>
            <description>Genetic diversity analysis of an indigenous Chinese buffalo breed and hybrids based on microsatellite data.
    Genet Mol Res. 2011 Dec 5;10(4)
    Authors: Yang WC, Tang KQ, Mei J, Zeng WB, Yang LG
    Abstract
    Chinese native buffaloes have faced the threat of extinction, along with an increase in crossbreeding with domesticated river buffaloes; consequently, conservation of local buffalo genetic resources has become a priority. A Chinese native breed, Jianghan, is often crossed intentionally and unintentionally with imported breeds from India and Pakistan, Murrah, and Nili-Ravi. A total of 128 buffaloes of the breeds Jianghan, Murrah, and Nili-Ravi and their presumed hybrid offspring were genotyped for 10 microsatellite markers. Heterozygosity and Wright's F-statistics were calculate...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524555</comments>
            <pubDate>Mon, 05 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5524555</guid>        </item>
        <item>
            <title>Assessing wheat (Triticum  aestivum) genotypes for &quot;Yr&quot; resistance genes using conserved regions and simple-sequence motifs.</title>
            <link>http://www.medworm.com/index.php?rid=5524554&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22180070%26dopt%3DAbstract</link>
            <description>Assessing wheat (Triticum aestivum) genotypes for &quot;Yr&quot; resistance genes using conserved regions and simple-sequence motifs.
    Genet Mol Res. 2011 Dec 5;10(4)
    Authors: Cabuk E, Aydin Y, Uncuoglu AA
    Abstract
    Analysis of DNA sequence variation among genotypes is useful for differentiation of wheat accessions, selection strategies and genetic development of crop plants. We screened molecular markers for yellow rust resistance genes (Yr7, Yr9, Yr15, Yr18, Yr26, and YrH52), which are in the gene-rich regions of wheat chromosomes 1B, 2B, and 7D, to investigate DNA sequence differences and repeat motifs and numbers between wheat cultivars resistant (Izgi2001, Sonmez2001, PI178383) and susceptible (Aytin98, ES14, Harmankaya99) to yellow rust. The F(2) individuals derived from the cros...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524554</comments>
            <pubDate>Mon, 05 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5524554</guid>        </item>
        <item>
            <title>Association of CYP2C19*3 gene polymorphism with breast  cancer in Chinese women.</title>
            <link>http://www.medworm.com/index.php?rid=5524553&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22180071%26dopt%3DAbstract</link>
            <description>Association of CYP2C19*3 gene polymorphism with breast cancer in Chinese women.
    Genet Mol Res. 2011 Dec 5;10(4)
    Authors: Gan CQ, Wang XY, Cao YD, Ye WX, Liu H, Sun YY
    Abstract
    Cytochrome P450 (CYP) 2C19 metabolizes arachidonic acid to biologically active epoxyeicosatrienoic acids, which significantly promote proliferation of cancer cells in vitro and in vivo. We looked for a possible association between human CYP2C19*3 gene polymorphism and breast cancer in the Chinese Han population. In a Chinese Han case-control study of breast cancer patients (N = 600) and age- and gender-matched healthy controls (N = 600), we investigated polymorphism in the CYP2C19 gene by PCR-RFLP analysis. The CYP2C19*3 AG + AA genotype was significantly more prevalent in breast cancer patients than ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524553</comments>
            <pubDate>Mon, 05 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5524553</guid>        </item>
        <item>
            <title>Association between retinoid-X  receptor-gamma genetic polymorphisms and diabetic retinopathy.</title>
            <link>http://www.medworm.com/index.php?rid=5524552&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22180072%26dopt%3DAbstract</link>
            <description>We examined 213 diabetic patients, who were divided into retinopathy or no retinopathy groups. Nine selected single nucleotide polymorphisms (SNPs) in the RXR-gamma gene were evaluated. The diabetic retinopathy group had longer diabetes duration, higher body mass indexes, and higher systolic blood pressure, as well as higher concentrations of fasting plasma glucose, blood urine nitrogen, and creatine. One SNP - rs3818569 of the RXR-gamma gene was found to be associated with increased risk for diabetic retinopathy in both allele and genotype frequencies (P = 0.0023 and 0.0057, respectively). Analysis with multivariate logistic regression revealed that the dominant RXR-gamma GG genotype is a risk factors for the development of diabetic retinopathy (odds ratio = 2.388; 95% confidence interval...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524552</comments>
            <pubDate>Mon, 05 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5524552</guid>        </item>
        <item>
            <title>Combining P values to improve classification of differential gene  expression in the HTself software.</title>
            <link>http://www.medworm.com/index.php?rid=5524551&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22180073%26dopt%3DAbstract</link>
            <description>Combining P values to improve classification of differential gene expression in the HTself software.
    Genet Mol Res. 2011 Dec 5;10(4)
    Authors: Cortez DA, Tonon AP, Colepicolo P, Vêncio RZ
    Abstract
    HTself is a web-based bioinformatics tool designed to deal with the classification of differential gene expression in low replication microarray studies. It is based on a statistical test that uses self-self experiments to derive intensity-dependent cutoffs. We developed an extension of HTself, originally released in 2005, by calculating P values instead of using a fixed acceptance level α. As before, the statistic used to compute single-spot P values is obtained from the Gaussian kernel density estimator method applied to self-self data. Different spots corresponding to the same...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524551</comments>
            <pubDate>Mon, 05 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5524551</guid>        </item>
        <item>
            <title>Molecular cloning, expression and  variation analyses of the dopamine D2 receptor gene in pig breeds in China.</title>
            <link>http://www.medworm.com/index.php?rid=5524550&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22180074%26dopt%3DAbstract</link>
            <description>Molecular cloning, expression and variation analyses of the dopamine D2 receptor gene in pig breeds in China.
    Genet Mol Res. 2011 Dec 5;10(4)
    Authors: Xu HP, He XM, Fang MX, Hu YS, Jia XZ, Nie QH, Zhang XQ
    Abstract
    The dopamine D2 receptor (DRD2) is a crucial mediator for normal physiological processes. We cloned the pig DRD2 gene, investigated its distribution in tissues and identified polymorphisms by RT-PCR, quantitative real-time PCR and direct sequencing. Two Yorkshire pigs from Guangdong Academy of Agricultural Sciences (Guangzhou, China) were selected to clone the gene and investigate its expression; 16 individuals from four pig breeds (Yorkshire, Landrace, small-ear spotted, and Xinchang) were used to scan the variations. The two transcripts (DRD2L and DRD2S), obtai...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524550</comments>
            <pubDate>Mon, 05 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5524550</guid>        </item>
        <item>
            <title>Molecular sexing of unusually  large numbers of Spheniscus magellanicus (Spheniscidae) washed ashore  along the Brazilian coast in 2008.</title>
            <link>http://www.medworm.com/index.php?rid=5524549&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22180075%26dopt%3DAbstract</link>
            <description>Molecular sexing of unusually large numbers of Spheniscus magellanicus (Spheniscidae) washed ashore along the Brazilian coast in 2008.
    Genet Mol Res. 2011 Dec 5;10(4)
    Authors: Reis EC, Aires RM, Moura JF, Matias CA, Tavares M, Ott PH, Siciliano S, Lôbo-Hajdu G
    Abstract
    There have been few studies on Magellanic penguins (Spheniscus magellanicus). In 2008, these penguins washed ashore along the Brazilian coast in unusually high numbers, some reaching as far as northeast Brazil. As Magellanic penguins show little sexual dimorphism, sex determination by morphological features is not accurate. Here, we tested a molecular procedure for sexing specimens of S. magellanicus washed ashore along the coasts of Sergipe, Rio de Janeiro and Rio Grande do Sul in 2008, comparing the sex ra...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524549</comments>
            <pubDate>Mon, 05 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5524549</guid>        </item>
        <item>
            <title>Isolation of fertility-related  genes of multiple-allele-inherited male sterility in Brassica rapa ssp pekinensis by cDNA-AFLP.</title>
            <link>http://www.medworm.com/index.php?rid=5524548&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22180076%26dopt%3DAbstract</link>
            <description>Isolation of fertility-related genes of multiple-allele-inherited male sterility in Brassica rapa ssp pekinensis by cDNA-AFLP.
    Genet Mol Res. 2011 Dec 5;10(4)
    Authors: Ji RQ, Song Q, Xin XF, Zhou X, Feng H
    Abstract
    To better understand the molecular mechanisms of multiple-allele-inherited male sterility in Chinese cabbage (Brassica rapa ssp pekinensis), differentially expressed genes in fertile and sterile plants must be isolated. We used cDNA-AFLP analysis to isolate differentially expressed genes in fertile and sterile buds of the two-type line, AB01. Sixteen high-quality sequences were generated, 11 of which were up-regulated in fertile buds, and five of which were up-regulated in sterile buds. Based on BLAST screening and functional annotation, these genes have homology...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524548</comments>
            <pubDate>Mon, 05 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5524548</guid>        </item>
        <item>
            <title>Interaction between CYP 2C19*3  polymorphism and smoking in relation to laryngeal carcinoma in the Chinese Han  population.</title>
            <link>http://www.medworm.com/index.php?rid=5524547&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22183943%26dopt%3DAbstract</link>
            <description>Interaction between CYP 2C19*3 polymorphism and smoking in relation to laryngeal carcinoma in the Chinese Han population.
    Genet Mol Res. 2011 Dec 5;10(4)
    Authors: Feng J, Li L, Zhao YS, Tang SQ, Yang HB, Liu SX
    Abstract
    Cytochrome P450 (CYP) 2C19 metabolizes arachidonic acid to biologically active epoxyeicosatrienoic acids, which strongly promote proliferation of cancer cells in vitro and in vivo. Knowing that smoking is the most important risk factor for laryngeal carcinoma, we examined the relationships between CYP2C19*3 polymorphism, smoking and laryngeal carcinoma in the Chinese Han population. In a Chinese Han case-control study of 300 laryngeal carcinoma patients and 300 healthy controls, we investigated polymorphism in the CYP2C19 gene by PCR-RFLP analysis. The CYP2C...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524547</comments>
            <pubDate>Mon, 05 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5524547</guid>        </item>
        <item>
            <title>Molecular evolution of two  consecutive carotenoid cleavage dioxygenase genes in strigolactone biosynthesis  in plants.</title>
            <link>http://www.medworm.com/index.php?rid=5524557&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22180067%26dopt%3DAbstract</link>
            <description>We examined the phylogenetic relationships of two carotenoid cleavage dioxygenase genes (CCD7 and CCD8) that are involved in consecutive upstream steps of the proposed strigolactone biosynthesis pathway. The CCD7 and CCD8 sequences from 11 model species, divided into two clades, correspond to sequences from monocotyledons and dicotyledons. However, the sequences from the primitive moss, Physcomitrella patens, appeared to be evolutionarily distinct from those of the angiosperms. CCD7 and CCD8 are much conserved, since no significant positive selection was detected among these plants. Ks values indicated that CCD7 and CCD8 diverged about 290 to 430 million years ago. As essential genes in the strigolactone pathway, the divergence timing of the conserved CCD7 and CCD8 genes reflects the appro...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524557</comments>
            <pubDate>Fri, 02 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5524557</guid>        </item>
        <item>
            <title>Distribution of HLA-B27 and  CYP2D6*4 mutations in the middle Black Sea area (Tokat) of Turkey.</title>
            <link>http://www.medworm.com/index.php?rid=5524556&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22180068%26dopt%3DAbstract</link>
            <description>Distribution of HLA-B27 and CYP2D6*4 mutations in the middle Black Sea area (Tokat) of Turkey.
