ring in carriers of BRCA1 gene muta-tions may have a distinctly different pathway of molecular pathogenesis from those occurring in noncarriers. Data from murine models implicate loss of p53 (also known as TP53) gene function as a critical early event in the malignant transformation of cells with a BRCA1 mutation. Therefore, breast tumors from BRCA1 mutation carriers might be ex-pected to exhibit a high frequency of p53 mutations. This study examined the fre-quency of p53 mutations in the breast tumors of Ashkenazi Jewish carriers and noncarriers of BRCA1 mutations. Meth
BRCA1, BRCA2 and TP53 mutations in very early-onset breast cancer with associated risks to relatives...
Breast cancer is a polymorphic disease and, until now, nodal invasion and steroid receptor levels re...
Somatic changes in the genome of breast cancer cells include amplifications, deletions and gene muta...
For the p53 Special Issue Mutation in p53 (TP53) remains one of the most commonly described genetic ...
Mutation in p53 (TP53) remains one of the most commonly described genetic events in human neoplasia....
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
Germline mutations at BRCA1 or BRCA2 genes result in susceptibility to breast and ovarian cancers. B...
SummaryBased on breast cancer families with multiple and/or early-onset cases, estimates of the life...
In the Ashkenazim, three recurrent germline mutations have been identified in the breast carcinoma s...
Breast cancers arising in women with and without a germline mutation in the BRCA1 or BRCA2 gene disp...
The inheritance of a mutant copy of the BRCA1 gene greatly increases a woman’s lifetime risk for ova...
This article is hosted on a website external to the CBCRA Open Access Archive. Selecting “View/Open...
carry one of three founding mutations in the BRCA1 and BRCA2 genes, and each mutation is associated ...
Certain mutations in BRCA1 and BRCA2 genes are frequent in the Ashkenazi Jewish population. Several ...
ABSTRACT: BACKGROUND: Basal-like breast cancers (BLBC) are aggressive breast cancers for which, so f...
BRCA1, BRCA2 and TP53 mutations in very early-onset breast cancer with associated risks to relatives...
Breast cancer is a polymorphic disease and, until now, nodal invasion and steroid receptor levels re...
Somatic changes in the genome of breast cancer cells include amplifications, deletions and gene muta...
For the p53 Special Issue Mutation in p53 (TP53) remains one of the most commonly described genetic ...
Mutation in p53 (TP53) remains one of the most commonly described genetic events in human neoplasia....
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
Germline mutations at BRCA1 or BRCA2 genes result in susceptibility to breast and ovarian cancers. B...
SummaryBased on breast cancer families with multiple and/or early-onset cases, estimates of the life...
In the Ashkenazim, three recurrent germline mutations have been identified in the breast carcinoma s...
Breast cancers arising in women with and without a germline mutation in the BRCA1 or BRCA2 gene disp...
The inheritance of a mutant copy of the BRCA1 gene greatly increases a woman’s lifetime risk for ova...
This article is hosted on a website external to the CBCRA Open Access Archive. Selecting “View/Open...
carry one of three founding mutations in the BRCA1 and BRCA2 genes, and each mutation is associated ...
Certain mutations in BRCA1 and BRCA2 genes are frequent in the Ashkenazi Jewish population. Several ...
ABSTRACT: BACKGROUND: Basal-like breast cancers (BLBC) are aggressive breast cancers for which, so f...
BRCA1, BRCA2 and TP53 mutations in very early-onset breast cancer with associated risks to relatives...
Breast cancer is a polymorphic disease and, until now, nodal invasion and steroid receptor levels re...
Somatic changes in the genome of breast cancer cells include amplifications, deletions and gene muta...