...BRCA1 and BRCA2 mutations.,From our population-based case-control study comparing women with CBC to women with unilatera...
Uncertainty exists about the origin of BRCA1 c.4035delA mutation which is prevalent in Baltic countries, with the highes...
...BRCA1 and BRCA2. Underlying genetic heterogeneity in these cases is the probable explanation for the failure of all atte...
...BRCA1/2 mutations, and recommended at-risk individuals be referred for genetic counseling and evaluation for BRCA testin...
...BRCA1 and BRCA2 explain less than 25 % of familial aggregation of breast cancer, which suggests the involvement of addit...
...BRCA1) in cardiac tissue and fibroblast, which subsequently activate the transcription factor Nuclear factor (erythroid-...
...BRCA1/BRCA2 mutations. We have found that the allelic variation of rs926103, which alters amino acid 52 of the encoded p...
...BRCA1 and tumour suppressor p53, and interfering with the erk pathway, the cyclin-dependent cell cycle regulation proces...
...BRCA1, BRCA2, TP53, ATM, BRIP1, CHEK2 and PALB2, about 70% of breast cancer heritability remains unexplained. Because of...
...BRCA1 relocalisation. While RPA32 phosphorylation (p-RPA32) and RPA foci formation were reduced in parallel with increas...
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