    Genet Mol Res. 2011 Dec 2;10(4)
    Authors: Sahin S, Aydogan L, Benli I, Ozyurt H
    Abstract
    We analyzed distribution of HLA-B27 and CYP2D6*4 mutations in 249 patients from Tokat province in Turkey with symptoms of arthritis, sacroiliac, joint and back pain, using a LightCycler 480 II Real-Time PCR thermal cycler. The Genes-4U was applied for studying HLA-B27 mutation, and the Tib-Molbiol commercial kit was used to examine the CYP2D6*4 mutation. Among the 249 patients, 18.5% had the HLA-B27 mutation. The CYP2D6*4 mutation was found in 22.0% (six homozygotes). Ten patients had both mutations. These frequencies are similar to what has been reported from other populations.
    PMID: 22180...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524556</comments>
            <pubDate>Fri, 02 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5524556</guid>        </item>
        <item>
            <title>A new approach for cloning hLIF cDNA from genomic DNA  isolated from the oral mucous membrane.</title>
            <link>http://www.medworm.com/index.php?rid=5524559&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22180065%26dopt%3DAbstract</link>
            <description>A new approach for cloning hLIF cDNA from genomic DNA isolated from the oral mucous membrane.
    Genet Mol Res. 2011 Nov 25;10(4)
    Authors: Cui YH, Zhu GQ, Chen QJ, Wang YF, Yang MM, Song YX, Wang JG, Cao BY
    Abstract
    Complementary DNA (cDNA) is valuable for investigating protein structure and function in the study of life science, but it is difficult to obtain by traditional reverse transcription. We employed a novel strategy to clone human leukemia inhibitory factor (hLIF) gene cDNA from genomic DNA, which was directly isolated from the mucous membrane of mouth. The hLIF sequence, which is 609 bp long and is composed of three exons, can be acquired within a few hours by amplifying each exon and splicing all of them using overlap-PCR. This new approach developed is simple, time...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524559</comments>
            <pubDate>Fri, 25 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5524559</guid>        </item>
        <item>
            <title>The role of α-satellite DNA and heterochromatin polymorphism in  leukemia patients and illicit drug addicts.</title>
            <link>http://www.medworm.com/index.php?rid=5524558&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22180066%26dopt%3DAbstract</link>
            <description>The role of α-satellite DNA and heterochromatin polymorphism in leukemia patients and illicit drug addicts.
    Genet Mol Res. 2011 Nov 25;10(4)
    Authors: Movafagh A, Mortazavi-Tabatabaei SA, Kolahi AA
    Abstract
    Heterochromatin is considered to play a role in protecting the genome against mutagens. Changes in the quantity and proportion of different types of satellite DNA could increase genetic susceptibility in individuals with heterochromatic variations; they cause chromosome instability and predispose patients to malignancies. We evaluated the heterochromatin associated with chromosomes in 50 leukemia patients, 93 drug addicts and 93 healthy controls from Tehran, Iran. Barium hydroxide saline Giemsa staining was used to examine heterochromatin polymorphism of chromosomes 1, 9...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524558</comments>
            <pubDate>Fri, 25 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5524558</guid>        </item>
        <item>
            <title>Environmental and genetic  factors affecting the weaning-estrus interval in sows.</title>
            <link>http://www.medworm.com/index.php?rid=5435868&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22095595%26dopt%3DAbstract</link>
            <description>We examined the effects of environmental and genetic factors on the weaning-to-estrus interval (WEI) in sows. In order to perform the analyses of the environmental factors, 8104 observations of the 1st to the 6th WEI were carried out, while 6548 observations of the 1st to the 3rd WEI were carried out for the analyses of genetic factors. The environmental model included as fixed effects, herd, genetic line, year and season of birth, as well as the covariates, age of sow at farrowing, litter size at birth and lactation length. Genetic analysis was performed by repeatability and multitrait models. The mean and coefficient of variation for WEI were 7.02 days and 100.6%, respectively. The linear effect of lactation length and the quadratic effect of the age of sow at farrowing affected the WEI....</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5435868</comments>
            <pubDate>Wed, 23 Nov 2011 01:36:03 +0100</pubDate>
            <guid isPermaLink="false">5435868</guid>        </item>
        <item>
            <title>Lactic acid bacteria dynamics  during spontaneous fermentation of cocoa beans verified by culture-independent  denaturing gradient gel electrophoresis.</title>
            <link>http://www.medworm.com/index.php?rid=5435867&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22095596%26dopt%3DAbstract</link>
            <description>Lactic acid bacteria dynamics during spontaneous fermentation of cocoa beans verified by culture-independent denaturing gradient gel electrophoresis.
    Genet Mol Res. 2011;10(4):2702-9
    Authors: Santos TF, Santana LK, Santos AC, Silva GS, Romano CC, Dias JC, Rezende RP
    Abstract
    Cocoa is naturally fermented in the field before the cocoa seeds are removed for processing. We assessed the dynamics of lactic acid bacteria during cocoa fermentation in Bahia, Brazil. During five days of fermentation, temperature and pH were measured and beans were collected for genomic DNA extraction every 12 h. The DNA was used as a template for amplification with Lac1-Lac2 and Lac3-Lac2 for denaturing gradient gel electrophoresis analyses. pH values ranged from 3.34 to 4.98, while the temperature v...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5435867</comments>
            <pubDate>Wed, 23 Nov 2011 01:36:03 +0100</pubDate>
            <guid isPermaLink="false">5435867</guid>        </item>
        <item>
            <title>Clonal monosomy of chromosome 21 in a case of  myelodysplastic syndrome.</title>
            <link>http://www.medworm.com/index.php?rid=5435866&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22095597%26dopt%3DAbstract</link>
            <description>This study reports on a cytogenetic finding in a bone marrow examination of a 47-year-old male patient treated in the Hematology and Blood Transfusion Service of the Hospital de Base in São José do Rio Preto, São Paulo State, Brazil. The only alteration found at diagnosis of myelodysplastic syndrome (MDS) subtype refractory anemia with excess blasts (RAEB-2) was clonal monosomy of chromosome 21. The patient evolved to acute myeloid leukemia type M2 and died nine months after diagnosis. Clonal monosomy of chromosome 21, as the only cytogenetic abnormality in MDS, has only been reported three times previously. This uncommon cytogenetic abnormality in MDS has been associated with a poor clinical course, although more data will be needed to determine if this prognosis is invariable.
    PMI...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5435866</comments>
            <pubDate>Wed, 23 Nov 2011 01:36:03 +0100</pubDate>
            <guid isPermaLink="false">5435866</guid>        </item>
        <item>
            <title>A novel polymorphism of the  myogenin gene is associated with body measurement traits in native Chinese breeds.</title>
            <link>http://www.medworm.com/index.php?rid=5435865&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22095598%26dopt%3DAbstract</link>
            <description>A novel polymorphism of the myogenin gene is associated with body measurement traits in native Chinese breeds.
    Genet Mol Res. 2011;10(4):2721-8
    Authors: Xue M, Zan LS, Gao L, Wang HB
    Abstract
    Using PCR-SSCP and DNA sequencing technology, we examined the association of single nucleotide polymorphisms (SNPs) in the bovine MyoG gene with body measurement traits in 779 individuals of six native Chinese cattle breeds, namely Luxi, Luxi × Simmental crossbred, Nanyang, Xia'nan, Jiaxian red, and Qinchuan. A novel SNP, T314C, was detected. Allelic frequencies of MyoG-T/C in the six breeds were 0.8308/0.1692, 0.8774/0.1226, 0.8021/0.1979, 0.8209/0.1791, 0.8630/0.1370, 0.8044/0.1956, respectively. Least squares analysis revealed a significant (P &amp;lt; 0.05) association of the MyoG SNP...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5435865</comments>
            <pubDate>Wed, 23 Nov 2011 01:36:03 +0100</pubDate>
            <guid isPermaLink="false">5435865</guid>        </item>
        <item>
            <title>Assessing molecular and morpho-agronomical diversity and identification  of ISSR markers associated with fruit traits in quince  (Cydonia  oblonga).</title>
            <link>http://www.medworm.com/index.php?rid=5435864&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22095599%26dopt%3DAbstract</link>
            <description>Assessing molecular and morpho-agronomical diversity and identification of ISSR markers associated with fruit traits in quince (Cydonia oblonga).
    Genet Mol Res. 2011;10(4):2729-46
    Authors: Ganopoulos I, Merkouropoulos G, Pantazis S, Tsipouridis C, Tsaftaris A
    Abstract
    Quince is a deciduous tree known to the countries around the Mediterranean since antiquity. Nowadays, quince is used as an ornamental plant, and as a rootstock for pear trees, with its fruit being appreciated mainly for production of jam and sweets rather than for raw consumption. Quince leaves contain compounds with antioxidant, antimicrobial and anticancerous properties that have been the focus of recent research on pharmaceutical and medical uses as well as for food preservatives. An orchard has been establ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5435864</comments>
            <pubDate>Wed, 23 Nov 2011 01:36:03 +0100</pubDate>
            <guid isPermaLink="false">5435864</guid>        </item>
        <item>
            <title>AGPAT6 polymorphism and  its association with milk traits of dairy goats.</title>
            <link>http://www.medworm.com/index.php?rid=5435863&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22095600%26dopt%3DAbstract</link>
            <description>AGPAT6 polymorphism and its association with milk traits of dairy goats.
    Genet Mol Res. 2011;10(4):2747-56
    Authors: He C, Wang C, Chang ZH, Guo BL, Li R, Yue XP, Lan XY, Chen H, Lei CZ
    Abstract
    As one of the eight members in the 1-acylglycerol-3-phosphate-O-acyltransferase (AGPATs) family, AGPAT6 is a crucial enzyme for the biosynthesis of glycerolipids and triacylglycerol in eukaryotes, as well as catalyzing the conversion from lysophosphatidic acid to phosphatidic acid. AGPAT6 can be considered as a candidate gene for regulating milk composition. DNA sequencing and PCR-RFLP methods were applied to detect genetic variation in the AGPAT6 gene in 549 Chinese dairy goats. Four polymorphisms (NC_007328.3:g.152G&amp;gt;C, 8124G&amp;gt;A, 9263C&amp;gt;G, 16436G&amp;gt;A) were detected in 5'UTR,...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5435863</comments>
            <pubDate>Wed, 23 Nov 2011 01:36:03 +0100</pubDate>
            <guid isPermaLink="false">5435863</guid>        </item>
        <item>
            <title>Genomic DNA extraction from medicinal plants available in Malaysia using a TriOmic(TM) improved extraction kit.</title>
            <link>http://www.medworm.com/index.php?rid=5435862&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22095601%26dopt%3DAbstract</link>
            <description>Authors: Mohd-Hairul AR, Sade AB, Yiap BC, Raha AR
    Abstract
    DNA extraction was carried out on 32 medicinal plant samples available in Malaysia using the TriOmic(TM) extraction kit. Amounts of 0.1 g flowers or young leaves were ground with liquid nitrogen, lysed at 65°C in RY1(plus) buffer and followed by RNAse treatment. Then, RY2 buffer was added to the samples and mixed completely by vortexing before removal of cell debris by centrifugation. Supernatants were transferred to fresh microcentrifuge tubes and 0.1 volume RY3 buffer was added to each of the transferred supernatant. The mixtures were applied to spin columns followed by a centrifugation step to remove buffers and other residues. Washing step was carried out twice by applying 70% ethanol to the spin columns. Genomic DNA ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5435862</comments>
            <pubDate>Wed, 23 Nov 2011 01:36:03 +0100</pubDate>
            <guid isPermaLink="false">5435862</guid>        </item>
        <item>
            <title>Lack of an association between -308G&gt;A polymorphism  of the TNF-α gene and liver cirrhosis risk based on a meta-analysis.</title>
            <link>http://www.medworm.com/index.php?rid=5435861&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22095602%26dopt%3DAbstract</link>
            <description>In conclusion, we found no association between TNF-α -308G&amp;gt;A polymorphism and liver cirrhosis risk, both in Caucasian and Asian populations.
