Mutations in the BRCA1 gene confer a high risk for the development of breast or ovarian cancer. The aim of this study wa...
...BRCA1/2 mutation, and sociodemographic characteristics. Use of BRCA1/2 counseling between 1996 and 1997 was positively a...
...Brca1 full-length isoform causes senescence in mutant embryos and cultured cells as well as aging and tumorigenesis in a...
...BRCA1-2 in breast and ovary; other cancers in Bloom syndrome, neurofibromatosis and xeroderma pigmentosum). The mutation...
...BRCA1 and 3 in BRCA2, including mutations recurring in Central Italy (BRCA1 3345delAG and BRCA2 6696delTC). The a priori...
...BRCA1 and BRCA2 mutation carriers, individuals with familial non-BRCA1/2 epithelial ovarian cancer, and women with nonfa...
...BRCA1 or SMN2 pre-mRNA transcripts. This general approach can be used as a tool to investigate splicing mechanisms and m...
...BRCA1 and BRCA2 (breast and ovarian cancer), PKD1 (polycystic kidney disease), NF1 and NF2 (neurofibromatosis), and DMD ...
...BRCA1 and BRCA2, thereby providing a link with other disorders in which defective DNA damage repair is a feature. This r...
...BRCA1 and BRCA2 genes, there has been an increasing demand for breast cancer risk assessment programs. In an effort to u...
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