<?xml version="1.0" encoding="iso-8859-1"?>
<!-- generator="FeedCreator 1.7.2" -->
<rss version="2.0">
    <channel>
        <title>Plant Methods 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 'Plant Methods' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Plant+Methods&t=Plant+Methods&s=Search&f=source]]></link>
        <lastBuildDate>Mon, 06 Feb 2012 14:26:19 +0100</lastBuildDate>
        <item>
            <title>PhosphoRice: A meta-predictor of rice-specific phosphorylation sites</title>
            <link>http://www.medworm.com/index.php?rid=5656304&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F8%2F1%2F5</link>
            <description>PhosphoRice is a web-based tool specifically designed to predict phosphorylation sites in rice. It can be accessed at http://bioinformatics.fafu.edu.cn/PhosphoRice. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5656304</comments>
            <pubDate>Fri, 03 Feb 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5656304</guid>        </item>
        <item>
            <title>A simple and efficient method for the long-term preservation of plant cell suspension cultures</title>
            <link>http://www.medworm.com/index.php?rid=5643749&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F8%2F1%2F4</link>
            <description>The authors describe a very convenient way to preserve plant cell cultures that doesn't require any specialised equipment and avoids the use of freezing. A combination of low temperature (5oC) and a phosphate-free medium allows the cells to remain viable for 6 months and, importantly to resume active growth without a lag when they are returned to standard culture conditions. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5643749</comments>
            <pubDate>Mon, 30 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5643749</guid>        </item>
        <item>
            <title>Hyperspectral imaging for small-scale analysis of symptoms caused by different sugar beet diseases</title>
            <link>http://www.medworm.com/index.php?rid=5624610&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F8%2F1%2F3</link>
            <description>Hyperspectral imaging (HSI) offers high potential as a non-invasive diagnostic tool for disease detection. In this paper leaf characteristics and spectral reflectance of sugar beet leaves diseased with Cercospora leaf spot, powdery mildew and leaf rust at different development stages were connected. Light microscopy was used to describe the morphological changes in the host tissue due to pathogen colonisation. Under controlled conditions a hyperspectral imaging line scanning spectrometer (ImSpector V10E) with a spectral resolution of 2.8 nm from 400 to 1000 nm and a spatial resolution of 0.19 mm was used for continuous screening and monitoring of disease symptoms during pathogenesis. A pixel-wise mapping of spectral reflectance in the visible and near-infrared range enabled the detection a...</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5624610</comments>
            <pubDate>Tue, 24 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5624610</guid>        </item>
        <item>
            <title>A convenient method for simultaneous quantification of multiple phytohormones and metabolites: application in study of rice-bacterium interaction</title>
            <link>http://www.medworm.com/index.php?rid=5603832&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F8%2F1%2F2</link>
            <description>Conclusion:
This UFLC-ESI-MS method is convenient, sensitive, reliable, and inexpensive for quantification of multiple phytohormones and metabolites compared to current methods. The results obtained by application of this method in studying rice-bacterial interaction provide a basis for understanding the molecular mechanisms of rice defense responses. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5603832</comments>
            <pubDate>Sun, 15 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5603832</guid>        </item>
        <item>
            <title>Precursor uptake assays and metabolic analyses in isolated tomato fruit chromoplasts</title>
            <link>http://www.medworm.com/index.php?rid=5592854&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F8%2F1%2F1</link>
            <description>Conclusions:
We have set up a method for high yield purification of intact tomato fruit chromoplasts suitable for precursor uptake assays and metabolic analyses. Using targeted radiolabeled precursors we have been able to unravel novel biochemical and metabolic aspects related with carotenoid and lipid biosynthesis in tomato fruit chromoplasts. The reported chromoplast system could represent a valuable platform to address the validation and characterization of functional processes predicted from recent transcriptomic and proteomic data. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5592854</comments>
            <pubDate>Fri, 13 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5592854</guid>        </item>
        <item>
            <title>An improved protocol for efficient transformation and regeneration of diverse indica rice cultivars</title>
            <link>http://www.medworm.com/index.php?rid=5556712&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F49</link>
            <description>Conclusions:
This speedy, yet less labor-intensive, protocol overcomes major limitations associated with genetic manipulation in rice. Moreover, our protocol uses mature seeds as the explant, which can easily be obtained in quantity throughout the year and kept viable for a long time. Such an easy, efficient and generalized protocol has the potential to be a major tool for crop improvement and gene-function studies on the model monocot plant rice. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5556712</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5556712</guid>        </item>
        <item>
            <title>Comparative evaluation of extraction methods for apoplastic proteins from maize leaves</title>
            <link>http://www.medworm.com/index.php?rid=5533157&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F48</link>
            <description>Proteins in the plant apoplast are essential for many physiological processes. We have analysed and compared six different infiltration solutions for proteins contained in the apoplast to recognize the most suitable method for leaves and to establish proteome maps for each extraction. The efficiency of protocols was evaluated by comparing the protein patterns resolved by 1-DE and 2-DE, and revealed distinct characteristics for each infiltration solution. Nano-LC-ESI-Q-TOF MS analysis of all fractions was applied to cover all proteins differentially extracted by infiltration solutions and led to the identification of 328 proteins in total in apoplast preparations. The predicted subcellular protein localisation distinguished the examined infiltration solutions in those with high or low amoun...</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5533157</comments>
            <pubDate>Thu, 22 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5533157</guid>        </item>
        <item>
            <title>Reverse protection assay: a tool to analyze transcriptional rates from individual promoters</title>
            <link>http://www.medworm.com/index.php?rid=5533158&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F47</link>
            <description>Transcriptional activity of entire genes in chloroplasts is usually assayed by run-on analyses. To determine not only the overall intensity of transcription of a gene, but also the rate of transcription from a particular promoter, we created the Reverse RNase Protection Assay (RePro): in-organello run-on transcription coupled to RNase protection to define distinct transcript ends during transcription. We demonstrate successful application of RePro in plastid promoter analysis and transcript 3' end processing. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5533158</comments>
            <pubDate>Tue, 20 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5533158</guid>        </item>
        <item>
            <title>Reproducible hairy root transformation and spot-inoculation methods to study root symbioses of pea</title>
            <link>http://www.medworm.com/index.php?rid=5512266&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F46</link>
            <description>The authors describe a set of tools that should greatly facilitate investigations of both the mycorrhizal and rhizobial symbioses with pea. The tools include an improved transformation method and techniques for targeted inoculation of roots with the symbiont to enable the processes involved in establishing the symbiosis to be studied in more detail. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5512266</comments>
            <pubDate>Thu, 15 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5512266</guid>        </item>
        <item>
            <title>An in vivo root hair assay for determining rates of apoptotic-like programmed cell death in plants</title>
            <link>http://www.medworm.com/index.php?rid=5500990&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F45</link>
            <description>In Arabidopsis thaliana we demonstrate that dying root hairs provide an easy and rapid in vivo model for the morphological identification of apoptotic-like programmed cell death (AL-PCD) in plants. The model described here is transferable between species, can be used to investigate rates of AL-PCD in response to various treatments and to identify modulation of AL-PCD rates in mutant/transgenic plant lines facilitating rapid screening of mutant populations in order to identify genes involved in AL-PCD regulation. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5500990</comments>
            <pubDate>Tue, 13 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5500990</guid>        </item>
        <item>
            <title>A novel machine-vision-based facility for the automatic evaluation of yield-related traits in rice</title>
            <link>http://www.medworm.com/index.php?rid=5500991&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F44</link>
            <description>The authors describe an automated facility that can enable the high-throughput evaluation of yield-related traits in rice. The facility could greatly facilitate the phenotyping process in breeding, genetics and functional genomics. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5500991</comments>
            <pubDate>Mon, 12 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5500991</guid>        </item>
        <item>
            <title>High Resolution Melt (HRM) analysis is an efficient tool to genotype EMS mutants in complex crop genomes</title>
            <link>http://www.medworm.com/index.php?rid=5492476&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F43</link>