    PMID: 22095602 [PubMed - in process] (Source: Genetics and Molecular Research)</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5435861</comments>
            <pubDate>Wed, 23 Nov 2011 01:36:03 +0100</pubDate>
            <guid isPermaLink="false">5435861</guid>        </item>
        <item>
            <title>Population structure and  demographic inferences concerning the endangered onychophoran species Epiperipatus  acacioi (Onychophora: Peripatidae).</title>
            <link>http://www.medworm.com/index.php?rid=5435860&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22095603%26dopt%3DAbstract</link>
            <description>Population structure and demographic inferences concerning the endangered onychophoran species Epiperipatus acacioi (Onychophora: Peripatidae).
    Genet Mol Res. 2011;10(4):2775-85
    Authors: Lacorte GA, Oliveira IS, Fonseca CG
    Abstract
    Epiperipatus acacioi (Onychophora: Peripatidae) is an endemic species of the Atlantic rainforest in southeastern Brazil, with a restricted known distribution, found only in two nearby areas (Tripuí and Itacolomi). Mitochondrial gene COI sequences of 93 specimens collected across the known range of E. acacioi were used to assess the extant genetic diversity and patterns of genetic structure, as well as to infer the demographic history of this species. We found considerable variability within the populations, even though there has been recent envi...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5435860</comments>
            <pubDate>Wed, 23 Nov 2011 01:36:03 +0100</pubDate>
            <guid isPermaLink="false">5435860</guid>        </item>
        <item>
            <title>Molecular differentiation of  species of the genus Zungaro (Siluriformes, Pimelodidae) from the Amazon  and Paraná-Paraguay River basins in Brazil.</title>
            <link>http://www.medworm.com/index.php?rid=5435859&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22095604%26dopt%3DAbstract</link>
            <description>Molecular differentiation of species of the genus Zungaro (Siluriformes, Pimelodidae) from the Amazon and Paraná-Paraguay River basins in Brazil.
    Genet Mol Res. 2011;10(4):2795-805
    Authors: Boni TA, Padial AA, Prioli SM, Lucio LC, Maniglia TC, Bignotto TS, Panarari-Antunes RS, Prioli RA, Prioli AJ
    Abstract
    Fish species of the Zungaro genus (Siluriformes, Pimelodidae) are amongst the largest migratory fish in Latin America and have considerable economic importance for commercial fishing in Brazil. However, natural populations of this large catfish are experiencing a severe decline. There are significant taxonomical inconsistencies for this fish. Two geographically separated species of the fish were initially described, one endemic in the Amazon and another in the Paraná-Pa...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5435859</comments>
            <pubDate>Wed, 23 Nov 2011 01:36:03 +0100</pubDate>
            <guid isPermaLink="false">5435859</guid>        </item>
        <item>
            <title>Molecular authentication of the medicinal herb Ruta graveolens (Rutaceae)  and an adulterant   using nuclear and chloroplast DNA markers.</title>
            <link>http://www.medworm.com/index.php?rid=5435858&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22095605%26dopt%3DAbstract</link>
            <description>Molecular authentication of the medicinal herb Ruta graveolens (Rutaceae) and an adulterant  using nuclear and chloroplast DNA markers.
    Genet Mol Res. 2011;10(4):2806-16
    Authors: Al-Qurainy F, Khan S, Tarroum M, Al-Hemaid FM, Ali MA
    Abstract
    Dried parts of different plant species often look alike, especially in powdered form, making them very difficult to identify. Ruta graveolens, sold as a dried medicinal herb, can be adulterated with Euphorbia dracunculoides. The genomic DNA was isolated from the leaf powder (100 mg each) using the modified CTAB method. Internal transcribed spacer sequences of nuclear ribosomal DNA (nrDNA-ITS), and chloroplast spacer sequences (rpoB and rpoC1) are regarded as potential genes for plant DNA barcoding. We amplified and sequenced these space...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5435858</comments>
            <pubDate>Wed, 23 Nov 2011 01:36:03 +0100</pubDate>
            <guid isPermaLink="false">5435858</guid>        </item>
        <item>
            <title>Aluminum triggers broad changes in microRNA expression  in rice roots.</title>
            <link>http://www.medworm.com/index.php?rid=5435857&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22095606%26dopt%3DAbstract</link>
            <description>We examined the expression of at least one miRNA member from each miRNA family in rice roots of Oryza sativa spp indica cv. Embrapa Taim and Oryza sativa spp japonica cv. Nipponbare under high concentrations of aluminum. Forty-six miRNA families were effectively detected by quantitative PCR. Among these, 13 were down-regulated and six were up-regulated in roots of the Nipponbare cultivar after 8 h of aluminum treatment. In roots of the Embrapa Taim cultivar, five miRNAs were down-regulated and three were up-regulated. Analyses of their putative targets suggest that these rice miRNAs are involved in the regulation of various metabolic pathways in response to high concentrations of aluminum.
    PMID: 22095606 [PubMed - in process] (Source: Genetics and Molecular Research)</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5435857</comments>
            <pubDate>Wed, 23 Nov 2011 01:36:03 +0100</pubDate>
            <guid isPermaLink="false">5435857</guid>        </item>
        <item>
            <title>Association between a single  nucleotide  polymorphism in the bovine chemerin gene and carcass  traits in Qinchuan cattle.</title>
            <link>http://www.medworm.com/index.php?rid=5435856&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22095607%26dopt%3DAbstract</link>
            <description>Association between a single nucleotide polymorphism in the bovine chemerin gene and carcass traits in Qinchuan cattle.
    Genet Mol Res. 2011;10(4):2833-40
    Authors: Tian WQ, Wang HC, Song FB, Zan LS, Wang H, Wang HB, Xin YP, Ujan JA
    Abstract
    Qinchuan is a red or yellow draft and beef breed in China. In order to identify a predictor of carcass traits on the basis of associations between carcass traits and gene polymorphism, variation in the bovine chemerin gene was investigated using PCR-single-strand conformational polymorphism and DNA sequencing. An SNP of A868G located in exon 2 of the Bos taurus chemerin gene was detected in 716 samples of six breeds (Jiaxian red, Luxi, Nan yang, Qinchuan, Simmental and Luxi crossbred steers, and Xia'nan), all in China, and three genotypes...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5435856</comments>
            <pubDate>Wed, 23 Nov 2011 01:36:03 +0100</pubDate>
            <guid isPermaLink="false">5435856</guid>        </item>
        <item>
            <title>Lack of association between RANTES-28, SDF-1 gene polymorphisms and systemic  lupus erythematosus in the Malaysian  population.</title>
            <link>http://www.medworm.com/index.php?rid=5435855&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22095608%26dopt%3DAbstract</link>
            <description>Lack of association between RANTES-28, SDF-1 gene polymorphisms and systemic lupus erythematosus in the Malaysian population.
    Genet Mol Res. 2011;10(4):2841-50
    Authors: Lian LH, Kee BP, Ng HL, Chua KH
    Abstract
    Regulated on activation, normal T-cell expressed and secreted (RANTES) and stromal cell-derived factor 1 (SDF-1) are members of the CC- and CXC-chemokine families, respectively. Both genes have been postulated to be involved in the pathogenesis of systemic lupus erythematosus (SLE). We analyzed position 28 of the RANTES gene promoter region, as well as the SNP observed in the 3' UTR of the SDF-1 gene at position 801, in 130 patients presenting SLE at the Malaya University Medical Centre. Screening of 130 healthy volunteer controls using RFLP was also performed. RANTES...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5435855</comments>
            <pubDate>Wed, 23 Nov 2011 01:36:03 +0100</pubDate>
            <guid isPermaLink="false">5435855</guid>        </item>
        <item>
            <title>Multiple displacement amplification for preimplantation genetic diagnosis of  fragile X syndrome.</title>
            <link>http://www.medworm.com/index.php?rid=5435854&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22095609%26dopt%3DAbstract</link>
            <description>Multiple displacement amplification for preimplantation genetic diagnosis of fragile X syndrome.
    Genet Mol Res. 2011;10(4):2851-9
    Authors: Lee HS, Kim MJ, Lim CK, Cho JW, Song IO, Kang IS
    Abstract
    Preimplantation genetic diagnosis (PGD) has become an assisted reproductive technique for couples that have genetic risks. Despite the many advantages provided by PGD, there are several problems, including amplification failure, allele drop-out and amplification inefficiency. We evaluated multiple displacement amplification (MDA) for PGD of the fragile X syndrome. Whole genome amplification was performed using MDA. MDA products were subjected to fluorescent PCR of fragile X mental retardation-1 (FMR1) CGG repeats, amelogenin and two polymorphic markers. In the pre-clinical tests, ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5435854</comments>
            <pubDate>Wed, 23 Nov 2011 01:36:03 +0100</pubDate>
            <guid isPermaLink="false">5435854</guid>        </item>
        <item>
            <title>Establishing references for gene  expression  analyses by RT-qPCR in Theobroma cacao tissues.</title>
            <link>http://www.medworm.com/index.php?rid=5435871&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22095481%26dopt%3DAbstract</link>
            <description>Establishing references for gene expression analyses by RT-qPCR in Theobroma cacao tissues.
    Genet Mol Res. 2011 Nov 17;10(4)
    Authors: Pinheiro TT, Litholdo Jr CG, Sereno ML, Leal Jr GA, Albuquerque PS, Figueira A
    Abstract
    Lack of continuous progress in Theobroma cacao (Malvaceae) breeding, especially associated with seed quality traits, requires more efficient selection methods based on genomic information. Reverse transcript quantitative PCR (RT-qPCR) has become the method of choice for gene expression analysis, but relative expression analysis requires various reference genes, which must be stable across various biological conditions. We sought suitable reference genes for various tissues of cacao, especially developing seeds. Ten potential reference genes were analyzed f...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5435871</comments>
            <pubDate>Thu, 17 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5435871</guid>        </item>
        <item>
            <title>High degree of genetic diversity among genotypes of  the forage grass Brachiaria ruziziensis (Poaceae) detected with ISSR  markers.</title>
            <link>http://www.medworm.com/index.php?rid=5435870&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22095482%26dopt%3DAbstract</link>
            <description>High degree of genetic diversity among genotypes of the forage grass Brachiaria ruziziensis (Poaceae) detected with ISSR markers.
    Genet Mol Res. 2011 Nov 17;10(4)
    Authors: Azevedo AL, Costa PP, Machado MA, de Paula CM, Sobrinho FS
    Abstract
    The grasses of the genus Brachiaria account for 80% of the cultivated pastures in Brazil. Despite its importance for livestock production, little information is available for breeding purposes. Embrapa has a population of B. ruziziensis from different regions of Brazil, representing most of existing variability. This population was used to initiate an improvement program based on recurrent selection. In order to assist the genetic improvement program, we estimated the molecular variability among 93 genotypes of Embrapa's collection using ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5435870</comments>
            <pubDate>Thu, 17 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5435870</guid>        </item>
        <item>
            <title>Successful preimplantation  genetic aneuploidy screening in Turkish patients.</title>
            <link>http://www.medworm.com/index.php?rid=5435869&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22095483%26dopt%3DAbstract</link>
            <description>Successful preimplantation genetic aneuploidy screening in Turkish patients.
