...BRCA2 gene mutation long after the initial diagnosis. These women's experiences across time reflect the concepts of the ...
...BRCA2 mutation carriers were identified. Complete clinical response was documented in 12/35 (34%) mutation carriers and ...
...BRCA2-like or non-BRCA-like profiles using previous classifiers derived from FBC, and correlated these profiles with pat...
...BRCA2 mutation. After genetic test results, the available options for treatment/surveillance were discussed by a multidi...
...BRCA2), chromatin remodeling (ARID1A), cell adhesion (CDH1, FAT4, CTNNA1), cytoskeleton and cell motility (RHOA), Wnt pa...
...BRCA2 mutations and the genetic cause of breast cancer remains unexplained. Routine testing for the CHEK2*1100delC mutat...
...BRCA2, key factors for non-homologous end joining and homologous recombination respectively. Importantly, the apparent D...
The objective of this study was to design and validate a next-generation sequencing assay (NGS) to detect BRCA1 and BRCA...
...BRCA2 gene mutations from a clinical pipeline gave 100 % concordance with Sanger data; only 8/25 BRCA2 mutations were co...
山东省济南市章丘区文博路2号
齐鲁师范学院 genelibs生信实验室
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