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Cited 27 time in webofscience Cited 26 time in scopus
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dc.contributor.authorKhan, AA-
dc.contributor.authorLee, AJ-
dc.contributor.authorRoh, TY-
dc.date.accessioned2016-04-01T07:45:59Z-
dc.date.available2016-04-01T07:45:59Z-
dc.date.created2015-06-22-
dc.date.issued2015-01-
dc.identifier.issn1750-1911-
dc.identifier.other2015-OAK-0000033167-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/26848-
dc.description.abstractPolycomb group (PcG) proteins play an important role in the regulation of gene expression, especially genes encoding lineage-specific factors. Perturbations in PcG protein expression may trigger an unexpected developmental pathway, resulting in birth defects and developmental disabilities. Two Polycomb repressive complexes, PRC1 and PRC2, have been identified and are related with diverse cellular processes through histone modifications. Many developmental genes are trimethylated at histone H3 lysine 27 (H3K27me3) mediated by PRC2, which provides a binding site for PRC1. These processes contribute to chromatin compaction and transcriptional repression. In this review, we discuss about the complex formation of PcG proteins, the mechanism through which they are recruited to target sites and their functional roles in cell differentiation.-
dc.description.statementofresponsibilityarchiving status unknown-
dc.languageEnglish-
dc.publisherFUTURE MEDICINE LTD-
dc.relation.isPartOfEPIGENOMICS-
dc.titlePolycomb group protein-mediated histone modifications during cell differentiation-
dc.typeArticle-
dc.contributor.college융합생명공학부-
dc.identifier.doi10.2217/EPI.14.61-
dc.author.googleKhan, AA-
dc.author.googleLee, AJ-
dc.author.googleRoh, TY-
dc.relation.volume7-
dc.relation.issue1-
dc.relation.startpage75-
dc.relation.lastpage84-
dc.contributor.id10138348-
dc.relation.journalEPIGENOMICS-
dc.relation.sciSCIE-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationEPIGENOMICS, v.7, no.1, pp.75 - 84-
dc.identifier.wosid000349832500009-
dc.date.tcdate2019-02-01-
dc.citation.endPage84-
dc.citation.number1-
dc.citation.startPage75-
dc.citation.titleEPIGENOMICS-
dc.citation.volume7-
dc.contributor.affiliatedAuthorRoh, TY-
dc.identifier.scopusid2-s2.0-84923262122-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc13-
dc.description.scptc10*
dc.date.scptcdate2018-05-121*
dc.type.docTypeReview-
dc.subject.keywordPlusHOX GENE-EXPRESSION-
dc.subject.keywordPlusSTEM-CELLS-
dc.subject.keywordPlusTRANSCRIPTIONAL REGULATION-
dc.subject.keywordPlusH2A UBIQUITYLATION-
dc.subject.keywordPlusTARGET GENES-
dc.subject.keywordPlusNUCLEAR REORGANIZATION-
dc.subject.keywordPlusEPIGENETIC REGULATION-
dc.subject.keywordPlusCOMPLEX PRC2-
dc.subject.keywordPlusEZH2-
dc.subject.keywordPlusCHROMATIN-
dc.subject.keywordAuthorcell differentiation-
dc.subject.keywordAuthordevelopment-
dc.subject.keywordAuthorhomeobox genes-
dc.subject.keywordAuthorPcG recruitment-
dc.subject.keywordAuthorPolycomb group proteins-
dc.relation.journalWebOfScienceCategoryGenetics & Heredity-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaGenetics & Heredity-

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노태영ROH, TAE YOUNG
Dept of Life Sciences
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