    Genet Mol Res. 2011 Nov 17;10(4)
    Authors: Ercelen N, Turtar E, Gultomruk M, Comert H, Coskun H, Mercan R, Nuhoglu A
    Abstract
    Preimplantation genetic diagnosis is a preventive approach for identifying genetic abnormalities in early stages of reproduction. We used preimplantation genetic aneuploidy screening in 230 cycles of patients with indications of advanced maternal age, recurrent implantation failure, recurrent spontaneous abortions, or severe male factor. Biopsied blastomeres from embryos with six to eight blastomeres on day 3 were fixed and fluorescence in situ hybridization was utilized on chromosomes 13, 16, 18, 21, 22, X, and Y. Among 945 morphologically normal embryos, 314 were diagnosed ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5435869</comments>
            <pubDate>Thu, 17 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5435869</guid>        </item>
        <item>
            <title>Use of molecular markers in  reciprocal recurrent selection of maize increases heterosis effects.</title>
            <link>http://www.medworm.com/index.php?rid=5410488&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22057955%26dopt%3DAbstract</link>
            <description>We examined the effect of incorporation of molecular markers on variability between and within populations in order to maximize heterotic effects and longevity of a maize reciprocal recurrent selection program. Molecular variability was quantified by inter-simple sequence repeat (ISSR) markers between and within the maize populations Cimmyt and Piranão in the 10th cycle of a reciprocal recurrent selection program. Forty-two S(1) progenies of each population were analyzed, these being families of full-sibs selected according to their agronomic traits. Thirteen primers were selected, which produced 140 bands; 114 of them were polymorphic and 26 monomorphic. Based on UPGMA grouping analysis and by genetic distances, it was possible to identify &quot;contaminant&quot; progenies. These progenies belong ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410488</comments>
            <pubDate>Thu, 17 Nov 2011 04:36:02 +0100</pubDate>
            <guid isPermaLink="false">5410488</guid>        </item>
        <item>
            <title>A66G and C524T polymorphisms of the methionine synthase reductase gene are associated with congenital heart defects in the Chinese Han population.</title>
            <link>http://www.medworm.com/index.php?rid=5410487&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22057956%26dopt%3DAbstract</link>
            <description>In conclusion, MTRR A66G and C524T polymorphisms are associated with increased risk of CHDs.
    PMID: 22057956 [PubMed - in process] (Source: Genetics and Molecular Research)</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410487</comments>
            <pubDate>Thu, 17 Nov 2011 04:36:02 +0100</pubDate>
            <guid isPermaLink="false">5410487</guid>        </item>
        <item>
            <title>Two genetic stocks of Steindachneridion  melanodermatum living in sympatry in nature and genetic variability of wild  parents and F(1) generation.</title>
            <link>http://www.medworm.com/index.php?rid=5410486&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22057957%26dopt%3DAbstract</link>
            <description>Two genetic stocks of Steindachneridion melanodermatum living in sympatry in nature and genetic variability of wild parents and F(1) generation.
    Genet Mol Res. 2011;10(4):2606-12
    Authors: Matoso DA, da Silva M, Cortinhas MC, Cestari MM, de Almeida MC, Vicari MR, Artoni RF
    Abstract
    Steindachneridion melanodermatum is a large Brazilian catfish, highly prized for sport fishing and for its meat. Specimens of this species, both caught in nature from Iguacu River and F(1) fish born in captivity, were analyzed with regard to patterns of RAPD molecular markers. Genetic similarity ranged from 0.57 to 0.95; two groups were determined for the wild specimens. The results suggest different genetic lineages in sympatry in nature. Heterozygosity and percentage of polymorphic loci were 0.3...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410486</comments>
            <pubDate>Thu, 17 Nov 2011 04:36:02 +0100</pubDate>
            <guid isPermaLink="false">5410486</guid>        </item>
        <item>
            <title>Genome-wide identification,  phylogeny and expression analysis of the lipoxygenase gene family in cucumber.</title>
            <link>http://www.medworm.com/index.php?rid=5410485&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22057958%26dopt%3DAbstract</link>
            <description>Genome-wide identification, phylogeny and expression analysis of the lipoxygenase gene family in cucumber.
    Genet Mol Res. 2011;10(4):2613-36
    Authors: Liu SQ, Liu XH, Jiang LW
    Abstract
    Plant lipoxygenase (LOX) is involved in growth and developmental control processes, through the biosynthesis of regulatory molecules and defense responses to pathogens, wounding and stress. To date, few LOX proteins and little tissue expression profiling have been reported in detail for cucumber (Cucumis sativus L.). Recent completion of the cucumber genome sequence now permits genome-wide analysis of the LOX gene family in cucumber as well as comparison with LOX in Arabidopsis and rice. We identified 23 candidate LOX genes in the cucumber genome; phylogenetic analysis indicated that these LOX...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410485</comments>
            <pubDate>Thu, 17 Nov 2011 04:36:02 +0100</pubDate>
            <guid isPermaLink="false">5410485</guid>        </item>
        <item>
            <title>Functional characterization and signal transduction ability of nucleotide-binding  site-leucine-rich repeat resistance genes in plants.</title>
            <link>http://www.medworm.com/index.php?rid=5410484&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22057959%26dopt%3DAbstract</link>
            <description>Functional characterization and signal transduction ability of nucleotide-binding site-leucine-rich repeat resistance genes in plants.
    Genet Mol Res. 2011;10(4):2637-52
    Authors: Joshi RK, Nayak S
    Abstract
    Pathogen infection in plants is often limited by a multifaceted defense response triggered by resistance genes. The most prevalent class of resistance proteins includes those that contain a nucleotide-binding site-leucine-rich repeat (NBS-LRR) domain. Over the past 15 years, more than 50 novel NBS-LRR class resistance genes have been isolated and characterized; they play a significant role in activating conserved defense-signaling networks. Recent molecular research on NBS-LRR resistance proteins and their signaling networks has the potential to broaden the use of resistan...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410484</comments>
            <pubDate>Thu, 17 Nov 2011 04:36:02 +0100</pubDate>
            <guid isPermaLink="false">5410484</guid>        </item>
        <item>
            <title>Detection of fetal RHD pseudogene  (RHDΨ) and hybrid  RHD-CE-D(s) from RHD-negative  pregnant women with a free DNA fetal kit.</title>
            <link>http://www.medworm.com/index.php?rid=5410483&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22057960%26dopt%3DAbstract</link>
            <description>We examined 40 female blood samples to verify the specificity of RHD exons (7 and 10) amplified by real-time PCR. Thirty fetuses were predicted to be RHD-positive based on analysis of plasma DNA. Seven fetuses were predicted to be RHD-negative. One fetus was negative for RHD on exon 10, and positive for RHD on exon 7 (early gestation age); two fetuses were RHD-negative on exon 7, and RHD-positive on exon 10 (RHD-CE-D(s) or RHDΨ), indicative of a maternal RHD allele. We conclude that it is necessary to analyze at least two exon regions in the RHD gene.
    PMID: 22057960 [PubMed - in process] (Source: Genetics and Molecular Research)</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410483</comments>
            <pubDate>Thu, 17 Nov 2011 04:36:02 +0100</pubDate>
            <guid isPermaLink="false">5410483</guid>        </item>
        <item>
            <title>Using PCR for early diagnosis  of bovine leukemia virus infection in some native cattle.</title>
            <link>http://www.medworm.com/index.php?rid=5410482&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22057961%26dopt%3DAbstract</link>
            <description>Using PCR for early diagnosis of bovine leukemia virus infection in some native cattle.
    Genet Mol Res. 2011;10(4):2658-63
    Authors: Mohammadabadi MR, Soflaei M, Mostafavi H, Honarmand M
    Abstract
    Bovine leukemia virus (BLV), the causative agent of enzootic bovine leukosis, is an exogenous, B lymphotropic retrovirus belonging to the Retroviridae family that induces persistent lymphocytosis in cattle and sheep. PCR has proven to be particularly suitable for investigating herds of cattle with a very low incidence of BLV infection and for clarifying doubtful serological results obtained by immunodiffusion or ELISA. The native Iranian and Russian cattle have a series of valuable traits that discriminate them as unique breeds that are well able to compete with western analogues. Ho...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410482</comments>
            <pubDate>Thu, 17 Nov 2011 04:36:02 +0100</pubDate>
            <guid isPermaLink="false">5410482</guid>        </item>
        <item>
            <title>Smith-Magenis syndrome:  clinical evaluation in seven Brazilian patients.</title>
            <link>http://www.medworm.com/index.php?rid=5410481&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22057962%26dopt%3DAbstract</link>
            <description>Smith-Magenis syndrome: clinical evaluation in seven Brazilian patients.
    Genet Mol Res. 2011;10(4):2664-70
    Authors: Gamba BF, Vieira GH, Souza DH, Monteiro FF, Lorenzini JJ, Carvalho DR, Morreti-Ferreira D
    Abstract
    Smith-Magenis syndrome (SMS) is a complex congenital anomaly characterized by craniofacial anomalies, neurological and behavioral disorders. SMS is caused by a deletion in region 17p11.2, which includes the RAI1 gene (90% of cases), or by point mutation in the RAI1 gene (10% of cases). Laboratory diagnosis is through cytogenetic analysis by GTG banding and molecular cytogenetic analysis by FISH. We carried out an active search for patients in Associations of Parents and Friends of Exceptional Children (APAE) of São Paulo and genetic centers in Brazil. Forty-eigh...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410481</comments>
            <pubDate>Thu, 17 Nov 2011 04:36:02 +0100</pubDate>
            <guid isPermaLink="false">5410481</guid>        </item>
        <item>
            <title>Chemical synthesis and improved  expression of recombinant human granulocyte colony-stimulating factor cDNA.</title>
            <link>http://www.medworm.com/index.php?rid=5410480&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22057963%26dopt%3DAbstract</link>
            <description>In conclusion, a synthetic G-CSF cDNA in combination with the recombinant DNA protocol offers a rapid and reliable strategy for synthesizing the target protein. However, commercial utilization of this methodology will require rigorous validation and quality control.
    PMID: 22057963 [PubMed - in process] (Source: Genetics and Molecular Research)</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410480</comments>
            <pubDate>Thu, 17 Nov 2011 04:36:02 +0100</pubDate>
            <guid isPermaLink="false">5410480</guid>        </item>
        <item>
            <title>Microbial diversity in the larval  gut of field and laboratory populations of the sugarcane weevil Sphenophorus levis  (Coleoptera, Curculionidae).</title>
            <link>http://www.medworm.com/index.php?rid=5410479&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22057964%26dopt%3DAbstract</link>
            <description>We examined the diversity of the gut microbiota of S. levis, which was characterized using culture-dependent and culture-independent methods. Analysis of 16S rRNA amplified directly from the gut community revealed the presence of 14 genera, one group from the Candidatus category, one uncultured group assigned to the family Flavobacteriaceae, and one uncultured group assigned to the family Enterobacteriaceae; all of them are members of the Alpha-Proteobacteria, Beta-Proteobacteria, Gamma-Proteobacteria, Firmicutes, and Bacteroidetes phyla. Microorganisms isolated through culture-dependent methods were classified according to morphological parameters and by 16S rRNA gene sequences. In addition to bacteria, four filamentous fungi were isolated. A higher bacterial diversity was observed in fie...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410479</comments>
            <pubDate>Thu, 17 Nov 2011 04:36:02 +0100</pubDate>
            <guid isPermaLink="false">5410479</guid>        </item>
        <item>
            <title>Serum ferritin and transferrin saturation levels in β⁰ and β(+) thalassemia patients.</title>
            <link>http://www.medworm.com/index.php?rid=5375827&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21491373%26dopt%3DAbstract</link>
            <description>Authors: Estevão IF, Peitl Junior P, Bonini-Domingos CR
    Abstract
    There have been few studies on the mutations that cause heterozygous beta-thalassemia and how they affect the iron profile. One hundred and thirty-eight individuals were analyzed, 90 thalasemic β⁰ and 48 thalasemic β(+), identified by classical and molecular methods. Mutations in the hemochromatosis (HFE) gene, detected using PCR-RFLP, were found in 30.4% of these beta-thalassemic patients; heterozygosity for H63D (20.3%) was the most frequent. Ferritin levels and transferrin saturation were similar in beta-thalassemics with and without mutations in the HFE gene. Ferritin concentrations were significantly higher in men and in individuals over 40 years of age. Transferrin saturation also was significantly higher i...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375827</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375827</guid>        </item>
        <item>
            <title>Polymorphisms  associated with egg number at 300 days of age in chickens.</title>
            <link>http://www.medworm.com/index.php?rid=5375826&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22002122%26dopt%3DAbstract</link>
            <description>Polymorphisms associated with egg number at 300 days of age in chickens.
