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        <title>Gene 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 'Gene' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Gene&t=Gene&s=Search&f=source]]></link>
        <lastBuildDate>Mon, 06 Feb 2012 09:32:08 +0100</lastBuildDate>
        <item>
            <title>Analysis of the 5' untranslated region (5'UTR) of the alcohol oxidase 1 (AOX1) gene in recombinant protein expression in Pichia pastoris.</title>
            <link>http://www.medworm.com/index.php?rid=5650550&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22285974%26dopt%3DAbstract</link>
            <description>Authors: Staley CA, Huang A, Nattestad M, Oshiro K, Ray L, Mulye T, Li ZH, Le T, Stephens JJ, Gomez SR, Moy A, Nguyen JC, Franz AH, Lin-Cereghino J, Lin-Cereghino GP
    Abstract
    Pichia pastoris is a methylotrophic yeast that has been genetically engineered to express over one thousand heterologous proteins valued for industrial, pharmaceutical and basic research purposes. In most cases, the 5' untranslated region (UTR) of the alcohol oxidase 1 (AOX1) gene is fused to the coding sequence of the recombinant gene for protein expression in this yeast. Because the effect of the AOX1 5'UTR on protein expression is not known, site-directed mutagenesis was performed in order to decrease or increase the length of this region. Both of these types of changes were shown to affect translational ef...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650550</comments>
            <pubDate>Wed, 25 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5650550</guid>        </item>
        <item>
            <title>An arrayed human genomic library constructed in the PAC shuttle vector pJCPAC-Mam2 for genome-wide association studies and gene therapy.</title>
            <link>http://www.medworm.com/index.php?rid=5650554&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22285925%26dopt%3DAbstract</link>
            <description>Authors: Fuesler J, Nagahama Y, Szulewski J, Mundorff J, Bireley S, Coren JS
    Abstract
    The various iterations of the HapMap Project and many genome-wide association studies (GWAS) have identified hundreds of potential genes involved in monogenic and multifactorial traits. We constructed an arrayed 115,000-member human genomic library in the PAC shuttle vector pJCPAC-Mam2 that can be propagated in both bacterial and human cells. The library appears to represent a two-fold coverage of the human genome. Transient transfection of a p53-containing PAC clone into p53-null Saos-2 human osteosarcoma cells demonstrated that both p53 mRNA and protein were produced. Additionally, expression of the p53 protein triggered apoptosis in a subset of the Saos-2 cells. This library should serve as a v...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650554</comments>
            <pubDate>Tue, 24 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5650554</guid>        </item>
        <item>
            <title>High frequency of Neuropeptide Y Leu7Pro polymorphism in an Iranian population and its association with coronary artery disease.</title>
            <link>http://www.medworm.com/index.php?rid=5650549&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22289186%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: The frequency of Leu7Pro polymorphism of NPY was 5.9% in our Iranian population; higher than reported for other Asian populations. The Leu7Pro polymorphism was associated with CAD in an Iranian population.
    PMID: 22289186 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650549</comments>
            <pubDate>Tue, 24 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5650549</guid>        </item>
        <item>
            <title>Association between the catechol-O-methyltransferase (rs4680: Val158Met) polymorphism and serum alanine aminotransferase activity.</title>
            <link>http://www.medworm.com/index.php?rid=5650548&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22293393%26dopt%3DAbstract</link>
            <description>Authors: Hiyoshi M, Uemura H, Arisawa K, Nakamoto M, Hishida A, Okada R, Matsuo K, Kita Y, Niimura H, Kuriyama N, Nanri H, Ohnaka K, Suzuki S, Mikami H, Kubo M, Tanaka H, Hamajima N, 
    Abstract
    In our previous proteomic study in rat liver damaged by carbon tetrachloride, soluble catechol-O-methyltransferase (COMT) increased as a phosphorylated form and decreased as a dephosphorylated form. This finding raised the possibility that the COMT protein is associated with liver function. Thus, we hypothesized that (1) the COMT gene contributes to liver homeostasis and (2) a COMT polymorphism (rs4680: Val158Met) causing thermolability of enzymatic activity affects liver enzymes (e.g., aspartate aminotransferase (AST), alanine aminotransferase (ALT) and gamma-glutamyl transpeptidase (γ-GT))...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650548</comments>
            <pubDate>Tue, 24 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5650548</guid>        </item>
        <item>
            <title>Molecular characterization and expression profiles of MaCOL1, a CONSTANS-like gene in banana fruit.</title>
            <link>http://www.medworm.com/index.php?rid=5650556&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22285923%26dopt%3DAbstract</link>
            <description>Authors: Chen J, Chen JY, Wang JN, Kuang JF, Shan W, Lu WJ
    Abstract
    CONSTANS (CO) gene is a key transcription regulator that controls the long-day induction of flowering in Arabidopsis plant. However, CO gene involved in fruit ripening and stress responses is poorly understood. In the present study, a novel cDNA encoding CONSTANS-like gene, designated as MaCOL1 was isolated and characterized from banana fruit. The full length cDNA sequence was 1887bp with an open reading frame (ORF) of 1242bp, encoding 414 amino acids with a molecular weight of 46.20kDa and a theoretical isoelectric point of 5.40. Sequence alignment showed that MaCOL1 contained two B-box zinc finger motifs and a CCT domain. In addition, MaCOL1 showed transcriptional activity in yeast and was a nucleus-localized pro...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650556</comments>
            <pubDate>Fri, 20 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5650556</guid>        </item>
        <item>
            <title>Cytogenomic characterization of an unexpected 17.6Mb 9p deletion associated to a 14.8Mb 20p duplication in a dysmorphic patient with multiple congenital anomalies presenting a normal G-banding karyotype.</title>
            <link>http://www.medworm.com/index.php?rid=5650552&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22285927%26dopt%3DAbstract</link>
            <description>This study also shows the relevance of using molecular techniques to make an accurate diagnosis in patients with dysmorphic features and multiple anomalies suggestive of chromosome aberration, even if on G-banding their karyotype appears to be normal. Fluorescence in situ hybridization (FISH) was necessary to identify a masked balanced translocation in the patient's mother, indicating the importance of associating cytogenetic and molecular techniques in clinical genetics, given the implications for patient management and genetic counseling.
    PMID: 22285927 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650552</comments>
            <pubDate>Fri, 20 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5650552</guid>        </item>
        <item>
            <title>Long non-coding RNA UCA1 regulated cell cycle distribution via CREB through PI3-K dependent pathway in bladder carcinoma cells.</title>
            <link>http://www.medworm.com/index.php?rid=5650551&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22285928%26dopt%3DAbstract</link>
            <description>Authors: Yang C, Li X, Wang Y, Zhao L, Chen W
    Abstract
    Long non-coding RNA urothelial carcinoma associated 1 (UCA1) promotes human bladder cancer cell proliferation, but the underlying mechanism remains unknown. After knocking down of UCA1 in BLZ-211 cells, several cell cycle-related genes (CDKN2B, EP300 and TGFβ-2) were screened by microarray assay and validated by real-time PCR. Interestingly, in western blot analysis, p300 (encoded by EP300) and its coactivator cAMP response element-binding protein (CREB) level were significantly down-regulated. Both suppression of UCA1 expression by shRNA in BLZ-211 cells and ectopic expression of UCA1 in UMUC-2 cells showed that UCA1 alteration paralleled to the expression and phosphorylation of CREB, and UCA1 obviously influenced AKT express...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650551</comments>
            <pubDate>Fri, 20 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5650551</guid>        </item>
        <item>
            <title>Venom evolution through gene duplications.</title>
            <link>http://www.medworm.com/index.php?rid=5650558&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22285376%26dopt%3DAbstract</link>
            <description>Authors: Wong ES, Belov K
    Abstract
    Venoms contain highly complex mixtures that typically include hundreds of different components and have evolved independently in a diverse range of animals including platypuses, shrews, snakes, lizards, fishes, echinoderms, spiders, wasps, centipedes, sea snails, cephalopods, jellyfish and sea anemones. Many venom genes evolved through gene duplication. Gene duplication occurs in all domains of life and provides the raw substrate from which novel function arise. In this review, we focus on the role that gene duplication has played in the origin and diversification of venom genes. We outline the selective advantages of venom gene duplicates and the role that selection has played in the retention of these duplicates. We use toxin gene intermediates ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650558</comments>
            <pubDate>Wed, 18 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5650558</guid>        </item>
        <item>
            <title>Structural biology of the chromodomain: Form and function.</title>
            <link>http://www.medworm.com/index.php?rid=5650555&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22285924%26dopt%3DAbstract</link>
            <description>Authors: Eissenberg JC
    Abstract
    The chromodomain motif is found among certain chromosomal proteins of all eukaryotes. The chromodomain fold - three beta strands packed against a C-terminal alpha helix - mediates protein-protein and/or protein-nucleic acid interactions. In some cases, the affinity of chromodomain binding is regulated by lysine methylation, which appears to target chromodomain proteins and associated complexes to specific sites in chromatin. In this review, our current knowledge of chromodomain structure and function is summarized.
    PMID: 22285924 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650555</comments>
            <pubDate>Wed, 18 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5650555</guid>        </item>
        <item>
            <title>A 40-bp insertion/deletion polymorphism in the constitutive promoter of MDM2 confers risk for hepatocellular carcinoma in a Chinese population.</title>
            <link>http://www.medworm.com/index.php?rid=5650553&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22285926%26dopt%3DAbstract</link>
            <description>Authors: Dong D, Gao X, Zhu Z, Yu Q, Bian S, Gao Y
    Abstract
    The pathogenesis of HCC is a multistage process with the involvement of genetic factors. The aim of the present study is to investigate the possible association between a 40-bp insertion/deletion polymorphism (indel) at constitutive promoter of MDM2 and risk of hepatocellular carcinoma (HCC) in a Chinese population. Using 420 HCC patients and 423 control subjects, we genotyped the indel polymorphism (rs3730485) using polymerase chain reaction method. Logistic regression was used to analyze the association between the polymorphism and HCC susceptibility. Under co-dominant model, we found that the ins/del and del/del genotype of indel was associated with a significantly increased risk of HCC compared with its homozygote ins/...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650553</comments>
            <pubDate>Wed, 18 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5650553</guid>        </item>
        <item>
            <title>Vanishing white matter disease caused by EIF2B2 mutation with the presentation of an adrenoleukodystrophy phenotype.</title>
            <link>http://www.medworm.com/index.php?rid=5650557&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22285377%26dopt%3DAbstract</link>
            <description>This report widens the clinical spectrum of VWMD and raises the possibility of an allele-specific association with adrenal insufficiency.
    PMID: 22285377 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5650557</comments>
            <pubDate>Tue, 17 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5650557</guid>        </item>
        <item>
            <title>Inactivation of the MSLNL gene encoding mesothelin-like protein during African great ape evolution.</title>
            <link>http://www.medworm.com/index.php?rid=5636004&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22265842%26dopt%3DAbstract</link>
            <description>Authors: Kim DW, Jeong S, Kim DS, Kim HS, Seo SB, Hahn Y
    Abstract
    Loss of gene function is implicated in the emergence of novel phenotypes during organism evolution. Here, we report the inactivation of the MSLNL gene encoding mesothelin-like protein in African great ape evolution. Human MSLNL has a nonsense mutation in exon 10 and two polymorphic mutations: a frameshift in exon 3 and a nonsense codon in exon 8. The gorilla gene also shows multiple deleterious mutations, including a premature stop codon, a deletion, and a splice site mutation. Molecular evolutionary analysis indicated relaxed selection pressure on MSLNL in African great ape lineages, which suggested that MSLNL might have become inactivated before the divergence of human, chimpanzee and gorilla. The mouse Mslnl gene ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5636004</comments>
            <pubDate>Sat, 14 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5636004</guid>        </item>
        <item>
            <title>Non-association of Crohn's disease with NOD2 gene variants in Moroccan patients.</title>
            <link>http://www.medworm.com/index.php?rid=5636003&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22266421%26dopt%3DAbstract</link>
            <description>CONCLUSION: This preliminary study shows no evidence association of NOD2 gene with Crohn's disease in the Moroccan population.
    PMID: 22266421 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5636003</comments>
            <pubDate>Sat, 14 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5636003</guid>        </item>
        <item>
            <title>Molecular characterization, tissue distribution and expression analysis of Interleukin-12 receptor β2 chain in sheep.</title>
            <link>http://www.medworm.com/index.php?rid=5636005&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22265841%26dopt%3DAbstract</link>
            <description>Authors: Meng X, Guo A, Gong W, Jia W, Luo X, Zhai J, Dou Y, Cai X
    Abstract
    Ovine β2 subunit of the interleukin (IL)-12 receptor (IL-12Rβ2) was cloned from mRNA preparation of mitogen-activated peripheral blood mononuclear cells (PBMCs). The complete coding sequence for ovine IL-12 Rβ2 was found to be 2586 nucleotides in length encoding 862-amino-acid residue protein. It showed 96.4% homology at the nucleotide level and 94.1% homology at the amino acid level with bovine IL-12 Rβ2. The ovine IL-12 Rβ2 subunit shares common structural and functional elements with their counterparts from the other species. Phylogenetic tree showed that ovine IL-12Rβ2 was clustered into the Artiodactyla group, together with those of cattle and pig, which was distinct from the other groups. Real-t...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5636005</comments>
            <pubDate>Thu, 12 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5636005</guid>        </item>
        <item>
            <title>The first mutations in the MYH gene reported in Moroccan colon cancer patients.</title>
            <link>http://www.medworm.com/index.php?rid=5636002&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22266422%26dopt%3DAbstract</link>
            <description>CONCLUSION: We report the first biallelic MYH mutations in four Moroccan patients with clinical criteria of MAP; three of them had colorectal cancer with attenuated polyposis. No MYH mutations were found in colorectal patients without polyposis. Despite the relatively small sample size of the current study, our findings suggest that the MAP is not a frequent cause of colon cancer in Morocco as we had expected, and the molecular analysis of MYH gene should be restricted to patients displaying the classical phenotype of MAP.
    PMID: 22266422 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5636002</comments>
            <pubDate>Tue, 10 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5636002</guid>        </item>
        <item>
            <title>Isolation and molecular characterisation of flavonoid 3'-hydroxylase and flavonoid 3', 5'-hydroxylase genes from a traditional Chinese medicinal plant, Epimedium sagittatum.</title>
            <link>http://www.medworm.com/index.php?rid=5617773&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22248626%26dopt%3DAbstract</link>
            <description>Authors: Huang W, Sun W, Wang Y
    Abstract
    The epimedii herb, a traditional Chinese medicinal plant, has significant pharmacological effects on human health. The bioactive components in the herb (Epimedium sagittatum (Sieb. et Zucc.) Maxim) are mainly prenylated flavonol glycosides, which are end-products of the flavonoid biosynthetic pathway. This has not been clearly elucidated until recently. The genes encoding flavonoid 3'-hydroxylase (F3'H) and flavonoid 3', 5'-hydroxylase (F3'5'H) involved in the flavonoid biosynthetic pathway, designated as EsF3'H and EsF3'5'H, were isolated from E. sagittatum using a homology-based cloning method and deposited in the GenBank databases (GenBank ID: HM011054 and HM011055), respectively. EsF3'H and EsF3'5'H proteins shared high homology with oth...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5617773</comments>
            <pubDate>Mon, 09 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5617773</guid>        </item>
        <item>
            <title>Associations of variants of CNR1 with obesity and obesity-related traits in Chinese women.</title>
            <link>http://www.medworm.com/index.php?rid=5617780&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22244745%26dopt%3DAbstract</link>
            <description>In conclusion, the rs2023239 and rs806381 polymorphisms of CNR1 were not associated with increased overweight and obesity risk. But the rs2023239 polymorphism was significantly associated with GPT, and the rs806381 polymorphism was significantly associated with TG.
