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dc.contributor.authorHanssen-Bauer, Audun
dc.contributor.authorSolvang-Garten, Karin
dc.contributor.authorAkbari, Mansour
dc.contributor.authorOtterlei, Marit
dc.date.accessioned2015-09-29T12:21:53Z
dc.date.accessioned2015-10-20T11:44:09Z
dc.date.available2015-09-29T12:21:53Z
dc.date.available2015-10-20T11:44:09Z
dc.date.issued2012
dc.identifier.citationInternational Journal of Molecular Sciences 2012, 13(12):17210-17229nb_NO
dc.identifier.issn1422-0067
dc.identifier.urihttp://hdl.handle.net/11250/2357220
dc.description.abstractX-ray Repair Cross Complementing protein 1 (XRCC1) acts as a scaffolding protein in the converging base excision repair (BER) and single strand break repair (SSBR) pathways. XRCC1 also interacts with itself and rapidly accumulates at sites of DNA damage. XRCC1 can thus mediate the assembly of large multiprotein DNA repair complexes as well as facilitate the recruitment of DNA repair proteins to sites of DNA damage. Moreover, XRCC1 is present in constitutive DNA repair complexes, some of which associate with the replication machinery. Because of the critical role of XRCC1 in DNA repair, its common variants Arg194Trp, Arg280His and Arg399Gln have been extensively studied. However, the prevalence of these variants varies strongly in different populations, and their functional influence on DNA repair and disease remains elusive. Here we present the current knowledge about the role of XRCC1 and its variants in BER and human disease/cancer.nb_NO
dc.language.isoengnb_NO
dc.publisherMDPInb_NO
dc.titleX-ray repair cross complementing protein 1 in base excision repairnb_NO
dc.typeJournal articlenb_NO
dc.typePeer revieweden_GB
dc.date.updated2015-09-29T12:21:53Z
dc.source.volume13nb_NO
dc.source.journalInternational Journal of Molecular Sciencesnb_NO
dc.source.issue12nb_NO
dc.identifier.doi10.3390/ijms131217210
dc.identifier.cristin988643
dc.description.localcodeThis is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.nb_NO


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