BROWSE

Related Scientist

cnir's photo.

cnir
뇌과학이미징연구단
more info

ITEM VIEW & DOWNLOAD

Eukaryotic DNA damage responses: Homologous recombination factors and ubiquitin modification

DC Field Value Language
dc.contributor.authorNam soo Lee-
dc.contributor.authorSoomi Kim-
dc.contributor.authorYong Woo Jung-
dc.contributor.authorHongtae Kim-
dc.date.available2019-01-03T05:34:09Z-
dc.date.created2018-06-26-
dc.date.issued2018-05-
dc.identifier.issn0027-5107-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/5276-
dc.description.abstractTo prevent genomic instability disorders, cells have developed a DNA damage response. The response involves various proteins that sense damaged DNA, transduce damage signals, and effect DNA repair. In addition, ubiquitin modifications modulate the signaling pathway depending on cellular context. Among various types of DNA damage, double-stranded breaks are highly toxic to genomic integrity. Homologous recombination (HR) repair is an essential mechanism that fixes DNA damage because of its high level of accuracy. Although factors in the repair pathway are well established, pinpointing the exact mechanisms of repair and devising therapeutic applications requires more studies. Moreover, essential functions of ubiquitin modification in the DNA damage signaling pathway have emerged. In this review, to explore the eukaryotic DNA damage response, we will mention the functions of main factors in the HR repair pathway and ubiquitin modification © 2017 Elsevier B.V.-
dc.description.uri1-
dc.language영어-
dc.publisherELSEVIER SCIENCE BV-
dc.subjectDNA damage response-
dc.subjectHomologous recombination repair pathway-
dc.subjectUbiquitin modification-
dc.titleEukaryotic DNA damage responses: Homologous recombination factors and ubiquitin modification-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000432598800012-
dc.identifier.scopusid2-s2.0-85019882487-
dc.identifier.rimsid63804-
dc.contributor.affiliatedAuthorHongtae Kim-
dc.identifier.doi10.1016/j.mrfmmm.2017.04.003-
dc.identifier.bibliographicCitationMUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, v.809, pp.88 - 98-
dc.citation.titleMUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS-
dc.citation.volume809-
dc.citation.startPage88-
dc.citation.endPage98-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordPlusDOUBLE-STRAND BREAKS-
dc.subject.keywordPlusTRAF-INTERACTING PROTEIN-
dc.subject.keywordPlusMAINTAINS GENOMIC STABILITY-
dc.subject.keywordPlusDEPENDENT SIGNALING CASCADE-
dc.subject.keywordPlusCANCER SUSCEPTIBILITY GENE-
dc.subject.keywordPlusREPAIR PATHWAY CHOICE-
dc.subject.keywordPlusEND RESECTION-
dc.subject.keywordPlusBINDING PROTEIN-
dc.subject.keywordPlusMRN COMPLEX-
dc.subject.keywordPlusE3 LIGASE-
dc.subject.keywordAuthorDNA damage response-
dc.subject.keywordAuthorHomologous recombination repair pathway-
dc.subject.keywordAuthorUbiquitin modification-
Appears in Collections:
Center for Neuroscience Imaging Research (뇌과학 이미징 연구단) > 1. Journal Papers (저널논문)
Files in This Item:
16_김홍태_Eukaryotic DNA damage responses Homologous recombination factors andubiquitin modification.pdfDownload

qrcode

  • facebook

    twitter

  • Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
해당 아이템을 이메일로 공유하기 원하시면 인증을 거치시기 바랍니다.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse