...BRCA1/2 explain part of the hereditary risk, the contribution of rare coding variants in Arab EOBC remains unclear. Whol...
...BRCA1, and MSH6. Half (n = 11, 50.0%) of patients with P/LP variants or APC increased risk allele communicated results w...
...BRCA1/somatic TP53 (n=40 and n=38 studies, respectively). Statistical testing was performed in 41.6% (n=82) of studies t...
...BRCA1 and BRCA2). Two newly explored luminophores, the Eu-luminol complex and Ru/Zn MOF with blue and orange-red high-in...
...BRCA1, BRCA2, and HSD3B1 are the most prevalent alterations in men with advanced prostate cancer and are associated with...
...BRCA1 mutations and TERC amplification whereas LOH-low with low-grade endometrioid, MSI, ARID1A, PIK3CA, CTNNB1, and PTE...
...BRCA1 and BRCA2 are essential for homologous recombination (HR) repair. Mutations in BRCA1/2 compromise HR repair effica...
...BRCA1, and BRCA2. Germline testing performed in 15 cases identified Lynch syndrome in 5 (33%). MMR immunohistochemistry ...
...BRCA1/BRCA2 were identified in 19 cases (11.51%), including 8 in BRCA1 and 11 in BRCA2. The presence of BRCA P/LPVs asso...
...BRCA1/2. Here we highlight the clinical value of extending testing to beyond BRCA susceptibility genes for improved prev...
山东省济南市章丘区文博路2号
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