Human Fanconi anemia monoubiquitination pathway promotes homologous DNA repair
Fanconi anemia (FA) is a recessive disorder characterized by congenital abnormalities, progressive bone-marrow failure, and cancer susceptibility. Cells from FA patients are hypersensitive to agents that produce DNA crosslinks and, after treatment with these agents, have pronounced chromosome breaka...
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| Yayımlandı: | Proc Natl Acad Sci U S A |
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| Asıl Yazarlar: | , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
National Academy of Sciences
2005
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC545844/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/15650050/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.0407796102 |
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