    Genet Mol Res. 2011;10(4):2279-89
    Authors: Xu HP, Zeng H, Zhang DX, Jia XL, Luo CL, Fang MX, Nie QH, Zhang XQ
    Abstract
    We looked for variations that could be associated with chicken egg number at 300 days of age (EN300) in seven genes of the hypothalamic-pituitary-gonadal axis, including gonadotrophin-releasing hormone-I (GnRH-I), GnRH receptor (GnRHR), neuropeptide Y (NPY), dopamine D2 receptor (DRD2), vasoactive intestinal polypeptide (VIP), VIP receptor-1 (VIPR-1), prolactin (PRL), and the QTL region between 87 and 105 cM of the Z chromosome. Ten mutations in the seven genes were chosen to do marker-trait association analyses in a population comprising 1310 chickens, which were obtained from a compa...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375826</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375826</guid>        </item>
        <item>
            <title>Identification and expression analysis of the Broad-Complex  core protein isoform 6 (BR-C Z6) gene in the giant tiger  shrimp Penaeus monodon (Penaeidae: Decapoda).</title>
            <link>http://www.medworm.com/index.php?rid=5375825&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22002123%26dopt%3DAbstract</link>
            <description>Identification and expression analysis of the Broad-Complex core protein isoform 6 (BR-C Z6) gene in the giant tiger shrimp Penaeus monodon (Penaeidae: Decapoda).
    Genet Mol Res. 2011;10(4):2290-306
    Authors: Buaklin A, Klinbunga S, Mensveta P
    Abstract
    Broad-Complex (BR-C) is an early ecdysone-responsive gene encoding a family of zinc-finger transcription factors that function during metamorphosis in insects. We identified two full-length cDNAs of BR-C Z6 in the giant tiger shrimp (Penaeus monodon). They were 2422 and 2060 bp in length, containing open reading frames of 1440 and 1443 bp, corresponding to polypeptides of 479 and 480 amino acids, respectively. Tissue distribution analysis indicated that PmBR-C Z6 was abundantly expressed in hemocytes and ovaries in juveniles. I...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375825</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375825</guid>        </item>
        <item>
            <title>Prediction of genomic islands  in seven human pathogens using the Z-Island method.</title>
            <link>http://www.medworm.com/index.php?rid=5375824&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22002124%26dopt%3DAbstract</link>
            <description>Prediction of genomic islands in seven human pathogens using the Z-Island method.
    Genet Mol Res. 2011;10(4):2307-15
    Authors: Wei W, Guo FB
    Abstract
    We adopted the method of Zhang and Zhang (the Z-Island method) to identify genomic islands in seven human pathogens, analyzing their chromosomal DNA sequences. The Z-Island method is a theoretical method for predicting genomic islands in bacterial genomes; it consists of determination of the cumulative GC profile and computation of codon usage bias. Thirty-one genomic islands were found in seven pathogens using this method. Further analysis demonstrated that most have the known conserved features; this increases the probability that they are real genomic islands. Eleven genomic islands were found to code for products involved in...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375824</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375824</guid>        </item>
        <item>
            <title>Loss of heterozygosity on chromosome 5 in Iranian  esophageal cancer patients.</title>
            <link>http://www.medworm.com/index.php?rid=5375823&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22002125%26dopt%3DAbstract</link>
            <description>Loss of heterozygosity on chromosome 5 in Iranian esophageal cancer patients.
    Genet Mol Res. 2011;10(4):2316-25
    Authors: Attaran-Bandarabadi F, Ziaee AA, Yazdanbod M, Shahpanah M, Setayeshgar A, Nassiri M
    Abstract
    There is a high incidence of esophageal squamous cell carcinoma (ESCC) in Iran. Non-functionality of some tumor suppressor genes has been reported in esophageal cancer. Loss of heterozygosity on chromosome 5 has also been reported in esophageal carcinomas. We assessed loss of heterozygosity along a region of the long arm of chromosome 5 (5q), from 5q23.1 to 5q23.2, by PCR amplifying DNA fragments of tumor tissues from patients with ESCC and their corresponding normal samples. The PCR products were electrophoresed on 6% non-denaturing polyacrylamide gels, and band ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375823</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375823</guid>        </item>
        <item>
            <title>Sexual reproduction development in apomictic Eulaliopsis binata (Poaceae).</title>
            <link>http://www.medworm.com/index.php?rid=5375822&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22002126%26dopt%3DAbstract</link>
            <description>Authors: Li JJ, Liu L, Ouyang YD, Yao JL
    Abstract
    Apomixis is a particular mode of reproduction that allows progeny formation without meiosis and fertilization. Eulaliopsis binata, a tetraploid apomictic species, is widely used for making paper, rope and mats. There is great potential for fixation of heterosis in E. binata due to autonomous endosperm formation in this species. Although most of its embryo sac originates from nucellus cells, termed apospory, we observed sexual reproduction initiation in 86.8 to 96.8% of the ovules, evidenced by callose deposition on the walls of cells undergoing megasporogenesis. However, only 2-3% mature polygonum-type sexual embryo sacs were confirmed by embryological investigation. Callose was not detected on aposporous initial cell walls. The apo...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375822</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375822</guid>        </item>
        <item>
            <title>N-nitrosodiethylamine  genotoxicity  evaluation: a cytochrome P450 induction study in rat  hepatocytes.</title>
            <link>http://www.medworm.com/index.php?rid=5375821&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22002127%26dopt%3DAbstract</link>
            <description>We examined NDEA genotoxicity and cytotoxicity in primary cultures of female rat hepatocytes; we also looked at how it affected CYP mRNA expression. Single incubation with 0.9% NaCl resulted in a mean of 0.2% apoptotic cells, which doubled with 105 μg NDEA/mL. The frequency of necrosis with NDEA treatment was also doubled. Besides the cytotoxic effects, there was also a 4-fold decrease in mitotic index and a 3-fold decrease in the percentage of cells with micronuclei. A significant increase in micronucleus cells when hepatocytes were incubated with 2.1 μg NDEA/mL suggests that DNA repair was inactive. The chromosomal aberration evaluation revealed a discrete dose-response curve. Treatment with NDEA induced increases in CYP mRNA: CYP2B2 (1.8 times) and CYP2E1 (1.6 times) with non-cytotoxi...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375821</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375821</guid>        </item>
        <item>
            <title>A new reduced height gene found in the tetraploid  semi-dwarf wheat landrace Aiganfanmai.</title>
            <link>http://www.medworm.com/index.php?rid=5375820&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22002128%26dopt%3DAbstract</link>
            <description>A new reduced height gene found in the tetraploid semi-dwarf wheat landrace Aiganfanmai.
    Genet Mol Res. 2011;10(4):2349-57
    Authors: Peng ZS, Li X, Yang ZJ, Liao ML
    Abstract
    Aiganfanmai is a dwarf tetraploid wheat landrace (Triticum turgidum var. turgidum) that stably produces the semi-dwarf trait. Plant height varies from 80-105 cm under cultivation. Compared with tall durum wheat (T. turgidum var. durum) variety Langdon, we found it to have short spikes and seeds, besides a semi-dwarf character. We crossed Aiganfanmai with Langdon to analyze the genetic basis of the semi-dwarf trait. The F(2) population segregated at a 1:3 ratio for the short trait to the normal, which demonstrates that Aiganfanmai carries a recessive reduced height (Rht) gene. This gene was found to be lo...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375820</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375820</guid>        </item>
        <item>
            <title>Molecular traceability of beef  from synthetic Mexican bovine breeds.</title>
            <link>http://www.medworm.com/index.php?rid=5375819&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22002129%26dopt%3DAbstract</link>
            <description>Molecular traceability of beef from synthetic Mexican bovine breeds.
    Genet Mol Res. 2011;10(4):2358-65
    Authors: Rodríguez-Ramírez R, Arana A, Alfonso L, González-Córdova AF, Torrescano G, Guerrero Legarreta I, Vallejo-Cordoba B
    Abstract
    Traceability ensures a link between carcass, quarters or cuts of beef and the individual animal or the group of animals from which they are derived. Meat traceability is an essential tool for successful identification and recall of contaminated products from the market during a food crisis. Meat traceability is also extremely important for protection and value enhancement of good-quality brands. Molecular meat traceability would allow verification of conventional methods used for beef tracing in synthetic Mexican bovine breeds. We evalua...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375819</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375819</guid>        </item>
        <item>
            <title>Genetic characterization of an elite coffee germplasm assessed by gSSR  and  EST-SSR markers.</title>
            <link>http://www.medworm.com/index.php?rid=5375818&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22002130%26dopt%3DAbstract</link>
            <description>Genetic characterization of an elite coffee germplasm assessed by gSSR and EST-SSR markers.
    Genet Mol Res. 2011;10(4):2366-81
    Authors: Missio RF, Caixeta ET, Zambolim EM, Pena GF, Zambolim L, Dias LA, Sakiyama NS
    Abstract
    Coffee is one of the main agrifood commodities traded worldwide. In 2009, coffee accounted for 6.1% of the value of Brazilian agricultural production, generating a revenue of US$6 billion. Despite the importance of coffee production in Brazil, it is supported by a narrow genetic base, with few accessions. Molecular differentiation and diversity of a coffee breeding program were assessed with gSSR and EST-SSR markers. The study comprised 24 coffee accessions according to their genetic origin: arabica accessions (six traditional genotypes of C. arabica), res...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375818</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375818</guid>        </item>
        <item>
            <title>Comparison of RAPD and ISSR  markers for assessment of genetic diversity among endangered rare Dalbergia  oliveri (Fabaceae) genotypes in Vietnam.</title>
            <link>http://www.medworm.com/index.php?rid=5375817&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22002131%26dopt%3DAbstract</link>
            <description>Comparison of RAPD and ISSR markers for assessment of genetic diversity among endangered rare Dalbergia oliveri (Fabaceae) genotypes in Vietnam.
    Genet Mol Res. 2011;10(4):2382-93
    Authors: Phong DT, Hien VT, Thanh TT, Tang DV
    Abstract
    Dalbergia oliveri is a leguminous tree of the Fabaceae family. This species is popular and valuable in Vietnam and is currently listed on the Vietnam Red List and on the IUCN Red List as endangered. Two PCR techniques using RAPD and inter-simple sequence repeat (ISSR) markers were used to make a comparative analysis of genetic diversity in this species. Fifty-six polymorphic primers (29 RAPD and 27 ISSR) were used. The RAPD primers produced 63 bands across 35 genotypes, of which 24 were polymorphic. The number of amplified bands varied from one...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375817</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375817</guid>        </item>
        <item>
            <title>Genetic analysis of the  Venezuelan Criollo horse.</title>
            <link>http://www.medworm.com/index.php?rid=5375816&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22002132%26dopt%3DAbstract</link>
            <description>Genetic analysis of the Venezuelan Criollo horse.
    Genet Mol Res. 2011;10(4):2394-403
    Authors: Cothran EG, Canelon JL, Luis C, Conant E, Juras R
    Abstract
    Various horse populations in the Americas have an origin in Spain; they are remnants of the first livestock introduced to the continent early in the colonial period (16th and 17th centuries). We evaluated genetic variability within the Venezuelan Criollo horse and its relationship with other horse breeds. We observed high levels of genetic diversity within the Criollo breed. Significant population differentiation was observed between all South American breeds. The Venezuelan Criollo horse showed high levels of genetic diversity, and from a conservation standpoint, there is no immediate danger of losing variation unless ther...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375816</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375816</guid>        </item>
        <item>
            <title>Introgression of cotton leaf  curl virus-resistant genes from Asiatic cotton (Gossypium arboreum) into  upland cotton (G. hirsutum).</title>
            <link>http://www.medworm.com/index.php?rid=5375815&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22002133%26dopt%3DAbstract</link>
            <description>Introgression of cotton leaf curl virus-resistant genes from Asiatic cotton (Gossypium arboreum) into upland cotton (G. hirsutum).
