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Breast Cancer Research and Treatment|December 26, 2006
Mutation analysis of five candidate genes in familial breast cancerAnna Marsh, Sue Healey, Aaron Lewis, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|October 31, 2012
A role for common genomic variants in the assessment of familial breast cancerSarah Sawyer, Gillian Mitchell, Joanne McKinley, et al.Breast Cancer Research : BCR|November 11, 2005
Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancerAaron G Lewis, James Flanagan, Anna Marsh, et al.Genetic Epidemiology|March 26, 2003
Regressive logistic and proportional hazards disease models for within-family analyses of measured genotypes, with application to a CYP17 polymorphism and breast cancerJisheng S Cui, Amanda B Spurdle, Melissa C Southey, et al.American Journal of Human Genetics|March 9, 2010
DNA methylome of familial breast cancer identifies distinct profiles defined by mutation statusJames M Flanagan, Sibylle Cocciardi, Nic Waddell, et al.Plos Genetics|May 24, 2008
BRCA1 and BRCA2 missense variants of high and low clinical significance influence lymphoblastoid cell line post-irradiation gene expressionNic Waddell, Anette Ten Haaf, Anna Marsh, et al.Molecular Oncology|April 23, 2009
Role of genetic polymorphisms and ovarian cancer susceptibilityPeter A Fasching, Simon Gayther, Leigh Pearce, et al.International Journal of Epidemiology|November 30, 2017
Assessment of moderate coffee consumption and risk of epithelial ovarian cancer: a Mendelian randomization studyJue-Sheng Ong, Liang-Dar Hwang, Gabriel Cuellar-Partida, et al.The Journal of Pathology|July 2, 2010
Gene expression profiling of formalin-fixed, paraffin-embedded familial breast tumours using the whole genome-DASL assayNic Waddell, Sibylle Cocciardi, Julie Johnson, et al.Cancers|January 16, 2020
Candidate Causal Variants at the 8p12 Breast Cancer Risk Locus Regulate DUSP4Dylan M Glubb, Wei Shi, Jonathan Beesley, et al.Pageof 42