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Divergent cellular phenotypes of human and mouse cells lacking the Werner syndrome RecQ helicase
Werner syndrome (WS) is a human autosomal recessive genetic instability and cancer predisposition syndrome with features of premature aging. Several genetically determined mouse models of WS have been generated, however none develops features of premature aging or an elevated risk of neoplasia unles...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2818259/ https://ncbi.nlm.nih.gov/pubmed/19896421 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.dnarep.2009.09.013 |
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