            <description>The authors demonstrate how high resolution melt analysis can be a useful tool to characterise allelic series of EMS-induced mutations, as generated for example in TILLING populations. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5492476</comments>
            <pubDate>Thu, 08 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5492476</guid>        </item>
        <item>
            <title>A novel Gateway(R)-compatible binary vector allows direct selection of recombinant clones in Agrobacterium tumefaciens</title>
            <link>http://www.medworm.com/index.php?rid=5482928&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F42</link>
            <description>Conclusion:
Our results demonstrate that the new pEG101-SacB/R destination vector can be used for Gateway(R) cloning in Agrobacterium tumefaciens. pEG101-SacB/R will be a valuable tool for high-throughput functional analysis of genes in planta. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5482928</comments>
            <pubDate>Wed, 07 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5482928</guid>        </item>
        <item>
            <title>Simulation of future global warming scenarios in rice paddies with an open-field warming facility</title>
            <link>http://www.medworm.com/index.php?rid=5482929&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F41</link>
            <description>To simulate expected future global warming, hexagonal arrays of infrared heaters have previously been used to warm open-field canopies of upland crops such as wheat. Through the use of concrete-anchored posts, improved software, overhead wires, extensive grounding, and monitoring with a thermal camera, the technology was safely and reliably extended to paddy rice fields. The system maintained canopy temperature increases within 0.5degreesC of daytime and nighttime set-point differences of 1.3 and 2.7degreesC 67% of the time. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5482929</comments>
            <pubDate>Tue, 06 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5482929</guid>        </item>
        <item>
            <title>Protocol:  High throughput silica-based purification of RNA from Arabidopsis seedlings in a 96-well format.</title>
            <link>http://www.medworm.com/index.php?rid=5473507&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F40</link>
            <description>We present optimised manual and automated protocols for the extraction of total RNA from 9-day-old Arabidopsis seedlings in a 96 well plate format using silica membrane-based methodology. Consistent and reproducible yields of high quality RNA are isolated averaging 8.9 ug total RNA per sample (~20 mg plant tissue). The purified RNA is suitable for subsequent qPCR analysis of the expression of over 500 genes in triplicate from each sample. Using the automated procedure, 192 samples (2x 96 well plates) can easily be fully processed (samples homogenised, RNA purified and quantified) in less than half a day. Additionally we demonstrate that plant samples can be stored in RNAlater at -20 degrees C (but not 4 degrees C) for 10 months prior to extraction with no significant effect on RNA yield or...</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5473507</comments>
            <pubDate>Fri, 02 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5473507</guid>        </item>
        <item>
            <title>Universal endogenous gene controls for bisulphite conversion in analysis of plant DNA methylation</title>
            <link>http://www.medworm.com/index.php?rid=5465083&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F39</link>
            <description>Accurate analysis of DNA methylation by bisulphite sequencing depends on the complete conversion of all cytosines into uracil. Until now there has been no standard or universal gene identified as an endogenous control to monitor the conversion frequency in plants. Here, we report the development of PCR based assays for one nuclear gene IND (INDEHISCENT) and two mitochondrial genes, NAD (NICOTINAMIDE ADENINE DINUCLEOTIDE) and ATP1 (ATPase SUBUNIT 1). We demonstrated their efficacy as bisulphite conversion controls in Brassica and other plant taxa. The target regions amplified by four primer pairs were found to be consistently free from DNA methylation. Primer pairs for IND.a and NAD were effective within Brassica species, whereas two primer pairs for ATP1 provided reliable controls across a...</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5465083</comments>
            <pubDate>Fri, 02 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5465083</guid>        </item>
        <item>
            <title>An efficient procedure for plant organellar genome assembly, based on whole genome data from the 454 GS FLX sequencing platform</title>
            <link>http://www.medworm.com/index.php?rid=5465084&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F38</link>
            <description>The authors describe an improved method for sequencing and assembly of organellar genomes using the Roche 454 GS FLX platform. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5465084</comments>
            <pubDate>Tue, 29 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5465084</guid>        </item>
        <item>
            <title>Rapid and sensitive hormonal profiling of complex plant samples by liquid chromatography coupled to electrospray ionization tandem mass spectrometry</title>
            <link>http://www.medworm.com/index.php?rid=5427886&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F37</link>
            <description>Conclusions:
This new method is applicable to the analysis of dynamic changes in endogenous concentrations of hormones to study plant developmental processes or plant responses to biotic and abiotic stresses in complex tissues. An example is shown in which a hormone profiling is obtained from leaves of plants exposed to salt stress in the aromatic plant, Rosmarinus officinalis. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5427886</comments>
            <pubDate>Fri, 18 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5427886</guid>        </item>
        <item>
            <title>Transformation and regeneration of the holoparasitic plant Phelipanche aegyptiaca</title>
            <link>http://www.medworm.com/index.php?rid=5396665&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F36</link>
            <description>Conclusions:
This work constitutes a breakthrough in holoparasitic plant research methods. The method described here is a robust system for transformation and regeneration of a holoparasitic plant and will facilitate research on unique parasitic plant capabilities such as host plant recognition, haustorial formation, penetration and vascular connection. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5396665</comments>
            <pubDate>Tue, 08 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5396665</guid>        </item>
        <item>
            <title>Protocol: methodology for chromatin immunoprecipitation (ChIP) in Chlamydomonas reinhardtii</title>
            <link>http://www.medworm.com/index.php?rid=5375009&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F35</link>
            <description>The authors have investigated the most critical parameters for succesful application of the ChIP technique to Chlamydmonas, an important model organsism for plant research, and they provide a step-by-step protocol. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5375009</comments>
            <pubDate>Thu, 03 Nov 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5375009</guid>        </item>
        <item>
            <title>A simple and efficient micrografting method for stably transformed Nicotiana attenuata plants to examine shoot-root signaling</title>
            <link>http://www.medworm.com/index.php?rid=5343444&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F34</link>
            <description>An efficient micrografting method has been developed for the wild tobacco species, Nicotiana attenuata. This will allow important questions about long distance signals and their adaptive functions to be addressed in an ecological context. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5343444</comments>
            <pubDate>Thu, 20 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5343444</guid>        </item>
        <item>
            <title>A Pair of New BAC and BIBAC Vectors that Facilitate BAC/BIBAC Library Construction and Intact Large Genomic DNA Insert Exchange</title>
            <link>http://www.medworm.com/index.php?rid=5310619&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F33</link>
            <description>The new vectors described here should greatly facilitate the process of constructs BAC genomic libraries and transferring selected fragments to binary BAC (BIBAC) vectors. This will be of particular interest to those doing positional cloning and wanting to perform complementation tests by reintroducing genomic fragments via Agrobacterium transformation. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5310619</comments>
            <pubDate>Tue, 11 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5310619</guid>        </item>
        <item>
            <title>Arabidopsis seedling flood-inoculation technique: A rapid and reliable assay for studying plant-bacterial interactions</title>
            <link>http://www.medworm.com/index.php?rid=5292742&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F32</link>
            <description>Conclusions:
The Arabidopsis seedling flood-inoculation assay provides a rapid, efficient and economical method for studying Arabidopsis-Pseudomonas interactions with minimal growth chamber space and time. This assay could also provide an excellent system for investigating the virulence mechanisms of P. syringae. Using this method, we demonstrated that FLS2 plays a critical role in conferring NHR against nonhost pathovars of P. syringae, but not to Xanthomonas campestris pv. vesicatoria. This method is potentially ideal for high-throughput screening of both Arabidopsis and pathogen mutants. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5292742</comments>
            <pubDate>Thu, 06 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5292742</guid>        </item>
        <item>
            <title>Maize Microarray Annotation Database</title>
            <link>http://www.medworm.com/index.php?rid=5281321&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F31</link>
            <description>Conclusions:
The Maize Microarray Annotation Database will assist users of the Agilent-016047 maize microarray in (i) refining gene lists for global expression analysis, and (ii) confirming the annotation of candidate genes before functional studies. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5281321</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5281321</guid>        </item>
