The Fanconi Anemia Proteins FANCD2 and FANCJ Interact and Regulate Each Other's Chromatin Localization

Fanconi anemia is a genetic disease resulting in bone marrow failure, birth defects, and cancer that is thought to encompass a defect in maintenance of genomic stability. Mutations in 16 genes (FANCA, B, C, D1, D2, E, F, G, I, J, L, M, N, O, P, and Q) have been identified in patients, with the Fanco...

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Detalhes bibliográficos
Main Authors: Chen, Xiaoyong, Wilson, James B., McChesney, Patricia, Williams, Stacy A., Kwon, Youngho, Longerich, Simonne, Marriott, Andrew S., Sung, Patrick, Jones, Nigel J., Kupfer, Gary M.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Biochemistry and Molecular Biology 2014
Assuntos:
DNA and Chromosomes
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4162179/
https://ncbi.nlm.nih.gov/pubmed/25070891
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M114.552570
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