    PMID: 22244745 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5617780</comments>
            <pubDate>Sun, 08 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5617780</guid>        </item>
        <item>
            <title>Differential requirement for the N-terminal catalytic domain of the DNA polymerase ε p255 subunit in the mitotic cell cycle and the endocycle.</title>
            <link>http://www.medworm.com/index.php?rid=5617777&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22245183%26dopt%3DAbstract</link>
            <description>Authors: Suyari O, Kawai M, Ida H, Yoshida H, Sakaguchi K, Yamaguchi M
    Abstract
    In Drosophila, the 255kDa catalytic subunit (dpolεp255) and the 58kDa subunit of DNA polymerase ε (dpolεp58) have been identified. The N-terminus of dpolεp255 carries well-conserved six DNA polymerase subdomains and five 3'→5' exonuclease motifs as observed with Polε in other species. We here examined roles of dpolεp255 during Drosophila development using transgenic fly lines expressing double stranded RNA (dsRNA). Expression of dpolεp255 dsRNA in eye discs induced a small eye phenotype and inhibited DNA synthesis, indicating a role in the G1-S transition and/or S-phase progression of the mitotic cycle. Similarly, expression of dpolεp255 dsRNA in the salivary glands resulted in small size and ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5617777</comments>
            <pubDate>Sun, 08 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5617777</guid>        </item>
        <item>
            <title>Genetic variants of TCF7L2 are associated with type 2 diabetes in a northeastern Chinese population.</title>
            <link>http://www.medworm.com/index.php?rid=5617774&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22245614%26dopt%3DAbstract</link>
            <description>In this study, an association of these two loci with T2D was investigated in a Harbin Chinese population. Whereas the two populations in the initial studies were southern Han Chinese, Harbin Chinese are from northeastern China. The SNPs rs290487 and rs11196218 were genotyped by ligase detection reactions in 700 T2D patients and 570 unrelated non-diabetic controls. Association analyses, which were carried out using the case-control sample set, yielded a significant association between rs290487 and T2D, with a trend opposite to that described in a previous report. Specifically, rs290487T was found to be significantly associated with disease susceptibility (p=0.039), and the allelic OR of rs290487T carriers was 1.184 (95% CI 1.008-1.391). There was no significant association between rs1119621...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5617774</comments>
            <pubDate>Sun, 08 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5617774</guid>        </item>
        <item>
            <title>Putative function of TAP63α during endochondral bone formation.</title>
            <link>http://www.medworm.com/index.php?rid=5617781&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22244744%26dopt%3DAbstract</link>
            <description>Authors: Li F, Lu Y, Ding M, Wu G, Sinha S, Wang S, Zheng Q
    Abstract
    P63, a member of the P53 tumor suppressor family, is known to play important functions in cancer and development. Interestingly, previous studies have shown that p63 null mice are absent or have truncated limbs, while mutations in human P63 cause several skeletal syndromes that also show limb and digit abnormalities, suggesting its essential role in long bone development. Indeed, we detected increased level of p63 transcript in hypertrophic MCT cells (an established cell model of chondrocyte maturation) than in proliferative MCT cells. To investigate the in vivo role of P63 upon endochondral bone formation, we have established transgenic mouse lines in which HA- and Flag-tagged TAP63α (the longest P63 isoform) is...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5617781</comments>
            <pubDate>Thu, 05 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5617781</guid>        </item>
        <item>
            <title>Integrated analysis of mRNA and microRNA expression in mature neurons, neural progenitor cells and neuroblastoma cells.</title>
            <link>http://www.medworm.com/index.php?rid=5617779&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22244746%26dopt%3DAbstract</link>
            <description>Authors: Liu DZ, Ander BP, Tian Y, Stamova B, Jickling G, Davis RR, Sharp FR
    Abstract
    Mature neurons (MNs), neural progenitor cells (NPCs) and neuroblastoma cells (NBCs) are all neural-derived cells. However, MNs are unable to divide once differentiated; NPCs are able to divide a limited number of times and differentiate to normal brain cell types; whereas NBCs can divide an unlimited number of times but rarely differentiate. Here, we perform whole transcriptome (mRNA, miRNA) profiling of these cell types and compare expression levels of each cell type to the others. Integrated mRNA-miRNA functional analyses reveal that: 1) several very highly expressed genes (e.g., Robo1, Nrp1, Epha3, Unc5c, Dcc, Pak3, Limk4) and a few under-expressed miRNAs (e.g., miR-152, miR-146b, miR-339-5p) i...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5617779</comments>
            <pubDate>Thu, 05 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5617779</guid>        </item>
        <item>
            <title>Associations between two novel rSNPs in 5'-flanking region of the bovine casein gene cluster and milk performance traits.</title>
            <link>http://www.medworm.com/index.php?rid=5617778&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22245182%26dopt%3DAbstract</link>
            <description>Authors: Fomichev KA, Sazanova AL, Malewski T, Kaminski S, Sazanov AA
    Abstract
    Ten evolutionary conservative sequences with high identity level to homological sequences in other mammal species were revealed in 5'-flanking region of casein's genes cluster. Five novel SNPs located inside of the evolutionary conservative regions were identified. The binding sites were revealed to be present in one allelic variant of four detected SNPs. So these SNPs were considered as rSNPs. Significant differences of allelic frequencies were revealed between beef cow's group and dairy cow's group in two rSNPs (NCE4, NCE7, p&amp;lt;0.001). Different alleles of those two rSNPs were shown to be associated with some milk performance traits in Black-and-White Holstein dairy cows. Significant difference of pro...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5617778</comments>
            <pubDate>Thu, 05 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5617778</guid>        </item>
        <item>
            <title>Assessment of phylogenetic inter-relationships in the genus Cymbidium (Orchidaceae) based on internal transcribed spacer region of rDNA.</title>
            <link>http://www.medworm.com/index.php?rid=5617776&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22245612%26dopt%3DAbstract</link>
            <description>This study validates the utility of ITS rDNA region as a reliable indicator of phylogenetic relationships, especially ITS 2 as probable DNA barcode at higher levels and can serve as an additional approach for identification of broader range of plant taxa especially orchids.
    PMID: 22245612 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5617776</comments>
            <pubDate>Thu, 05 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5617776</guid>        </item>
        <item>
            <title>BsmI polymorphisms in vitamin D receptor gene are associated with diabetic nephropathy in type 2 diabetes in the Han Chinese population.</title>
            <link>http://www.medworm.com/index.php?rid=5617775&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22245613%26dopt%3DAbstract</link>
            <description>Authors: Zhang H, Wang J, Yi B, Zhao Y, Liu Y, Zhang K, Cai X, Sun J, Huang L, Liao Q
    Abstract
    We investigated the relationship between BsmI/ApaI polymorphisms in vitamin D receptor gene and diabetic nephropathy in a Han Chinese population. PCR-restriction fragment length polymorphism was used to test the genotype and allele frequency of BsmI and ApaI polymorphisms in 304 patients with type 2 diabetes mellitus (DM group) and 100 control individuals (ND group). The DM group was further divided into DN0 (no diabetic nephropathy), DN1 (diabetes with small amount of albuminuria), DN2 (diabetes with large amount of albuminuria), L/NDN (late-onset DN after 5years/no DN over the whole follow-up period of 5years) and EDN (early-onset diabetic nephropathy occurring within first year) subgro...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5617775</comments>
            <pubDate>Thu, 05 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5617775</guid>        </item>
        <item>
            <title>MCPH1/BRIT1 represses transcription of the human telomerase reverse transcriptase gene.</title>
            <link>http://www.medworm.com/index.php?rid=5594103&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22240313%26dopt%3DAbstract</link>
            <description>In this study, to determine the mechanism by which MCPH1 regulates hTERT gene expression, we examined the role of MCPH1 in regulating the hTERT promoter in vitro. Co-transfection of the hTERT promoter with MCPH1 in Hela cells could inhibit the hTERT promoter activity. The EMSA assay demonstrated that MCPH1 could bind to the proximal hTERT promoter. Overexpression of MCPH1 could repress telomerase activity, and the repression was abolished by knocking down the MCPH1 expression using siRNA in U2OS cells. We propose that MCPH1 functions as a transcriptional repressor of hTERT in vitro. Since the activation of telomerase, widely observed in human tumor cell lines, is a critical step in tumorigenesis, our findings provide new insights into delineating the tumor-suppressing function of MCPH1 thr...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5594103</comments>
            <pubDate>Thu, 05 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5594103</guid>        </item>
        <item>
            <title>Association of genetic variants of fibrinolytic system with stroke and stroke subtypes.</title>
            <link>http://www.medworm.com/index.php?rid=5594102&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22240314%26dopt%3DAbstract</link>
            <description>Authors: Babu MS, Prabha TS, Kaul S, Al-Hazzani A, Shafi G, Roy S, Balakrishna N, Jyothy A, Munshi A
    Abstract
    Genetic variants of tPA (PLAT) and PAI-1 genes have been suggested to be the risk factors for stroke. In the present case-control study we investigated the association of -7351C/T polymorphism (rs2020918) and I/D polymorphism of tPA gene and Insertion/deletion polymorphism (4G/5G) of PAI-1 gene with genetic predisposition to ischemic stroke. 516 stroke patients and 513, sex and age matched healthy controls were involved in the study. We did not find a significant association of tPA -7351C/T polymorphism and PAI-1 4G/5G polymorphism with stroke. However, in case of I/D polymorphism significant difference was observed in the genotypic distribution and allelic frequency betwee...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5594102</comments>
            <pubDate>Thu, 05 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5594102</guid>        </item>
        <item>
            <title>Molecular cloning, tissue expression and protein structure prediction of the porcine 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGR) gene.</title>
            <link>http://www.medworm.com/index.php?rid=5594101&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22240315%26dopt%3DAbstract</link>
            <description>Authors: Chen X, Wang X, Li Z, Kong L, Liu G, Fu J, Wang A
    Abstract
    3-hydroxy-3-methylglutaryl-Coenzyme A reductase (HMGR) is the rate-limiting enzyme for cholesterol synthesis. Its activity is regulated via a negative feedback mechanism through sterols and non-sterol metabolites derived from mevalonate, the product of the reaction catalyzed by reductase. Here, we cloned a full-length transcript of porcine HMGR by RT-PCR and RACE. The porcine HMGR cDNA (2864bp,GenBank accession no. DQ432054) contains a 2658bp open reading frame and shares 91% identify with those of human and cattle, and 85%, 85% and 84% identify with the HMGR coding sequences of Norway rat, golden hamster, and house mouse, respectively. The deduced porcine HMGR protein consists of 885 amino acids with a calculated ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5594101</comments>
            <pubDate>Thu, 05 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5594101</guid>        </item>
        <item>
            <title>Nanostructure and β1-integrin distribution analysis of pig's spermatogonial stem cell by atomic force microscopy.</title>
            <link>http://www.medworm.com/index.php?rid=5594107&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22237019%26dopt%3DAbstract</link>
            <description>In this study, atomic force microscopy (AFM) was used to obtain the morphology and ultrastructure of SSCs at nanometer level, and the CD29 Ab-functionalized AFM tip was used to examine β1-integrin distribution on the cell membrane. There were many force-binding spots on about 50% of cell membrane binding to the CD29 Ab-functionalized AFM tip, and the mean bind rupture force was 283.63±12.56PN which was much larger than the non-specific average force 70.75±10.95PN. Meanwhile, β1-integrin on SSCs membrane was distributed non-uniformly, and there were some β1-integrins appeared to be expressed as 150-350nm nanoclusters on the membrane. Our results discovered the structure of SSCs at nanometer level by AFM. The force between β1-integrin antigen-antibody interactions and the distribution ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5594107</comments>
            <pubDate>Tue, 03 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5594107</guid>        </item>
        <item>
            <title>Polymorphism T→C of gene CYP17 promoter and polycystic ovary syndrome risk: A meta-analysis.</title>
            <link>http://www.medworm.com/index.php?rid=5594106&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22237020%26dopt%3DAbstract</link>
            <description>We examined the association by performing a meta-analysis. Two investigators independently searched the Medline, Embase, CNKI, and Chinese Biomedicine Databases. Summary odds ratios (ORs) and 95% confidence intervals (95% CIs) for CYP17 polymorphism and PCOS were calculated in a fixed-effects model and a random-effects model when appropriate. The pooled ORs were performed for co-dominant model (CC vs. TT, TC vs. TT), dominant model (CC+TC vs. TT), and recessive model (CC vs. TC+TT). Subgroup analyses were performed by ethnicity, country, Hardy-Weinberg equilibrium (HWE) in controls and study sample size. This meta-analysis included 10 case-control studies, which included 1321 PCOS cases and 1017 controls. Overall, the variant genotypes (CC and TC) were not associated with PCOS risk, compar...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5594106</comments>
            <pubDate>Tue, 03 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5594106</guid>        </item>
        <item>
            <title>High resolution array in the clinical approach to chromosomal phenotypes.</title>
            <link>http://www.medworm.com/index.php?rid=5594105&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22240311%26dopt%3DAbstract</link>
            <description>We report our experience in the clinical diagnostic use of high resolution AGH up to 100kb on 131 patients with chromosomal phenotypes but previously normal karyotype. We evaluated the usefulness in our clinics and laboratories by the detection rate of causal CNVs and CNVs of unknown clinical significance and to what extent their interpretation would challenge the systematic use of high-resolution arrays in clinical application. Prioritizing phenotype-genotype correlation in our interpretation strategy to criteria previously described, we identified 33 (25.2%) potentially pathogenic aberrations. 16 aberrations were confirmed pathogenic (16.4% syndromic, 8.5% non-syndromic patients); 9 were new and individual aberrations, 3 of them were pathogenic although inherited and one is as small as a...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5594105</comments>
            <pubDate>Tue, 03 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5594105</guid>        </item>
        <item>
            <title>Evolutionary analysis of prokaryotic heat-shock transcription regulatory protein σ(32).</title>
            <link>http://www.medworm.com/index.php?rid=5594104&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22240312%26dopt%3DAbstract</link>
            <description>This study therefore may help in elucidating the hitherto unknown molecular mechanism of the functionalities of σ(32)family of proteins.
    PMID: 22240312 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5594104</comments>
            <pubDate>Tue, 03 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5594104</guid>        </item>
        <item>
            <title>Functional analysis of cus operon promoter of Klebsiella pneumoniae using E. coli lacZ assay.</title>
            <link>http://www.medworm.com/index.php?rid=5594110&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22230226%26dopt%3DAbstract</link>
            <description>Authors: Zahid N, Zulfiqar S, Shakoori AR
    Abstract
    The transcriptional fusion of reporter lacZ gene with cusRS regulatory promoter of cus operon of Klebsiella pneumoniae enabled us to analyze the inductive effect of copper on promoter via lacZ assay. The stimulus response curve of promoter to a range of copper metal concentrations indicated a normal sigmoidal response profile with apparent Hill coefficient 1.0. There was a positive correlation of promoter response to the increasing concentration of copper in the medium. AC(50) value of copper was calculated to be 1mM, whereas the promoter response was exponential beyond 1mM and up to 2.5mM concentration. The promoter activity did not increase exponentially in copper concentration higher than 2.5mM. The promoter PcusRS requires two ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5594110</comments>
            <pubDate>Sat, 31 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5594110</guid>        </item>
        <item>
            <title>Molecular differentiation of Chenopodium album complex and some related species using ISSR profiles and ITS sequences.</title>
            <link>http://www.medworm.com/index.php?rid=5594108&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22233894%26dopt%3DAbstract</link>
            <description>Authors: Rana TS, Narzary D, Ohri D
    Abstract
    The present study was undertaken to understand the genetic differentiation and relationships in various components of C. album complex, C. giganteum and some related species using inter simple sequence repeats (ISSR) profiles and internal transcribed spacer (ITS) sequences. The relationships based on UPGMA dendrograms have shown the heterogenous nature of C. album complex. The 2x taxa while showing close relation among themselves are sharply segregated from 4x and 6x taxa belonging to C. album and C. giganteum. Among the three cytotypes from North Indian plains the 4x shows greater similarity to 6x than to 2x which is corroborated by the karyotypic studies. Furthermore, the 6x C. album and C. giganteum accessions of American and European...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5594108</comments>
            <pubDate>Sat, 31 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5594108</guid>        </item>
        <item>
            <title>Recombinant lactoferrin (Lf) of Vechur cow, the critical breed of Bos indicus and the Lf gene variants.</title>
            <link>http://www.medworm.com/index.php?rid=5594111&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22230225%26dopt%3DAbstract</link>
            <description>Authors: Anisha S, Bhasker S, Mohankumar C
    Abstract
    Vechur cow, categorized as a critically maintained breed by the FAO, is a unique breed of Bos indicus due to its extremely small size, less fodder intake, adaptability, easy domestication and traditional medicinal property of the milk. Lactoferrin (Lf) is an iron-binding glycoprotein that is found predominantly in the milk of mammals. The full coding region of Lf gene of Vechur cow was cloned, sequenced and expressed in a prokaryotic system. Antibacterial activity of the recombinant Lf showed suppression of bacterial growth. To the best of our knowledge this is the first time that the full coding region of Lf gene of B. indicus Vechur breed is sequenced, successfully expressed in a prokaryotic system and characterized. Comparative...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5594111</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5594111</guid>        </item>
        <item>
            <title>Genetic polymorphism of MMP family and coronary disease susceptibility: A meta-analysis.</title>
            <link>http://www.medworm.com/index.php?rid=5594120&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22226810%26dopt%3DAbstract</link>
            <description>Authors: Li M, Shi J, Fu L, Wang H, Zhou B, Wu X
    Abstract
    The issue that genetic polymorphism of matrix metalloproteinase (MMP) family is in association with coronary disease is controversial. So we did a meta-analysis to clarify it clearly. We made a literature search of PubMed, the Web of Science, and Cochrane Collaboration's database to identify eligible reports. The methodological quality of each included studies was assessed. We calculated the pooled ORs with their 95%CI for each genetic polymorphism in STATA 11 software. Separate analysis was performed to address the consistency of results across the subgroup with different continents. A total of 39 studies were included, with a sample of 42269 individuals. This meta-analysis provided evidence that genetic polymorphism of MMP...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5594120</comments>
            <pubDate>Thu, 29 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5594120</guid>        </item>
        <item>
            <title>Molecular regulation of catechins biosynthesis in tea (Camellia sinensis (L.) O. Kuntze).</title>
            <link>http://www.medworm.com/index.php?rid=5594119&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22226811%26dopt%3DAbstract</link>
            <description>The objective of the work was to clone and analyze these genes so as to generate a comprehensive knowledge on the critical genes of catechins biosynthesis pathway. Gene expression analysis was carried out in response to leaf age and external cues (drought stress, abscisic acid, gibberellic acid treatments and wounding). A holistic analysis suggested that CsCHI, CsF3H, CsDFR, CsANS and CsANR were amongst the critical regulatory genes in regulating catechins content.
    PMID: 22226811 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5594119</comments>
            <pubDate>Thu, 29 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5594119</guid>        </item>
        <item>
            <title>The soybean aldehyde dehydrogenase (ALDH) protein superfamily.</title>
            <link>http://www.medworm.com/index.php?rid=5594118&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22226812%26dopt%3DAbstract</link>
            <description>Authors: Kotchoni SO, Jimenez-Lopez JC, Kayodé AP, Gachomo EW, Baba-Moussa L
    Abstract
    Aldehyde dehydrogenases (ALDHs) are members of NAD(P)(+)-dependent protein superfamily that catalyze the oxidation of a wide range of endogenous and exogenous highly reactive aliphatic and aromatic aldehyde molecules to their corresponding non toxic carboxylic acids. Research evidence has shown that ALDHs represent a promising class of genes to improve growth development, seed storage and environmental stress adaptation in higher plants. The recently completed genome sequences of several plant species have resulted in the identification of a large number of ALDH genes, most of which still need to be functionally characterized. In this paper, we identify members of the ALDH gene superfamily in soy...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5594118</comments>
            <pubDate>Thu, 29 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5594118</guid>        </item>
        <item>
            <title>Association study of microRNA polymorphisms with risk of idiopathic recurrent spontaneous abortion in Korean women.</title>
            <link>http://www.medworm.com/index.php?rid=5594121&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22222140%26dopt%3DAbstract</link>
            <description>CONCLUSION: miR-196a2CC, miR-499AG+GG, and the miR-196a2CC/miR-499AG+GG combination are significantly associated with idiopathic RSA in Korean women.
