نتایج جستجو برای: chek2

تعداد نتایج: 669  

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2006
Deborah Thompson Sheila Seal Mieke Schutte Lesley McGuffog Rita Barfoot Anthony Renwick Rosalind Eeles Nayanta Sodha Richard Houlston Susan Shanley Jan Klijn Marijke Wasielewski Jenny Chang-Claude P Andrew Futreal Barbara L Weber Katherine L Nathanson Michael Stratton Hanne Meijers-Heijboer Nazneen Rahman Douglas F Easton

The CHEK2 1100delC protein-truncating mutation has a carrier frequency of approximately 0.7% in Northern and Western European populations and confers an approximately 2-fold increased risk of breast cancer. It has also been suggested to increase risks of colorectal and prostate cancer, but its involvement with these or other types of cancer has not been confirmed. The incidence of cancer other ...

2006
Deborah Thompson Sheila Seal Mieke Schutte Lesley McGuffog Rita Barfoot Anthony Renwick Rosalind Eeles Nayanta Sodha Richard Houlston Susan Shanley Jan Klijn Marijke Wasielewski Jenny Chang-Claude P. Andrew Futreal Barbara L. Weber Katherine L. Nathanson Michael Stratton Hanne Meijers-Heijboer Nazneen Rahman Douglas F. Easton

The CHEK2 1100delC protein-truncating mutation has a carrier frequency of f0.7% in Northern and Western European populations and confers an f2-fold increased risk of breast cancer. It has also been suggested to increase risks of colorectal and prostate cancer, but its involvement with these or other types of cancer has not been confirmed. The incidence of cancer other than breast cancer in 11,1...

Journal: :The American Journal of Human Genetics 2003

Journal: :Breast Cancer: Targets and Therapy 2017

Journal: : 2023

Introduction. At least 3% of all cancer cases are associated with hereditary changes in genes predisposing to malignant neoplasms. In addition the widely known BRCA1,2 genes, other involved equally DNA repair system and maintenance genome integrity, such as PALB2, CHEK2, being introduced into routine diagnosis. this review we present current information from recent studies on structure function...

Journal: :Asian Pacific journal of cancer biology 2023

Introduction: The TP53 and CHEK2 genes have been described as breast cancer susceptibility some of their polymorphisms associated with an increased risk in certain populations.Aim: objective this study was to investigate the p.R72P PIN3 Ins16bp (TP53) I157T (CHEK2) mutation developping cancer. Methods: This case-control had enrolled 144 participants including 65 cases (breast patients) 79 contr...

2016
Cameron M Scott JiHoon Eric Joo Neil O'Callaghan Daniel D Buchanan Mark Clendenning Graham G Giles John L Hopper Ee Ming Wong Melissa C Southey

DNA methylation can mimic the effects of both germline and somatic mutations for cancer predisposition genes such as BRCA1 and p16INK4a. Constitutional DNA methylation of the BRCA1 promoter has been well described and is associated with an increased risk of early-onset breast cancers that have BRCA1-mutation associated histological features. The role of methylation in the context of other breas...

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