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Previous transcriptome-wide association studies (TWAS) have identified breast cancer risk genes

Breast cancer is a common disease partially caused by genetic risk factors. Germline pathogenic

proposed that Lynch Syndrome-related germline mutations (LS-mutations) are associated with breast cancer

to cancer therapy in patients with five aggressive types of cancer: breast, colorectal, lung, ovarian

Genome-wide association studies have identified breast cancer risk variants in over 150 genomic

Genome-wide association studies (GWAS) have identified more than 170 breast cancer susceptibility

Breast cancer (BC) risk for BRCA1 and BRCA2 mutation carriers varies by genetic and familial

, such as hormone-insensitive breast cancer and prostate cancer, cholangiocarcinoma, and multiple myeloma

Breast cancer susceptibility variants frequently show heterogeneity in associations by tumor

Despite many advances in diagnosis and therapy (surgery, radiation therapy, chemotherapy), cancer

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