    PMID: 22222140 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5594121</comments>
            <pubDate>Wed, 28 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5594121</guid>        </item>
        <item>
            <title>Molecular cloning and characterization of the sheep α-TTP gene and its expression in response to different vitamin E status.</title>
            <link>http://www.medworm.com/index.php?rid=5594117&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22227492%26dopt%3DAbstract</link>
            <description>In this study, the full-length cDNA of sheep α-TTP gene was cloned from sheep liver by using of rapid amplification of complementary DNA ends (RACE). As a result, the sheep α-TTP gene was 1098bp in nucleotide which contained 23bp 5'-untranslated region (UTR), 226bp 3'-UTR and 849bp open reading frame (ORF) that encoded a basic protein of 282 amino acids. Further bioinformatic analysis indicated that the sheep α-TTP gene had a high homologous of both nucleotide and amino acid sequences compared with that of other species and had a Sec14p-like lipid-binding domain which called the CRAL-TRIO domain. Moreover, the expression of sheep α-TTP mRNA and protein in response to different vitamin E supplemented levels were observed according to quantitative real-time PCR (qRT-PCR) and Western blot...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5594117</comments>
            <pubDate>Wed, 28 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5594117</guid>        </item>
        <item>
            <title>Arbuscular mycorrhizal protein mRNA over-expression in bread wheat seedlings by Trichoderma harzianum Raifi (KRL-AG2) elicitation.</title>
            <link>http://www.medworm.com/index.php?rid=5594116&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22227493%26dopt%3DAbstract</link>
            <description>Authors: Al-Asbahi AA
    Abstract
    Association between arbuscular mycorrhizal fungi (AMF) and majority of terrestrial plant species provides many benefits to plants that range from stress alleviation and bioremediation in soils polluted with heavy metals to plant growth promotion and yield quantity. Some non-arbuscular mycorrhizal fungi such as, Trichoderma harzianum, are known to enhance the AMF symbiosis with vascular plants. However, information about their role in AMF symbiosis is still limited. Shoots of (Avocet S) wheat seedlings were sprayed with the fungal culture filtrate and gene expression patterns were analyzed in the treated tissues. An increase in the level of mRNA of arbuscular mycorrhizal protein comparing with control was found. The over-expression of this protein in w...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5594116</comments>
            <pubDate>Wed, 28 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5594116</guid>        </item>
        <item>
            <title>The Bxb1 gp47 recombination directionality factor is required not only for prophage excision, but also for phage DNA replication.</title>
            <link>http://www.medworm.com/index.php?rid=5594115&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22227494%26dopt%3DAbstract</link>
            <description>Authors: Savinov A, Pan J, Ghosh P, Hatfull GF
    Abstract
    Mycobacteriophage Bxb1 encodes a serine-integrase that catalyzes both integrative and excisive site-specific recombination. However, excision requires a second phage-encoded protein, gp47, which serves as a recombination directionality factor (RDF). The viability of a Bxb1 mutant containing an S153A substitution in gp47 that eliminates the RDF activity of Bxb1 gp47 shows that excision is not required for Bxb1 lytic growth. However, the inability to construct a Δ47 deletion mutant of Bxb1 suggests that gp47 provides a second function that is required for lytic growth, although the possibility of an essential cis-acting site cannot be excluded. Characterization of a mutant prophage of mycobacteriophage L5 in which gene 54 - a h...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5594115</comments>
            <pubDate>Wed, 28 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5594115</guid>        </item>
        <item>
            <title>Identification of a novel isoform of DHRS4 protein with a nuclear localization signal.</title>
            <link>http://www.medworm.com/index.php?rid=5594114&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22227495%26dopt%3DAbstract</link>
            <description>This study identifies the alternative transcript variant NRDRA2 encoding a subcellular nuclear localized NRDRA2 protein.
    PMID: 22227495 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5594114</comments>
            <pubDate>Wed, 28 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5594114</guid>        </item>
        <item>
            <title>Regulation of gene transcription by the oncoprotein MYC.</title>
            <link>http://www.medworm.com/index.php?rid=5594112&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22227497%26dopt%3DAbstract</link>
            <description>Authors: Lüscher B, Vervoorts J
    Abstract
    The proteins of the MYC/MAX/MAD network are central regulators of many key processes associated with basic cell physiology. These include the regulation of protein biosynthesis, energy metabolism, proliferation, and apoptosis. Molecularly the MYC/MAX/MAD network achieves these broad activities by controlling the expression of many target genes, which are primarily responsible for the diverse physiological consequences elicited by the network. The MYC proteins of the network possess oncogenic activity and their functional deregulation is associated with the majority of human tumors. Over the last years we have witnessed the accumulation of a considerable number of molecular observations that suggest many different biochemical means and tools...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5594112</comments>
            <pubDate>Wed, 28 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5594112</guid>        </item>
        <item>
            <title>Differences in mtDNA whole sequence between Tibetan and Han populations suggesting adaptive selection to high altitude.</title>
            <link>http://www.medworm.com/index.php?rid=5594109&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22233893%26dopt%3DAbstract</link>
            <description>Authors: Gu M, Dong X, Shi L, Shi L, Lin K, Huang X, Chu J
    Abstract
    We performed a mitochondrial whole-genome comparison study in 40 Tibetan and 50 Han Chinese. All subjects could be classified into 13 haplogroups pertained to the Macrohaplogroup M and N that pitched different quadrants by principal component analysis. We observed a difference in the M9 haplogroup and identified 18 significant variants by comparing whole sequences between Tibetan and Han populations. Variants in ND2, COX2, tRNA alanine and 12S rRNA were predicted to confer increased protein stability in Tibetans. We compared the base substitutions of nonsynonymous (NS) versus synonymous (S) of 13 protein-encoding genes and found the NS/S values of the ATP6, ATP8, and Cyt b genes were larger (&amp;gt;1) in Tibetans than...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5594109</comments>
            <pubDate>Wed, 28 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5594109</guid>        </item>
        <item>
            <title>&quot;Delayed death&quot; phenomenon: A synergistic action of cyclophosphamide and exogenous DNA.</title>
            <link>http://www.medworm.com/index.php?rid=5594113&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22227496%26dopt%3DAbstract</link>
            <description>&quot;Delayed death&quot; phenomenon: A synergistic action of cyclophosphamide and exogenous DNA.
    Gene. 2011 Dec 27;
    Authors: Dolgova EV, Proskurina AS, Nikolin VP, Popova NA, Alyamkina EA, Orishchenko KE, Rogachev VA, Efremov YR, Dubatolova TD, Prokopenko AV, Chernykh ER, Ostanin AA, Taranov OS, Omigov VV, Zagrebelniy SN, Bogachev SS, Shurdov MA
    Abstract
    Morbidity and mortality in mice were observed upon administration of exogenous DNA following their pre-treatment with a cytostatic agent cyclophosphamide. Upon intraperitoneal injections, the fragments of exogenous DNA reached bone marrow cells. These cells were also found to internalize up to 1800kb of exogenous DNA ex vivo. The 18-24h time frame represents a final stage in the repair of DNA double-strand breaks, so when exogenous ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5594113</comments>
            <pubDate>Tue, 27 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5594113</guid>        </item>
        <item>
            <title>Association of myostatin gene polymorphisms with obesity in Chinese north Han human subjects.</title>
            <link>http://www.medworm.com/index.php?rid=5574842&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22209717%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Our data firstly suggest that genetic variant rs3791783 A/G in myostatin gene are associated with obesity. The A allele carriers in rs3791783 SNP have an increased susceptibility to obesity compared with the G allele carriers. Participants with AA genotype in rs3791783 SNP site will have higher risk suffered from overweight or obesity than those with GG genotype.
    PMID: 22209717 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5574842</comments>
            <pubDate>Sat, 24 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5574842</guid>        </item>
        <item>
            <title>A homemade MLPA assay detects known CTNS mutations and identifies a novel deletion in a previously unresolved cystinosis family.</title>
            <link>http://www.medworm.com/index.php?rid=5574841&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22209718%26dopt%3DAbstract</link>
            <description>Authors: Kiehntopf M, Varga RE, Koch HG, Beetz C
    Abstract
    Infantile nephropatic cystinosis is a rare, recessive, and genetically homogeneous disorder impairing renal function. It is caused by mutations in CTNS. Several large copy number aberrations have been identified but, for the majority of these, heterozygous patients and carriers can not easily be identified. We therefore developed a multiplex ligation-dependent probe amplification assay targeting eight of the twelve CTNS exons. We show that this assay is valid in detecting known deletions in both the homozygous and heterozygous state. The application to a family previously found mutation-negative by conventional screening revealed a novel large deletion which, as the first of its kind, does not involve the coding region. We c...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5574841</comments>
            <pubDate>Sat, 24 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5574841</guid>        </item>
        <item>
            <title>A high-throughput apple SNP genotyping platform using the GoldenGate™ assay.</title>
            <link>http://www.medworm.com/index.php?rid=5574840&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22209719%26dopt%3DAbstract</link>
            <description>Authors: Khan MA, Han Y, Zhao YF, Korban SS
    Abstract
    EST data generated from 14 apple genotypes were downloaded from NCBI and mapped against a reference EST assembly to identify Single Nucleotide Polymorphisms (SNPs). Mapping of these SNPs was undertaken using 90% of sequence similarity and minimum coverage of four reads at each SNP position. In total, 37,807 SNPs were identified with an average of one SNP every 187bp from a total of 6888 unique EST contigs. Identified SNPs were checked for flanking sequences of ≥60bp along both sides of SNP alleles for reliable design of a custom high-throughput genotyping assay. A total of 12,299 SNPs, representing 6525 contigs, fit the selected criterion of ≥60bp sequences flanking a SNP position. Of these, 1411 SNPs were validated using fou...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5574840</comments>
            <pubDate>Sat, 24 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5574840</guid>        </item>
        <item>
            <title>Impaired DNA repair and genomic stability in hereditary tyrosinemia type 1.</title>
            <link>http://www.medworm.com/index.php?rid=5574836&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22209984%26dopt%3DAbstract</link>
            <description>Authors: van Dyk E, Pretorius PJ
    Abstract
    The autosomal recessive disorder, hereditary tyrosinemia type 1 (HT1), is caused by a defective fumarylacetoacetate hydrolase enzyme. Consequently intermediate metabolites such as fumarylacetoacetate, succinylacetone and p-hydroxyphenylpyruvic acid accumulate. Characteristic to HT1 is the development of hepatocellular carcinoma, irrespective of dietary intervention or pharmacological treatment. Carcinogenesis may occur through a chromosomal instability mutator phenotype or a microsatellite instability phenotype, and deficient DNA repair may be a contributing factor thereof. The purpose of this study was to investigate the expression of DNA repair proteins, and the possible occurrence of microsatellite instability in HT1. Gene expression ana...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5574836</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5574836</guid>        </item>
        <item>
            <title>The complete mitochondrial genome of Gomphocerus tibetanus Uvarov, 1935 (Orthoptera: Acrididae: Gomphocerinae).</title>
            <link>http://www.medworm.com/index.php?rid=5574839&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22209720%26dopt%3DAbstract</link>
            <description>Authors: Yin H, Zhi Y, Jiang H, Wang P, Yin X, Zhang D
    Abstract
    The complete nucleotide sequence of the mitochondrial genome (mitogenome) of Gomphocerus tibetanus Uvarov, 1935 (Orthoptera: Acrididae: Gomphocerinae) was determined. It is 15,571bp in length and contains 74.8% A+T. All Gomphocerus tibetanus protein-coding sequences start with a typical ATN codon. The usual termination codons (TAA and TAG) were found from 13 PCGs except COI and COII which took incomplete codon T as termination codons. All tRNA genes could be folded into the typical cloverleaf secondary structure, except tRNA(Ser(AGN)) lacking of dihydrouridine (D) arm. The sizes of the large and small ribosomal RNA genes are 1313 and 822bp, respectively. The A+T content of the A+T-rich region is 82.3%. A preliminary an...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5574839</comments>
            <pubDate>Thu, 22 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5574839</guid>        </item>
        <item>
            <title>Sequence variations and selection analysis of microRNA target genes involved in rice flower development.</title>
            <link>http://www.medworm.com/index.php?rid=5574838&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22209962%26dopt%3DAbstract</link>
            <description>Authors: Ling LZ
    Abstract
    The variation of key regulatory elements contributes to phenotypic diversity by altering the mechanism of gene regulation and selection operates more efficiently on them during evolution. Recently discovered microRNAs (miRNAs) are endogenous posttranscriptional repressors and play essential roles in diverse biological processes. Although genome-wide studies in animals and plants have identified candidate regions under selection, few attempts have been made, from the point of a biological process (e.g. plant flower development), to describe the regimes of selection on miRNA-associated motifs. Here I investigated the variation patterns of miRNA target sequences and characterized selection mechanisms by resequencing 31 miRNA targets involved in flower develop...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5574838</comments>
            <pubDate>Thu, 22 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5574838</guid>        </item>
        <item>
            <title>Role of luteinizing hormone β-subunit gene variants among South Indian women with polycystic ovary syndrome.</title>
            <link>http://www.medworm.com/index.php?rid=5574837&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22209983%26dopt%3DAbstract</link>
            <description>This study is first of its kind to study association of LH β-subunit gene variants with PCOS among South-Indian women. 250 PCOS cases and 299 controls were recruited for the study. All the exons of LH β gene were screened. Allele and genotype frequencies of the SNPs were compared between the cases and controls. We identified seven SNPs in the LH β gene; one SNP in exon 3 (rs#1056917) exhibited significant difference in the allele frequency between the PCOS cases and controls (p=0.015). Although, the LH β variants that are found to be more frequent among PCOS cases are silent in nature and not of any functional significance, they might influence other significant functional polymorphisms in the hypothalamic-pituitary-gonadal axis which needs to be explored.
    PMID: 22209983 [PubMed - ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5574837</comments>
            <pubDate>Tue, 20 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5574837</guid>        </item>
        <item>
            <title>Cloning and characterization of homeologous cellulose synthase catalytic subunit 2 genes from allotetraploid cotton (Gossypium hirsutum L.).</title>
            <link>http://www.medworm.com/index.php?rid=5557585&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22200568%26dopt%3DAbstract</link>
            <description>Authors: Kim HJ, Triplett BA, Zhang HB, Lee MK, Hinchliffe DJ, Li P, Fang DD
    Abstract
    Cellulose synthase catalytic subunits (CesAs) are the catalytic sites within a multisubunit complex for cellulose biosynthesis in plants. CesAs have been extensively studied in diploid plants, but are not well characterized in polyploid plants. Gossypium hirsutum is an allotetraploid cotton species producing over 90% of the world's cotton fibers. Although G. hirsutum CesAs (GhCesAs) are responsible for cellulose production in cotton fiber, very limited numbers of GhCesA genes have been identified. Here, we report isolating and characterizing a pair of homeologous CesA2 genes and their full-length cDNAs from allotetraploid cotton. The GhCesA2-A(T) gene from the A-subgenome and GhCesA2-D(T) gene fro...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5557585</comments>
            <pubDate>Tue, 20 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5557585</guid>        </item>
        <item>
            <title>Gender-specific methylation differences in relation to prenatal exposure to cigarette smoke.</title>
            <link>http://www.medworm.com/index.php?rid=5557584&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22202639%26dopt%3DAbstract</link>
            <description>Authors: Murphy SK, Adigun A, Huang Z, Overcash F, Wang F, Jirtle RL, Schildkraut JS, Murtha AP, Iversen ES, Hoyo C
    Abstract
    Epigenetic alterations may mechanistically explain the developmental origins of adult disease, namely the hypothesis that many complex adult chronic diseases originate as a result of conditions encountered in utero. If true, epigenetically regulated imprinted genes, critical to normal growth and development, may partially mediate these outcomes. We determine the influence of in utero exposure to cigarette smoking on methylation at two differentially methylated regions (DMRs) regulating Insulin-like Growth Factor 2 (IGF2) and H19, and how this might relate to birth weight of infants born to 418 pregnant women. Smoking status was ascertained through self-report...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5557584</comments>
            <pubDate>Tue, 20 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5557584</guid>        </item>
        <item>
            <title>Significant associations of the rs2943634 (2q36.3) genetic polymorphism with adiponectin, high density lipoprotein cholesterol and ischemic stroke.</title>
            <link>http://www.medworm.com/index.php?rid=5557583&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22207032%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Our findings suggest that rs2943634 is associated with IS risk and with plasma levels of HDL-cholesterol and adiponectin in this German population. Further investigations are needed to confirm these results and to clarify the mechanisms underlying the association.
    PMID: 22207032 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5557583</comments>
            <pubDate>Tue, 20 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5557583</guid>        </item>
        <item>
            <title>A regulatory cascade of three transcription factors in a single specific neuron, DVC, in Caenorhabditis elegans.</title>
            <link>http://www.medworm.com/index.php?rid=5557582&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22207033%26dopt%3DAbstract</link>
            <description>Authors: Feng H, Reece-Hoyes JS, Walhout AJ, Hope IA
    Abstract
    Homeobox proteins are critical regulators of developmental gene transcription and cell specification. Many insights into transcriptional regulation have been gained from studies in the nematode Caenorhabditis elegans. We investigated the expression and regulation of the C. elegans homeobox gene ceh-63, which encodes a single-homeodomain transcription factor of 152 amino acids. ceh-63 is expressed in the interneuron DVC in both sexes, from late embryogenesis through adulthood, and two pairs of uterine cells in reproductive hermaphrodites only. A reporter gene fusion, encoding GFP fused to the full-length CEH-63, also drove weak inconsistent expression in additional unidentified cells in the head and tail. A potential ceh-...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5557582</comments>
            <pubDate>Mon, 19 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5557582</guid>        </item>
        <item>
            <title>A novel silk-like shell matrix gene is expressed in the mantle edge of the Pacific oyster prior to shell regeneration.</title>
            <link>http://www.medworm.com/index.php?rid=5543657&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22197657%26dopt%3DAbstract</link>
            <description>Authors: Takahashi J, Takagi M, Okihana Y, Takeo K, Ueda T, Touhata K, Maegawa S, Toyohara H
    Abstract
    During shell formation, little is known about the functions of organic matrices, especially about the biomineralization of shell prismatic layer. We identified a novel gene, shelk2, from the Pacific oyster presumed to be involved in the shell biosynthesis. The Pacific oyster has multiple copies of shelk2. Shelk2 mRNA is specifically expressed on the mantle edge and is induced during shell regeneration, thereby suggesting that Shelk2 is involved in shell biosynthesis. To our surprise, the database search revealed that it encodes a spider silk-like alanine-rich protein. Interestingly, most of the Shelk2 primary structure is composed of two kinds of poly-alanine motifs-GXNA(n)(S) and ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5543657</comments>
            <pubDate>Mon, 19 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5543657</guid>        </item>
        <item>
            <title>Genetic variation in the C-terminal domain of arginine vasotocin receptor in avian species.</title>
            <link>http://www.medworm.com/index.php?rid=5543659&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22197655%26dopt%3DAbstract</link>
            <description>Authors: Abe H, Watanabe Y, Inoue-Murayama M
    Abstract
    Arginine vasotocin (AVT) is a neurohypophysial hormone that plays an essential role in various social behaviours. We investigated the degree of polymorphisms in the C-terminal domain of the AVT V2-type receptor (AVT2R) among avian species to determine the mechanism by which genetic polymorphisms in the neuropeptide receptor may contribute to different levels of signal transduction. In passerine birds, AVT2R was characterised by 2 variable regions, both of which were managed by insertion/deletion (indel); however, indels were rarely found in other avian taxa. The presence or absence of deletions in passerines largely affected the properties of the predicted palmitoylation sites at the proximal part of the C-terminal tail. Moreove...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5543659</comments>
            <pubDate>Sat, 17 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5543659</guid>        </item>
        <item>
            <title>Haplotype frequency distribution for 7 microsatellites in chromosome 8 and 11 in relation to the metabolic syndrome in four ethnic groups: Tehran Lipid and Glucose Study.</title>
            <link>http://www.medworm.com/index.php?rid=5543660&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22197654%26dopt%3DAbstract</link>
            <description>CONCLUSION: Our findings show a relation between the short allele of D8S1743 in all related haplotype frequencies of subjects with metabolic syndrome. These findings may require more studies of some candidate genes, including the lipoprotein lipase gene, in this chromosomal region.
