Kin-cohort estimates for familial breast cancer risk in relation to variants in DNA base excision repair, BRCA1 interacting and growth factor genes
暂无分享,去创建一个
[1] X. Shu,et al. A population-based case-control study of the Arg399Gln polymorphism in DNA repair gene XRCC1 and risk of breast cancer. , 2003, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.
[2] N. Chatterjee,et al. The HER2 I655V Polymorphism and Breast Cancer Risk in Ashkenazim , 2003, Epidemiology.
[3] K. Lohman,et al. DNA-repair genetic polymorphisms and breast cancer risk. , 2003, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.
[4] D. Cox,et al. Polymorphisms in the DNA repair gene XRCC1, breast cancer risk, and response to radiotherapy. , 2003, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.
[5] D. Hunter,et al. Polymorphic variation at the ‐202 locus in IGFBP3: Influence on serum levels of insulin‐like growth factors, interaction with plasma retinol and vitamin D and breast cancer risk , 2003, International journal of cancer.
[6] Jinghui Zhang,et al. Mutational analysis of the BRCA1‐interacting genes ZNF350/ZBRK1 and BRIP1/BACH1 among BRCA1 and BRCA2‐negative probands from breast‐ovarian cancer families and among early‐onset breast cancer cases and reference individuals , 2003, Human mutation.
[7] F. Berrino,et al. Combination of DNA repair gene single nucleotide polymorphisms and increased levels of DNA adducts in a population-based study. , 2003, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.
[8] J. Chang-Claude,et al. A Transforming Growth Factorβ1 Signal Peptide Variant Increases Secretion in Vitro and Is Associated with Increased Incidence of Invasive Breast Cancer , 2003 .
[9] I. M. Jones,et al. Challenges and complexities in estimating both the functional impact and the disease risk associated with the extensive genetic variation in human DNA repair genes. , 2003, Mutation research.
[10] C. Begg,et al. Kin‐cohort evaluation of relative risks of genetic variants , 2003, Genetic epidemiology.
[11] K. Lohman,et al. Polymorphisms of XRCC1 and XRCC3 genes and susceptibility to breast cancer. , 2003, Cancer letters.
[12] A. Spurdle,et al. BRCA2 arg372hispolymorphism and epithelial ovarian cancer risk , 2003, International journal of cancer.
[13] C. Ulrich,et al. Polymorphisms in DNA repair genes and associations with cancer risk. , 2002, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.
[14] I. M. Jones,et al. Identification of 127 amino acid substitution variants in screening 37 DNA repair genes in humans. , 2002, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.
[15] D. Noh,et al. XRCC1 genetic polymorphism and breast cancer risk. , 2002, Pharmacogenetics.
[16] K. Caldecott,et al. Central Role for the XRCC1 BRCT I Domain in Mammalian DNA Single-Strand Break Repair , 2002, Molecular and Cellular Biology.
[17] G. Giles,et al. The BRCA2 372 HH genotype is associated with risk of breast cancer in Australian women under age 60 years. , 2002, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.
[18] E. D. de Vries,et al. Genes other than BRCA1 and BRCA2 involved in breast cancer susceptibility , 2002, Journal of medical genetics.
[19] Douglas F. Easton,et al. Polygenic susceptibility to breast cancer and implications for prevention , 2002, Nature Genetics.
[20] N E Day,et al. Evidence for further breast cancer susceptibility genes in addition to BRCA1 and BRCA2 in a population‐based study , 2001, Genetic epidemiology.
[21] E. Ziv,et al. Association between the T29-->C polymorphism in the transforming growth factor beta1 gene and breast cancer among elderly white women: The Study of Osteoporotic Fractures. , 2001, JAMA.
[22] H. Mohrenweiser,et al. Amino acid substitution variants of APE1 and XRCC1 genes associated with ionizing radiation sensitivity. , 2001, Carcinogenesis.
[23] E J Duell,et al. Polymorphisms in the DNA repair gene XRCC1 and breast cancer. , 2001, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.
[24] S Wacholder,et al. A Marginal Likelihood Approach for Estimating Penetrance from Kin‐Cohort Designs , 2001, Biometrics.
[25] J. Chang-Claude,et al. A common variant in BRCA2 is associated with both breast cancer risk and prenatal viability , 2000, Nature Genetics.
[26] M. West,et al. XRCC1 keeps DNA from getting stranded. , 2000, Mutation research.
[27] M. Gail,et al. Kin-cohort designs for gene characterization. , 1999, Journal of the National Cancer Institute. Monographs.
[28] D. Evans,et al. Heritability of cellular radiosensitivity: a marker of low-penetrance predisposition genes in breast cancer? , 1999, American journal of human genetics.
[29] D. Easton. How many more breast cancer predisposition genes are there? , 1999, Breast Cancer Research.
[30] Nazneen,et al. Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer. , 1999, Journal of the National Cancer Institute.
[31] D. Bell,et al. XRCC1 polymorphisms: effects on aflatoxin B1-DNA adducts and glycophorin A variant frequency. , 1999, Cancer research.
[32] S Wacholder,et al. The kin-cohort study for estimating penetrance. , 1998, American journal of epidemiology.
[33] C. Mantzoros,et al. Insulin-like growth factor-I in relation to premenopausal ductal carcinoma in situ of the breast. , 1998, Epidemiology.
[34] I. M. Jones,et al. Variation in DNA repair is a factor in cancer susceptibility: a paradigm for the promises and perils of individual and population risk estimation? , 1998, Mutation research.
[35] A. Sigurdson,et al. Family history of cancer in patients with glioma: a validation study of accuracy. , 1998, Journal of the National Cancer Institute.
[36] I. M. Jones,et al. Nonconservative amino acid substitution variants exist at polymorphic frequency in DNA repair genes in healthy humans. , 1998, Cancer research.
[37] L. Thompson,et al. Life without DNA repair. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[38] D. Arveiler,et al. Polymorphisms of the transforming growth factor-beta 1 gene in relation to myocardial infarction and blood pressure. The Etude Cas-Témoin de l'Infarctus du Myocarde (ECTIM) Study. , 1996, Hypertension.
[39] A. Howell,et al. Cancer experience in the relatives of an unselected series of breast cancer patients. , 1994, British Journal of Cancer.
[40] Y. Hochberg. A sharper Bonferroni procedure for multiple tests of significance , 1988 .
[41] K. Shiraki,et al. Breast cancer genetics: what we know and what we need , 2001, Nature Medicine.