for the genesis of cancer predicts that cancer can develop when the wild-type allele of a tumor suppressor gene is lost in an individual with a germline muta-tion in that gene. Neither loss of hetero-zygosity (LOH) for BRCA1 nor muta-tions of the TP53 (also known as p53) gene have been documented prior to invasion in ovarian cancers arising in women with germline BRCA1 muta-tions. Such documentation is difficult because lesions are rarely identified in ovarian epithelium. We, therefore, looked for LOH at microsatellite poly-morphisms linked to the BRCA1 an
OBJECTIVES: Mutations in the BRCA1 and BRCA2 genes predispose women to ovarian and/or breast cancer....
We analyzed 37 primary invasive carcinomas for BRCA1 and BRCA2 mutations by screening the entire cod...
The phenotypic variability of epithelial ovarian neoplasms correlates with a diversity of changes at...
Background Subclassification of ovarian carcinomas can be used to guide treatment and determine pro...
Loss of BRCA1/BRCA2 function through genetic or epigenetic mechanisms is common in epithelial ovari...
Hereditary ovarian cancers associated with germline mutations in either BRCA1 or BRCA2 were studied ...
PURPOSE: Germline mutations in the BRCA1 and BRCA2 genes confer increased susceptibility to ovarian ...
Ovarian cancer is the most lethal cause of death from gynecological malignancies in the Western worl...
AIM: Mutations in the BRCA1 and TP53 genes are early genetic events leading to (hereditary) ovarian ...
Mutations within the BRCA1 tumor suppressor gene occur frequently in familial epithelial ovarian car...
Four main histological subtypes of ovarian cancer exist: serous (the most frequent), endometrioid, m...
Complete loss of BRCA1 or BRCA2 function is associated with sensitivity to DNA damaging agents. Howe...
Germline BRCA1 and BRCA2 mutations highly increase the risk of breast and female adnexal cancer. The...
Ovarian carcinoma (OC) is the commonest gynaecological cause of death in the Western world. As a ste...
Ovarian cancer is a heterogeneous disease that encompasses a number of different cellular subtypes, ...
OBJECTIVES: Mutations in the BRCA1 and BRCA2 genes predispose women to ovarian and/or breast cancer....
We analyzed 37 primary invasive carcinomas for BRCA1 and BRCA2 mutations by screening the entire cod...
The phenotypic variability of epithelial ovarian neoplasms correlates with a diversity of changes at...
Background Subclassification of ovarian carcinomas can be used to guide treatment and determine pro...
Loss of BRCA1/BRCA2 function through genetic or epigenetic mechanisms is common in epithelial ovari...
Hereditary ovarian cancers associated with germline mutations in either BRCA1 or BRCA2 were studied ...
PURPOSE: Germline mutations in the BRCA1 and BRCA2 genes confer increased susceptibility to ovarian ...
Ovarian cancer is the most lethal cause of death from gynecological malignancies in the Western worl...
AIM: Mutations in the BRCA1 and TP53 genes are early genetic events leading to (hereditary) ovarian ...
Mutations within the BRCA1 tumor suppressor gene occur frequently in familial epithelial ovarian car...
Four main histological subtypes of ovarian cancer exist: serous (the most frequent), endometrioid, m...
Complete loss of BRCA1 or BRCA2 function is associated with sensitivity to DNA damaging agents. Howe...
Germline BRCA1 and BRCA2 mutations highly increase the risk of breast and female adnexal cancer. The...
Ovarian carcinoma (OC) is the commonest gynaecological cause of death in the Western world. As a ste...
Ovarian cancer is a heterogeneous disease that encompasses a number of different cellular subtypes, ...
OBJECTIVES: Mutations in the BRCA1 and BRCA2 genes predispose women to ovarian and/or breast cancer....
We analyzed 37 primary invasive carcinomas for BRCA1 and BRCA2 mutations by screening the entire cod...
The phenotypic variability of epithelial ovarian neoplasms correlates with a diversity of changes at...