    PMID: 22197654 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5543660</comments>
            <pubDate>Fri, 16 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5543660</guid>        </item>
        <item>
            <title>PCR-RFLP analysis of mitochondrial DNA cytochrome b gene among Haruan (Channa striatus) in Malaysia.</title>
            <link>http://www.medworm.com/index.php?rid=5543658&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22197656%26dopt%3DAbstract</link>
            <description>Authors: Rahim MH, Ismail P, Alias R, Muhamad N, Mat Jais AM
    Abstract
    Haruan (Channa striatus) is in great demand in the Malaysian domestic fish market. In the present study, mtDNA cyt b was used to investigate genetic variation of C. striatus among populations in Peninsular Malaysia. The overall population of C. striatus demonstrated a high level of haplotype diversity (h) and a low-to-moderate level of nucleotide diversity (π). Analysis of molecular variance (AMOVA) results showed a significantly different genetic differentiation among 6 populations (F(ST)=0.37566, P=0.01). Gene flow (Nm) was high and ranged from 0.32469 to infinity (∞). No significant relationship between genetic distance and geographic distance was detected. A UPGMA tree based on the distance matrix of net i...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5543658</comments>
            <pubDate>Fri, 16 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5543658</guid>        </item>
        <item>
            <title>Properties of the inulinase gene levH1 of Lactobacillus casei IAM 1045; cloning, mutational and biochemical characterization.</title>
            <link>http://www.medworm.com/index.php?rid=5543656&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22197658%26dopt%3DAbstract</link>
            <description>Authors: Kuzuwa S, Yokoi KJ, Kondo M, Kimoto H, Yamakawa A, Taketo A, Kodaira KI
    Abstract
    Though some genetic features of lactobacillar fructan hydrolases were elucidated, information about their enzymology or mutational analyses were scarce. Lactobacillus casei IAM1045 exhibits extracellular activity degrading inulin. After partial purification of the inulin-degrading protein from the spent culture medium, several fragments were obtained by protease digestion. Based on their partial amino-acid sequences, oligonucleotide primers were designed, and its structural gene (levH1) was determined using the gene library constructed in the E. coli system. The levH1 gene encoded a protein (designated as LevH1), of which calculated molecular mass and pI were 138.8-kDa and 4.66, respectively. ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5543656</comments>
            <pubDate>Fri, 16 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5543656</guid>        </item>
        <item>
            <title>Transcriptome analysis of tree peony during chilling requirement fulfillment: Assembling, annotation and markers discovering.</title>
            <link>http://www.medworm.com/index.php?rid=5543655&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22197659%26dopt%3DAbstract</link>
            <description>Authors: Gai S, Zhang Y, Mu P, Liu C, Liu S, Dong L, Zheng G
    Abstract
    Tree peony (Paeonia suffruticosa Andrews) is a well-known horticultural and medicinal plant. The flower buds must go through a period of endo-dormancy before bud sprouting in winter, but very little information concerned with dormancy release is available. We obtained 625,342 sequencing reads with massive parallel pyrosequencing on the Roche 454 GS FLX platform (mean length: 358.1bp). De novo assemblies yielded 23,652 contigs and singletons. 15,284 contigs longer than 300bp were further annotated, among them 12,345 ESTs showed significant similarity with sequences present in public databases (with an E-value &amp;lt;1e-10). 484 putative transcription factors were obtained. In addition, 2253 potential Simple Sequence ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5543655</comments>
            <pubDate>Fri, 16 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5543655</guid>        </item>
        <item>
            <title>Evolutionary diversification of the avian fatty acid-binding proteins.</title>
            <link>http://www.medworm.com/index.php?rid=5372928&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21986036%26dopt%3DAbstract</link>
            <description>Authors: Hughes AL, Piontkivska H
    Abstract
    Phylogenetic analysis of avian and other vertebrate fatty acid binding proteins (FABPs) supported the hypothesis that several gene duplications within this family occurred prior to the most recent common ancestor (MRCA) of tetrapods and bony fishes. The chicken genome encodes two liver-expressed FABPs: (1) L-FABP or FABP1; and (2) Lb-FABP. We propose that the latter be designated FABP10, because in our phylogenetic analysis it clustered with zebrafish FABP10. Bioinformatic analysis of across-tissue gene expression patterns in the chicken showed some congruence with phylogenetic relationships. On the basis of expression, chicken FABP genes seemed to form two major groups: (1) a cluster of genes many of which showed predominant expression in...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5372928</comments>
            <pubDate>Fri, 04 Nov 2011 15:07:03 +0100</pubDate>
            <guid isPermaLink="false">5372928</guid>        </item>
        <item>
            <title>Prenatal diagnosis of a rare de novo centromeric chromosome 6 variant.</title>
            <link>http://www.medworm.com/index.php?rid=5372927&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21989483%26dopt%3DAbstract</link>
            <description>We present a prenatal diagnosis of a rare de novo centromeric chromosome 6 variant. Cytogenetic and molecular techniques were used to characterize this variant and confirm the de novo nature of this event. This case illustrates the importance of reporting unusual variant chromosomes for genetic counseling and for determination of the frequency of variant chromosomes in the general population.
    PMID: 21989483 [PubMed - in process] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5372927</comments>
            <pubDate>Fri, 04 Nov 2011 15:06:05 +0100</pubDate>
            <guid isPermaLink="false">5372927</guid>        </item>
        <item>
            <title>Significant differences in gene expression of GABA receptors in peripheral blood leukocytes of migraineurs.</title>
            <link>http://www.medworm.com/index.php?rid=5293180&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21971078%26dopt%3DAbstract</link>
            <description>This study also identifies GABRA3 and GABBR2 as potential biomarkers to select migraineurs that may be more responsive to GABA agonists with future investigations in this area warranted.
    PMID: 21971078 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5293180</comments>
            <pubDate>Sat, 24 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5293180</guid>        </item>
        <item>
            <title>A novel splice site mutation in gene C2orf37 underlying Woodhouse-Sakati syndrome (WSS) in a consanguineous family of Pakistani origin.</title>
            <link>http://www.medworm.com/index.php?rid=5293186&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21963443%26dopt%3DAbstract</link>
            <description>This study presents a first report of Woodhouse-Sakati syndrome identified in Pakistani population.
    PMID: 21963443 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5293186</comments>
            <pubDate>Thu, 22 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5293186</guid>        </item>
        <item>
            <title>Helper-dependent canine adenovirus vector-mediated transgene expression in a neurodegenerative lysosomal storage disorder.</title>
            <link>http://www.medworm.com/index.php?rid=5293185&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21963444%26dopt%3DAbstract</link>
            <description>In this study, we have evaluated a gene therapy approach using a helper-dependent canine adenovirus vector that expresses human SGSH as a means of delivering sustained transgene expression to the brain. Initial testing in a mixed neural cell culture model demonstrated that the vector could significantly increase SGSH activity in transduced cells, resulting in near-normalization of heparan sulfate-derived fragments. While administration of vector by direct injection into the brain of adult MPS-IIIA mice enabled transgene expression for at least 8.5months post-treatment, it was only in discrete areas of brain. Heparan sulfate storage was reduced in some regions following treatment, however there was no improvement in secondary neuropathological changes. These data demonstrate that helper-dep...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5293185</comments>
            <pubDate>Thu, 22 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5293185</guid>        </item>
        <item>
            <title>Species-specific differences in the processing of acid α-glucosidase are due to the amino acid identity at position 201.</title>
            <link>http://www.medworm.com/index.php?rid=5293183&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21963446%26dopt%3DAbstract</link>
            <description>Authors: Moreland RJ, Higgins S, Zhou A, Vanstraten P, Cauthron RD, Brem M, McLarty BJ, Kudo M, Canfield WM
    Abstract
    Acid α-glucosidase (GAA) is a lysosomal enzyme that hydrolyzes glycogen to glucose. Deficiency of GAA causes Pompe disease. Mammalian GAA is synthesized as a precursor of ~110,000Da that is N-glycosylated and targeted to the lysosome via the M6P receptors. In the lysosome, human GAA is sequentially processed by proteases to polypeptides of 76-, 19.4-, and 3.9-kDa that remain associated. Further cleavage between R(200) and A(204) inefficiently converts the 76-kDa polypeptide to the mature 70-kDa form with an additional 10.4-kDa polypeptide. GAA maturation increases its affinity for glycogen by 7-10 fold. In contrast to human GAA, processing of bovine and hamster GAA ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5293183</comments>
            <pubDate>Thu, 22 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5293183</guid>        </item>
        <item>
            <title>In silico and in vivo identification of the intermediate filament vimentin that is downregulated downstream of Brachyury during Xenopus embryogenesis.</title>
            <link>http://www.medworm.com/index.php?rid=5293182&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21963995%26dopt%3DAbstract</link>
            <description>Authors: Yamada A, Koyanagi KO, Watanabe H
    Abstract
    Brachyury, a member of the T-box transcription family, has been suggested to be essential for morphogenetic movements in various processes of animal development. However, little is known about its critical transcriptional targets. In order to identify targets of Brachyury and understand the molecular mechanisms underlying morphogenetic movements, we first searched the genome sequence of Xenopus tropicalis, the only amphibian genomic sequence available, for Brachyury-binding sequences known as T-half sites, and then screened for the ones conserved between vertebrate genomes. We found three genes that have evolutionarily conserved T-half sites in the promoter regions and examined these genes experimentally to determine whether their...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5293182</comments>
            <pubDate>Thu, 22 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5293182</guid>        </item>
        <item>
            <title>Effect of probiotic fermented milk and chlorophyllin on gene expressions and genotoxicity during AFB(1)-induced hepatocellular carcinoma.</title>
            <link>http://www.medworm.com/index.php?rid=5293181&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21963996%26dopt%3DAbstract</link>
            <description>Authors: Kumar M, Verma V, Nagpal R, Kumar A, Gautam SK, Behare PV, Grover CR, Aggarwal PK
    Abstract
    The aim of this study was to investigate the chemopreventive effect of probiotic fermented milk and chlorophyllin on aflatoxin B(1) (AFB(1)) induced hepatocellular carcinoma. In vivo trials were conducted on 200 Wistar rats allocated to eight groups. Rats in the positive control group were given intraperitoneal injection of aflatoxin B(1) at 450μg/kg body weight twice a week for 6weeks. The rats were sacrificed and dissected at the 25th week of the experiment, and comet assay was carried out in hepatic cells to assess the genotoxicity or DNA damage. The tumour incidence was decreased by approximately one-third than the AFB(1) control group. The expression of c-myc bax, bcl-2, cyclin...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5293181</comments>
            <pubDate>Thu, 22 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5293181</guid>        </item>
        <item>
            <title>SVEP1 promoter regulation by methylation of CpG sites.</title>
            <link>http://www.medworm.com/index.php?rid=5293187&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21963386%26dopt%3DAbstract</link>
            <description>Authors: Glait-Santar C, Benayahu D
    Abstract
    SVEP1 gene encodes a cell adhesion molecule (CAM) that was previously shown to be expressed by cells related to skeletal tissues. Here we focus on SVEP1 expression regulation in pre-osteoblastic MBA-15 and mammary adenocarcinoma DA3 cells. We show that SVEP1 message and protein are highly expressed by MBA-15 when compared with DA3 cells. DNA methylation of CpGs sites is an epigenetic mechanism associated with gene silencing. Therefore, we analyzed the methylation status of a region potentially harbors SVEP1 promoter and further activity alterations induced by estrogen (17βE(2)) and TNFα. We also mapped in silico the transcription binding sites namely TFIIB, NF-κB, ERE, AP1 and Sp1 at the putative promoter. Treatments with demethylatio...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5293187</comments>
            <pubDate>Wed, 21 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5293187</guid>        </item>
        <item>
            <title>Evaluation of the 16S and 12S rRNA genes as universal markers for the identification of commercial fish species in South Africa.</title>
            <link>http://www.medworm.com/index.php?rid=5293184&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21963445%26dopt%3DAbstract</link>
            <description>Authors: Cawthorn DM, Steinman HA, Witthuhn RC
    Abstract
    The development of DNA-based methods for the identification of fish species is important for fisheries research and control, as well as for the detection of unintentional or fraudulent species substitutions in the marketplace. The aim of this study was to generate a comprehensive reference database of DNA sequences from the mitochondrial 16S and 12S ribosomal RNA (rRNA) genes for 53 commercial fish species in South Africa and to evaluate the applicability of these genetic markers for the identification of fish at the species level. The DNA extracted from all target species was readily amplified using universal primers targeting both rRNA gene regions. Sequences from the 16S and 12S rRNA genes were submitted to GenBank for the ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5293184</comments>
            <pubDate>Wed, 21 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5293184</guid>        </item>
        <item>
            <title>In vitro evolution of an atrazine-degrading population under cyanuric acid selection pressure: Evidence for the selective loss of a 47kb region on the plasmid ADP1 containing the atzA, B and C genes.</title>
            <link>http://www.medworm.com/index.php?rid=5272301&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21959051%26dopt%3DAbstract</link>
            <description>Authors: Changey F, Devers-Lamrani M, Rouard N, Martin-Laurent F
    Abstract
    The adaptation of microorganisms to pesticide biodegradation relies on the recruitment of catabolic genes by horizontal gene transfer and homologous recombination mediated by insertion sequences (IS). This environment-friendly function is maintained in the degrading population but it has a cost which could diminish its fitness. The loss of genes in the course of evolution being a major mechanism of ecological specialization, we mimicked evolution in vitro by sub-culturing the atrazine-degrading Pseudomonas sp. ADP in a liquid medium containing cyanuric acid as the sole source of nitrogen. After 120 generations, a new population evolved, which replaced the original one. This new population grew faster on cyanu...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5272301</comments>
            <pubDate>Sun, 18 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5272301</guid>        </item>
        <item>
            <title>Genetic organization and molecular characterization of secA2 locus in Listeria species.</title>
            <link>http://www.medworm.com/index.php?rid=5272306&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21939744%26dopt%3DAbstract</link>
            <description>Authors: Mishra KK, Mendonca M, Aroonnual A, Burkholder KM, Bhunia AK
    Abstract
    The translocation of proteins across the bacterial cell wall is carried out by the general secretory (Sec) system. Most bacteria have a single copy of the secA gene, with the exception of a few Gram-positive bacteria, which have an additional copy of secA, designated secA2. secA2 is present in Listeria monocytogenes and is responsible for secretion and translocation of several proteins including virulence factors; however, little is known about the secA2 gene and its genetic organization in nonpathogenic members of the genus Listeria. The goal of this study was to determine the presence of secA2 locus and analyze the genetic relatedness among pathogenic and nonpathogenic Listeria species. Cloning experim...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5272306</comments>
            <pubDate>Sat, 17 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5272306</guid>        </item>
        <item>
            <title>Mitochondrial genome organization and divergence in hybridizing central European waterfrogs of the Pelophylax esculentus complex (Anura, Ranidae).</title>
            <link>http://www.medworm.com/index.php?rid=5272302&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21951340%26dopt%3DAbstract</link>
            <description>Authors: Hofman S, Pabijan M, Dziewulska-Szwajkowska D, Szymura JM
    Abstract
    Natural transfer of mitochondrial DNA has occurred between three western Palaearctic waterfrog taxa: Pelophylax lessonae, Pelophylaxridibundus and their hybridogenetic hybrid, Pelophylax kl. esculentus. The transfer is asymmetric with most P. kl. esculentus and approximately one third of all central European P. ridibundus having mtDNA derived from P. lessonae (L-mtDNA). We obtained complete nucleotide sequences of multiple mitochondrial genomes (15,376-78bp without control regions) from all 3 taxa, including a P. ridibundus frog with introgressed L-mtDNA. The gene content and organization of the mitogenomes correspond to those typical of neobatrachians. Divergence between the mtDNAs of P. lessonae and P. ri...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5272302</comments>
            <pubDate>Sat, 17 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5272302</guid>        </item>
        <item>
            <title>Identification of porcine polycystic kidney disease 1 (PKD1) gene: Molecular cloning, expression profile, and implication in disease model.</title>
            <link>http://www.medworm.com/index.php?rid=5272304&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21945688%26dopt%3DAbstract</link>
            <description>Authors: He J, Wang Q, Ye J, Hu X, Li N
    Abstract
    The polycystic kidney disease 1 (PKD1) gene, which accounts for ~85% of human autosomal dominant polycystic kidney disease (ADPKD) cases, has been extensively studied in human and mouse. Much information about the pathogenesis of and treatments for ADPKD has been gained from the use of mouse models. However, because mouse models pose some limitations, further studies in other model systems are needed to investigate the biological basis of ADPKD. The pig is regarded as an important biomedical model. Thus, we isolated a pig PKD1 homolog and characterized its cDNA sequence, genomic structure, expression profile, alternative splicing, methylation status, protein characteristics, and immunohistochemical features in both neonatal and adult...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5272304</comments>
            <pubDate>Fri, 16 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5272304</guid>        </item>
        <item>
            <title>Sequence variations and two levels of MCT1 and CD147 expression in red blood cells and gluteus muscle of horses.</title>
            <link>http://www.medworm.com/index.php?rid=5272303&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21945690%26dopt%3DAbstract</link>
            <description>Authors: Koho NM, Mykkänen AK, Reeben M, Raekallio MR, Ilves M, Pösö AR
    Abstract
    MCT1-CD147 complex is the prime lactate transporter in mammalian plasma membranes. In equine red blood cells (RBCs), activity of the complex and expression of MCT1 and CD147 is bimodal; high in 70% and low in 30%. We studied whether sequence variations contribute to the bimodal expression of MCT1 and CD147. Samples of blood and cremaster muscle were collected in connection of castration from 24 horses. Additional gluteus muscle samples were collected from 15 Standardbreds of which seven were known to express low amounts of CD147 in RBCs. The cDNA of MCT1 and CD147 together with a promoter region of CD147 was sequenced. The amounts of MCT1 and CD147 expressed in RBC and muscle membranes were measured...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5272303</comments>
            <pubDate>Fri, 16 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5272303</guid>        </item>
        <item>
            <title>Association of angiotensin converting enzyme (ACE) gene I/D polymorphism and polycystic ovary syndrome (PCOS).</title>
            <link>http://www.medworm.com/index.php?rid=5272307&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21939743%26dopt%3DAbstract</link>
            <description>This study was conducted in Turkish patients with polycystic ovary syndrome to determine the frequency of I/D polymorphism genotypes of angiotensin converting enzyme gene, and to examine the role of this polymorphism in polycystic ovary syndrome development. Genomic DNA obtained from 200 persons (100 patients with polycystic ovary syndrome and 100 healthy controls) was used in the study. DNA was multiplied by polymerase chain reaction using I and D allele-specific primers. Polymerase chain reaction products were assessed with a charge coupled device (CCD) camera by being exposed to 2% agarose gel electrophoresis. There was statistically significant difference between the groups with respect to genotype distribution (p&amp;lt;0.001). The D allele frequency was indicated as 68% and I allele was ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5272307</comments>
