FANCG Is Phosphorylated at Serines 383 and 387 during Mitosis

Fanconi anemia (FA) is an autosomal recessive disease marked by congenital defects, bone marrow failure, and high incidence of leukemia and solid tumors. Eight genes have been cloned, with the accompanying protein products participating in at least two complexes, which appear to be functionally depe...

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Autors principals: Mi, Jun, Qiao, Fengyu, Wilson, James B., High, Anthony A., Schroeder, Melanie J., Stukenberg, Peter T., Moss, Amy, Shabanowitz, Jeffrey, Hunt, Donald F., Jones, Nigel J., Kupfer, Gary M.
Format: Artigo
Idioma:Inglês
Publicat: American Society for Microbiology 2004
Matèries:
DNA Dynamics and Chromosome Structure
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC516759/
https://ncbi.nlm.nih.gov/pubmed/15367677
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/MCB.24.19.8576-8585.2004
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