Homologous Recombination Resolution Defect in Werner Syndrome

Werner syndrome (WRN) is an uncommon autosomal recessive disease whose phenotype includes features of premature aging, genetic instability, and an elevated risk of cancer. We used three different experimental strategies to show that WRN cellular phenotypes of limited cell division potential, DNA dam...

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Dettagli Bibliografici

Pubblicato in:	Mol Cell Biol
Autori principali:	Saintigny, Yannick, Makienko, Kate, Swanson, Cristina, Emond, Mary J., Monnat, Jr., Raymond J.
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	Taylor & Francis 2002
Soggetti:	DNA Dynamics and Chromosome Structure
Accesso online:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC139822/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12242278/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/MCB.22.20.6971-6978.2002
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