            <pubDate>Mon, 12 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5272307</guid>        </item>
        <item>
            <title>Quantitative analysis of transcript variants of CHM gene containing LTR12C element in humans.</title>
            <link>http://www.medworm.com/index.php?rid=5272305&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21939745%26dopt%3DAbstract</link>
            <description>Authors: Jung YD, Huh JW, Kim DS, Kim YJ, Ahn K, Ha HS, Lee JR, Yi JM, Moon JW, Kim TO, Song GA, Han K, Kim HS
    Abstract
    Choroideremia (CHM) is essential for the posttranslational activation of retina-specific Rab protein. Transcript variants (a and b) of the CHM gene were detected in human cancer cells and tissues. Sequence analysis of the both variants found that isoform b is caused by an LTR12C element offering an alternative splicing site within the CHM gene. We performed real-time RT-PCR analysis to study expression levels of the CHM transcript variants in tumor and adjacent normal tissue samples. Our results showed that CHM isoform b was highly expressed in tumor tissues but its expression levels were relatively low in those of adjacent normal tissues including colon, testis, ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5272305</comments>
            <pubDate>Mon, 12 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5272305</guid>        </item>
        <item>
            <title>Integrative analysis of transcriptome and genome indicates two potential genomic islands are associated with pathogenesis of Mycobacterium tuberculosis.</title>
            <link>http://www.medworm.com/index.php?rid=5237986&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21924330%26dopt%3DAbstract</link>
            <description>In this study, we predicted two potential genomic islands in M.tb genome, respectively named as GI-1 and GI-2. It is indicated that the genes belong to PE_PGRS family in GI-1 and genes involved in sulfolipid-1 (SL-1) synthesis in GI-2 are strongly associated with M.tb pathogenesis. Sequence analysis revealed that the five PGRS genes are more polymorphic than other PGRS members in full virulence M.tb complex strains at significance level 0.01 but not in attenuated strains. Expression analysis of microarrays collected from literatures displayed that GI-1 genes, especially Rv3508 might be correlated with the response to the inhibition of aerobic respiration. Microarray analysis also showed that SL-1 cluster genes are drastically down-expressed in attenuated strains relative to full virulence ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5237986</comments>
            <pubDate>Thu, 08 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5237986</guid>        </item>
        <item>
            <title>High resolution positioning of intron ends on the nucleosomes.</title>
            <link>http://www.medworm.com/index.php?rid=5237983&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21925247%26dopt%3DAbstract</link>
            <description>Authors: Hapala J, Trifonov EN
    Abstract
    High resolution sequence-directed nucleosome mapping is applied to 36,000 sequences containing splice junctions, from five different species. As it has been also shown in previous studies, the junctions are found to be preferentially located within nucleosomes. Moreover, the orientation of guanine residues at the GT- and AG-ends of introns within the nucleosomes is such that the guanines are positioned nearest to the surface of histone octamers, 3 and 4 bases upstream from the local DNA pseudo-dyads passing through minor grooves oriented outwards. Since the guanine residues are the most vulnerable to spontaneous damage within the cell (primarily, depurination and oxidation) such positioning of the splice junctions minimizes the damage that is...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5237983</comments>
            <pubDate>Thu, 08 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5237983</guid>        </item>
        <item>
            <title>Gene transport and expression by arginine-rich cell-penetrating peptides in Paramecium.</title>
            <link>http://www.medworm.com/index.php?rid=5237982&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21925248%26dopt%3DAbstract</link>
            <description>In this study, we demonstrate that three arginine-rich CPPs (SR9, HR9 and PR9) can form stable complexes with plasmid DNA at the optimized nitrogen/phosphate ratio of 3 and deliver plasmid DNA into Paramecium caudatum in a noncovalent manner. Accordingly, the transported plasmid encoding the green fluorescent protein (GFP) gene could be expressed in cells functionally assayed at both the protein and DNA levels. The efficiency of gene delivery varied among these CPPs in the order of HR9&amp;gt;PR9&amp;gt;SR9. In addition, these CPPs and CPP/DNA complexes were not cytotoxic in Paramecium detected by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diohenyltetrazolium bromide (MTT) assay. Thus, these results suggest that the functionality of arginine-rich CPPs offers an efficient and safe tool for transgenesis i...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5237982</comments>
            <pubDate>Thu, 08 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5237982</guid>        </item>
        <item>
            <title>Polymorphisms of hemochromatosis, and alpha-1 antitrypsin genes in Egyptian HCV patients with and without hepatocellular carcinoma.</title>
            <link>http://www.medworm.com/index.php?rid=5237981&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21925577%26dopt%3DAbstract</link>
            <description>Authors: Gharib AF, Karam RA, Pasha HF, Radwan MI, Elsawy WH
    Abstract
    Hereditary hemochromatosis and alpha-1antitrypsin deficiency are genetic diseases characterized by endoplasmic reticulum (ER) stress with subsequent development of liver disease. Our aim was to estimate the frequency of hemochromatosis gene (HFE) mutant alleles (C282Y and H63D) and alpha-1 antitrypsin S/Z variants among Egyptian HCV cirrhotic patients and in hepatocellular carcinoma patients and to evaluate their effects on disease progression. HFE and alpha-1 antitrypsin polymorphisms were characterized in 200 Egyptian patients with HCV infection (100 patients complicated with cirrhosis, 100 patients with HCC) and 100 healthy subjects who had no history of any malignancy. The frequencies of HD genotype of H63D m...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5237981</comments>
            <pubDate>Thu, 08 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5237981</guid>        </item>
        <item>
            <title>Expression of yeast high mobility group protein HMO1 is regulated by TOR signaling.</title>
            <link>http://www.medworm.com/index.php?rid=5237985&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21924331%26dopt%3DAbstract</link>
            <description>Authors: Xiao L, Kamau E, Donze D, Grove A
    Abstract
    Expression of ribosomal proteins is controlled by the Target of Rapamycin (TOR) kinase. The Saccharomyces cerevisiae Forkhead-like transcription factor Fhl1 is important for this regulation, and its localization to ribosomal protein gene promoters requires the high mobility group protein HMO1. We show here that HMO1 expression is similarly controlled by TOR signaling. Reporter constructs in which lacZ is under control of the HMO1 promoter show that HMO1 promoter activity is repressed on inactivation of TOR and that HMO1 is required for this repression. Chromatin immunoprecipitation shows that Fhl1 localizes to the HMO1 promoter in an HMO1-dependent fashion and that it centers on a predicted Fhl1 site, and removal of the Fhl1 site ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5237985</comments>
            <pubDate>Mon, 05 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5237985</guid>        </item>
        <item>
            <title>Semaphorin-plexin signalling genes associated with human breast tumourigenesis.</title>
            <link>http://www.medworm.com/index.php?rid=5237984&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21925246%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Semaphorins and their receptors, the plexins, have been implicated in numerous aspects of neural development, however their expression in many other epithelial tissues suggests that the semaphorin-plexin signalling system also contributes to blood vessel growth and development. These findings warrant further investigation of the role of semaphorins and plexins and their role in normal and tumour-induced angiogenesis in vivo and in vitro. This may represent a new front of attack in anti-angiogenic therapies of breast and other cancers.
    PMID: 21925246 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5237984</comments>
            <pubDate>Fri, 02 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5237984</guid>        </item>
        <item>
            <title>Transcriptional analysis of the Aurora inhibitor Danusertib leading to biomarker identification in TP53 wild type cells.</title>
            <link>http://www.medworm.com/index.php?rid=5224405&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21914463%26dopt%3DAbstract</link>
            <description>Authors: Bosotti R, Carpinelli P, Healy S, Locatelli G, Cappella P, Lanfrancone L, Calogero R, Moll J, Isacchi A
    Abstract
    Aurora kinases represent an appealing target for anticancer therapies and several Aurora inhibitors are in clinical development, including the potent pan-Aurora inhibitor Danusertib. Treatment with Aurora inhibitors has been shown to induce diverse biological responses in different tumor cells, in part depending on TP53 status. To characterize the effects of Danusertib at the transcriptional level we carried out gene expression profiling of wt and TP53 mutant tumor cells showing differential cell cycle response upon drug treatment. We found that treatment with Danusertib induces a strong transcriptional response only in TP53 wt cells, with an overlapping pattern...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5224405</comments>
            <pubDate>Fri, 02 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5224405</guid>        </item>
        <item>
            <title>IGD: A resource for intronless genes in the human genome.</title>
            <link>http://www.medworm.com/index.php?rid=5224404&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21914464%26dopt%3DAbstract</link>
            <description>Authors: Louhichi A, Fourati A, Rebaï A
    Abstract
    Intronless genes (IGs) fraction varies between 2.7 and 97.7% in eukaryotic genomes. Although many databases on exons and introns exist, there was no curated database for such genes which allowed their study in a concerted manner. Such a database would be useful to identify the functional features and the distribution of these genes across the genome. Here, a new database of IGs in eukaryotes based on GenBank data was described. This database, called IGD (Intronless Gene Database), is a collection of gene sequences that were annotated and curated. The current version of IGD contains 687 human intronless genes with their protein and CDS sequences. Some features of the entries are given in this paper. Data was extracted from GenBank re...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5224404</comments>
            <pubDate>Fri, 02 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5224404</guid>        </item>
        <item>
            <title>Cloning of the 5' regulatory regions and functional characterization of the core promoters of ovine PLAU (u-PA) and SERPIN1 (PAI-1).</title>
            <link>http://www.medworm.com/index.php?rid=5224403&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21914465%26dopt%3DAbstract</link>
            <description>Authors: Lampidonis AD, Theodorou G, Pecorini C, Rebucci R, Baldi A, Politis I
    Abstract
    The activation of plasminogen plays a crucial role in various extracellular proteolytic events (fibrinolysis, cell migration, ovulation and involution of the mammary gland). In the present study we describe the isolation of the 5' proximal and distal promoter regions of ovine PLAU (urokinase plasminogen activator, u-PA) and SERPIN1 (plasminogen activator inhibitor 1, PAI-1) genes for the first time in ruminants. Analysis of the 5.645kb 5'-flanking region of u-PA revealed a putative TATA-less promoter. In contrast the isolated 2.787kb 5'-flanking region of PAI-1 included a TATA-box. It should be noted that both genes lack the initiator motif around the transcription start site. The two genes shar...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5224403</comments>
            <pubDate>Fri, 02 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5224403</guid>        </item>
        <item>
            <title>Molecular characterization of two isoforms of ZFAND3 cDNA from the Japanese quail and the leopard gecko, and different expression patterns between testis and ovary.</title>
            <link>http://www.medworm.com/index.php?rid=5224402&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21914466%26dopt%3DAbstract</link>
            <description>Authors: Otake S, Endo D, Park MK
    Abstract
    Zing finger AN1-type domain 3 (ZFAND3), also known as testis expressed sequence 27 (Tex27), is a gene found in the mouse testis, but its physiological function is unknown. We identified the full-length sequences of two isoforms (short and long) of ZFAND3 cDNA from Japanese quail and leopard gecko. This is the first cloning of avian and reptilian ZFAND3 cDNA. The two isoforms are generated by alternative polyadenylation in the 3'UTR and have the same ORF sequences encoding identical proteins. There were highly conserved regions in the 3'UTR of the long form near the polyadenylation sites from mammals to amphibians, suggesting that the features for determining the stability of mRNA or translation efficiency differ between isoforms. The deduc...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5224402</comments>
            <pubDate>Fri, 02 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5224402</guid>        </item>
        <item>
            <title>Molecular characterization of a novel gene from Synechocystis sp. PCC 6803.</title>
            <link>http://www.medworm.com/index.php?rid=5224401&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21914467%26dopt%3DAbstract</link>
            <description>In conclusion, our study suggests that we have cloned a novel gene and this gene may play an important role in attachment of the chromophores to the apo-proteins.
    PMID: 21914467 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5224401</comments>
            <pubDate>Fri, 02 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5224401</guid>        </item>
        <item>
            <title>Molecular characterization of genes encoding trypsin-like enzymes from Aedes aegypti larvae and identification of digestive enzymes.</title>
            <link>http://www.medworm.com/index.php?rid=5224400&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21914468%26dopt%3DAbstract</link>
            <description>In conclusion, for the first time, digestive enzymes of 4th larval instar of Ae. aegypti were purified and characterized. The knowledge of digestive enzymes present in Ae. aegypti larvae may be helpful in the development of a larvicide.
    PMID: 21914468 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5224400</comments>
            <pubDate>Fri, 02 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5224400</guid>        </item>
        <item>
            <title>Disease-driven detection of differential inherited SNP modules from SNP network.</title>
            <link>http://www.medworm.com/index.php?rid=5224399&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21920414%26dopt%3DAbstract</link>
            <description>Authors: Li C, Li Y, Xu J, Lv J, Ma Y, Shao T, Gong B, Tan R, Xiao Y, Li X
    Abstract
    Detection of the synergetic effects between variants, such as single-nucleotide polymorphisms (SNPs), is crucial for understanding the genetic characters of complex diseases. Here, we proposed a two-step approach to detect differentially inherited SNP modules (synergetic SNP units) from a SNP network. First, SNP-SNP interactions are identified based on prior biological knowledge, such as their adjacency on the chromosome or degree of relatedness between the functional relationships of their genes. These interactions form SNP networks. Second, disease-risk SNP modules (or sub-networks) are prioritised by their differentially inherited properties in IBD (Identity by Descent) profiles of affected and u...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5224399</comments>
            <pubDate>Fri, 02 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5224399</guid>        </item>
        <item>
            <title>Microsatellites in different Potyvirus genomes: Survey and analysis.</title>
            <link>http://www.medworm.com/index.php?rid=5224398&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21920415%26dopt%3DAbstract</link>
            <description>Authors: Zhao X, Tan Z, Feng H, Yang R, Li M, Jiang J, Shen G, Yu R
    Abstract
    Simple sequence repeats (SSRs) have been extensively used for various genetic and evolutionary studies in eukaryotic and prokaryotic organisms, while few relevant researches have been made in viruses. The Potyvirus is a fine system to study roles and evolution of SSRs in viruses. The densities, relative abundances, compositions and evolutionary inferences of SSRs in 45 different Potyvirus genomes have been analyzed in this study. Results showed that the densities and relative abundances of SSRs are similar in all those Potyvirus genomes. The number of SSRs decreases with an increase in the length of repeat unit. Dinucleotide repeats are the most abundant and followed by trinucleotide repeats, and the numbe...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5224398</comments>
            <pubDate>Fri, 02 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5224398</guid>        </item>
        <item>
            <title>Analysis of lamprey clustered Fox genes: Insight into Fox gene evolution and expression in vertebrates.</title>
            <link>http://www.medworm.com/index.php?rid=5214547&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21907770%26dopt%3DAbstract</link>
            <description>Authors: Wotton KR, Shimeld SM
    Abstract
    In the human genome, members of the FoxC, FoxF, FoxL1, and FoxQ1 gene families are found in two paralagous clusters. One cluster contains the genes FOXQ1, FOXF2, FOXC1 and the second consists of FOXF1, FOXC2, and FOXL1. In jawed vertebrates these genes are known to be expressed in different pharyngeal tissues and all, except FoxQ1, are involved in patterning the early embryonic mesoderm. We have previously traced the evolution of this cluster in the bony vertebrates, and the gene content is identical in the dogfish, a member of the most basally branching lineage of the jawed vertebrates. Here we extend these analyses to jawless vertebrates. Using genomic searches and molecular approaches we have identified homologues of these genes from lampr...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5214547</comments>
            <pubDate>Wed, 31 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5214547</guid>        </item>
        <item>
            <title>RNA polymerase I activity is regulated at multiple steps in the transcription cycle: Recent insights into factors that influence transcription elongation.</title>
            <link>http://www.medworm.com/index.php?rid=5214549&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21893173%26dopt%3DAbstract</link>
            <description>Authors: Schneider DA
    Abstract
    Synthesis of the translation apparatus is a central activity in growing and/or proliferating cells. Because of its fundamental importance and direct connection to cell proliferation, ribosome synthesis has been a focus of ongoing research for several decades. As a consequence, much is known about the essential factors involved in this process. Many studies have shown that transcription of the ribosomal DNA by RNA polymerase I is a major target for cellular regulation of ribosome synthesis rates. The initiation of transcription by RNA polymerase I has been implicated as a regulatory target, however, recent studies suggest that the elongation step in transcription is also influenced and regulated by trans-acting factors. This review describes the factor...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5214549</comments>
            <pubDate>Fri, 26 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5214549</guid>        </item>
        <item>
            <title>Multiple cis-elements in the 5'-flanking region of embryonic/larval fast-type of the myosin heavy chain gene of torafugu, MYH(M743-2), function in the transcriptional regulation of its expression.</title>
            <link>http://www.medworm.com/index.php?rid=5214548&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21893174%26dopt%3DAbstract</link>
            <description>Authors: Asaduzzaman M, Kinoshita S, Siddique BS, Asakawa S, Watabe S
    Abstract
    The myosin heavy chain gene, MYH(M743-2), is highly expressed in fast muscle fibers of torafugu embryos and larvae, suggesting its functional roles for embryonic and larval muscle development. However, the transcriptional regulatory mechanism involved in its expression remained unknown. Here, we analyzed the 2075bp 5'-flanking region of torafugu MYH(M743-2) to examine the spatial and temporal regulation by using transgenic and transient expression techniques in zebrafish embryos. Combining both transient and transgenic analyses, we demonstrated that the 2075bp 5'-flanking sequences was sufficient for its expression in skeletal, craniofacial and pectoral fin muscles. The immunohistochemical observation re...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5214548</comments>
            <pubDate>Fri, 26 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5214548</guid>        </item>
        <item>
            <title>&quot;Anticipated&quot; nucleosome positioning pattern in prokaryotes.</title>
            <link>http://www.medworm.com/index.php?rid=5183579&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21884764%26dopt%3DAbstract</link>
            <description>&quot;Anticipated&quot; nucleosome positioning pattern in prokaryotes.