        <item>
            <title>A highly efficient rice green tissue protoplast system for transient gene expression and studying light/chloroplast-related processes</title>
            <link>http://www.medworm.com/index.php?rid=5268486&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F30</link>
            <description>Conclusions:
We show here a simplified and highly efficient transient gene expression system using photosynthetically active rice green tissue protoplasts and its broad applications in protein immunoblot, localization and protein-protein interaction assays. These rice green tissue protoplasts will be particularly useful in studies of light/chloroplast-related processes. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5268486</comments>
            <pubDate>Fri, 30 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5268486</guid>        </item>
        <item>
            <title>A tiling microarray for global analysis of chloroplast genome expression in cucumber and other plants</title>
            <link>http://www.medworm.com/index.php?rid=5268487&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F29</link>
            <description>Plastids are small organelles equipped with their own genomes (plastomes). Although these organelles are involved in numerous plant metabolic pathways, current knowledge about the transcriptional activity of plastomes is limited. To solve this problem, we constructed a plastid tiling microarray (PlasTi-microarray) consisting of 1629 oligonucleotide probes. The oligonucleotides were designed based on the cucumber chloroplast genomic sequence and targeted both strands of the plastome in a non-contiguous arrangement. Up to 4 specific probes were designed for each gene/exon, and the intergenic regions were covered regularly, with 70-nt intervals. We also developed a protocol for direct chemical labeling and hybridization of as little as 2 micrograms of chloroplast RNA. We used this protocol fo...</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5268487</comments>
            <pubDate>Wed, 28 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5268487</guid>        </item>
        <item>
            <title>Variable-angle total internal reflection fluorescence microscopy of intact cells of Arabidopsis thaliana</title>
            <link>http://www.medworm.com/index.php?rid=5257178&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F27</link>
            <description>Conclusions:
These findings demonstrate that variable-angle TIRFM is appropriate for quantitative live imaging of cells in intact tissues of Arabidopsis thaliana. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5257178</comments>
            <pubDate>Sat, 24 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5257178</guid>        </item>
        <item>
            <title>Classification of images of wheat, ryegrass and brome grass species at early growth stages using principal component analysis</title>
            <link>http://www.medworm.com/index.php?rid=5257177&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F28</link>
            <description>Wheat is one of the most important crops in Australia, and the identification of young plants is an important step towards developing an automated system for monitoring crop establishment and also for differentiating crop from weeds. In this paper, a framework to differentiate early narrow-leaf wheat from two common weeds from their digital images is developed. A combination of colour, texture and shape features is used. These features are reduced to three descriptors using Principal Component Analysis. The three components provide an effective and significant means for distinguishing the three grasses. Further analysis enables threshold levels to be set for the discrimination of the plant species. The PCA model was evaluated on an independent data set of plants and the results show accura...</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5257177</comments>
            <pubDate>Sat, 24 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5257177</guid>        </item>
        <item>
            <title>Combining multivariate analysis and monosaccharide composition modeling to identify plant cell wall variations by Fourier Transform Near Infrared spectroscopy</title>
            <link>http://www.medworm.com/index.php?rid=5155507&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F26</link>
            <description>We outline a high throughput procedure that improves outlier detection in cell wall screens using FT-NIR spectroscopy of plant leaves. The improvement relies on generating a calibration set from a subset of a mutant population by taking advantage of the Mahalanobis distance outlier scheme to construct a monosaccharide range predictive model using PLS regression. This model was then used to identify specific monosaccharide outliers from the mutant population. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5155507</comments>
            <pubDate>Wed, 17 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5155507</guid>        </item>
        <item>
            <title>Visualization of plant viral suppressor silencing activity in intact leaf lamina by quantitative fluorescent imaging</title>
            <link>http://www.medworm.com/index.php?rid=5094191&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F25</link>
            <description>${item.shortDescription} (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5094191</comments>
            <pubDate>Tue, 02 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5094191</guid>        </item>
        <item>
            <title>Reverse Genetics in Chlamydomonas: A Platform for Isolating Insertional Mutants</title>
            <link>http://www.medworm.com/index.php?rid=5068490&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F24</link>
            <description>${item.shortDescription} (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5068490</comments>
            <pubDate>Tue, 26 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5068490</guid>        </item>
        <item>
            <title>A novel method for prenylquinone profiling in plant tissues by ultra-high pressure liquid chromatography-mass spectrometry</title>
            <link>http://www.medworm.com/index.php?rid=5048205&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F23</link>
            <description>Prenylquinones are mainly located in biological membranes where they function as electron and proton carriers in the photosynthetic and respiratory electron transport chains. The authors describe a rapid method for the simultaneous profiling of eleven prenylquinones in plant tissues, including alpha-tocopherol, phylloquinone, plastochromanol-8 and plastoquinone-9. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5048205</comments>
            <pubDate>Wed, 20 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5048205</guid>        </item>
        <item>
            <title>A rapid chemical method for lysing Arabidopsis cells for protein analysis</title>
            <link>http://www.medworm.com/index.php?rid=5035362&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F22</link>
            <description>Conclusions:
Our method is rapid and economical, and allows many samples to be prepared simultaneously for protein analysis. Our method is useful not only for Arabidopsis research but also research on certain other species. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5035362</comments>
            <pubDate>Thu, 14 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5035362</guid>        </item>
        <item>
            <title>Matrix-assisted laser desorption/ionisation mass spectrometry imaging and its development for plant protein imaging</title>
            <link>http://www.medworm.com/index.php?rid=5006240&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F21</link>
            <description>Matrix-Assisted Laser Desorption/Ionisation (MALDI) mass spectrometry imaging (MSI) uses the power of high resolution time of flight mass spectrometry coupled to the raster of laser shots across the cut surface of tissues to provide new insights into the spatial distribution of biomolecules within biological tissues. We consider the history of this technique in animals and plants and discuss the potential for analysis of proteins by this technique in plants. We discuss the bottleneck of protein biomarker identification from MALDI-MSI and alternative approaches to address this problem. We review the technical considerations needed for such analysis and present these alongside examples from our own work and a protocol for MALDI-MSI of proteins in plant samples. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5006240</comments>
            <pubDate>Mon, 04 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5006240</guid>        </item>
        <item>
            <title>A novel procedure for the quantitative analysis of metabolites, storage products and transcripts of laser microdissected seed tissues of Brassica napus</title>
            <link>http://www.medworm.com/index.php?rid=4991702&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F19</link>
            <description>Conclusion:
The described methodology allows for the rapid, combined analysis of metabolic intermediates, major storage products and transcripts in a tissue-specific manner. The protocols are robust for oilseed rape, and should be readily adjustable for other crop species. The suite of methods applied to LM tissues represents an important step in the context of both the systems biology and the biotechnology of oilseeds. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4991702</comments>
            <pubDate>Wed, 29 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4991702</guid>        </item>
        <item>
            <title>sunTILL: a TILLING resource for gene function analysis in sunflower</title>
            <link>http://www.medworm.com/index.php?rid=4991701&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F20</link>
            <description>Conclusion:
A first TILLING population for a high throughput identification of EMS-induced point mutations in sunflower genome has been successfully obtained. This represents a powerful tool to a better understanding of gene function in sunflower. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4991701</comments>
            <pubDate>Wed, 29 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4991701</guid>        </item>
        <item>
            <title>Convergence of developmental mutants into a single tomato model system: 'Micro-Tom' as an effective toolkit for plant development research</title>
            <link>http://www.medworm.com/index.php?rid=4983181&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F18</link>
            <description>Conclusions:
