Author:
Offit Kenneth,Pierce Heather,Kirchhoff Tomas,Kolachana Prema,Rapaport Beth,Gregersen Peter,Johnson Steven,Yossepowitch Orit,Huang Helen,Satagopan Jaya,Robson Mark,Scheuer Lauren,Nafa Khedoudja,Ellis Nathan
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference8 articles.
1. Chehab NH, Malikzay A, Appel M, Halazonetis TD: Chk2/hCds1 functions as a DNA damage checkpoint in G(1) by stabilizing p53. Genes Dev. 2000, 14: 278-288.
2. Lee JS, Collins KM, Brown AL, Lee CH, Chung JH: hCds1-mediated phosphorylation of BRCA1 regulates the DNA damage response. Nature. 2000, 404: 201-204. 10.1038/35004614.
3. Bell DW, Varley JM, Szydlo TE, Kang DH, Wahrer DC, Shannon KE, et al: Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome. Science. 1999, 286: 2528-2523. 10.1126/science.286.5449.2528.
4. Vahteristo P, Bartkova J, Eerola H, Syrjakoski K, Ojala S, Kilpivaara O, et al: CHEK2 Genetic Variant Contributing to a Substantial Fraction of Familial Breast Cancer. Am J Hum Genet. 2002, 71: 432-438. 10.1086/341943.
5. The CHEK2 Breast Cancer Consortium: Low-penetrance susceptibility to breast cancer due to CHEK2*1100delC in noncarriers of BRCA1 or BRCA2 mutations. Nature Genet. 2002, 31: 55-59. 10.1038/ng879.
Cited by
98 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献