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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Detalles Bibliográficos
Autores principales: van der Groep, Petra, Hoelzel, Michael, Buerger, Horst, Joenje, Hans, de Winter, Johan P., van Diest, Paul J.
Formato: Texto
Lenguaje:English
Publicado: Springer US 2007
Materias:
Preclinical Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2096638/
https://www.ncbi.nlm.nih.gov/pubmed/17333336
http://dx.doi.org/10.1007/s10549-007-9534-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2096638/
https://www.ncbi.nlm.nih.gov/pubmed/17333336
http://dx.doi.org/10.1007/s10549-007-9534-7

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