    Genet Mol Res. 2011;10(4):2404-14
    Authors: Ahmad S, Mahmood K, Hanif M, Nazeer W, Malik W, Qayyum A, Hanif K, Mahmood A, Islam N
    Abstract
    Cotton is under the constant threat of leaf curl virus, which is a major constraint for successful production of cotton in the Pakistan. A total of 3338 cotton genotypes belonging to different research stations were screened, but none were found to be resistant against the Burewala strain of cotton leaf curl virus (CLCuV). We explored the possibility of transferring virus-resistant genes from Gossypium arboreum (2n = 26) into G. hirsutum (2n = 52) through conventional breeding techniques. Hybridization was don...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375815</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375815</guid>        </item>
        <item>
            <title>Analysis of CD38 and ZAP70 mRNA  expression among cytogenetic subgroups of Iranian chronic-lymphocytic-leukemia patients.</title>
            <link>http://www.medworm.com/index.php?rid=5375814&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22002134%26dopt%3DAbstract</link>
            <description>Analysis of CD38 and ZAP70 mRNA expression among cytogenetic subgroups of Iranian chronic-lymphocytic-leukemia patients.
    Genet Mol Res. 2011;10(4):2415-23
    Authors: Teimori H, Akbari MT, Hamid M, Forouzandeh M, Bibordi E
    Abstract
    Chromosomal abnormalities and ZAP70 expression profile are two major independent prognostic markers in B-cell chronic lymphocytic leukemia. We investigated a possible correlation between these two markers. ZAP70 expression using real-time RT-PCR was examined in 20 B-cell chronic lymphocytic leukemia patients with del13q14, 13 patients with del11q22, 15 patients with trisomy 12, and 16 patients with no detected chromosomal abnormalities. Molecular analysis revealed that ZAP70 expression in the del13q subgroup was the same as in the control group, whi...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375814</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375814</guid>        </item>
        <item>
            <title>Prevalence of cystathionine  beta synthase gene mutation 852Ins68 as a possible risk for neural tube defects  in eastern India.</title>
            <link>http://www.medworm.com/index.php?rid=5375813&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22002135%26dopt%3DAbstract</link>
            <description>Prevalence of cystathionine beta synthase gene mutation 852Ins68 as a possible risk for neural tube defects in eastern India.
    Genet Mol Res. 2011;10(4):2424-9
    Authors: Saxena AK, Gupta J, Pandey S, Gangopadhaya AN, Pandey LK
    Abstract
    Cystathionine beta synthase gene (CβS) catalyzes the condensation of homocysteine with serine, forming cystathionine by the transsulfuration pathway. Disruption of CβS enzyme activity due to defective folic acid metabolism increases the risk factor for neural tube defects. We evaluated the CβS gene mutation in 25 children with neural tube defects (NTDs), including lumbosacral and thoracic myelomeningocele and open NTDs and mothers of cases, along with 25 healthy children and their mothers, serving as controls. Genomic DNA was isolated to ass...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375813</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375813</guid>        </item>
        <item>
            <title>Identification of complex  vertebral malformation carriers in Holstein cattle in south China.</title>
            <link>http://www.medworm.com/index.php?rid=5375812&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22009856%26dopt%3DAbstract</link>
            <description>Identification of complex vertebral malformation carriers in Holstein cattle in south China.
    Genet Mol Res. 2011;10(4):2443-8
    Authors: Wang C, Tong Q, Hu XZ, Yang LG, Zhong XQ, Yu Y, Wu JJ, Liu WJ, Li X, Hua GH, Zhao HQ, Zhang SJ
    Abstract
    Complex vertebral malformation (CVM) is a recently described monogenic autosomal recessive hereditary defect of Holstein dairy cattle that causes premature birth, aborted fetuses and stillborn calves. Guanine is substituted by thymine (G&amp;gt;T) in the solute carrier family 35 member A3 gene (SLC35A3). A valine is changed to a phenylalanine at position 180 of uridine 5'-diphosphate-N-acetyl-glucosamine transporter protein. CVM is expected to occur in many countries due to the widespread use of sire semen. We developed a created restriction s...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375812</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375812</guid>        </item>
        <item>
            <title>Meta-analysis of the relationship  between p21 Ser31Arg polymorphism and lung cancer susceptibility.</title>
            <link>http://www.medworm.com/index.php?rid=5375811&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22009857%26dopt%3DAbstract</link>
            <description>Meta-analysis of the relationship between p21 Ser31Arg polymorphism and lung cancer susceptibility.
    Genet Mol Res. 2011;10(4):2449-56
    Authors: Lin G, Fang F, Yu XJ, Yu L
    Abstract
    The cyclin-dependent kinase inhibitor 1A (also known as p21) is thought to be involved in tumor development by mediating cell cycle arrest through the inhibition of cyclin/CDK activity. To explore the relationship of Ser31Arg polymorphism in the p21 gene with the risk of developing lung cancer, we performed an overall and stratified meta-analysis based on ethnicity, lung cancer subtypes and source of controls, with six eligible studies (2366 cases and 3320 controls). No significant variation in lung cancer risk was detected in any of the genetic models in the overall, and the ethnicity-based and ca...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375811</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375811</guid>        </item>
        <item>
            <title>Multivariate analysis of  morphological characteristics of two species of passion flower with ornamental potential and of hybrids between them.</title>
            <link>http://www.medworm.com/index.php?rid=5375810&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22009858%26dopt%3DAbstract</link>
            <description>Multivariate analysis of morphological characteristics of two species of passion flower with ornamental potential and of hybrids between them.
    Genet Mol Res. 2011;10(4):2457-71
    Authors: Santos EA, Souza MM, Viana AP, Almeida AA, Freitas JC, Lawinscky PR
    Abstract
    We estimated genetic parameters through multivariate analysis of two species of Passiflora and their hybrids, considered of ornamental potential, based on the morphological characteristics: flower diameter, corona diameter, corona filament size, flower peduncle length, petal length and width, sepal length and width, internode length, stem diameter, leaf length, leaf width (mm), and leaf area (cm(2)). Five specimens of Passiflora sublanceolata [ex P. palmeri var. sublanceolata], five of P. foetida var. foetida and 20...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375810</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375810</guid>        </item>
        <item>
            <title>Esterase polymorphisms for analysis  of  genetic diversity and structure of soybean (Glycine  max) cultivars.</title>
            <link>http://www.medworm.com/index.php?rid=5375809&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22009859%26dopt%3DAbstract</link>
            <description>Esterase polymorphisms for analysis of genetic diversity and structure of soybean (Glycine max) cultivars.
    Genet Mol Res. 2011;10(4):2472-81
    Authors: Valentini LC, Mangolin CA, Collet SA, Machado MF
    Abstract
    We used native polyacrylamide gel electrophoresis to identify polymorphism levels in α- and β-esterase loci from leaf tissues of Brazilian soybean cultivars for the analysis of population genetic diversity and structure, and to investigate relationships between conventional and genetically modified cultivars. The cultivars included lines developed by a soybean-grower cooperative (CD), by EMBRAPA (BR), and &quot;Roundup Ready&quot; (RR) cultivars. Esterase isozymes recorded with α-naphthyl acetate and β-naphthyl acetate were produced from 14 loci. Two to three allelic variants...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375809</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375809</guid>        </item>
        <item>
            <title>Genetic variability of an endangered Bromeliaceae  species (Pitcairnia albiflos) from the Brazilian Atlantic rainforest.</title>
            <link>http://www.medworm.com/index.php?rid=5375808&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22009860%26dopt%3DAbstract</link>
            <description>Genetic variability of an endangered Bromeliaceae species (Pitcairnia albiflos) from the Brazilian Atlantic rainforest.
    Genet Mol Res. 2011;10(4):2482-91
    Authors: Domingues R, Machado MA, Forzza RC, Melo TD, Wohlres-Viana S, Viccini LF
    Abstract
    Pitcairnia albiflos is a Bromeliaceae species endemic to Brazil that has been included as data-deficient in the extinction risk list of Brazilian flora. We analyzed genetic variability in P. albiflos populations using RAPD markers to investigate population structure and reproductive mechanisms and also to evaluate the actual extinction risk level of this species. Leaves of 56 individuals of P. albiflos from three populations were collected: Urca Hill (UH, 20 individuals), Chacrinha State Park (CSP, 24 individuals) and Tijuca National...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375808</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375808</guid>        </item>
        <item>
            <title>Population genetic structure of  wild and hatchery black rockfish Sebastes inermis  in Korea, assessed using cross-species  microsatellite markers.</title>
            <link>http://www.medworm.com/index.php?rid=5375807&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22009861%26dopt%3DAbstract</link>
            <description>Population genetic structure of wild and hatchery black rockfish Sebastes inermis in Korea, assessed using cross-species microsatellite markers.
    Genet Mol Res. 2011;10(4):2492-504
    Authors: An HS, Kim EM, Lee JH, Noh JK, An CM, Yoon SJ, Park KD, Myeong JI
    Abstract
    The population structure of the black rockfish, Sebastes inermis (Sebastidae), was estimated using 10 microsatellite loci developed for S. schlegeli on samples of 174 individuals collected from three wild and three hatchery populations in Korea. Reduced genetic variation was detected in hatchery strains [overall number of alleles (N(A)) = 8.07; allelic richness (A(R)) = 7.37; observed heterozygosity (H(O)) = 0.641] compared with the wild samples (overall N(A) = 8.43; A(R) = 7.83; H(O) = 0.670), but the difference w...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375807</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375807</guid>        </item>
        <item>
            <title>Non-invasive sex identification of the white-bellied  sea eagle (Haliaeetus leucogaster) through genetic analysis of feathers.</title>
            <link>http://www.medworm.com/index.php?rid=5375806&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22009862%26dopt%3DAbstract</link>
            <description>Non-invasive sex identification of the white-bellied sea eagle (Haliaeetus leucogaster) through genetic analysis of feathers.
    Genet Mol Res. 2011;10(4):2505-10
    Authors: Naim DM, Nor SA, Baharuddin MH
    Abstract
    The white-bellied sea eagle, Haliaeetus leucogaster, displays reversed sexual size dimorphism and is monomorphic for adult plumage coloration. Early attempts to identify sex in sexually monomorphic birds were based on morphological or chromosomal characters, but since avian W-specific DNA sequences were identified, PCR amplification has become commonly used for molecular sexing. We used a PCR test employing primers that amplify two homologous fragments of both the CHD-W gene, unique to females, and the CHD-Z gene, occurring in both sexes. This test was applied to five ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375806</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375806</guid>        </item>
        <item>
            <title>A novel single-nucleotide polymorphism in the 5' upstream region of the prolactin receptor gene is associated with fiber traits in Liaoning cashmere goats.</title>
            <link>http://www.medworm.com/index.php?rid=5375805&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22009863%26dopt%3DAbstract</link>
            <description>Authors: Zhou JP, Zhu XP, Zhang W, Qin F, Zhang SW, Jia ZH
    Abstract
    The most important traits of Chinese Liaoning cashmere goat fiber are fiber diameter, weight, and length. We looked for polymorphisms and their possible association with cashmere fiber traits in the 5' upstream region (5' UTR) of the prolactin receptor gene (PRLR), which encodes an anterior pituitary peptide hormone involved in different physiological activities; it is the principal endocrine regulator in pelage replacement in mammals. A novel single-nucleotide polymorphism (SNP) was found in the 5' UTR of PRLR by PCR-RFLP in an analysis of 590 goats. Two genotypes (CC and CT) were observed. The frequencies of allele C and T were 0.93 and 0.07, respectively. Association analysis revealed that the PRLR 5' UTR polymo...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375805</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375805</guid>        </item>
        <item>
            <title>Two novel NPHS1 mutations  in a Chinese family with congenital nephrotic syndrome.</title>
            <link>http://www.medworm.com/index.php?rid=5375804&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22009864%26dopt%3DAbstract</link>
            <description>Two novel NPHS1 mutations in a Chinese family with congenital nephrotic syndrome.
