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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Dades bibliogràfiques

Publicat a:	Proc Natl Acad Sci U S A
Autors principals:	Nakanishi, Koji, Yang, Yun-Gui, Pierce, Andrew J., Taniguchi, Toshiyasu, Digweed, Martin, D'Andrea, Alan D., Wang, Zhao-Qi, Jasin, Maria
Format:	Artigo
Idioma:	Inglês
Publicat:	National Academy of Sciences 2005
Matèries:	Biological Sciences
Accés en línia:	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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