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dc.citation.startPage 111878 -
dc.citation.title Mutation research -
dc.citation.volume 829 -
dc.contributor.author Dodds, Sherry G. -
dc.contributor.author Hubbard, Gene B. -
dc.contributor.author Choi, Yongjun -
dc.contributor.author Myung, Kyungjae -
dc.contributor.author Elliot, Gene -
dc.contributor.author Garrett-Beal, Lisa J. -
dc.contributor.author Kim, Tae-moon -
dc.contributor.author Hasty, Paul E. -
dc.date.accessioned 2026-02-13T19:32:40Z -
dc.date.available 2026-02-13T19:32:40Z -
dc.date.created 2026-02-13 -
dc.date.issued 2024-12 -
dc.description.abstract RAD51 is critical to the homologous recombination (HR) pathway that repairs DNA double strand breaks (DSBs) and protects replication forks (RFs). Previously, we showed that the S181P (SP) mutation in RAD51 causes defective RF maintenance but is proficient for DSB repair. Here we report that SP/SP female mice exhibit a shortened lifespan compared to +/+ females but not males. Histological analysis found that most mice in this study died from lymphoma, independent of genotype and sex. We propose that a potential cause for shortened lifespan in SP/SP females is due to the RF defect. © © 2024 The Authors. Published by Elsevier B.V. All rights reserved. -
dc.identifier.bibliographicCitation Mutation research, v.829, pp.111878 -
dc.identifier.doi 10.1016/j.mrfmmm.2024.111878 -
dc.identifier.issn 0027-5107 -
dc.identifier.scopusid 2-s2.0-85210776733 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/90470 -
dc.language 영어 -
dc.publisher ELSEVIER -
dc.title The RAD51 S181P mutation shortens lifespan of female mice -
dc.type Article -
dc.description.isOpenAccess TRUE -
dc.type.docType Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor Lifespan -
dc.subject.keywordAuthor Replication fork maintenance -
dc.subject.keywordAuthor Double strand break repair -
dc.subject.keywordAuthor Homologous recombination -

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