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

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

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http://www.wikidata.org/entity/Q28188416

Q28188416

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Kin-cohort estimates for familial breast cancer risk in relation to variants in DNA base excision repair, BRCA1 interacting and growth factor genes Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer.BACH1 Ser919Pro variant and breast cancer risk.Interplay between Fanconi anemia and homologous recombination pathways in genome integrity Tagging single nucleotide polymorphisms in the BRIP1 gene and susceptibility to breast and ovarian cancer BRIP1 (BACH1) variants and familial breast cancer risk: a case-control study.Insight into the roles of helicase motif Ia by characterizing Fanconi anemia group J protein (FANCJ) patient mutations A competing risks model for correlated data based on the subdistribution hazard.G-quadruplex nucleic acids and human disease Fanconi anemia group J mutation abolishes its DNA repair function by uncoupling DNA translocation from helicase activity or disruption of protein-DNA complexes.Hereditary breast cancer and the BRCA1-associated FANCJ/BACH1/BRIP1.Breast cancer susceptibility and the DNA damage response.Fanconi anaemia genes and susceptibility to cancer.A novel breast cancer-associated BRIP1 (FANCJ/BACH1) germ-line mutation impairs protein stability and function Correlation of the BACH1 Pro919Ser polymorphism with breast cancer risk: A literature-based meta-analysis and meta-regression analysis.Association between BRIP1 (BACH1) polymorphisms and breast cancer risk: a meta-analysis.A commentary on Analysis of ZNF350/ZBRK1 promoter variants and breast cancer susceptibility in non-BRCA1/2 French Canadian breast cancer families.Note of clarification of data in the paper entitled association between BRIP1 (BACH1) polymorphisms and breast cancer risk.Germline mutations in BRIP1 and PALB2 in Jewish high cancer risk families.BRIP1 overexpression is correlated with clinical features and survival outcome of luminal breast cancer subtypes.Functional SNP in 3'-UTR MicroRNA-Binding Site of ZNF350 Confers Risk for Age-Related Cataract.CtIP- and ATR-dependent FANCJ phosphorylation in response to DNA strand breaks mediated by DNA replication.BRIP1, PALB2, and RAD51C mutation analysis reveals their relative importance as genetic susceptibility factors for breast cancer.

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P2860

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

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http://www.wikidata.org/entity/Q28188416

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2003 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2003 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

artículu científicu espublizáu en 2003

@ast

im August 2003 veröffentlichter wissenschaftlicher Artikel

@de

scientific article (publication date: August 2003)

@en

vedecký článok (publikovaný 2003-08)

@sk

vědecký článek publikovaný v roce 2003

@cs

wetenschappelijk artikel (gepubliceerd in 2003-08)

@nl

наукова стаття, опублікована в серпні 2003

@uk

مقالة علمية (نشرت في أغسطس 2003)

@ar