    Genet Mol Res. 2011;10(4):2517-22
    Authors: Wu LQ, Hu JJ, Xue JJ, Liang DS
    Abstract
    Congenital nephrotic syndrome of the Finnish type (CNF) is a lethal, autosomal recessive disorder mainly caused by mutations in the NPHS1 gene; it is found at a relatively high frequency in Finns. We investigated the disease-causing mutations in a Chinese family with CNF and developed a prenatal genetic diagnosis for their latest pregnancy. Mutation analysis was made of all exons and exon/intron boundaries of NPHS1 in the fetus, parents and 50 unrelated controls using PCR and direct sequencing. A heterozygous nonsense mutation within exon 20 (c.2783C&amp;gt;A) and a missense mutation within exon 17 (c.2225T&amp;gt;C) in...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375804</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375804</guid>        </item>
        <item>
            <title>Isolation and characterization  of polymorphic microsatellite loci in Aleurodicus dispersus (Hemiptera,  Aleyrodidae).</title>
            <link>http://www.medworm.com/index.php?rid=5375803&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22009865%26dopt%3DAbstract</link>
            <description>Isolation and characterization of polymorphic microsatellite loci in Aleurodicus dispersus (Hemiptera, Aleyrodidae).
    Genet Mol Res. 2011;10(4):2523-6
    Authors: Ma GC, Wu X, Ma CL, Wu HL, Hu HY, Niu LM, Fu YG
    Abstract
    Ten microsatellite markers were isolated and characterized from Aleurodicus dispersus, the spiraling whitefly, an exotic pest species that is considered to be one of the most serious agricultural pests on Hainan Island, China. The polymorphism of these loci was examined in individual whiteflies from Hainan Island and from the Canary Islands. All loci were polymorphic, with two to four alleles per locus. Mean observed and expected heterozygosity values were 0.773 and 0.585, respectively. These microsatellite markers provide powerful tools for ecological, epidemio...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375803</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375803</guid>        </item>
        <item>
            <title>Vero cells infected with the Lederle strain of  canine distemper virus have increased Fas receptor  signaling expression at 15 h post-infection.</title>
            <link>http://www.medworm.com/index.php?rid=5375802&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22009866%26dopt%3DAbstract</link>
            <description>Vero cells infected with the Lederle strain of canine distemper virus have increased Fas receptor signaling expression at 15 h post-infection.
    Genet Mol Res. 2011;10(4):2527-33
    Authors: Del Puerto HL, Martins AS, Braz GF, Alves F, Heinemann MB, Rajão DS, Araújo FC, Martins SF, Nascimento DR, Leite RC, Vasconcelos AC
    Abstract
    We evaluated the expression of the Fas receptor gene in Vero cells infected with the Lederle vaccine strain of canine distemper virus using RT-PCR. Vero cells were plated, and after being grown for 24 h in MEM with 5% FBS, 80-90% confluent monolayer cultures were infected with the virus. The cells were harvested at 3, 6, 9, and 15 h post-infection. Uninfected Vero cells were used as a control. Total RNA was isolated from Vero cells using 1 mL Trizol(...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375802</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375802</guid>        </item>
        <item>
            <title>Microsatellites behaving badly:  empirical evaluation of genotyping errors and  subsequent impacts on population studies.</title>
            <link>http://www.medworm.com/index.php?rid=5375789&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22033936%26dopt%3DAbstract</link>
            <description>This study facilitates the application of microsatellite technology in population studies by examining common sources of genotyping error, identifying unreported problems with microsatellites, and offering solutions to prevent error and bias in population studies.
    PMID: 22033936 [PubMed - in process] (Source: Genetics and Molecular Research)</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375789</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375789</guid>        </item>
        <item>
            <title>Optimization of PCR conditions  to amplify Cyt b, COI and 12S rRNA gene fragments of Malayan gaur (Bos  gaurus hubbacki) mtDNA.</title>
            <link>http://www.medworm.com/index.php?rid=5375788&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22033937%26dopt%3DAbstract</link>
            <description>Optimization of PCR conditions to amplify Cyt b, COI and 12S rRNA gene fragments of Malayan gaur (Bos gaurus hubbacki) mtDNA.
    Genet Mol Res. 2011;10(4):2554-68
    Authors: Rosli MK, Zamzuriada AS, Syed-Shabthar SM, Mahani MC, Abas-Mazni O, Md-Zain BM
    Abstract
    PCR has been extensively used for amplification of DNA sequences. We conducted a study to obtain the best amplification conditions for cytochrome b (Cyt b), cytochrome c oxidase I (COI) and 12S rRNA (12S) gene fragments of Malayan gaur mtDNA. DNA from seven Malayan gaur samples were extracted for PCR amplification. Various trials and combinations were tested to determine the best conditions of PCR mixture and profile to obtain the best PCR products for sequencing purposes. Four selected target factors for enhancing PCR, a...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375788</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375788</guid>        </item>
        <item>
            <title>Common ABCB1 polymorphisms  associated with susceptibility to infantile spasms in the Chinese Han population.</title>
            <link>http://www.medworm.com/index.php?rid=5375787&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22033938%26dopt%3DAbstract</link>
            <description>This study demonstrated that variations in the C3435T gene play an important role in the pathogenesis of infantile spasms in the Han Chinese population; 3435TT is associated with increased risk of having this epilepsy syndrome.
    PMID: 22033938 [PubMed - in process] (Source: Genetics and Molecular Research)</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375787</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375787</guid>        </item>
        <item>
            <title>Detection of Salmonella Enteritidis  in asymptomatic carrier animals: comparison of quantitative real-time PCR and  bacteriological culture methods.</title>
            <link>http://www.medworm.com/index.php?rid=5375786&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22033939%26dopt%3DAbstract</link>
            <description>We examined the sensitivity, specificity and accuracy of real-time qPCR, without pre-enrichment or selective enrichment stages, for the quantification of S. enterica serovar Enteritidis in resistant mice, as a model of asymptomatic carrier animal. The results were compared with those obtained by traditional bacteriological culture methods, the gold standard test. Two hundred and forty-three samples, including spleen, liver, mesenteric lymph nodes, portions of intestine, intestinal content of the ileocecal portion, and feces, were collected from a group of 27 C57BL/6 mice, that had been intragastrically inoculated with high doses of S. enterica serovar Enteritidis. The real-time qPCR assay presented a consistent linearity of the standard curve (r(2) = 0.999), with very low differences betwe...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375786</comments>
            <pubDate>Fri, 04 Nov 2011 22:25:04 +0100</pubDate>
            <guid isPermaLink="false">5375786</guid>        </item>
        <item>
            <title>Sexing single bovine  blastomeres using TSPY gene amplification.</title>
            <link>http://www.medworm.com/index.php?rid=5375794&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22033907%26dopt%3DAbstract</link>
            <description>Sexing single bovine blastomeres using TSPY gene amplification.
    Genet Mol Res. 2011 Oct 25;10(4)
    Authors: Carneiro MC, Takeuchi PL, Araújo A, Lôbo RB, Elias FP, Vila RA, Miranda-Furtado CL, Ramos ES
    Abstract
    The testis-specific protein Y-encoded gene (TSPY) is a Y-specific gene present in variable copy number in many mammalian species, including cattle. We tested the applicability of the TSPY gene as a Y-specific marker to predict preimplantation embryo sex in Nelore (Bos indicus) cattle. Two blastomeres were removed from each embryo. A total of 36 single blastomeres and the remaining cells of their 18 matched in vitro conceived embryos were screened for TSPY amplification by nested-PCR. The results obtained from a single blastomere and the remaining cells of the same emb...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375794</comments>
            <pubDate>Tue, 25 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5375794</guid>        </item>
        <item>
            <title>Genetic dissimilarity of putative gamma-ray-induced  'Preciosa - AAAB-Pome type' banana (Musa sp) mutants based on  multivariate statistical analysis.</title>
            <link>http://www.medworm.com/index.php?rid=5375793&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22033908%26dopt%3DAbstract</link>
            <description>Genetic dissimilarity of putative gamma-ray-induced 'Preciosa - AAAB-Pome type' banana (Musa sp) mutants based on multivariate statistical analysis.
    Genet Mol Res. 2011 Oct 25;10(4)
    Authors: Pestana RK, Amorim EP, Ferreira CF, Amorim VB, Oliveira LS, Ledo CA, Silva SO
    Abstract
    Bananas are among the most important fruit crops worldwide, being cultivated in more than 120 countries, mainly by small-scale producers. However, short-stature high-yielding bananas presenting good agronomic characteristics are hard to find. Consequently, wind continues to damage a great number of plantations each year, leading to lodging of plants and bunch loss. Development of new cultivars through conventional genetic breeding methods is hindered by female sterility and the low number of seeds. Mu...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375793</comments>
            <pubDate>Tue, 25 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5375793</guid>        </item>
        <item>
            <title>A novel DDX5 gene in the freshwater crayfish Cherax  quadricarinatus is highly expressed during ontogenesis and spermatogenesis.</title>
            <link>http://www.medworm.com/index.php?rid=5375792&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22033909%26dopt%3DAbstract</link>
            <description>A novel DDX5 gene in the freshwater crayfish Cherax quadricarinatus is highly expressed during ontogenesis and spermatogenesis.
    Genet Mol Res. 2011 Oct 25;10(4)
    Authors: Fang DA, Wang Q, Wang J, He L, Liu LH, Wang Y
    Abstract
    The freshwater crayfish Cherax quadricarinatus, originally from Australia, is an invasive species that is also widely used in aquaculture. DEAD-box helicase family genes are found throughout evolution and encode RNA-binding proteins. The human DDX5 (p68) is important for normal cell growth, differentiation and proliferation. We identified a C. quadricarinatus homolog of DDX5 (Cq-DDX5); the temporal expression of Cq-DDX5 mRNA transcripts was measured during early ontogenesis, during spermatogenesis, during testes development, and during the annual cycle....</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375792</comments>
            <pubDate>Tue, 25 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5375792</guid>        </item>
        <item>
            <title>Application of the Sleeping Beauty  system in  Saanen goat fibroblast cells for establishing  persistent transgene expression.</title>
            <link>http://www.medworm.com/index.php?rid=5375791&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22033910%26dopt%3DAbstract</link>
            <description>Application of the Sleeping Beauty system in Saanen goat fibroblast cells for establishing persistent transgene expression.
    Genet Mol Res. 2011 Oct 25;10(4)
    Authors: Jiang BC, Kaleri HA, Zhang HX, Chen J, Liu HL
    Abstract
    The Sleeping Beauty (SB) transposon system is a promising new method for establishing persistent transgene expression in vivo. We applied the SB system for enhancing transgenesis in Saanen dairy goat fibroblast cells. We constructed a pKT2/CMV-EGFP-IRES-PURO vector and investigated the influence of transposon and transposase vector ratios on transfection efficiency in the Saanen goat fibroblast cells. To enhance SB system performance, we developed a new transfection technique (double-transfection method) for the SB system. The cultured cells were transfecte...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375791</comments>
            <pubDate>Tue, 25 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5375791</guid>        </item>
        <item>
            <title>Microarray analysis in caudal medulla of cattle orally challenged with bovine spongiform encephalopathy.</title>
            <link>http://www.medworm.com/index.php?rid=5375790&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22033911%26dopt%3DAbstract</link>
            <description>Authors: Almeida LM, Basu U, Williams JL, Moore SS, Guan LL
    Abstract
    Bovine spongiform encephalopathy (BSE) is a fatal disorder in cattle characterized by progressive neurodegeneration of the central nervous system. We investigated the molecular mechanisms involved in neurodegeneration during prion infection through the identification of genes that are differentially expressed (DE) between experimentally infected and non-challenged cattle. Gene expression of caudal medulla from control and orally infected animals was compared by microarray analysis using 24,000 bovine oligonucleotides representing 16,846 different genes to identify DE genes associated with BSE disease. In total, 182 DE genes were identified between normal and BSE-infected tissues (&amp;gt;2.0-fold change, P &amp;lt; 0.01);...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375790</comments>
            <pubDate>Tue, 25 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5375790</guid>        </item>
        <item>
            <title>A new inducible expression  system in a transformed green alga, Chlorella vulgaris.</title>
            <link>http://www.medworm.com/index.php?rid=5375801&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22033900%26dopt%3DAbstract</link>
            <description>This study presented an inducible recombinant gene expression system, also providing more gene regulation elements with potential for biotechnological applications.