    Gene. 2011 Aug 23;
    Authors: Rapoport AE, Trifonov EN
    Abstract
    Linguistic (word count) analysis of prokaryotic genome sequences, by Shannon N-gram extension, reveals that the dominant hidden motifs in A+T rich genomes are T(A)(T)A and G(A)(T)C with uncertain number of repeating A and T. Since prokaryotic sequences are largely protein-coding, the motifs would correspond to amphipathic alpha-helices with alternating lysine and phenylalanine as preferential polar and non-polar residues. The motifs are also known in eukaryotes, as nucleosome positioning patterns. Their existence in prokaryotes as well may serve for binding of histone-like proteins to DNA. In this case the above patterns in prokaryotes may be considered...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5183579</comments>
            <pubDate>Mon, 22 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5183579</guid>        </item>
        <item>
            <title>Identification of an entire set of tRNA molecules and characterization of cleavage sites of the intron-containing tRNA precursors in acidothermophilic crenarchaeon Sulfolobus tokodaii strain7.</title>
            <link>http://www.medworm.com/index.php?rid=5183583&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21872648%26dopt%3DAbstract</link>
            <description>Authors: Yamazaki S, Yoshinari S, Kita K, Watanabe YI, Kawarabayasi Y
    Abstract
    The acidothermophilic crenarchaeon, Sulfolobus tokodaii strain7, was isolated from a hot spring in Beppu, Kyushu, Japan. Whole genomic data of this microorganism indicated that among 46 putative tRNA genes identified, 24 were interrupted tRNA genes containing an intron. A sequence comparison between the cDNA sequences for unspliced and spliced tRNAs indicated that all predicted tRNAs were expressed and all intron portions were spliced in this microorganism. However, the actual cleavage site in the splicing process was not determined for 13 interrupted tRNAs because of the presence of the same nucleotides at both 5' and 3' border regions of each intron. The cleavage sites for all the introns, which were d...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5183583</comments>
            <pubDate>Wed, 17 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5183583</guid>        </item>
        <item>
            <title>Additional box B of RNA polymerase III promoter in SINE B1 can be functional.</title>
            <link>http://www.medworm.com/index.php?rid=5170181&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21855615%26dopt%3DAbstract</link>
            <description>Authors: Koval AP, Veniaminova NA, Kramerov DA
    Abstract
    Many genes of small RNAs and short interspersed elements (SINEs) are transcribed by RNA polymerase III due to an internal promoter that is composed of two boxes (A and B) spaced by 30-45bp. Rodent SINE B1 originated from 7SL RNA, and a 29-bp tandem duplication took place in B1 at an early stage of its evolution. As a result of this duplication, an additional box B (named B') located at a distance of 79-82bp from box A arose in SINE B1. Here we have shown that despite the unusually large distance between boxes A and B', they can form an active promoter. In chinchillas, guinea pigs, and other rodents belonging to clade Ctenohystrica, structure of the B' box was well preserved and closely resembles the canonical B box. One may su...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5170181</comments>
            <pubDate>Mon, 08 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5170181</guid>        </item>
        <item>
            <title>A simple and rapid technique for the authentication of the ginseng cultivar, Yunpoong, using an SNP marker in a large sample of ginseng leaves.</title>
            <link>http://www.medworm.com/index.php?rid=5133150&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21835232%26dopt%3DAbstract</link>
            <description>In this study, we developed a single nucleotide polymorphism (SNP) marker for Yunpoong based on analysis of expressed sequence tags (ESTs) in an exon region of the glyceraldehyde 3-phosphate dehydrogenase (GAPDH) gene. This SNP marker had high specificity to authenticate Yunpoong in twelve different main ginseng cultivars. For application of the molecular marker, a rapid identification method was established based on the NaOH-Tris method and real-time polymerase chain reaction (PCR) in order to ensure more efficiency in the cultivar selection. The biggest feature of the NaOH-Tris method was that it made the extraction of DNA very simple and rapid in young leaf tissues. We only spent 1min to extract DNA and directly used it to do PCR. In this report, the conventional DNA extraction method w...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5133150</comments>
            <pubDate>Sun, 07 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5133150</guid>        </item>
        <item>
            <title>Murine Sirt3 protein isoforms have variable half-lives.</title>
            <link>http://www.medworm.com/index.php?rid=5133143&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21840382%26dopt%3DAbstract</link>
            <description>In this study, we stably expressed these variants in several cell lines. We found that Sirt3 M1 or M2 could be stably expressed with predominant mitochondrial localization. However, stable expression of Sirt3 M3 protein was consistently at very low levels. Fast proteasomal degradation contributed to the low expression of Sirt3 M3 protein, as proteasome inhibitor treatment increased Sirt3 M3 protein levels in these cells. Sirt3 M3 protein is ubiquitinated and the E3 ubiquitin ligase subunit Skp2 is involved in Sirt3 M3 protein degradation. Additionally, we found Sirt3 M3 protein could be produced from Sirt3 transcripts encoding longer M1 and M2 isoforms. To explore the mechanism underlying the instability of Sirt3 M3 protein, we found that Sirt3 M1 and M2 proteins, but not M3, specifically ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5133143</comments>
            <pubDate>Thu, 04 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5133143</guid>        </item>
        <item>
            <title>Structural features of cytochrome P450 1A associated with the absence of EROD activity in liver of the loricariid catfish Pterygoplichthys sp.</title>
            <link>http://www.medworm.com/index.php?rid=5133142&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21840383%26dopt%3DAbstract</link>
            <description>Authors: Parente TE, Rebelo MF, da-Silva ML, Woodin BR, Goldstone JV, Bisch PM, Paumgartten FJ, Stegeman JJ
    The Amazon catfish genus Pterygoplichthys (Loricariidae, Siluriformes) is closely related to the loricariid genus Hypostomus, in which at least two species lack detectable ethoxyresorufin-O-deethylase (EROD) activity, typically catalyzed by cytochrome P450 1 (CYP1) enzymes. Pterygoplichthys sp. liver microsomes also lacked EROD, as well as activity with other substituted resorufins, but aryl hydrocarbon receptor agonists induced hepatic CYP1A mRNA and protein suggesting structural/functional differences in Pterygoplichthys CYP1s from those in other vertebrates. Comparing the sequences of CYP1As of Pterygoplichthys sp. and of two phylogenetically related siluriform species that do...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5133142</comments>
            <pubDate>Thu, 04 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5133142</guid>        </item>
        <item>
            <title>Negative transcriptional regulation of the human periostin gene by YingYang-1 transcription factor.</title>
            <link>http://www.medworm.com/index.php?rid=5133145&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21839814%26dopt%3DAbstract</link>
            <description>In this study we demonstrate that the ability of the human POSTN promoter to drive transcription mostly depends on the activity of YingYang-1 (YY1) zinc finger transcription factor. YY1, whose regulatory role in biology includes, besides transcriptional control, also chromatin remodeling, DNA damage repair and tumorigenesis, acts as a strong negative modulator of the POSTN expression. We retain that the identification of the functional role of YY1 in the transcriptional control of the human POSTN gene adds new insights in the studies focused on gene expression in normal and transformed cells.
    PMID: 21839814 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5133145</comments>
            <pubDate>Tue, 02 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5133145</guid>        </item>
        <item>
            <title>Transcriptome profiling of wood maturation in Pinus radiata identifies differentially expressed genes with implications in juvenile and mature wood variation.</title>
            <link>http://www.medworm.com/index.php?rid=5133144&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21839815%26dopt%3DAbstract</link>
            <description>Authors: Li X, Wu HX, Southerton SG
    Trees usually produce wood with distinct properties at different developmental stages. Juvenile wood (JW) formed in younger trees has poorer properties than mature wood (MW) formed in later years. We used cDNA microarrays to compare the xylem transcriptomes of Pinus radiata trees synthesising JW and MW respectively. JW and MW formation involved considerable transcriptome flux, with the greatest change occurring in spring (19.3%) compared to autumn (9.2%). We identified 147 candidate genes in response to wood maturation, of which 34.0% were implicated in cell wall formation and 19.7% were functional unknowns. Majority of the candidate genes were identified from MW and JW in spring (127) with fewer genes in autumn (30). Many genes involved in secondary...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5133144</comments>
            <pubDate>Tue, 02 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5133144</guid>        </item>
        <item>
            <title>RANTES gene mRNA expression and its -403 G/A promoter polymorphism in coronary artery disease.</title>
            <link>http://www.medworm.com/index.php?rid=5133149&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21839152%26dopt%3DAbstract</link>
            <description>CONCLUSION: More studies on larger number of samples are required to further evaluate role of RANTES in pathogenesis of CAD.
    PMID: 21839152 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5133149</comments>
            <pubDate>Mon, 01 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5133149</guid>        </item>
        <item>
            <title>Glutathione-S-transferase M1 and T1 genes and gastric cancer: A case control study in North Indian population.</title>
            <link>http://www.medworm.com/index.php?rid=5133148&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21839153%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Our data suggest that GSTM1 and GSTT1 status may not influence the risk of developing gastric cancer.
    PMID: 21839153 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5133148</comments>
            <pubDate>Mon, 01 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5133148</guid>        </item>
        <item>
            <title>Molecular characterization and tissue-specific expression of the acetyl-CoA carboxylase α gene from Grass carp, Ctenopharyngodon idella.</title>
            <link>http://www.medworm.com/index.php?rid=5133146&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21839155%26dopt%3DAbstract</link>
            <description>In conclusion, the liver is one of the main ACC1 producing tissues in grass carp and ACC1 gene was highly homologous to that of mammals.
    PMID: 21839155 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5133146</comments>
            <pubDate>Mon, 01 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5133146</guid>        </item>
        <item>
            <title>Computational analysis of the transcriptional regulation of the adenine nucleotide translocator isoform 4 gene and its role in spermatozoid glycolytic metabolism.</title>
            <link>http://www.medworm.com/index.php?rid=5133152&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21827840%26dopt%3DAbstract</link>
            <description>Authors: Dupont PY, Stepien G
    Computational phylogenetic analysis coupled to promoter sequence alignment was used to understand mechanisms of transcriptional regulation and to identify potentially coregulated genes. Our strategy was validated on the human ANT4 gene which encodes the fourth isoform of the mitochondrial adenine nucleotide translocator specifically expressed during spermatogenesis. The movement of sperm flagella is driven mainly by ATP generated by glycolytic pathways, and the specific induction of the mitochondrial ANT4 protein presented an interesting puzzle. We analysed the sequences of the promoters, introns and exons of 30 mammalian ANT4 genes and constructed regulatory models. The whole human genome and promoter database were screened for genes that were potentially...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5133152</comments>
            <pubDate>Sat, 30 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5133152</guid>        </item>
        <item>
            <title>The polypyrimidine/polypurine motif in the mouse mu opioid receptor gene promoter is a supercoiling-regulatory element.</title>
            <link>http://www.medworm.com/index.php?rid=5133147&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21839154%26dopt%3DAbstract</link>
            <description>Authors: Choe CY, Kim H, Dong J, van Wijnen AJ, Law PY, Loh HH
    The mu opioid receptor (MOR) is the principle molecular target of opioid analgesics. The polypyrimidine/polypurine (PPy/u) motif enhances the activity of the MOR gene promoter by adopting a non-B DNA conformation. Here, we report that the PPy/u motif regulates the processivity of torsional stress, which is important for endogenous MOR gene expression. Analysis by topoisomerase assays, S1 nuclease digests, and atomic force microscopy showed that, unlike homologous PPy/u motifs, the position- and orientation-induced structural strains to the mouse PPy/u element affect its ability to perturb the relaxation activity of topoisomerase, resulting in polypurine strand-nicked and catenated DNA conformations. Raman spectrum microscop...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5133147</comments>
            <pubDate>Sat, 30 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5133147</guid>        </item>
        <item>
            <title>The complete mitochondrial genome of Macrobrachium nipponense.</title>
            <link>http://www.medworm.com/index.php?rid=5133153&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21827838%26dopt%3DAbstract</link>
            <description>Authors: Ma K, Feng J, Lin J, Li J
    The complete mitochondrial (mt) genome sequence plays an important role in the accurate determination of phylogenetic relationships among metazoans. Herein, we determined the complete mt genome sequence, structure and organization of Macrobrachium nipponense (M. nipponense) (GenBank ID: NC_015073.1) and compared it to that of Macrobrachium lanchesteri (M. lanchesteri) and Macrobrachium rosenbergii (M. rosenbergii). The 15,806 base pair (bp) M. nipponense mt genome, which is comprised of 37 genes, including 13 protein-coding genes (PCGs), 22 transfer RNAs (tRNAs) and 2 ribosomal RNAs (rRNAs), is slightly larger than that of M. lanchesteri (15,694bp, GenBank ID: NC_012217.1) and M. rosenbergii (15,772bp, GenBank ID: NC_006880.1). The M. nipponense genom...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5133153</comments>
            <pubDate>Fri, 29 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5133153</guid>        </item>
        <item>
            <title>Glucosinolate biosynthetic genes in Brassica rapa.</title>
            <link>http://www.medworm.com/index.php?rid=5133151&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21835231%26dopt%3DAbstract</link>
            <description>Authors: Wang H, Wu J, Sun S, Liu B, Cheng F, Sun R, Wang X
    Glucosinolates (GS) are a group of amino acid-derived secondary metabolites found throughout the Cruciferae family. Glucosinolates and their degradation products play important roles in pathogen and insect interactions, as well as in human health. In order to elucidate the glucosinolate biosynthetic pathway in Brassica rapa, we conducted comparative genomic analyses of Arabidopsis thaliana and B. rapa on a genome-wide level. We identified 102 putative genes in B. rapa as the orthologs of 52 GS genes in A. thaliana. All but one gene was successfully mapped on 10 chromosomes. Most GS genes exist in more than one copy in B. rapa. A high co-linearity in the glucosinolate biosynthetic pathway between A. thaliana and B. rapa was als...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5133151</comments>
            <pubDate>Fri, 29 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5133151</guid>        </item>
        <item>
            <title>Comparative genomic analysis of dinucleotide repeats in Tritryps.</title>
            <link>http://www.medworm.com/index.php?rid=5133154&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21824509%26dopt%3DAbstract</link>
            <description>Authors: Duhagon MA, Smircich P, Forteza D, Naya H, Williams N, Garat B
    The protozoans Trypanosoma cruzi, Trypanosoma brucei and Leishmania major (Tritryps), are evolutionarily ancient eukaryotes which cause worldwide human parasitosis. They present unique biological features. Indeed, canonical DNA/RNA cis-acting elements remain mostly elusive. Repetitive sequences, originally considered as selfish DNA, have been lately recognized as potentially important functional sequence elements in cell biology. In particular, the dinucleotide patterns have been related to genome compartmentalization, gene evolution and gene expression regulation. Thus, we perform a comparative analysis of the occurrence, length and location of dinucleotide repeats (DRs) in the Tritryp genomes and their putative a...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5133154</comments>
            <pubDate>Wed, 27 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5133154</guid>        </item>
        <item>
            <title>Serum paraoxonase-1 (PON1) activities (PONase/AREase) and polymorphisms in patients with type 2 diabetes mellitus in North-West Indian population.</title>
            <link>http://www.medworm.com/index.php?rid=5086641&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21803130%26dopt%3DAbstract</link>
            <description>CONCLUSION: Both PONase and AREase activities are lower in patients and this could lead to increased lipid peroxidation and accelerated atherosclerosis in them. PONase activity, but not AREase activity is influenced by PON1 polymorphisms. QR, RR, GC, CC genotypes and L-C-A-R-G, L-T-A-R-G, L-T-G-Q-C haplotypes are commoner in diabetics as compared to controls and may be related to genetic susceptibility to type 2 diabetes.
