Research Resource: RNA-Seq Reveals Unique Features of the Pancreatic beta-Cell Transcriptome

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dc.contributor.authorKu, Gregory M.ko
dc.contributor.authorKim, Hailko
dc.contributor.authorVaughn, Ian W.ko
dc.contributor.authorHangauer, Matthew J.ko
dc.contributor.authorOh, Chang Myungko
dc.contributor.authorGerman, Michael S.ko
dc.contributor.authorMcManus, Michael T.ko
dc.date.accessioned2013-03-12T23:17:08Z-
dc.date.available2013-03-12T23:17:08Z-
dc.date.created2012-11-20-
dc.date.created2012-11-20-
dc.date.issued2012-10-
dc.identifier.citationMOLECULAR ENDOCRINOLOGY, v.26, no.10, pp.1783 - 1792-
dc.identifier.issn0888-8809-
dc.identifier.urihttp://hdl.handle.net/10203/103829-
dc.description.abstractThe pancreatic beta-cell is critical for the maintenance of glycemic control. Knowing the compendium of genes expressed in beta-cells will further our understanding of this critical cell type and may allow the identification of future antidiabetes drug targets. Here, we report the use of next-generation sequencing to obtain nearly 1 billion reads from the polyadenylated RNA of islets and purified beta-cells from mice. These data reveal novel examples of beta-cell-specific splicing events, promoter usage, and over 1000 long intergenic noncoding RNA expressed in mouse beta-cells. Many of these long intergenic noncoding RNA are beta-cell specific, and we hypothesize that this large set of novel RNA may play important roles in beta-cell function. Our data demonstrate unique features of the beta-cell transcriptome. (Molecular Endocrinology 26: 1783-1792, 2012)-
dc.languageEnglish-
dc.publisherENDOCRINE SOC-
dc.subjectNONCODING RNAS-
dc.subjectEXPRESSION ANALYSIS-
dc.subjectGENE-
dc.subjectPREGNANCY-
dc.subjectLINCRNAS-
dc.subjectPROMOTER-
dc.titleResearch Resource: RNA-Seq Reveals Unique Features of the Pancreatic beta-Cell Transcriptome-
dc.typeArticle-
dc.identifier.wosid000309509500014-
dc.identifier.scopusid2-s2.0-84866977211-
dc.type.rimsART-
dc.citation.volume26-
dc.citation.issue10-
dc.citation.beginningpage1783-
dc.citation.endingpage1792-
dc.citation.publicationnameMOLECULAR ENDOCRINOLOGY-
dc.identifier.doi10.1210/me.2012-1176-
dc.contributor.localauthorKim, Hail-
dc.contributor.nonIdAuthorKu, Gregory M.-
dc.contributor.nonIdAuthorVaughn, Ian W.-
dc.contributor.nonIdAuthorHangauer, Matthew J.-
dc.contributor.nonIdAuthorOh, Chang Myung-
dc.contributor.nonIdAuthorGerman, Michael S.-
dc.contributor.nonIdAuthorMcManus, Michael T.-
dc.type.journalArticleArticle-
dc.subject.keywordPlusNONCODING RNAS-
dc.subject.keywordPlusEXPRESSION ANALYSIS-
dc.subject.keywordPlusGENE-
dc.subject.keywordPlusPREGNANCY-
dc.subject.keywordPlusLINCRNAS-
dc.subject.keywordPlusPROMOTER-
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