    PMID: 22033900 [PubMed - as supplied by publisher] (Source: Genetics and Molecular Research)</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375801</comments>
            <pubDate>Fri, 21 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5375801</guid>        </item>
        <item>
            <title>Cytochrome c oxidase subunit I  barcoding of the green bee-eater (Merops orientalis).</title>
            <link>http://www.medworm.com/index.php?rid=5375800&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22033901%26dopt%3DAbstract</link>
            <description>Cytochrome c oxidase subunit I barcoding of the green bee-eater (Merops orientalis).
    Genet Mol Res. 2011 Oct 21;10(4)
    Authors: Arif IA, Khan HA, Shobrak M, Williams J
    Abstract
    DNA barcoding using mitochondrial cytochrome c oxidase subunit I (COI) is regarded as a standard method for species identification. Recent reports have also shown extended applications of COI gene analysis in phylogeny and molecular diversity studies. The bee-eaters are a group of near passerine birds in the family Meropidae. There are 26 species worldwide; five of them are found in Saudi Arabia. Until now, GenBank included a COI barcode for only one species of bee-eater, the European bee-eater (Merops apiaster). We sequenced the 694-bp segment of the COI gene of the green bee-eater M. orientalis and ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375800</comments>
            <pubDate>Fri, 21 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5375800</guid>        </item>
        <item>
            <title>Leptin mRNA expression in the rat mammary gland at  different activation stages.</title>
            <link>http://www.medworm.com/index.php?rid=5375799&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22033902%26dopt%3DAbstract</link>
            <description>Leptin mRNA expression in the rat mammary gland at different activation stages.
    Genet Mol Res. 2011 Oct 21;10(4)
    Authors: Wang YY, Wang YL, Li HP, Zhu HS, Jiang QD, Zhang L, Wang LF, Han LQ, Zhong K, Guo YJ, Lu WF, Li HJ, Yang GY
    Abstract
    Leptin is expressed in various tissues, suggesting that this protein is effective not only at the central nervous system level, but also peripherically. Recent studies have shown leptin production by other tissues, including the placenta, stomach, and mammary tissues, but there is no information available concerning expression levels of leptin in the rat mammary gland at different activation stages. We used semi-quantitative RT-PCR to investigate leptin mRNA expression levels in the rat mammary gland at different activity stages. Rat mamma...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375799</comments>
            <pubDate>Fri, 21 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5375799</guid>        </item>
        <item>
            <title>Molecular, anatomical and  physiological properties of a genetically modified soybean line transformed  with rd29A:AtDREB1A for the improvement of drought tolerance.</title>
            <link>http://www.medworm.com/index.php?rid=5375798&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22033903%26dopt%3DAbstract</link>
            <description>Molecular, anatomical and physiological properties of a genetically modified soybean line transformed with rd29A:AtDREB1A for the improvement of drought tolerance.
    Genet Mol Res. 2011 Oct 21;10(4)
    Authors: Polizel AM, Medri ME, Nakashima K, Yamanaka N, Farias JR, de Oliveira MC, Marin SR, Abdelnoor RV, Marcelino-Guimarães FC, Fuganti R, Rodrigues FA, Stolf-Moreira R, Beneventi MA, Rolla AA, Neumaier N, Yamaguchi-Shinozaki K, Carvalho JF, Nepomuceno AL
    Abstract
    We evaluated the molecular, anatomical and physiological properties of a soybean line transformed to improve drought tolerance with an rd29A:AtDREB1A construct. This construct expressed dehydration- responsive element binding protein DREB1A from the stress-inducible rd29A promoter. The greenhouse growth test included...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375798</comments>
            <pubDate>Fri, 21 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5375798</guid>        </item>
        <item>
            <title>Transcription factors  expressed in soybean roots under drought stress.</title>
            <link>http://www.medworm.com/index.php?rid=5375797&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22033904%26dopt%3DAbstract</link>
            <description>Transcription factors expressed in soybean roots under drought stress.
    Genet Mol Res. 2011 Oct 21;10(4)
    Authors: Pereira SS, Guimarães FC, Carvalho JF, Stolf-Moreira R, Oliveira MC, Rolla AA, Farias JR, Neumaier N, Nepomuceno AL
    Abstract
    To gain insight into stress-responsive gene regulation in soybean plants, we identified consensus sequences that could categorize the transcription factors MYBJ7, BZIP50, C2H2, and NAC2 as members of the gene families myb, bzip, c2h2, and nac, respectively. We also investigated the evolutionary relationship of these transcription factors and analyzed their expression levels under drought stress. The NCBI software was used to find the predicted amino acid sequences of the transcription factors, and the Clustal X software was used to align s...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375797</comments>
            <pubDate>Fri, 21 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5375797</guid>        </item>
        <item>
            <title>Association of -619C/T polymorphism in CDSN gene and  psoriasis risk: a meta-analysis.</title>
            <link>http://www.medworm.com/index.php?rid=5375796&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22033905%26dopt%3DAbstract</link>
            <description>In conclusion, this meta-analysis suggests that CDSN -619C/T polymorphism may not be associated with susceptibility to psoriasis.
    PMID: 22033905 [PubMed - as supplied by publisher] (Source: Genetics and Molecular Research)</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375796</comments>
            <pubDate>Fri, 21 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5375796</guid>        </item>
        <item>
            <title>A potential indicator of  denervated muscle atrophy: the ratio of myostatin to follistatin in peripheral  blood.</title>
            <link>http://www.medworm.com/index.php?rid=5375795&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22033906%26dopt%3DAbstract</link>
            <description>In this study, we investigated the possibility of myostatin being an indicator of denervated muscle atrophy. ELISA was used to detect the concentration of myostatin and follistatin in sera collected from individual rats at different times after sciatic nerve crush. A strong correlation was shown between the expression level of secreted myostatin in circulation and the wet weight ratio of the gastrocnemius muscle. The ratio of follistatin/myostatin could be used to monitor the progress of target muscle atrophy and recovery. Our study provides a potential serological test to detect denervated muscle atrophy for clinical purposes.
    PMID: 22033906 [PubMed - as supplied by publisher] (Source: Genetics and Molecular Research)</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375795</comments>
            <pubDate>Fri, 21 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5375795</guid>        </item>
        <item>
            <title>Response to treatment with imatinib mesylate in previously treated chronic-phase chronic myeloid leukemia patients in a hospital in Brazil.</title>
            <link>http://www.medworm.com/index.php?rid=5293463&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21968620%26dopt%3DAbstract</link>
            <description>Authors: Silveira CA, Daldegan MB, Ferrari I
    Abstract
    We analyzed the results of treatment with imatinib mesylate in 70 patients with chronic-phase chronic myeloid leukemia who had previously been treated (with second-line or higher imatinib), many of them in a late chronic phase. The median follow-up period was 60.5 months (range 3-100 months). Our objective was to assess the efficacy and safety of treatment. The mean dose was 400 mg per day. The hematologic response rate was 92.1% at six months, while the cumulative rates of major and complete cytogenetic responses were 73.6 and 66.3%, respectively. Molecular response rate improved slowly and steadily over time, reaching 65.8% at 60 months, remaining stable for up to 96 months. The five-year progression-free survival and overall ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5293463</comments>
            <pubDate>Fri, 07 Oct 2011 19:20:02 +0100</pubDate>
            <guid isPermaLink="false">5293463</guid>        </item>
        <item>
            <title>Comparative genetic analysis of trichome-less and normal pod genotypes of Mucuna pruriens (Fabaceae).</title>
            <link>http://www.medworm.com/index.php?rid=5293462&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21968621%26dopt%3DAbstract</link>
            <description>Authors: Dhawan SS, Rai GK, Darokar MP, Lal RK, Misra HO, Khanuja SP
    Abstract
    Velvet bean (Mucuna pruriens) seeds contain the catecholic amino acid L-DoPA (L-3,4-dihydroxyphenylalanine), which is a neurotransmitter precursor and used for the treatment of Parkinson's disease and mental disorders. The great demand for L-DoPA is largely met by the pharmaceutical industry through extraction of the compound from wild populations of this plant; commercial exploitation of this compound is hampered because of its limited availability. The trichomes present on the pods can cause severe itching, blisters and dermatitis, discouraging cultivation. We screened genetic stocks of velvet bean for the trichome-less trait, along with high seed yield and L-DoPA content. The highest yielding trichome-...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5293462</comments>
            <pubDate>Fri, 07 Oct 2011 19:20:02 +0100</pubDate>
            <guid isPermaLink="false">5293462</guid>        </item>
        <item>
            <title>Single nucleotide polymorphisms in CAPN and leptin genes associated with meat color and tenderness in Nellore cattle.</title>
            <link>http://www.medworm.com/index.php?rid=5293461&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21968622%26dopt%3DAbstract</link>
            <description>Authors: Pinto LF, Ferraz JB, Pedrosa VB, Eler JP, Meirelles FV, Bonin MN, Rezende FM, Carvalho ME, Cucco DC, Silva RC
    Abstract
    We analyzed single nucleotide polymorphisms in calpain, leptin, leptin receptor, and growth hormone receptor genes and their association with color, drip and cooking losses of longissimus muscle at 7, 14 and 21 days postmortem in 638 purebred Nellore bulls slaughtered between 22 and 26 months of age. Meat samples were vacuum-packed and aged at 4°C. The single nucleotide polymorphisms T945M, GHR2, E2FB, and CAPN4751 were evaluated. All genotypic classes were observed; however, the T/T genotype of T945M and E2FB was found at a low frequency. A significant association of E2FB with drip loss (a measure of water-holding capacity) was detected at seven days of ...</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5293461</comments>
            <pubDate>Fri, 07 Oct 2011 19:20:02 +0100</pubDate>
            <guid isPermaLink="false">5293461</guid>        </item>
        <item>
            <title>Isolation and characterization of microsatellite markers for the Korean rockfish, Sebastes schlegeli.</title>
            <link>http://www.medworm.com/index.php?rid=5293460&amp;cid=s_28401_50_f&amp;fid=28401&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21968623%26dopt%3DAbstract</link>
            <description>Authors: Bai CC, Liu SF, Zhuang ZM, Lin L, Wang H, Chang YQ
    Abstract
    The Korean rockfish (Sebastes schlegeli) is an important commercial fish that is widely used in aquaculture. We isolated and characterized 18 polymorphic microsatellite loci from the Korean rockfish using a (GT)(13)-enriched genomic library. Polymorphism was assessed in 48 individuals from a single population collected from the northern coastal waters of the Yellow Sea. The observed and expected heterozygosities ranged from 0.0244 to 0.7660 (mean 0.4194) and 0.0244 to 0.8758 (mean 0.5002), respectively. Polymorphism at these loci indicated from two to 15 alleles (mean 5.7); 14 of 18 loci conformed to Hardy-Weinberg equilibrium. These markers should be useful for management and conservation studies of this species....</description>
            <author>Genetics and Molecular Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5293460</comments>
            <pubDate>Fri, 07 Oct 2011 19:20:02 +0100</pubDate>
            <guid isPermaLink="false">5293460</guid>        </item>
    </channel>
</rss>