    PMID: 21803130 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5086641</comments>
            <pubDate>Wed, 27 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5086641</guid>        </item>
        <item>
            <title>Evaluation of Sox2 genetic effect on the development of type 2 diabetes.</title>
            <link>http://www.medworm.com/index.php?rid=5086639&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21803132%26dopt%3DAbstract</link>
            <description>Authors: Gu HF, Gu T, Ostenson CG, Kärvestedt L, Brismar K
    Sox2 is a transcription factor, which plays an important role in the induction of pluripotent stem cells from somatic cells. The Sox2 gene is located in chromosome 3q26.33 and resides in a linkage region of diabetes. In the present study, we attempted to evaluate the genetic effect of Sox2 in the development of type 2 diabetes (T2D). A total of 1598 Swedish subjects of T2D, pre-diabetes and non-diabetic control subjects were enrolled in the present study. Genotyping experiments for allelic discrimination of SNP rs11915160 were performed with TaqMan allelic discrimination. Sox2 mRNA expression levels in pancreatic islets of T2D patients (n=16) and control subjects (n=8) were detected by using real time RT-PCR. Among the non-dia...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5086639</comments>
            <pubDate>Wed, 27 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5086639</guid>        </item>
        <item>
            <title>RhoBTB2 (DBC2) functions as tumor suppressor via inhibiting proliferation, preventing colony formation and inducing apoptosis in breast cancer cells.</title>
            <link>http://www.medworm.com/index.php?rid=5086642&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21801820%26dopt%3DAbstract</link>
            <description>In this study, we constructed a recombinant expression vector pEGFP-N1-RhoBTB2 and transfected it into RhoBTB2-negative breast tumor cell line T-47D. Stable transformanted cells were identified by fluorescence microscope, RT-PCR and Western blot. Cell viability was measured by MTT assay. Colony forming efficiency of breast tumor cells was detected by colony formation assay. Morphological change of apoptotic cells was observed by hematoxylin-eosin staining. Apoptotic ratio was determined by flow cytometry. Cell invasion and migration ability assay were performed using transwell system. Overexpression of RhoBTB2 in breast tumor cells significantly inhibited the proliferation and colony formation of tumor cells. In addition, RhoBTB2 also elevated the apoptotic ratio and caused typical changes...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5086642</comments>
            <pubDate>Fri, 22 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5086642</guid>        </item>
        <item>
            <title>Basal transcription of the human TBX3 gene, a key developmental regulator which is overexpressed in several cancers, requires functional NF-Y and Sp1 sites.</title>
            <link>http://www.medworm.com/index.php?rid=5086647&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21784138%26dopt%3DAbstract</link>
            <description>Authors: Smith J, Mowla S, Prince S
    TBX3 is a member of the T-box family of genes that encode developmentally important transcription factors. Mutations resulting in decreased levels of functional TBX3 lead to Ulnar-Mammary Syndrome and increased levels of TBX3 have been linked to several cancers. To understand the mechanisms regulating TBX3 expression we have previously cloned the 5'-flanking region of the human TBX3 gene and here we describe cis-elements required for its basal transcription. Using site-directed mutagenesis, luciferase reporter assays and in vitro and in vivo DNA binding experiments we identify a Sp1 element and two CCAAT boxes to be essential for basal TBX3 promoter activity. Our results are consistent with reports that these sites are necessary for efficient basal t...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5086647</comments>
            <pubDate>Wed, 20 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5086647</guid>        </item>
        <item>
            <title>The complete mitochondrial genome of Calicogorgia granulosa (Anthozoa: Octocorallia): Potential gene novelty in unidentified ORFs formed by repeat expansion and segmental duplication.</title>
            <link>http://www.medworm.com/index.php?rid=5086643&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21798322%26dopt%3DAbstract</link>
            <description>In conclusion the present mitogenome of C. granulosa adds more information to our understanding of the diversity and evolution of mitogenomes of nonbilaterian animals.
    PMID: 21798322 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5086643</comments>
            <pubDate>Wed, 20 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5086643</guid>        </item>
        <item>
            <title>Transcriptional repression by the proximal exonic region at the human TERT gene.</title>
            <link>http://www.medworm.com/index.php?rid=5086645&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21787851%26dopt%3DAbstract</link>
            <description>In this study, we bioinformatically identify putative CTCF binding sites in the hTERT proximal exonic region (PER) and determine their functional relevance in mediating transcriptional silencing at this gene. Tests using a reporter gene assay in HeLa cancer cells demonstrate that a sub-region of the PER exhibits strong transcriptional repressive activity. This repression is independent of the previously identified CTCF binding site near the transcriptional start site of the hTERT gene. In addition, site directed mutagenesis of three predicted CTCF binding sites, including a previously characterized in vivo site in exon 2, does not result in a loss of the repression mediated by the PER. The results from this study indicate that expression of the hTERT gene in HeLa cells is regulated by sequ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5086645</comments>
            <pubDate>Tue, 19 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5086645</guid>        </item>
        <item>
            <title>Temporary effect of postharvest UV-C irradiation on gene expression profile in tomato fruit.</title>
            <link>http://www.medworm.com/index.php?rid=5086644&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21787852%26dopt%3DAbstract</link>
            <description>Authors: Liu C, Cai L, Han X, Ying T
    To obtain an overall view on gene expression during the early stage (24h) of tomato fruit in response to postharvest UV-C irradiation (4kJ/m(2)), we performed a microarray analysis by using Affymetrix Tomato Genechip. The results showed that 274 and 403 genes were up- or down-regulated, respectively, more than two folds in postharvest tomato fruit irradiated with UV-C as compared with that in control fruit. The up-regulated genes mainly involve in signal transduction, defense response and metabolism. Conversely, genes related to cell wall disassembly, photosynthesis and lipid metabolism were generally down-regulated. These results opened ways to probe into the molecular mechanisms of the effects of postharvest UV-C irradiation on increased disease r...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5086644</comments>
            <pubDate>Tue, 19 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5086644</guid>        </item>
        <item>
            <title>Molecular cloning and expression of a cucumber (Cucumis sativus L.) heme oxygenase-1 gene, CsHO1, which is involved in adventitious root formation.</title>
            <link>http://www.medworm.com/index.php?rid=5086646&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21784139%26dopt%3DAbstract</link>
            <description>In this study, the cucumber HO-1 gene (named as CsHO1) was isolated and sequenced. It contains four exons and three introns and encodes a polypeptide of 291 amino acids. Further results show that CsHO1 shares a high homology with plant HO-1 proteins and codes a 33.3kDa protein with a 65-amino transit peptide, predicting a mature protein of 26.1kDa. The mature CsHO1 was expressed in Escherichia coli to produce a fusion protein, which exhibits HO activity. The CsHO1:GFP fusion protein was localized in the chloroplast. Related biochemical analyses of mature CsHO1, including Vmax, Km, Topt and pHopt, were also investigated. CsHO1 mRNA was found in germinating seeds, roots, stem, and especially in leaf tissues. Several well-known adventitious root inducers, including auxin, ABA, hemin, nitric o...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5086646</comments>
            <pubDate>Mon, 18 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5086646</guid>        </item>
        <item>
            <title>Genome-wide analysis of interferon regulatory factor I binding in primary human monocytes.</title>
            <link>http://www.medworm.com/index.php?rid=5086640&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21803131%26dopt%3DAbstract</link>
            <description>Authors: Shi L, Perin JC, Leipzig J, Zhang Z, Sullivan KE
    IRF1 is a transcription factor that participates in interferon signaling. Previous studies of IRF1 binding have utilized in vitro assays. We used ChIP-seq in human monocytes to better define the recognition motif for IRF1. The newly identified 18bp motif (RAAASNGAAAGTGAAASY) is a refinement of the 13bp IRF1 motif commonly used. We utilized the 18bp consensus motif and identified 345 potential target genes. To compare the 18bp motif with the 13bp motif, we compared putative gene targets. Only 56 potential gene targets were defined by both consensus motifs. To compare biological effects of interferon on the 13bp and the 18bp consensus targets, we mined expression data from cells exposed to interferons or transfected with IRF1. In ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5086640</comments>
            <pubDate>Mon, 18 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5086640</guid>        </item>
        <item>
            <title>Protein map: An alignment-free sequence comparison method based on various properties of amino acids.</title>
            <link>http://www.medworm.com/index.php?rid=5086638&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21803133%26dopt%3DAbstract</link>
            <description>Authors: Yu C, Cheng SY, He RL, Yau SS
    In this paper, we propose a new protein map which incorporates with various properties of amino acids. As a powerful tool for protein classification, this new protein map both considers phylogenetic factors arising from amino acid mutations and provides computational efficiency for the huge amount of data. The ten amino acid physico-chemical properties (the chemical composition of the side chain, two polarity measures, hydropathy, isoelectric point, volume, aromaticity, aliphaticity, hydrogenation, and hydroxythiolation) are utilized according to their relative importance. Moreover, during the course of calculation of genetic distances between pairs of proteins, this approach does not require any alignment of sequences. Therefore, the proposed mod...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5086638</comments>
            <pubDate>Mon, 18 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5086638</guid>        </item>
        <item>
            <title>Integration of molecular genetics and proteomics with cell metabolism: How to proceed; How not to proceed!</title>
            <link>http://www.medworm.com/index.php?rid=5086650&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21782907%26dopt%3DAbstract</link>
            <description>Authors: Costello LC, Franklin RB
    There now exists a resurgence of interest in the role of intermediary metabolism in medicine; especially in relation to medical disorders. Coupled with this is the contemporary focus on molecular biology, genetics and proteomics and their integration into studies of regulation and alterations in cellular metabolism in health and disease. This is a marriage that has vast potential for elucidation of the factors and conditions that are involved in cellular metabolic and functional changes, which heretofore could not be addressed by the earlier generations of biochemists who established the major pathways of intermediary metabolism. The achievement of this present potential requires the appropriate application and interpretation of genetic and proteomic s...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5086650</comments>
            <pubDate>Sun, 17 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5086650</guid>        </item>
        <item>
            <title>Enhancement of angiogenic effect of co-transfection human NGF and VEGF genes in rat bone marrow mesenchymal stem cells.</title>
            <link>http://www.medworm.com/index.php?rid=5086649&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21782908%26dopt%3DAbstract</link>
            <description>Authors: Fan BS, Lou JY
    The current study explored the feasibility and efficacy of co-transfection of the human nerve growth factor (NGF) and vascular endothelial growth factor 165 (VEGF165) genes in rat bone marrow mesenchymal stem cells (BMSCs). The obtained hNGF and vascular endothelial growth factor (VEGF) cDNAs were cloned into the pEGFP-C1 expression vector to construct the recombinant vectors. Co-transfection in rat BMSCs was performed and the expressions of both genes were detected by RT-PCR, Western blot, and enzyme-linked immunospecific assay. The biological activity of recombinant NGF and VEGF proteins was confirmed using the Chick Chorioallantoic Membrane (CAM) assay. NGF and VEGF genes could be expressed successfully in rat BMSCs. The recombinant NGF and VEGF from the rat ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5086649</comments>
            <pubDate>Sun, 17 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5086649</guid>        </item>
        <item>
            <title>The evolution of alternative splicing exons in vascular endothelial growth factor A.</title>
            <link>http://www.medworm.com/index.php?rid=5086648&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21782909%26dopt%3DAbstract</link>
            <description>Authors: Xu J, Dou T, Liu C, Fu M, Huang Y, Gu S, Zhou Y, Xie Y
    The C-terminus alternative splicing in VEGFA (vascular endothelial growth factor A) is known for its impact on physiological and pathological angiogenesis. Based on our prediction and RT-PCR verification, we identified anti-angiogenic VEGFA165b isoforms in mouse and rabbit for the first time. We also found that the relative expression level of VEGFA165b isoform had been increasing from rodents to human, and exon8b may have experienced a minor-to-major form exon conversion, possibly correlated with its gain-of-function. It is suggested that introduction of alternative splicing exons (esp. exon6 and exon8b) made important contributions to the transcriptional diversity of VEGFA and played a crucial role in the evolution of it...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5086648</comments>
            <pubDate>Sun, 17 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5086648</guid>        </item>
        <item>
            <title>FMR1 CGG repeat lengths mediate different regulation of reporter gene expression in comparative transient and locus specific integration assays.</title>
            <link>http://www.medworm.com/index.php?rid=5086652&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21767618%26dopt%3DAbstract</link>
            <description>This study shows that locus directed integration of model FMR1 CGG transgenes could be a new basic tool to further elucidating the basic molecular mechanisms behind transcriptional deregulation of the FMR1 gene in fragile X-syndrome and FXTAS.
    PMID: 21767618 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5086652</comments>
            <pubDate>Tue, 12 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5086652</guid>        </item>
        <item>
            <title>Identification and characterization of a functional zebrafish smrt corepressor (ncor2).</title>
            <link>http://www.medworm.com/index.php?rid=5086651&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21767619%26dopt%3DAbstract</link>
            <description>Authors: Linney E, Perz-Edwards A, Kelley B
    The retinoic acid receptors (RARs or rars) and the thyroid hormone receptors are members of the steroid receptor superfamily that interact with their DNA response elements (for RARs: retinoic acid response elements or RAREs) in the regulatory regions of promoters in the absence of their ligand. In this ligand minus configuration, it has been suggested that the RAR provides a binding site for a corepressor (SMRT or N-CoR) that also brings in other proteins to repress the gene. In the presence of the ligand, the receptor goes through an allosteric change eliminating the corepressor binding site and providing a coactivator binding site. In this manuscript we describe the isolation of the zebrafish corepressor, smrt. We show that its association ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5086651</comments>
            <pubDate>Tue, 12 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5086651</guid>        </item>
        <item>
            <title>The evolution of MDM2 family genes.</title>
            <link>http://www.medworm.com/index.php?rid=5086653&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21762762%26dopt%3DAbstract</link>
            <description>Authors: Momand J, Villegas A, Belyi VA
    MDM2 and MDM4 are proto-oncoproteins that bind to and inhibit members of the p53 protein family, p53, p73 and possibly p63. p53 is a mammalian tumor suppressor and p63 and p73 are critical for development. With the sequencing of genomes from multiple organisms there is mounting evidence for a consensus scenario of p53 gene family evolution. A single p53/p63/p73 gene is in invertebrates and required for maintenance of germline DNA. Gene duplication occurred in an ancestor in common with cartilaginous fishes, giving rise to a separate p53 gene and at least one ancestral p63/p73 gene. In bony vertebrates, all three p53 gene family paralogs, p53, p63, and p73 are distinct genes. This raises the question of how MDM2 and MDM4 genes evolved. We show evi...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5086653</comments>
            <pubDate>Sun, 03 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5086653</guid>        </item>
        <item>
            <title>Pseudotrisomy 13 syndrome: Use of homozygosity mapping to target candidate genes.</title>
            <link>http://www.medworm.com/index.php?rid=5037287&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21756987%26dopt%3DAbstract</link>
            <description>Authors: Marquis-Nicholson R, Aftimos S, Ashton F, Love JM, Stone P, McFarlane J, George AM, Love DR
    Pseudotrisomy 13 syndrome is characterised by holoprosencephaly with or without polydactyly, but with a normal karyotype. The genetic cause of this syndrome remains unclear, but it is thought to be autosomal recessive. In order to identify possible candidate genes, we identified regions of homozygosity in the DNA of an affected foetus, which was the seventh pregnancy of a healthy non-consanguineous Cook Island Maori couple; this ethnic group derives from a small founder population. Several large regions of homozygosity were identified using a high density array. We excluded two candidate genes that lay within these regions, and suggest that Pseudotrisomy 13 syndrome might not be monogen...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5037287</comments>
            <pubDate>Sun, 03 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5037287</guid>        </item>
        <item>
            <title>Transcriptional and epigenetic effects of deleting large regions, alone or in combination, from their natural context in the chicken Ig-β gene.</title>
            <link>http://www.medworm.com/index.php?rid=5037289&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21749917%26dopt%3DAbstract</link>
            <description>In this study, we regrouped the cell-type-specific DHSs of Ig-β, those in the original six deletions and three additional ones, into three larger regional groups-the long upstream region, the intron, and the long downstream region-and deleted these groups individually or in combination. Combinatorial deletion of all three regional groups decreased Ig-β mRNA levels to 0.4% of the control, which was significantly higher than &amp;lt;0.1%, the level resulting from deletion of all six smaller groups. Histone H3 and H4 acetylation and H3K4 dimethylation levels at the Ig-β promoter were low in cells carrying deletions of all six smaller groups, but intermediate levels of acetylation and enhanced H3K4 dimethylation were observed in cells carrying deletions of all three larger groups. While CG meth...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5037289</comments>
            <pubDate>Fri, 01 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5037289</guid>        </item>
        <item>
            <title>Molecular mechanism underlying the differential MYF6 expression in postnatal skeletal muscle of Duroc and Pietrain breeds.</title>
            <link>http://www.medworm.com/index.php?rid=5037288&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21749918%26dopt%3DAbstract</link>
            <description>Authors: Fan H, Cinar MU, Phatsara C, Tesfaye D, Tholen E, Looft C, Schellander K
    Among modern western pigs, Duroc (high meat fat ratio) and Pietrain (low meat fat ratio) breeds extensively utilized in commercial pork production differ extremely for their muscle phenotypes. The molecular mechanism, especially the epigenetic mechanism, underlying these breed-specific differences is poorly known. Myogenic factor 6 (MYF6) is the most abundantly expressed myogenic factor in adult muscle. Moreover, MYF6 tends to be expressed more highly in muscle tissue of the lean selection line and is supposed to be one promising candidate gene for growth- and meat quality-related traits in adult pigs. Six months old female Duroc and Pietrain pure breed pigs were used in this study. Protein and mRNA level...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5037288</comments>
            <pubDate>Fri, 01 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5037288</guid>        </item>
        <item>
            <title>An SRp75/hnRNPG complex interacting with hnRNPE2 regulates the 5' splice site of tau exon 10, whose misregulation causes frontotemporal dementia.</title>
            <link>http://www.medworm.com/index.php?rid=5037292&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21723381%26dopt%3DAbstract</link>
            <description>In this study, we investigated three regulators of exon 10 splicing: serine/arginine-rich protein SRp75 and heterogeneous nuclear ribonucleoproteins hnRNPG and hnRNPE2. SRp75 and hnRNPG inhibit splicing of exon 10 whereas hnRNPE2 activates it. Using co-transfections, co-immunoprecipitations and RNAi we discovered that SRp75 binds to the proximal downstream intron of tau exon 10 at the FTDP-17 hotspot region; and that hnRNPG and hnRNPE2 interact with SRp75. Thus, increased exon 10 inclusion in FTDP mutants may arise from weakened SRp75 binding. This work provides insights into the splicing regulation of the tau gene and into possible strategies for correcting the imbalance in tauopathies caused by changes in the ratio of exon 10.
