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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Publikašuvnnas:	Mol Cell Biol
Váldodahkkit:	Saintigny, Yannick, Makienko, Kate, Swanson, Cristina, Emond, Mary J., Monnat, Jr., Raymond J.
Materiálatiipa:	Artigo
Giella:	Inglês
Almmustuhtton:	Taylor & Francis 2002
Fáttát:	DNA Dynamics and Chromosome Structure
Liŋkkat:	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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Homologous Recombination Resolution Defect in Werner Syndrome

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