障害者雇用における特例子会社制度の現代的課題 : 全国実態調査から

departmental bulletin pape

中山間地域の再生・持続モデル構築のための実証的研究 : 2010～2012年度文部科学省概算要求・特別経費（プロジェクト分） : 成果報告書

2010～2012年度文部科学省概算要求・特別経費（プロジェクト分）Other信州大学. 中山間地域の再生・持続モデル構築のための実証的研究 : 2010～2012年度文部科学省概算要求・特別経費（プロジェクト分） : 成果報告書. 信州大学, 2013, 65presearch repor

The Paradox of the Coffin Trick ——Tennessee Williams's The Glass Menagerie and Hans Hofmann's Painting Theory

本論文は「九州地区国立大学教育系・文系研究論文集」Vol.10,No.２に査読を経て受理された。journal articl

Observation of B+ → χc0K+

journal articl

Novel thionin-functionalised core shell magnetic nanoparticles for dispersive solid-phase extraction of Hg(II) in food and water samples

To develop an accurate and precise method for separation and pre-concentration of Hg(II), a novel thionin functionalised core shell structure magnetic material has been prepared and characterised. The extraction ability of the material was evaluated by magnetic solid-phase extraction coupled with inductively coupled plasma mass spectrometry determination of Hg(II) in food and water samples. Combining the advantages of magnetic separation with selective extraction of thionin towards Hg(II), the material exhibits enhanced enrich selectivity and efficiency for Hg(II). The experimental parameters influencing Hg(II) extraction efficiency, including pH of the aqueous solution, the dosage of the adsorbent, extraction time and sample volume, were systematically investigated. Under the optimised conditions, concentration of Hg(II) at 1.0 μg L−1 can be successfully enriched by the material without the interference of the common co-existing ions. The enrichment factor and adsorption capacity were 250 and 75.2 mg g−1, and precise of the method was confirmed by analysing the spiked food, water samples and standard water reference samples with the recoveries of 92.5–101.8%.</p

DFsn down-regulates the levels of the Wallenda/DLK kinase to restrain synaptic terminal growth

<p><b>Copyright information:</b></p><p>Taken from "DFsn collaborates with Highwire to down-regulate the Wallenda/DLK kinase and restrain synaptic terminal growth"</p><p>http://www.neuraldevelopment.com/content/2/1/16</p><p>Neural Development 2007;2():16-16.</p><p>Published online 15 Aug 2007</p><p>PMCID:PMC2031890.</p><p></p> Staining for endogenous Wallenda in central nervous system neuropil in ventral nerve cords of wild-type (WT), [], [presynaptic rescue: ] and third-instar larvae. Upper panels show Wallenda staining alone, and lower panels show co-staining of Wallenda (red) with the synaptic marker HRP (horseradish peroxidase) (blue). Quantification of average Wallenda staining in the neuropil of third-instar larvae for the genotypes shown in (a). The Wallenda intensity was measured for each genotype and the background intensity measured for was subtracted. Wallenda staining in the mutant was significantly higher than WT (< 0.001). Presynaptic expression of a transgene rescues the increase of Wallenda level (> 0.5 for versus WT). Representative confocal images of muscle 4 synapses co-stained with DVGLUT (green) and FasII (red), in WT, and third instar larvae. Quantification is shown for bouton number (d) and synaptic branch point number (e) and synaptic span (f) for WT, and (n = 23, 23, and 22 cells, respectively). The mutant fully suppresses the morphological defects in the mutant (> 0.1 for ; versus WT in number of boutons and branch points; < 0.001 for versus in synaptic span, number of boutons and branch points)

DFsn genetically interacts with Highwire to restrain synaptic terminal growth

<p><b>Copyright information:</b></p><p>Taken from "DFsn collaborates with Highwire to down-regulate the Wallenda/DLK kinase and restrain synaptic terminal growth"</p><p>http://www.neuraldevelopment.com/content/2/1/16</p><p>Neural Development 2007;2():16-16.</p><p>Published online 15 Aug 2007</p><p>PMCID:PMC2031890.</p><p></p> Representative confocal images of muscle 4 synapses co-stained with DVGLUT (green) and FasII (red), in wild-type (WT), , , ; , and ; third instar larvae. Quantification of bouton number of muscle 4 synapses in WT, , , ; , and ; third instar larvae (n = 27, 34, 27, 28, 22, and 39 cells, respectively). The number of boutons in the ; double mutant is increased compared to (< 0.001). The number of boutons in the ; double mutant is not significantly different from (> 0.5), demonstrating a lack of enhancement of the phenotype by

フル ハイビジョン ニヨル コウセイサイ ジュギョウ アーカイブ オ カイシ

video/mp4講演者所属: 木戸出正繼 本学愚属図書館長講演者所属: 藤川和利 本学付属図書館研究開発室長開催場所: 附属図書館マルチメディア提示室1開催日:　平成20年3月8日vide

MOESM4 of Genome-wide identification and expression profiling of glutathione transferase gene family under multiple stresses and hormone treatments in wheat (Triticum aestivum L.)

Additional file 4. The coding sequences of 330 TaGST genes

Extensive Post-Transcriptional Regulation Revealed by Transcriptomic and Proteomic Integrative Analysis in Cassava under Drought

Cassava is a major tropical/subtropical food crop and its yield is greatly restrained by drought; however, the mechanism underlying the drought stress remains largely unknown. In this study, totally 1242 and 715 differentially expressed genes (DEGs), together with 237 and 307 differentially expressed proteins (DEPs), were respectively identified in cassava leaves and roots through RNA-seq and iTRAQ techniques. The majority of DEGs and DEPs were exclusively regulated at the mRNA and protein level, respectively, whereas only a few were commonly regulated, indicating the major involvement of post-transcriptional regulation under drought. Subsequently, the functions of these specifically or commonly regulated DEGs and DEPs were analyzed, and the post-transcriptional regulation of genes involved in heat shock protein, secondary metabolism biosynthesis, and hormone biosynthesis was extensively discussed. This is the first report on an integration of transcriptomic and proteomic analysis in cassava, and it provides new insights into the post-transcriptional regulation of cassava drought stress