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The DNA structure and sequence preferences of WRN underlie its function in telomeric recombination events
Telomeric abnormalities caused by loss of function of the RecQ helicase WRN are linked to the multiple premature ageing phenotypes that characterize Werner syndrome. Here we examine WRN's role in telomeric maintenance, by comparing its action on a variety of DNA structures without or with telom...
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| Publicado no: | Nat Commun |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Pub. Group
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4589872/ https://ncbi.nlm.nih.gov/pubmed/26420422 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ncomms9331 |
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