Loss of expression of FANCD2 protein in sporadic and hereditary breast cancer

Fanconi anemia (FA) is a recessive disorder associated with progressive pancytopenia, multiple developmental defects, and marked predisposition to malignancies. FA is genetically heterogeneous, comprising at least 12 complementation groups (A–M). Activation of one of the FA proteins (FANCD2) by mono...

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Detalhes bibliográficos
Main Authors: van der Groep, Petra, Hoelzel, Michael, Buerger, Horst, Joenje, Hans, de Winter, Johan P., van Diest, Paul J.
Formato: Artigo
Idioma:Inglês
Publicado em: Springer US 2007
Assuntos:
Preclinical Study
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2096638/
https://ncbi.nlm.nih.gov/pubmed/17333336
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10549-007-9534-7
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