The most frequentDCLRE1C(ARTEMIS) mutations are based on homologous recombination events-Reference-Cited by-同舟云学术

The most frequentDCLRE1C(ARTEMIS) mutations are based on homologous recombination events

Published:2010-02 Issue:2 Volume:31 Page:197-207
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Pannicke Ulrich,Hönig Manfred,Schulze Ilka,Rohr Jan,Heinz Gitta A.,Braun Sylvia,Janz Ingrid,Rump Eva-Maria,Seidel Markus G.,Matthes-Martin Susanne,Soerensen Jan,Greil Johann,Stachel Daniel K.,Belohradsky Bernd H.,Albert Michael H.,Schulz Ansgar,Ehl Stephan,Friedrich Wilhelm,Schwarz Klaus

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.21168/fullpdf

Reference39 articles.

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2. Ataxia-telangiectasia-mutated dependent phosphorylation of Artemis in response to DNA damage;Chen;Cancer Sci,2005

3. Role of Artemis in DSB repair and guarding chromosomal stability following exposure to ionizing radiation at different stages of cell cycle;Darroudi;Mutat Res,2007

4. A histidine in the beta-CASP domain of Artemis is critical for its full in vitro and in vivo functions;de Villartay;DNA Repair (Amst),2009

5. Interplay between Ku, Artemis, and the DNA-dependent protein kinase catalytic subunit at DNA ends;Drouet;J Biol Chem,2006

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