The Fanconi Anemia Core Complex Acts as a Transcriptional Co-regulator in Hairy Enhancer of Split 1 Signaling

Mutations in one of the 13 Fanconi anemia (FA) genes cause a progressive bone marrow failure disorder associated with developmental abnormalities and a predisposition to cancer. Although FA has been defined as a DNA repair disease based on the hypersensitivity of patient cells to DNA cross-linking a...

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Detalhes bibliográficos
Main Authors: Tremblay, Cédric S., Huard, Caroline C., Huang, Feng-Fei, Habi, Ouassila, Bourdages, Valérie, Lévesque, Georges, Carreau, Madeleine
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Biochemistry and Molecular Biology 2009
Assuntos:
Transcription, Chromatin, and Epigenetics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2679438/
https://ncbi.nlm.nih.gov/pubmed/19321451
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M807921200
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