The community resource presented here is a useful toolkit for plant research, particularly for future studies in plant development, which will require the simultaneous observation of the effect of various hormones, signaling pathways and crosstalk. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4983181</comments>
            <pubDate>Tue, 28 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4983181</guid>        </item>
        <item>
            <title>Protocol: An updated integrated methodology for analysis of metabolites and enzyme activities of ethylene biosynthesis</title>
            <link>http://www.medworm.com/index.php?rid=4967516&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F17</link>
            <description>Conclusions:
This work collates an integrated set of detailed protocols for the measurement of components of the ethylene biosynthetic pathway, starting from well-established methods. These protocols have been optimised for smaller sample volumes, increased efficiency, repeatability and accuracy. The detailed protocol allows other scientists to rapidly implement these methods in their own laboratories in a consistent and efficient way. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4967516</comments>
            <pubDate>Wed, 22 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4967516</guid>        </item>
        <item>
            <title>A rapid, simple method for the genetic discrimination of intact Arabidopsis thaliana mutant seeds using metabolic profiling by direct analysis in real-time mass spectrometry</title>
            <link>http://www.medworm.com/index.php?rid=4919938&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F14</link>
            <description>Conclusion:
The described DART-MS combined by multivariate analysis allows for rapid screening and metabolic characterization of lots of Arabidopsis mutant seeds without complex metabolic preparation steps. Moreover, potential novel metabolic markers can be detected and used to clarify the genetic relationship between Arabidopsis cultivars. Furthermore this technique can be applied to predict the novel gene function of metabolic mutants regardless of morphological phenotypes. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4919938</comments>
            <pubDate>Thu, 09 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4919938</guid>        </item>
        <item>
            <title>Efficient virus-induced gene silencing in apple, pear and Japanese pear using Apple latent spherical virus vectors</title>
            <link>http://www.medworm.com/index.php?rid=4919937&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F15</link>
            <description>Conclusions:
The ALSV-based VIGS system developed have provides a valuable new addition to the tool box for functional genomics in apple, pear, and Japanese pear. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4919937</comments>
            <pubDate>Thu, 09 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4919937</guid>        </item>
        <item>
            <title>Agrobacterium-Mediated Transformation of Safflower and the Efficient Recovery of Transgenic Plants via Grafting</title>
            <link>http://www.medworm.com/index.php?rid=4847192&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F12</link>
            <description>Conclusions:
This protocol demonstrates significant improvements in both the efficiency and ease of use over existing safflower transformation protocols. This is the first complete method of genetic transformation of safflower that generates stably-transformed plants and progeny, allowing this crop to benefit from modern molecular applications. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4847192</comments>
            <pubDate>Thu, 19 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4847192</guid>        </item>
        <item>
            <title>A high resolution method for the localization of proanthocyanidins in plant tissues</title>
            <link>http://www.medworm.com/index.php?rid=4847191&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F13</link>
            <description>Conclusions:
This paper presents a simple, high-resolution method for analysis of proanthocyanidin accumulation in organs, tissues and cells of two plant species with different patterns of proanthocyanidin accumulation, namely Lotus corniculatus and Trifolium repens (white clover). This technique was used to characterize cell type-specific patterns of proanthocyanidin accumulation in white clover flowers at different stages of development. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4847191</comments>
            <pubDate>Thu, 19 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4847191</guid>        </item>
        <item>
            <title>ChIP-seq Analysis in R (CSAR): An R package for the statistical detection of protein-bound genomic regions</title>
            <link>http://www.medworm.com/index.php?rid=4801573&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F11</link>
            <description>Conclusions:
The software ChIP-seq Analysis in R (CSAR) enables fast and accurate detection of protein-bound genomic regions through the analysis of ChIP-seq experiments. Compared to existing methods, we found that our package shows greater robustness against PCR-artefacts and better control of the error rate. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4801573</comments>
            <pubDate>Sun, 08 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4801573</guid>        </item>
        <item>
            <title>De novo assembly of potential linear artificial chromosome constructs capped with expansive telomeric repeats</title>
            <link>http://www.medworm.com/index.php?rid=4718897&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F10</link>
            <description>Conclusions:
We successfully developed a procedure that circumvents the problem of cloning and maintaining long arrays of telomeric DNA sequences that are not stable in E. coli. Our procedure allows development of AC constructs in different eukaryotic species that are capped with long and designed sizes of telomeric DNA fragments. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4718897</comments>
            <pubDate>Thu, 14 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4718897</guid>        </item>
        <item>
            <title>FTIR-ATR-based prediction and modelling of lignin and energy contents reveals independent intra-specific variation of these traits in bioenergy poplars</title>
            <link>http://www.medworm.com/index.php?rid=4703479&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F9</link>
            <description>Conclusions:
These results show that FTIR-ATR spectroscopy is suitable as a high-throughput method for lignin and energy estimations in large data sets. Our study revealed that the intra-specific variations in lignin and energy contents were unrelated to each other and that the lignin content, therefore, was no predictor of the energy content. Employing principle component analyses we showed that factor loadings for the energy content were mainly associated with carbohydrate ring vibrations, whereas those for lignin were mainly related to aromatic compounds. Therefore, our analysis suggests that it may be possible to optimize the energy content of trees without concomitant increase in lignin. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4703479</comments>
            <pubDate>Sat, 09 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4703479</guid>        </item>
        <item>
            <title>Exploration of plant genomes in the FLAGdb++ environment</title>
            <link>http://www.medworm.com/index.php?rid=4651942&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F8</link>
            <description>Conclusion:
Combining original data with the output of experts and graphical displays that differ from classical plant genome browsers, FLAGdb++ presents a powerful complementary tool for exploring plant genomes and exploiting structural and functional resources, without the need for computer programming knowledge. First launched in 2002, a 15th version of FLAGdb++ is now available and comprises four model plant genomes and over eight million genomic features. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4651942</comments>
            <pubDate>Mon, 28 Mar 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4651942</guid>        </item>
        <item>
            <title>Development of expression vectors based on pepino mosaic virus</title>
            <link>http://www.medworm.com/index.php?rid=4574624&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F6</link>
            <description>Conclusions:
A stable PepMV vector was generated by expressing the transgene as a CP fusion using the sequence encoding the foot-and-mouth disease virus (FMDV) 2A catalytic peptide to separate them. We have generated a novel tool for the expression of recombinant proteins in plants and for the functional analysis of virus and plant genes. Our experiments have also highlighted virus requirements for replication in single cells as well as intercellular and long-distance movement. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4574624</comments>
            <pubDate>Fri, 11 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4574624</guid>        </item>
        <item>
            <title>An aeroponic culture system for the study of root herbivory on Arabidopsis thaliana</title>
            <link>http://www.medworm.com/index.php?rid=4570011&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F5</link>
            <description>Conclusions:
A root-herbivore system consisting of Arabidopsis thaliana and larvae of the opportunistic herbivore Bradysia spp. has been established that mimics herbivory in the rhizosphere. Bradysia infestation of Arabidopsis grown in this culture system significantly affects plant performance. The culture method will allow simple profiling and in vivo functional analysis of root defenses such as chemical defense metabolites that are released in response to belowground insect attack. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4570011</comments>
            <pubDate>Thu, 10 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4570011</guid>        </item>
        <item>
            <title>Rapid analysis of seed size in Arabidopsis for mutant and QTL discovery</title>
            <link>http://www.medworm.com/index.php?rid=4449687&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F7%2F1%2F3</link>
            <description>Conclusions:
This study describes a sensitive, high-throughput approach for measuring seed size and seed size distribution. The method provides a low cost and robust solution that can be easily implemented into the workflow of studies relating to various aspects of seed development. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4449687</comments>
