A functional interaction of Ku with Werner exonuclease facilitates digestion of damaged DNA
Werner syndrome (WS) is a premature aging disorder where the affected individuals appear much older than their chronological age. The single gene that is defective in WS encodes a protein (WRN) that has ATPase, helicase and 3′→5′ exonuclease activities. Our laboratory has recently uncovered a physic...
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| Publicado no: | Nucleic Acids Res |
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| Principais autores: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2001
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC37248/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11328876/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/29.9.1926 |
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