    PMID: 21723381 [PubMed - as supplied by publisher] (Sourc...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5037292</comments>
            <pubDate>Wed, 29 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5037292</guid>        </item>
        <item>
            <title>Molecular characterization of the iron binding protein ferritin in Eisenia andrei earthworms.</title>
            <link>http://www.medworm.com/index.php?rid=5037291&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21723382%26dopt%3DAbstract</link>
            <description>In this study, we report on the sequence characterization of a ferritin-coding cDNA in Eisenia andrei earthworms isolated by RT-PCR using degenerated primers, and we suggest the presence of a putative IRE in the 5'-UTR of ferritin mRNA. The obtained ferritin sequence was compared with those of other animals showing sequence and structure homology in consensus sites, including the iron-responsive element (IRE) and ferroxidase centers. Despite the sequence homology in the E. andrei mRNA of ferritin with the sequences of other animals in consensus IRE sites, the presented cytosine in the IRE of E. andrei ferritin in the expected position does not form a conventional bulge. The presence of ferritin in the coelomic fluid of E. andrei was proven by iron staining assay. Moreover, aconitase activi...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5037291</comments>
            <pubDate>Wed, 29 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5037291</guid>        </item>
        <item>
            <title>Feedback regulation of Ran gene expression by Ran protein.</title>
            <link>http://www.medworm.com/index.php?rid=5037290&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21741460%26dopt%3DAbstract</link>
            <description>In this study, the promoter of shrimp Ran gene was identified which contained a typical TATA box. The results showed that the shrimp Ran protein was bound with the Ran promoter in Drosophila S2 cells. Based on luciferase assays, our study indicated that the transcription of Ran gene could be regulated by the interaction between the Ran promoter and the Ran protein, suggesting the existence of a feedback regulation in Ran gene expression. Therefore our study presented a novel finding on the feedback regulation of gene transcription.
    PMID: 21741460 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5037290</comments>
            <pubDate>Tue, 28 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5037290</guid>        </item>
        <item>
            <title>Alteration of microRNA expression in the process of mouse brain growth.</title>
            <link>http://www.medworm.com/index.php?rid=4993292&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21718763%26dopt%3DAbstract</link>
            <description>In this study, we investigated expression profiles of miRNAs in the process of normal mouse brain growth from embryonic day 16.5 to ~19months old by means of DNA microarray and reverse-transcription quantitative polymerase chain reaction, and we examined whether there was any association between the expression of miRNAs and brain growth. The results indicated that a major change in the expression of miRNAs occurred in the brain within the first week to the fourth week postnatally. The data also exhibited the miRNAs that gradually increased and decreased in their levels, over the course of brain growth. Therefore, the current study suggests that miRNAs are capable of becoming a useful biological marker for study of brain growth, and leads to the possibility that gene silencing involving miR...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4993292</comments>
            <pubDate>Sun, 26 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4993292</guid>        </item>
        <item>
            <title>Identification and characterization of a novel mammalian isoform of the endocytic adaptor ITSN1.</title>
            <link>http://www.medworm.com/index.php?rid=4993298&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21712076%26dopt%3DAbstract</link>
            <description>Authors: Dergai M, Skrypkina I, Dergai O, Tsyba L, Novokhatska O, Filonenko V, Drobot L, Rynditch A
    Intersectin 1 (ITSN1) is an evolutionarily conserved adaptor protein engaged in clathrin-mediated endocytosis, cell signaling and actin cytoskeleton rearrangements. Two major ITSN1 isoforms were initially described, the ubiquitous short isoform (ITSN1-s) and the long isoform (ITSN1-l) expressed predominantly in neurons. Numerous alternative splicing events for ITSN1 pre-mRNA were later identified. Here we describe a novel isoform ITSN1-22a with an alternative C-terminus encoded by exon 22a. This exon is only found in placental mammals. The transcript of ITSN1-22a is detected in a wide range of human and mouse tissues. We show here that two alternative splicing events affect the coding se...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4993298</comments>
            <pubDate>Fri, 24 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4993298</guid>        </item>
        <item>
            <title>EST analysis on adipose tissue of rainbow trout Oncorhynchus mykiss and tissue distribution of adiponectin.</title>
            <link>http://www.medworm.com/index.php?rid=4993297&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21712077%26dopt%3DAbstract</link>
            <description>In this study, over 30,000 expressed sequence tags (ESTs) were obtained from adipose tissue in rainbow trout Oncorhynchus mykiss peritoneal cavity and searched for genes possibly related to lipid metabolism. Large numbers of ESTs encoded digestive enzymes and hormones usually found in the pancreas in higher vertebrates, consistent with the fact that pancreatic cells are dispersed in the adipose tissue. Many ESTs encoded apolipoprotein C-I, fatty acid-binding proteins and lymphocyte G0/G1 switch protein 2, which function in lipid transport, fatty acid accumulation and adipocyte differentiation, respectively. None of the ESTs encoded adipokines. We therefore obtained a cDNA encoding adiponectin, an adipokine that regulates oxidation of glucose and lipids in peripheral tissues, using rainbow ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4993297</comments>
            <pubDate>Fri, 24 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4993297</guid>        </item>
        <item>
            <title>Characterization of a CENP-B homolog in the holocentric Lepidoptera Spodoptera frugiperda.</title>
            <link>http://www.medworm.com/index.php?rid=4993296&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21712078%26dopt%3DAbstract</link>
            <description>Authors: d'Alençon E, Nègre N, Stanojcic S, Alassoeur B, Gimenez S, Léger A, Abd-Alla A, Juliant S, Fournier P
    The discovery of an homolog of the human centromeric protein B, CENP-B, in an EST database of the holocentric insect species Spodoptera frugiperda prompted us to further characterize that gene because i) CENP-B has not been described in invertebrates yet ii) it should be a milestone in the molecular characterization of the holocentric centromere of Lepidoptera. Like its human counterpart, the Sf CENP-B protein is related to the transposase of the pogo transposable element (TE) of D. melanogaster. In this paper, we show evidences that the lepidopteran cenpB gene has evolved from domestication of a transposase. Furthermore, the Sf CENP-B nuclear location and its ability to bi...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4993296</comments>
            <pubDate>Fri, 24 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4993296</guid>        </item>
        <item>
            <title>RNA polymerase III transcription control elements: Themes and variations.</title>
            <link>http://www.medworm.com/index.php?rid=4993295&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21712079%26dopt%3DAbstract</link>
            <description>Authors: Orioli A, Pascali C, Pagano A, Teichmann M, Dieci G
    Eukaryotic genomes are punctuated by a multitude of tiny genetic elements, that share the property of being recognized and transcribed by the RNA polymerase (Pol) III machinery to produce a variety of small, abundant non-protein-coding (nc) RNAs (tRNAs, 5S rRNA, U6 snRNA and many others). The highly selective, efficient and localized action of Pol III at its minute genomic targets is made possible by a handful of cis-acting regulatory elements, located within the transcribed region (where they are bound by the multisubunit assembly factor TFIIIC) and/or upstream of the transcription start site. Most of them participate directly or indirectly in the ultimate recruitment of TFIIIB, a key multiprotein initiation factor able to d...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4993295</comments>
            <pubDate>Fri, 24 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4993295</guid>        </item>
        <item>
            <title>Novel genes specifically expressed during the development of the male thalli and antheridia in the dioecious liverwort Pellia endiviifolia.</title>
            <link>http://www.medworm.com/index.php?rid=4993294&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21712080%26dopt%3DAbstract</link>
            <description>Authors: Sierocka I, Rojek A, Bielewicz D, Karlowski W, Jarmolowski A, Szweykowska-Kulinska Z
    In bryophytes (lower plants), sex determination is manifested in the gametophyte generation by the production of egg- and sperm-forming gametangia. We identified four genes specifically expressed in the male thalli of dioecious liverwort Pellia endiviifolia species B using RDA-cDNA method. These are: PenB_TUA1 coding for an α-tubulin family protein, PenB_Raba1/11 coding for a Rab family protein, PenB_HMG-box coding for an HMG-box family protein and PenB_MT coding for an unknown transcript that contains an ORF of 295 amino acid residues. The expression of identified genes shows developmental and environmental regulation. PenB_TUA1 and PenB_Raba1/11 are expressed in the male thalli, regardless ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4993294</comments>
            <pubDate>Fri, 24 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4993294</guid>        </item>
        <item>
            <title>Sequence conservation among orthologous vomeronasal type 1 receptor-like (Ora) genes does not support the differential tuning hypothesis in Salmonidae.</title>
            <link>http://www.medworm.com/index.php?rid=4993293&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21712081%26dopt%3DAbstract</link>
            <description>In this study, we used genomic DNA sequence data from nine salmonid species to compare nucleotide identities for orthologous main olfactory receptor (mOR) genes with nucleotide identities for orthologous vomeronasal type 1-like (Ora) receptor genes. We found that orthologs for both classes of olfactory receptor genes (mORs and Oras) appear to be highly conserved among species. Our findings do not support the differential tuning hypothesis in Salmonidae, which predicts higher sequence conservation for mORs than Oras. We did, however, find convincing evidence for site-specific positive selection acting on paralogous main olfactory receptor genes.
    PMID: 21712081 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4993293</comments>
            <pubDate>Fri, 24 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4993293</guid>        </item>
        <item>
            <title>Detection and characterization of interleukin-6 gene variants in Canis familiaris: Association studies with periodontal disease.</title>
            <link>http://www.medworm.com/index.php?rid=4993302&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21708229%26dopt%3DAbstract</link>
            <description>This study aims to contribute to the characterization of the genetic basis of PD in the dog, a classically accepted model in Periodontology. We searched for genetic variations in the interleukin-6 (IL6) gene, in order to verify its association with PD in a case-control study including 25 dogs in the PD case group and 45 dogs in the control group. We indentified and characterized three new genetic variations in IL6 gene. No statistically significant differences were detected between the control and PD cases groups. Our results do not support an evidence for a major role contribution of these variants in the susceptibility to PD in the analyzed population. Nevertheless, the sequence variant I/5_g.105G&amp;gt;A leads to an amino acid change (arginine to glutamine) and was predicted to be possibly...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4993302</comments>
            <pubDate>Thu, 23 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4993302</guid>        </item>
        <item>
            <title>Proteome profile of maize (Zea Mays L.) leaf tissue at the flowering stage after long-term adjustment to rice black-streaked dwarf virus infection.</title>
            <link>http://www.medworm.com/index.php?rid=4993301&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21708230%26dopt%3DAbstract</link>
            <description>Authors: Li K, Xu C, Zhang J
    Maize rough dwarf disease (MRDD) is a viral disease and causes great yield loss. To better understand the effects of MRDD on plant growth and metabolism, comparative proteomic analysis of leaves from virus-infected and normal plants was performed. In order to eliminate the interference of Ribulose-1, 5-bisphosphate carboxylase with low-abundance proteins, total proteins were pre-fractionated by 15% PEG and the proteins from supernatant and precipitated fractions were analyzed by 2-DE, subsequently. Out of approximately 1200 protein spots detected, less than 2% of the spots on the gels were overlapping between the fractions of precipitation and supernatant. We identified 91 differentially accumulated proteins that belong to multiple metabolic/biochemical pat...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4993301</comments>
            <pubDate>Thu, 23 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4993301</guid>        </item>
        <item>
            <title>Transcriptional regulation of antioxidant enzymes by FoxO1 under dehydration stress.</title>
            <link>http://www.medworm.com/index.php?rid=4993300&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21708231%26dopt%3DAbstract</link>
            <description>This study analyzed responses to dehydration stress by manganese-dependent superoxide dismutase (MnSOD) and catalase, and the role of forkhead box class O type 1 (FoxO1) transcription factor in regulating their up-regulation, in selected tissues of the African clawed frogs, Xenopus laevis. Protein and mRNA levels of MnSOD and catalase were analyzed by immunoblotting and PCR. Analysis of FoxO1 included protein and phosphoprotein (FoxO1(ser245)) levels, nuclear versus cytoplasmic distribution, and FoxO1 binding to DNA. MnSOD protein increased significantly in the liver during dehydration whereas catalase rose in the liver and skeletal muscle. This was supported in liver by 1.5-2.2 fold increases in MnSOD and catalase mRNA levels. FoxO1 transcriptional activity was enhanced in liver of dehydr...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4993300</comments>
            <pubDate>Thu, 23 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4993300</guid>        </item>
        <item>
            <title>Functional activity of the novel Alzheimer's amyloid β-peptide interacting domain (AβID) in the APP and BACE1 promoter sequences and implications in activating apoptotic genes and in amyloidogenesis.</title>
            <link>http://www.medworm.com/index.php?rid=4993299&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21708232%26dopt%3DAbstract</link>
            <description>Authors: Bailey JA, Maloney B, Ge YW, Lahiri DK
    Amyloid β peptide (Aβ) plaque in the brain is the primary (post mortem) diagnostic criterion of Alzheimer's disease (AD). Any physiological role of Aβ constituent is poorly understood. We have previously determined an Aβ interacting domain (AβID) in the promoters of AD-associated genes (Maloney and Lahiri, in press). This AβID interacts in a DNA sequence-specific manner with Aβ. We now demonstrate novel Aβ activity as a possible transcription factor. Herein, we demonstrate Aβ-chromatin interaction in cell culture by ChIP assay. We observed that human neuroblastoma (SK-N-SH) cells treated with FITC conjugated Aβ1-40 localized Aβ to the nucleus in the presence of H(2)O(2)-mediated oxidative stress. Furthermore, primary rat fetal ...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4993299</comments>
            <pubDate>Thu, 23 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4993299</guid>        </item>
        <item>
            <title>Relation between 3435C&gt;T multidrug resistance 1 gene polymorphism with high dose methylprednisolone treatment of childhood acute idiopathic thrombocytopenic purpura.</title>
            <link>http://www.medworm.com/index.php?rid=4993291&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21718764%26dopt%3DAbstract</link>
            <description>CONCLUSION: In our study, there was no difference in the HDMP treatment response between MDR1 gene genotypes. However, it should be noted that this study includes a small group of patients. Our data should therefore be considered preliminary, awaiting further confirmatory studies on an expanded patient base.
    PMID: 21718764 [PubMed - as supplied by publisher] (Source: Gene)</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4993291</comments>
            <pubDate>Mon, 20 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4993291</guid>        </item>
        <item>
            <title>The complete mitochondrial genome of the leafminer Liriomyza sativae (Diptera: Agromyzidae): Great difference in the A+T-rich region compared to Liriomyza trifolii.</title>
            <link>http://www.medworm.com/index.php?rid=4993304&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21703334%26dopt%3DAbstract</link>
            <description>Authors: Yang F, Du YZ, Wang LP, Cao JM, Yu WW
    The complete mitochondrial genome sequence of Liriomyza sativae Blanchard (15,551bp) was determined and analyzed in this study. The circular genome contained 37 genes including 13 protein-coding genes, 22 tRNA genes, 2 rRNA genes and an A+T-rich region. The initiation codons of COI and ND1 were 'ATCA' and 'GTG', respectively. ND2 gene used the truncated termination codon 'T'. All the tRNA genes had the typical cloverleaf secondary structures except for tRNA(Ser(AGN)) gene, which was found with the absence of a DHU arm. In addition, a tRNA-like secondary structure (tRNA(Met)) was found in the A+T-rich region. The great difference was that the length of L. sativae A+T-rich region was 597bp shorter than that of Liriomyza trifolii (Burgess). M...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4993304</comments>
            <pubDate>Wed, 15 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4993304</guid>        </item>
        <item>
            <title>Yeast cell cycle transcription factors identification by variable selection criteria.</title>
            <link>http://www.medworm.com/index.php?rid=4993303&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21703335%26dopt%3DAbstract</link>
            <description>Authors: Wang H, Wang YH, Wu WS
    Identifying cell cycle transcription factors (TFs) is important for understanding the transcriptional regulation of the cell cycle process which controls the growth and development of all organisms. Existing computational approaches for identifying cell cycle TFs are mainly based on methods with a fixed selection criterion. That is, the same criterion was applied to each TF to determine whether it is a cell cycle TF or not. Since the characteristic of each TF may be quite different, it is not suitable to use a fixed selection criterion in identifying cell cycle TFs. Instead of using a fixed selection criterion, we propose a method with variable selection criteria to identify cell cycle TFs in yeast by integrating the ChIP-chip and cell cycle gene express...</description>
            <author>Gene</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4993303</comments>
            <pubDate>Wed, 15 Jun 2011 23:00:00 +0100</pubDate>
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        <item>
            <title>The Alzheimer's amyloid β-peptide (Aβ) binds a specific DNA Aβ-interacting domain (AβID) in the APP, BACE1, and APOE promoters in a sequence-specific manner: Characterizing a new regulatory motif.</title>
            <link>http://www.medworm.com/index.php?rid=4993305&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21699964%26dopt%3DAbstract</link>
            <description>Authors: Maloney B, Lahiri DK
    Deposition of extracellular plaques, consisting of amyloid β peptide (Aβ), in the brain is the confirmatory diagnostic of Alzheimer's disease (AD); however, the physiological and pathological role of Aβ is not fully understood. Herein, we demonstrate novel Aβ activity as a putative transcription factor upon AD-associated genes. We used oligomers from 5'-flanking regions of the apolipoprotein E (APOE), Aβ-precursor protein (APP) and β-amyloid site cleaving enzyme-1 (BACE1) genes for electrophoretic mobility shift assay (EMSA) with different fragments of the Aβ peptide. Our results suggest that Aβ bound to an Aβ-interacting domain (AβID) with a consensus of &quot;KGGRKTGGGG&quot;. This peptide-DNA interaction was sequence specific, and mutation of the first ...</description>
            <author>Gene</author>
            <type>journals</type>
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            <pubDate>Tue, 14 Jun 2011 23:00:00 +0100</pubDate>
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            <title>Computational analysis of the fructosyltransferase enzymes in plants, fungi and bacteria.</title>
            <link>http://www.medworm.com/index.php?rid=4944185&amp;cid=s_35583_50_f&amp;fid=35583&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21679751%26dopt%3DAbstract</link>
            <description>In this study, we conducted a computational analysis of reported sequences for FTase from a diverse source of organisms, such as plants, fungi, and bacteria. Ninety-one proteins sequences were obtained; all belonging to the glycoside hydrolase 32 (GH32) and 68 (GH68) families. The sequences were grouped in seven clades, five for plants, one for fungi, and one for bacteria. Our findings suggest that FTases from fungi and bacteria likely evolved from dicotyledonous FTases. The analysis of catalytic domains A, D and E, which contain the amino acids involved in the catalytic binding site, allowed the identification of clade-specific conserved characteristics. The analysis of sequence motifs involved in donor/acceptor molecule affinity showed that additional sequences could be responsible for d...</description>
            <author>Gene</author>
            <type>journals</type>
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            <pubDate>Sun, 12 Jun 2011 23:00:00 +0100</pubDate>
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