The Simple Chordate Ciona intestinalis Has a Reduced Complement of Genes Associated with Fanconi Anemia

Fanconi anemia (FA) is a human genetic disease characterized by congenital defects, bone marrow failure, and increased cancer risk. FA is associated with mutation in one of 24 genes. The protein products of these genes function cooperatively in the FA pathway to orchestrate the repair of DNA interst...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Evol Bioinform Online
Prif Awduron: Stanley, Edward C., Azzinaro, Paul A., Vierra, David A., Howlett, Niall G., Irvine, Steven Q.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Libertas Academica 2016
Pynciau:
Original Research
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4898443/
https://ncbi.nlm.nih.gov/pubmed/27279728
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4137/EBO.S37920
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