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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Bibliografiska uppgifter
I publikationen:Int J Mol Sci
Huvudupphovsmän: Nepal, Manoj, Che, Raymond, Ma, Chi, Zhang, Jun, Fei, Peiwen
Materialtyp: Artigo
Språk:Inglês
Publicerad: MDPI 2017
Ämnen:
Review
Länkar: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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