Variation in Cancer Risks, by Mutation Position, in BRCA2 Mutation Carriers
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- 1 February 2001
- journal article
- research article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 68 (2) , 410-419
- https://doi.org/10.1086/318181
Abstract
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This publication has 34 references indexed in Scilit:
- Multiplying functions for BRCA1 and BRCA2?: Meeting Report, The Breakthrough Breast Cancer Second International Workshop on the Function of BRCA1 and BRCA2, Cambridge, UK, 9–10 September 1999Biochimica et Biophysica Acta (BBA) - Reviews on Cancer, 2000
- The N-terminal domain of the human Rad51 protein binds DNA: structure and a DNA binding surface as revealed by NMRJournal of Molecular Biology, 1999
- Genetic Heterogeneity and Penetrance Analysis of the BRCA1 and BRCA2 Genes in Breast Cancer FamiliesAmerican Journal of Human Genetics, 1998
- Differential subcellular localization, expression and biological toxicity of BRCA1 and the splice variant BRCA1-Δ11bOncogene, 1997
- Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 geneNature Genetics, 1997
- Internal repeats in the BRCA2 protein sequenceNature Genetics, 1996
- BRCA2 germline mutations in male breast cancer cases and breast cancer familiesNature Genetics, 1996
- The complete BRCA2 gene and mutations in chromosome 13q-linked kindredsNature Genetics, 1996
- A large multisite cancer family is linked to BRCA2.Journal of Medical Genetics, 1995
- Identification of the breast cancer susceptibility gene BRCA2Nature, 1995