Mutation of the RAD51C gene in a Fanconi anemia–like disorder-Reference-Cited by-同舟云学术

Mutation of the RAD51C gene in a Fanconi anemia–like disorder

Published:2010-04-18 Issue:5 Volume:42 Page:406-409
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Vaz Fiona,Hanenberg Helmut,Schuster Beatrice,Barker Karen,Wiek Constanze,Erven Verena,Neveling Kornelia,Endt Daniela,Kesterton Ian,Autore Flavia,Fraternali Franca,Freund Marcel,Hartmann Linda,Grimwade David,Roberts Roland G,Schaal Heiner,Mohammed Shehla,Rahman Nazneen,Schindler Detlev,Mathew Christopher G

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.570.pdf

Reference30 articles.

1. Moldovan, G.-L. & D'Andrea, A.D. How the Fanconi anemia pathway guards the genome. Annu. Rev. Genet. 43, 223–249 (2009).

2. Rosenberg, P.S. et al. Cancer risks in Fanconi anemia: findings from the German Fanconi Anemia Registry. Haematologica 93, 511–517 (2008).

3. Abraham, J. et al. Eme1 is involved in DNA damage processing and maintenance of genomic stability in mammalian cells. EMBO J. 22, 6137–6147 (2003).

4. Godthelp, B.C. et al. Mammalian Rad51C contributes to DNA cross-link resistance, sister chromatid cohesion and genomic stability. Nucleic Acids Res. 30, 2172–2182 (2002).

5. French, C.A. et al. Role of mammalian RAD51L2 (RAD51C) in recombination and genetic stability. J. Biol. Chem. 277, 19322–19330 (2002).

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