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ScharerDavid Orlando

Scharer, Orlando D.
Schärer Lab.
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DC Field Value Language
dc.citation.endPage 1995 -
dc.citation.number 14 -
dc.citation.startPage 1993 -
dc.citation.title EMBO JOURNAL -
dc.citation.volume 36 -
dc.contributor.author Scharer, Orlando D. -
dc.date.accessioned 2023-12-21T22:08:15Z -
dc.date.available 2023-12-21T22:08:15Z -
dc.date.created 2017-07-31 -
dc.date.issued 2017-07 -
dc.description.abstract To counteract damage to our genomes, numerous endo-and exonucleases incise the DNA backbone to remove damaged and aberrant DNA structures. It is imperative that such incisions be very tightly controlled, as unwanted DNA breaks are a key source of genome instability. Two new papers in The EMBO Journal shed light on how the activity of one such nuclease-ERCC1-XPF, an enzyme involved in various DNA repair pathways-is regulated to perform incision in the vicinity of DNA interstrand crosslinks. -
dc.identifier.bibliographicCitation EMBO JOURNAL, v.36, no.14, pp.1993 - 1995 -
dc.identifier.doi 10.15252/embj.201797489 -
dc.identifier.issn 0261-4189 -
dc.identifier.scopusid 2-s2.0-85021447721 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/22379 -
dc.identifier.url http://emboj.embopress.org/content/36/14/1993 -
dc.identifier.wosid 000405478400001 -
dc.language 영어 -
dc.publisher WILEY -
dc.title ERCC1-XPF endonuclease-positioned to cut -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Biochemistry & Molecular Biology; Cell Biology -
dc.relation.journalResearchArea Biochemistry & Molecular Biology; Cell Biology -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus NUCLEOTIDE EXCISION-REPAIR -
dc.subject.keywordPlus GENOME STABILITY -
dc.subject.keywordPlus FANCONI-ANEMIA -
dc.subject.keywordPlus NUCLEASE -
dc.subject.keywordPlus XPF-ERCC1 -
dc.subject.keywordPlus COMPLEX -
dc.subject.keywordPlus SLX4 -

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