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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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| Hlavní autoři: | , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
National Academy of Sciences
2005
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC545844/ https://ncbi.nlm.nih.gov/pubmed/15650050 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0407796102 |
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