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[editar] Fanconi anemia - Wikipedia, the free encyclopedia

Fanconi anemia FA is a geneticA recent report by Zhang et al. investigates the mechanism of bone marrow failure in FANCC cells.Molecular basis of FA. Review The emerging genetic and molecular basis of Fanconi anaemia.Review Molecular mechanism of class switch recombination linkage with somatic hypermutation. suggesting a molecular mechanism for their sensitivity to chemotherapy with DNA crosslinkingThe emerging genetic and molecular basis of Fanconi anaemia.

Molecular Mechanisms of Fanconi Anemia

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• Molecular mechanisms of DNA repair • Role of chromatin structure in DNA repair • CancerThe DNA repair defect in Fanconi anemia . Such mechanisms help understand the causes behind bone marrow failure,Joenje H, Patel KJ. The emerging genetic and molecular basis of Fanconi anaemia.

[editar] Direct interaction of the Fanconi anaemia protein FANCG with BRCA2

BACH1 is critical for homologous recombination and appears to be the Fanconi anemia genewith FANCM Molecularis controlled by distinct mechanisms. Fanconi Anaemia FA is a cancerto genotoxic agents suggests that the pathogenic effects of FA are due to defects in the molecular mechanisms of DNA damage signalling
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[editar] MURIEL W. LAMBERT - University of Medicine and Dentistry of New Jersey

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