To access publisher full text version of this article. Please click on the hyperlink in Additional Links field.Breast tumors from BRCA1 germ line mutation carriers typically exhibit features of the basal-like molecular subtype. However, the specific genes recurrently mutated as a consequence of BRCA1 dysfunction have not been fully elucidated. In this study, we used gene expression profiling to molecularly subtype 577 breast tumors, including 73 breast tumors from BRCA1/2 mutation carriers. Focusing on the RB1 locus, we analyzed 33 BRCA1-mutated, 36 BRCA2-mutated, and 48 non-BRCA1/2-mutated breast tumors using a custom-designed high-density oligomicroarray covering the RB1 gene. We found a strong association between the basal-like subtype a...
Basal-like breast cancer (BBC) is a subtype of breast cancer with poor prognosis. Inherited mutation...
Mutations in a number of genes are now known to cause susceptibility to breast cancer. In the contex...
Mutations in BRCA1 and BRCA2 cause deficiencies in homologous recombination repair (HR), resulting i...
Breast tumors from BRCA1 germ line mutation carriers typically exhibit features of the basal-like mo...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
Introduction Breast cancers can be classified using whole genome expression into distinct subtypes t...
To access full text version of this article. Please click on the hyperlink "Full Text" at the bottom...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
Breast tumours are highly heterogeneous with several distinct sub-types recognised according to thei...
ABSTRACT: BACKGROUND: Basal-like breast cancers (BLBC) are aggressive breast cancers for which, so f...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
BRCA1-mutated breast carcinomas may have distinct biological features, suggesting the involvement of...
Thesis (Ph. D.)--University of Washington, 2000Germline mutations in BRCA1 lead to an increased risk...
Extensive expression profiling studies have shown that sporadic breast cancer is composed of five cl...
Tumor suppressor genes that perform apparently generic cellular functions nonetheless cause tissue-s...
Basal-like breast cancer (BBC) is a subtype of breast cancer with poor prognosis. Inherited mutation...
Mutations in a number of genes are now known to cause susceptibility to breast cancer. In the contex...
Mutations in BRCA1 and BRCA2 cause deficiencies in homologous recombination repair (HR), resulting i...
Breast tumors from BRCA1 germ line mutation carriers typically exhibit features of the basal-like mo...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
Introduction Breast cancers can be classified using whole genome expression into distinct subtypes t...
To access full text version of this article. Please click on the hyperlink "Full Text" at the bottom...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
Breast tumours are highly heterogeneous with several distinct sub-types recognised according to thei...
ABSTRACT: BACKGROUND: Basal-like breast cancers (BLBC) are aggressive breast cancers for which, so f...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
BRCA1-mutated breast carcinomas may have distinct biological features, suggesting the involvement of...
Thesis (Ph. D.)--University of Washington, 2000Germline mutations in BRCA1 lead to an increased risk...
Extensive expression profiling studies have shown that sporadic breast cancer is composed of five cl...
Tumor suppressor genes that perform apparently generic cellular functions nonetheless cause tissue-s...
Basal-like breast cancer (BBC) is a subtype of breast cancer with poor prognosis. Inherited mutation...
Mutations in a number of genes are now known to cause susceptibility to breast cancer. In the contex...
Mutations in BRCA1 and BRCA2 cause deficiencies in homologous recombination repair (HR), resulting i...