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FANCD2 and DNA Damage

Investigators have dedicated considerable effort to understanding the molecular basis underlying Fanconi Anemia (FA), a rare human genetic disease featuring an extremely high incidence of cancer and many congenital defects. Among those studies, FA group D2 protein (FANCD2) has emerged as the focal p...

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Detalhes bibliográficos
Publicado no:Int J Mol Sci
Main Authors: Nepal, Manoj, Che, Raymond, Ma, Chi, Zhang, Jun, Fei, Peiwen
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5578191/
https://ncbi.nlm.nih.gov/pubmed/28825622
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms18081804
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