            <pubDate>Tue, 08 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4449687</guid>        </item>
        <item>
            <title>Normalization using ploidy and genomic DNA copy number allows absolute quantification of transcripts, proteins and metabolites in cells.</title>
            <link>http://www.medworm.com/index.php?rid=4298293&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F6%2F1%2F29</link>
            <description>Conclusion:
Genomic DNA copy number and ploidy are useful as general normalization factors, providing an easy method for determining the number of transcripts, proteins, and metabolites in a cell. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4298293</comments>
            <pubDate>Wed, 29 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4298293</guid>        </item>
        <item>
            <title>Protocol: using virus-induced gene silencing to study the arbuscular mycorrhizal symbiosis in Pisum sativum</title>
            <link>http://www.medworm.com/index.php?rid=4257901&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F6%2F1%2F28</link>
            <description>Virus-induced gene silencing (VIGS) is an alternative reverse genetics tool for silencing of genes in some plants, which are difficult to transform. The pea early-browning virus (PEBV) has been developed as a VIGS vector and used in pea for functional analysis of several genes. However, the available PEBV-VIGS protocols are inadequate for studying genes involved in the symbiosis with arbuscular mycorrhizal fungi (AMF).Here we describe a PEBV-VIGS protocol suitable for reverse genetics studies in pea of genes involved in the symbiosis with AMF and show its effectiveness in silencing genes involved in the early and late stages of AMF symbiosis. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4257901</comments>
            <pubDate>Tue, 14 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4257901</guid>        </item>
        <item>
            <title>pH-sensitivity of YFP provides an intracellular indicator of programmed cell death</title>
            <link>http://www.medworm.com/index.php?rid=4212728&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F6%2F1%2F27</link>
            <description>Conclusions:
The observation that YFP fluorescence is lost during the plant PCD process provides a new tool to study the genetic regulation and cell biology of the process. In addition, plant cell biologists should make a note of this effect of PCD on YFP fluorescence to avoid misinterpretation of their data and to select a pH insensitive reporter if appropriate. This method represents an efficient and streamlined tool expected to bring insights on the process leading to the pH shift occurring during PCD. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4212728</comments>
            <pubDate>Tue, 30 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4212728</guid>        </item>
        <item>
            <title>DPI-ELISA: a fast and versatile method to specify the binding of plant transcription factors to DNA in vitro</title>
            <link>http://www.medworm.com/index.php?rid=4202634&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F6%2F1%2F25</link>
            <description>Conclusions:
We successfully applied our DPI-ELISA protocol to investigate the DNA-binding specificities of three different classes of transcription factors from Arabidopsis thaliana. However, the analysis of the binding affinity of any DNA-binding protein to any given DNA sequence can be performed via this method. The DPI-ELISA is cost efficient, less time-consuming than other methods and provides a qualitative and quantitative readout. The presented DPI-ELISA protocol is accompanied by advice on trouble-shooting, which will enable scientists to rapidly establish this versatile and easy to use method in their laboratories. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4202634</comments>
            <pubDate>Thu, 25 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4202634</guid>        </item>
        <item>
            <title>A simple, rapid method to isolate salt glands for three-dimensional visualization, fluorescence imaging and cytological studies</title>
            <link>http://www.medworm.com/index.php?rid=4081280&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F6%2F1%2F24</link>
            <description>Conclusions:
The study of salt glands directly at the glandular level are made possible with the successful isolation of these specialized structures. Preparation of materials for subsequent microscopic observations of salt glands could be achieved within a day. Potential applications of confocal fluorescence microscopic techniques could also be performed using these isolated glands. Experiments designed and targeted directly at the salt glands were explored and cytological information obtained herein could be further incorporated towards the understanding of the mechanism underlying secretion in plant salt glands. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4081280</comments>
            <pubDate>Mon, 18 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4081280</guid>        </item>
        <item>
            <title>Whole genome sequencing of enriched chloroplast DNA using the Illumina GAII platform</title>
            <link>http://www.medworm.com/index.php?rid=4011454&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F6%2F1%2F22</link>
            <description>Conclusions:
We report successful whole genome sequencing of chloroplast DNA from karaka, obtained efficiently and with high fidelity. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4011454</comments>
            <pubDate>Mon, 27 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4011454</guid>        </item>
        <item>
            <title>A high-throughput method for isolation of salicylic acid metabolic mutants</title>
            <link>http://www.medworm.com/index.php?rid=3997858&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F6%2F1%2F21</link>
            <description>Conclusions:
The rapid SA extraction method by direct boiling of leaf discs further reduced the cost and time required for the biosensor Acinetobacter sp. ADPWH_lux-based SA estimation, and allowed the screening for npr1 suppressors that accumulated less SA than npr1 after pathogen infection in a high-throughput manner. The highly efficacious SA estimation protocol can be applied in genetic screen for SA metabolic mutants and characterization of enzymes involved in SA metabolism. The mutants isolated in this study may help identify new components in the SA-related signaling pathways. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3997858</comments>
            <pubDate>Wed, 22 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3997858</guid>        </item>
        <item>
            <title>Targeted identification of genomic regions using TAGdb</title>
            <link>http://www.medworm.com/index.php?rid=3888582&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F6%2F1%2F19</link>
            <description>Conclusions:
The ability to produce large numbers of paired read genome tags using second generation sequencing provides a cost effective method for the identification of genes and promoters in large, complex or orphan species without the need for whole genome assembly. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3888582</comments>
            <pubDate>Thu, 19 Aug 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3888582</guid>        </item>
        <item>
            <title>High-contrast three-dimensional imaging of the Arabidopsis leaf enables the analysis of cell dimensions in the epidermis and mesophyll</title>
            <link>http://www.medworm.com/index.php?rid=3721382&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F6%2F1%2F17</link>
            <description>Conclusions:
The pipeline for the three-dimensional imaging and analysis of plant leaves provides the means to include variables on internal tissues in leaf growth studies and the assessment of leaf phenotypes. It also allows the visualisation and quantification of alterations in leaf structure alongside changes in leaf functioning observed under environmental constraints. Data obtained using this procedure can further be integrated in leaf development and functioning models. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3721382</comments>
            <pubDate>Thu, 01 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3721382</guid>        </item>
        <item>
            <title>UCE:  A uracil excision (USER TM)-based toolbox for transformation of cereals</title>
            <link>http://www.medworm.com/index.php?rid=3647873&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F6%2F1%2F15</link>
            <description>Conclusions:
The USER TM technology is very well suited for generating a toolbox of vectors for transformation and it opens an opportunity to engineer complex vectors, where several genetic elements of different origin are combined in a single cloning reaction. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3647873</comments>
            <pubDate>Wed, 09 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3647873</guid>        </item>
        <item>
            <title>Rapid metabolic profiling of Nicotiana tabacum defence responses against Phytophthora nicotianae using direct infrared laser desorption ionization mass spectrometry and principal component analysis</title>
            <link>http://www.medworm.com/index.php?rid=3647874&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F6%2F1%2F14</link>
            <description>Conclusion:
The described methodology allows for rapid assessment of infection-specific changes in the plant metabolism, in particular of phenolics, alkaloids, oxylipins and carbohydrates. Moreover, potential novel biomarkers can be detected and used to predict the quality of plant infections. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3647874</comments>
            <pubDate>Tue, 08 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3647874</guid>        </item>
        <item>
            <title>Functional mapping of genotype-environment interactions for soybean growth by a semiparametric approach</title>
            <link>http://www.medworm.com/index.php?rid=3620966&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F6%2F1%2F13</link>
            <description>Conclusions:
The model provides a basis for deciphering the genetic architecture of trait expression adjusted to different biotic and abiotic environments for any organism. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3620966</comments>
            <pubDate>Tue, 01 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3620966</guid>        </item>
        <item>
            <title>Protocol: a simple gel-free method for SNP genotyping using allele-specific primers in rice and other plant species</title>
