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The phenotype of FancB-mutant mouse embryonic stem cells

Fanconi anemia (FA) is a rare autosomal recessive disease characterized by bone marrow failure, developmental defects and cancer. There are multiple FA genes that enable the repair of interstrand crosslinks (ICLs) in coordination with a variety of other DNA repair pathways in a way that is poorly un...

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Bibliografiska uppgifter
Huvudupphovsmän: Kim, Tae Moon, Ko, Jun Ho, Choi, Yong Jun, Hu, Lingchuan, Hasty, Paul
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2011
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3109163/
https://ncbi.nlm.nih.gov/pubmed/21458466
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mrfmmm.2011.03.010
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