Preventing Nonhomologous End Joining Suppresses DNA Repair Defects of Fanconi Anemia-Reference-Cited by-同舟云学术

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Preventing Nonhomologous End Joining Suppresses DNA Repair Defects of Fanconi Anemia

Published:2010-07 Issue:1 Volume:39 Page:25-35
ISSN:1097-2765
Container-title:Molecular Cell
language:en
Short-container-title:Molecular Cell

Author:

Adamo Adele,Collis Spencer J.,Adelman Carrie A.,Silva Nicola,Horejsi Zuzana,Ward Jordan D.,Martinez-Perez Enrique,Boulton Simon J.,La Volpe Adriana

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology

Reference57 articles.

1. BRC-1 acts in the inter-sister pathway of meiotic double-strand break repair;Adamo;EMBO Rep.,2008

2. Fanconi's anaemia and its variability;Alter;Br. J. Haematol.,1993

3. Frameshift mutation in PRKDC, the gene for DNA-PKcs, in the DNA repair-defective, human, glioma-derived cell line M059J;Anderson;Radiat. Res.,2001

4. XPF-ERCC1 participates in the Fanconi anemia pathway of cross-link repair;Bhagwat;Mol. Cell. Biol.,2009

5. Cellular functions of the BRCA tumour-suppressor proteins;Boulton;Biochem. Soc. Trans.,2006

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