...BRCA1 gene, a tumor suppressor gene that is mutated in the majority of patients with triple negative BC. Some clinical r...
...BRCA1 genes. Our findings indicate that an awareness of the possible concomitance of NF1 and BRCA1 gene mutations is imp...
Adding MRI to annual mammography screening improves early breast cancer detection in women with familial risk or BRCA1/2...
...BRCA1-BRCA2 pathway. These DSB resulted in an increase in chromatid-type aberrations, which are characteristic for BRCA1...
...BRCA1 founder and recurrent mutations. The CHEK2 c.1100delC mutation was detected in 0.16% (4 of 2,408) of females, all ...
...BRCA1 or BRCA2 mutation carriers. Forty-one single nucleotide polymorphisms (SNPs) were genotyped in 15,252 BRCA1 and 8,...
...BRCA1 and BRCA2 presented. Recommendations to surgical treatment of hereditary breast cancer are considered as a very di...
...BRCA1 and PALB2) was assessed in the same batches of cells isolated for previous studies, using the methylation-sensitiv...
...BRCA1 cells, suggesting that BRCA1 plays a crucial role in repairing and recovering drug-induced DNA damage by recruitin...
...BRCA1 and BRCA2 mutations have significantly elevated risk of developing breast and ovarian cancers. BRCA1-associated br...
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