            <link>http://www.medworm.com/index.php?rid=3490031&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F6%2F1%2F12</link>
            <description>Conclusion:
Our ASP methodology allows characterization of SNPs genotypes without electrophoresis, expensive probes or specialized equipment, and is highly versatile due to the flexibility in the design of primers. The method could be established easily in any molecular biology laboratory, and is applicable to diverse organisms. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3490031</comments>
            <pubDate>Tue, 20 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3490031</guid>        </item>
        <item>
            <title>Protocol: fine-tuning of a Chromatin Immunoprecipitation (ChIP) protocol in tomato</title>
            <link>http://www.medworm.com/index.php?rid=3456346&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F6%2F1%2F11</link>
            <description>Conclusion:
Here we provide a chromatin immunoprecipitation procedure for tomato leaves that could be combined with high-throughput sequencing to generate a detailed map of epigenetic modifications or genome-wide nucleosome positioning data. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3456346</comments>
            <pubDate>Thu, 08 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3456346</guid>        </item>
        <item>
            <title>SSHscreen and SSHdb, generic software for microarray based gene discovery: application to the stress response in cowpea</title>
            <link>http://www.medworm.com/index.php?rid=3428399&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F6%2F1%2F10</link>
            <description>Conclusions:
We developed the SSHscreen-SSHdb software pipeline, which greatly facilitates gene discovery using suppression subtractive hybridization by improving the selection of clones for sequencing after screening the library on a small number of microarrays. Annotation of the sequence information and collaboration was further enhanced through a web-based SSHdb database, and we illustrated this through identification of drought responsive genes from cowpea, which can now be investigated in gene function studies. SSH is a popular and powerful gene discovery tool, and therefore this pipeline will have application for gene discovery in any biological system, particularly non-model organisms. SSHscreen 2.0.1 and a link to SSHdb are available from http://microarray.up.ac.za/SSHscreen. (Sour...</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3428399</comments>
            <pubDate>Wed, 31 Mar 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3428399</guid>        </item>
        <item>
            <title>Rapid expression of transgenes driven by seed-specific constructs in leaf tissue: DHA production</title>
            <link>http://www.medworm.com/index.php?rid=3358312&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F6%2F1%2F8</link>
            <description>Conclusions:
The LEC2-extended N. benthamiana assay allows the transient activation of seed-specific promoters in leaf tissue. In this study we have used the assay as a rapid preliminary screen of a complex seed-specific transgenic construct prior to stable transformation, a feature that will become increasingly useful as genetic engineering moves from the manipulation of single genes to the engineering of complex pathways. We propose that the assay will prove useful for other applications wherein rapid expression of transgenes driven by seed-specific constructs in leaf tissue are sought. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3358312</comments>
            <pubDate>Thu, 11 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3358312</guid>        </item>
        <item>
            <title>Dealing with the problem of non-specific in situ mRNA hybridization signals associated with plant tissues undergoing programmed cell death</title>
            <link>http://www.medworm.com/index.php?rid=3243137&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F6%2F1%2F7</link>
            <description>Conclusions:
In plants, cell death is an integral part of both development and defence, and hence it is a common phenomenon in all stages of the life cycle. Our results suggest that extensive nucleic acid fragmentation during cell death processes can be a considerable source of non-specific signals in traditional in situ mRNA hybridization. Thus, the visualization of potential nucleic acid fragmentation simultaneously with the in situ mRNA hybridization assay may be necessary to ensure the correct interpretation of the signals in the case of non-specific hybridization of probes in plant tissues. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3243137</comments>
            <pubDate>Fri, 05 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3243137</guid>        </item>
        <item>
            <title>Proposal for field sampling of plants and processing in the lab for environmental metabolic fingerprinting</title>
            <link>http://www.medworm.com/index.php?rid=3219876&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F6%2F1%2F6</link>
            <description>Conclusions:
The proposed extraction protocol leads to highly reproducible metabolic fingerprints and allows optimal handling of field-collected plant material and further processing in the laboratory, which is demonstrated for an exemplary field data-set. Calculation of Xi values is a useful tool to judge similarities between chromatograms. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3219876</comments>
            <pubDate>Fri, 29 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3219876</guid>        </item>
        <item>
            <title>Documentation system for plant transformation service and research</title>
            <link>http://www.medworm.com/index.php?rid=3215814&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F6%2F1%2F4</link>
            <description>Conclusion:
The system has been evolved and tested over several years in a transformation service unit, where it increased efficiency. Additionally, the system provided rapid access to data for quality control and decision making. The system can be easily modified for the use in other research environments. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3215814</comments>
            <pubDate>Wed, 27 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3215814</guid>        </item>
        <item>
            <title>NEATTILL: A simplified procedure for nucleic acid extraction from arrayed tissue for TILLING and other high-throughput reverse genetic applications</title>
            <link>http://www.medworm.com/index.php?rid=3207824&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F6%2F1%2F3</link>
            <description>Conclusion:
NEATTILL is a convenient procedure that can be applied to all organisms, the genomes of which have been mutagenized and are being scanned for multiple alleles of various genes by TILLING for understanding gene-to-phenotype relationships. It is a time-saving, less labour intensive and reasonably cost-effective method. Tissue arraying can cut costs byup to 90% and minimizes the risk of exposing the DNA to nucleases. Before arraying, different tissues should be evaluated for DNA quality, as the case study in tomato showed that cotyledons rather than leaves are better suited for DNA isolation. The protocol described here for nucleic acid isolation can be generally adapted for large-scale projects such as insertional mutagenesis, transgenic confirmation, mapping and fingerprinting w...</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3207824</comments>
            <pubDate>Tue, 26 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3207824</guid>        </item>
        <item>
            <title>High frequency, cell type-specific visualization of fluorescent-tagged genomic sites in interphase and mitotic cells of living Arabidopsis plants</title>
            <link>http://www.medworm.com/index.php?rid=3184900&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F6%2F1%2F2</link>
            <description>Conclusions:
The results illustrate the propensity of operator repeat arrays to form heterochromatin that can silence the neighbouring gene encoding the RP-FP fusion protein. Supplying the RP-FP fusion protein in trans from a second T-DNA largely alleviates this problem. Depending on the promoter used to drive expression of the RP-FP fusion protein gene, the fluorescent tagged sites can be visualized at high frequency in different cell types. The ability to observe fluorescent dots on both interphase and mitotic chromosomes allows tagged sites to be tracked throughout the cell cycle. These improvements enhance the versatility of the fluorescent tagging technique for future studies of chromosome arrangement and dynamics in living plants. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3184900</comments>
            <pubDate>Tue, 19 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3184900</guid>        </item>
        <item>
            <title>Protocol: a rapid and economical procedure for purification of plasmid or plant DNA with diverse applications in plant biology</title>
            <link>http://www.medworm.com/index.php?rid=3175226&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F6%2F1%2F1</link>
            <description>Research in plant molecular biology involves DNA purification on a daily basis. Although different commercial kits enable convenient extraction of high-quality DNA from E. coli cells, PCR and agarose gel samples as well as plant tissues, each kit is designed for a particular type of DNA extraction work, and the cost of purchasing these kits over a long run can be considerable. Furthermore, a simple method for the isolation of binary plasmid from Agrobacterium tumefaciens cells with satisfactory yield is lacking. Here we describe an easy protocol using homemade silicon dioxide matrix and seven simple solutions for DNA extraction from E. coli and A. tumefaciens cells, PCR and restriction digests, agarose gel slices, and plant tissues. Compared with the commercial kits, this protocol allows r...</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3175226</comments>
            <pubDate>Thu, 14 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3175226</guid>        </item>
        <item>
            <title>Computer aided data acquisition tool for high-throughput phenotyping of plant populations</title>
            <link>http://www.medworm.com/index.php?rid=3074834&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F5%2F1%2F18</link>
            <description>Conclusions:
The phenotyping of large population of plants both in the laboratory and in the field is very efficiently managed using PDA. The data is transferred to a specialized database(s) where it can be further analyzed and catalogued. The &quot;PHENOME&quot; aids collection and analysis of data obtained in large-scale mutagenesis, assessing quantitative trait loci (QTLs), raising mapping population, sampling of several individuals in one or more ecological niches etc. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3074834</comments>
