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ScharerDavid Orlando

Scharer, Orlando D.
Schärer Lab.
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DC Field Value Language
dc.citation.number 10 -
dc.citation.title COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY -
dc.citation.volume 5 -
dc.contributor.author Scharer, Orlando D. -
dc.date.accessioned 2023-12-22T03:36:15Z -
dc.date.available 2023-12-22T03:36:15Z -
dc.date.created 2017-01-26 -
dc.date.issued 2013-10 -
dc.description.abstract Nucleotide excision repair (NER) is the main pathway used by mammals to remove bulky DNA lesions such as those formed by UV light, environmental mutagens, and some cancer chemotherapeutic adducts from DNA. Deficiencies in NER are associated with the extremely skin cancer-prone inherited disorder xeroderma pigmentosum. Although the core NER reaction and the factors that execute it have been known for some years, recent studies have led to a much more detailed understanding of the NER mechanism, how NER operates in the context of chromatin, and how it is connected to other cellular processes such as DNA damage signaling and transcription. This review emphasizes biochemical, structural, cell biological, and genetic studies since 2005 that have shed light on many aspects of the NER pathway. -
dc.identifier.bibliographicCitation COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, v.5, no.10 -
dc.identifier.doi 10.1101/cshperspect.a012609 -
dc.identifier.issn 1943-0264 -
dc.identifier.scopusid 2-s2.0-84870751887 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/21246 -
dc.identifier.url http://cshperspectives.cshlp.org/content/5/10/a012609 -
dc.identifier.wosid 000327740000006 -
dc.language 영어 -
dc.publisher COLD SPRING HARBOR LAB PRESS -
dc.title Nucleotide Excision Repair in Eukaryotes -
dc.type Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus GROUP-C PROTEIN -
dc.subject.keywordPlus DNA-BINDING PROTEIN -
dc.subject.keywordPlus GROUP-A PROTEIN -
dc.subject.keywordPlus CYCLOBUTANE PYRIMIDINE DIMERS -
dc.subject.keywordPlus TRICHOTHIODYSTROPHY GROUP-A -
dc.subject.keywordPlus COMPLEMENTATION GROUP-A -
dc.subject.keywordPlus HUMAN XPG PROTEIN -
dc.subject.keywordPlus GROUP D HELICASE -
dc.subject.keywordPlus XERODERMA-PIGMENTOSUM -
dc.subject.keywordPlus DAMAGED DNA -

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