            <pubDate>Thu, 10 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3074834</guid>        </item>
        <item>
            <title>A rapid and sensitive method for the simultaneous analysis of aliphatic and polar molecules containing free carboxyl groups in plant extracts by LC-MS/MS</title>
            <link>http://www.medworm.com/index.php?rid=3026094&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F5%2F1%2F17</link>
            <description>Conclusions:
The method presented was used to detect 16 compounds in leaf extracts of N. attenuata plants. Importantly, the method can be adapted based on the specific analytes of interest with the only consideration that the molecules must contain at least one free carboxyl group. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3026094</comments>
            <pubDate>Wed, 25 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3026094</guid>        </item>
        <item>
            <title>An inbred line of the diploid strawberry Fragaria vesca f.  semperflorens for genomic and molecular genetic studies in the Rosaceae</title>
            <link>http://www.medworm.com/index.php?rid=2946543&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F5%2F1%2F15</link>
            <description>Conclusions:
The development of the documented YW5AF7 line provides an important tool for Rosaceae functional genomic analyses. These day-neutral plants have a small genome, a seed to seed cycle of 3.0 - 3.5 months, and produce fruit in 7.5 cm pots in a growth chamber. YW5AF7 is runnerless and therefore easy to maintain in the greenhouse, forms abundant branch crowns for vegetative propagation, and produces highly aromatic yellow fruit throughout the year in the greenhouse. F. vesca can be transformed with Agrobacterium tumefaciens, making these plants suitable for insertional mutagenesis, RNAi and overexpression studies that can be compared against a stable baseline of phenotypic descriptors and can be readily genetically substantiated. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2946543</comments>
            <pubDate>Sat, 31 Oct 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">2946543</guid>        </item>
        <item>
            <title>A simple, flexible and efficient PCR-fusion/Gateway cloning procedure for gene fusion, site-directed mutagenesis, short sequence insertion and domain deletions and swaps</title>
            <link>http://www.medworm.com/index.php?rid=2934128&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F5%2F1%2F14</link>
            <description>Conclusions:
The PCR-fusion/Gateway cloning procedure described provides an elegant, simple and efficient solution for a wide range of diverse and complicated cloning tasks. Our method allows for efficient utilization of the growing sequence and expression data for gene families through streamlined cloning of sets of gene fusions and modification variants into binary vectors for systematic functional studies of gene families. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2934128</comments>
            <pubDate>Wed, 28 Oct 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">2934128</guid>        </item>
        <item>
            <title>Implementation of two high through-put techniques in a novel application: detecting point mutations in large EMS mutated plant populations</title>
            <link>http://www.medworm.com/index.php?rid=2868497&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F5%2F1%2F13</link>
            <description>Conclusion:
These results demonstrate that CSCE and HRM are fast, affordable and sensitive techniques for mutation detection in DNA pools and therefore allow the rapid identification of new allelic variants in a mutant population. Results from the first screens indicate that the mutagen treatment has been effective with an average mutation detection rate per diploid genome of 1.36 mutation/kb/1000lines. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2868497</comments>
            <pubDate>Tue, 06 Oct 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2868497</guid>        </item>
        <item>
            <title>3D fluorescent in situ hybridization using Arabidopsis leaf cryosections and isolated nuclei</title>
            <link>http://www.medworm.com/index.php?rid=2666861&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F5%2F1%2F11</link>
            <description>Conclusion:
Our work describes a 3D-FISH protocol that preserves the 3D structure of Arabidopsis interphase nuclei. Moreover, we report for the first time FISH using cryosections of Arabidopsis leaves. This protocol is a valuable tool to investigate nuclear architecture and chromatin organization. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2666861</comments>
            <pubDate>Sun, 02 Aug 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2666861</guid>        </item>
        <item>
            <title>High-throughput retrotransposon-based fluorescent markers: improved information content and allele discrimination</title>
            <link>http://www.medworm.com/index.php?rid=2648530&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F5%2F1%2F10</link>
            <description>Conclusion:
As well as developing a rapid, and high-throughput marker method for genetic studies, the fluorescent SSAP system improved the accuracy of amplicon scoring, increased the available marker number, improved allele discrimination, and was sensitive enough to identify heterozygous loci in F1 and F2 progeny, indicating the potential to develop high-throughput codominant SSAPs. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2648530</comments>
            <pubDate>Mon, 27 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2648530</guid>        </item>
        <item>
            <title>Development of a gene silencing DNA vector derived from a broad host range geminivirus</title>
            <link>http://www.medworm.com/index.php?rid=2569301&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F5%2F1%2F9</link>
            <description>Conclusion:
The unique properties of the pWSRi vector, the ability to silence genes in meristem tissue, the separation of virus and silencing phenotypes, and the broad natural host range of BCTV, suggest that it will have wide utility. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2569301</comments>
            <pubDate>Wed, 01 Jul 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2569301</guid>        </item>
        <item>
            <title>The DAWGPAWS pipeline for the annotation of genes and transposable elements in plant genomes</title>
            <link>http://www.medworm.com/index.php?rid=2503854&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F5%2F1%2F8</link>
            <description>Conclusion:
The DAWGPAWS genome annotation pipeline fills an important need in the annotation of plant genomes by generating computational evidences in a high throughput manner, translating these results to a common file format, and facilitating the human curation of these computational results. We have verified the value of DAWGPAWS by using this pipeline to annotate the genes and transposable elements in 220 BAC insertions from the hexaploid wheat genome (Triticum aestivum L.). DAWGPAWS can be applied to annotation efforts in other plant genomes with minor modifications of program-specific configuration files, and the modular design of the workflow facilitates integration into existing pipelines (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2503854</comments>
            <pubDate>Thu, 18 Jun 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2503854</guid>        </item>
        <item>
            <title>Instrumentation enabling study of plant physiological response to elevated nighttime temperature</title>
            <link>http://www.medworm.com/index.php?rid=2503855&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F5%2F1%2F7</link>
            <description>Conclusion:
The described infrared heating system meets the utilitarian requirements of a heating system for plant physiology studies in that the elevated temperature can be accurately, precisely, and reliably controlled with minimal perturbation of other environmental factors. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2503855</comments>
            <pubDate>Wed, 10 Jun 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2503855</guid>        </item>
        <item>
            <title>Simple allele-discriminating PCR for cost-effective and rapid genotyping and mapping</title>
            <link>http://www.medworm.com/index.php?rid=2090537&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F5%2F1%2F1</link>
            <description>Conclusions:
SAP offers an excellent alternative to existing SNP-discrimination methods such as Cleaved Amplified Polymorphic Sequence (CAPS), or derived CAPS (dCAPS) method. It can also be adapted for high throughput SNP analyses by incorporating fluorophore-labeled primers. SAP is reliable, cost-effective, fast, and simple, and can be applied to all organisms not limited to Arabidopsis thaliana. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2090537</comments>
            <pubDate>Thu, 08 Jan 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2090537</guid>        </item>
        <item>
            <title>A rapid biosensor-based method for quantification of free and glucose-conjugated salicylic acid</title>
            <link>http://www.medworm.com/index.php?rid=2076076&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F4%2F1%2F28</link>
            <description>Conclusions:
The ability of Acinetobacter sp. ADPWH_lux to detect SA in a complex mixture, combined with the enzymatic hydrolysis of SAG in crude extract, allowed the development of a simple, rapid, and inexpensive method to simultaneously measure free and glucose-conjugated SA. This approach is amenable to a high-throughput format, which would further reduce the cost and time required for biosensor-based SA quantification. Possible applications of this approach include characterization of enzymes involved in SA metabolism, analysis of temporal changes in SA levels, and isolation of mutants with aberrant SA accumulation. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2076076</comments>
            <pubDate>Wed, 31 Dec 2008 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2076076</guid>        </item>
        <item>
            <title>A rapid, non-invasive procedure for quantitative assessment of drought survival using chlorophyll fluorescence</title>
            <link>http://www.medworm.com/index.php?rid=1948154&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F4%2F1%2F27</link>
            <description>Conclusions:
The method presented here allows the acquisition of quantitative numerical estimates of Arabidopsis drought survival times that are amenable to statistical analysis. Furthermore, the required measurements can be obtained quickly and non-invasively using inexpensive equipment and with minimal expertise in chlorophyll fluorometry. This technique enables the rapid assessment and comparison of the relative viability of germplasm during drought, and may complement detailed physiological and water relations studies. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1948154</comments>
            <pubDate>Tue, 11 Nov 2008 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">1948154</guid>        </item>
        <item>
            <title>Gluten measurement and its relationship to food toxicity for celiac disease patients</title>
            <link>http://www.medworm.com/index.php?rid=1912217&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F4%2F1%2F26</link>
            <description>The gluten analysis of foods has long had limitations, which have precluded food standards authorities from issuing standards for gluten-free foods based on final gluten content. The Codex Alimentarius and the Food and Drug Administration have recently taken steps towards such standards in which they favour the R5-enzyme-linked immunosorbent assay for gluten analysis. If this method is to be widely employed, its limitations should be recognised. Above all, it should be noted the ability of the R5-enzyme-linked immunosorbent assay, and other methods, to measure gluten's toxicity toward celiac disease patients is not validated clinically. Gluten is a complex mixture of proteins and its toxicity is not fully understood. Analytical methods are a valuable tool in the definition of gluten-free f...</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1912217</comments>
            <pubDate>Tue, 28 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1912217</guid>        </item>
        <item>
            <title>Vectors for multi-color bimolecular fluorescence complementation to investigate protein-protein interactions in living plant cells</title>
            <link>http://www.medworm.com/index.php?rid=1876965&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F4%2F1%2F24</link>
            <description>Conclusion:
Multi-color BiFC is a useful technique to determine interactions simultaneously between a given&quot; bait&quot; protein and multiple &quot;prey&quot; proteins in living plant cells. The vectors we have constructed and tested will facilitate the study of protein-protein interactions in many different plant systems. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1876965</comments>
            <pubDate>Wed, 15 Oct 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1876965</guid>        </item>
        <item>
            <title>Mutational optimization of the coelenterazine-dependent luciferase from Renilla</title>
            <link>http://www.medworm.com/index.php?rid=1838259&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F4%2F1%2F23</link>
            <description>Renilla luciferase (RLUC) is a popular reporter enzyme for gene expression and biosensor applications, but it is an unstable enzyme whose catalytic mechanism remains to be elucidated. We titrated that one RLUC molecule can turn over about one hundred molecules of coelenterazine substrate. Mutagenesis of active site residue Pro220 extended the half-life of photon emission, yielding brighter luminescence in E. coli. Random mutagenesis uncovered two new mutations that stabilized and increased photon emission in vivo and in vitro, while ameliorating substrate inhibition. Further amended with a previously identified mutation, a new triple mutant showed a threefold improved kcat , as well as elevated luminescence in Arabidopsis. This advances the utility of RLUC as a reporter protein, biosensor,...</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1838259</comments>
            <pubDate>Tue, 30 Sep 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1838259</guid>        </item>
        <item>
            <title>Visualizing the actin cytoskeleton in living plant cells using a photo-convertible mEos::FABD-mTn  fluorescent fusion protein</title>
            <link>http://www.medworm.com/index.php?rid=1806941&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F4%2F1%2F21</link>
            <description>Conclusions:
The mEosFP::FABD-mTn probe retains all the imaging qualities associated with the well tested GFP::mTn probe while allowing for non-invasive, regional photo-conversion that allows colour based discrimination within a living cell. Whereas a number of precautions should be exercised in dealing with photo-convertible probes, mEosFP::FABD-mTn is a versatile live imaging tool for dissecting the organization and activity of the actin cytoskeleton in plants. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1806941</comments>
            <pubDate>Fri, 19 Sep 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1806941</guid>        </item>
        <item>
            <title>Protocol: A high-throughput DNA extraction system suitable for conifers</title>
            <link>http://www.medworm.com/index.php?rid=1672316&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F4%2F1%2F20</link>
            <description>Conclusions:
A high-throughput system for DNA extraction from conifer needles and seeds has been developed and validated. The quality of the isolated DNA was comparable with that obtained from two commonly used methods: the silica-spin column and the classic CTAB protocol. Our protocol provides a fully automatable and cost effective solution for processing large numbers of conifer samples. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1672316</comments>
            <pubDate>Fri, 01 Aug 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1672316</guid>        </item>
        <item>
            <title>A plastome primer set for comprehensive quantitative real time RT-PCR analysis of Zea mays: a starter primer set for other Poaceae species</title>
            <link>http://www.medworm.com/index.php?rid=1556931&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F4%2F1%2F14</link>
            <description>Conclusion:
Due to the highly conserved chloroplast genome in plant families it is possible to utilize primer pairs designed against one genomic sequence to detect the presence and abundance of plastid genes or transcripts from genomes that have yet to be sequenced. Analysis of steady state transcription of vital system genes is a necessary requirement to comprehensively elucidate gene expression in any organism. The primer pairs reported in this paper were designed for q2(RT)PCR of maize chloroplast genes but should be useful for other members of the Poaceae family. Both in silico and in vitro data are presented to support this assumption. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1556931</comments>
            <pubDate>Mon, 02 Jun 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1556931</guid>        </item>
        <item>
            <title>Development and evaluation of a high-throughput, low-cost genotyping platform based on oligonucleotide microarrays in rice</title>
            <link>http://www.medworm.com/index.php?rid=1556932&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F4%2F1%2F13</link>
            <description>Conclusion:
We anticipate this microarray-based genotyping platform, based on its low cost-per-sample, to be particularly useful in applications requiring whole-genome molecular marker coverage across large numbers of individuals. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1556932</comments>
            <pubDate>Thu, 29 May 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1556932</guid>        </item>
        <item>
            <title>A plant resource and experiment management system based on the Golm Plant Database as a basic tool for omics research</title>
            <link>http://www.medworm.com/index.php?rid=1556933&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F4%2F1%2F11</link>
            <description>Conclusion:
The Golm Plant Database system, which is based on a relational database, collects the genetic and environmental information on plant material during its production or experimental use at the Max-Planck-Institute of Molecular Plant Physiology. It thus provides information according to the MIAME standard for the component 'Sample' in a highly standardised format. The Plant Database system thus facilitates collaborative work and allows efficient queries in data analysis for systems biology research. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1556933</comments>
            <pubDate>Wed, 21 May 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1556933</guid>        </item>
        <item>
            <title>Multidimensional fluorescence microscopy of multiple organelles in Arabidopsis seedlings</title>
            <link>http://www.medworm.com/index.php?rid=1556934&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F4%2F1%2F9</link>
            <description>Conclusion:
We developed a tool and associated methods for analyzing the complex dynamic of organelle-organelle interactions in real time in planta. Homozygous transgenic Arabidopsis (Kaleidocell) is available through Arabidopsis Biological Resource Center. (Source: Plant Methods)</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1556934</comments>
            <pubDate>Mon, 19 May 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1556934</guid>        </item>
        <item>
            <title>High quality metabolomic data for Chlamydomonas reinhardtii</title>
            <link>http://www.medworm.com/index.php?rid=1556935&amp;cid=s_37185_62_f&amp;fid=37185&amp;url=http%3A%2F%2Fwww.plantmethods.com%2Fcontent%2F4%2F1%2F7</link>
            <description>The green eukaryote alga Chlamydomonas reinhardtii is a unicellular model to study control of metabolism in a photosynthetic organism. We here present method improvements for metabolite profiling based on GC-TOF mass spectrometry focusing on three parameters: quenching and cell disruption, extract solvent composition and metabolite annotation. These improvements facilitate using smaller cell numbers and hence, smaller culture volumes which enable faster and more precise sampling techniques that eventually lead to a higher number of samples that can be processed, e.g. for time course experiments. Quenching of metabolism was achieved by mixing 1 ml of culture to 1 ml of -70°C cold 70% methanol. After centrifugation, cells were lyophilized and disrupted by milling using 2-6E6 lyophilized cel...</description>
            <author>Plant Methods</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1556935</comments>
            <pubDate>Mon, 28 Apr 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1556935</guid>        </item>
    </channel>
</rss>

