Impact of germline and somatic BRCA1/2 mutations: tumor spectrum and detection platforms
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,Molecular Medicine
Link
https://www.nature.com/articles/gt201773.pdf
Reference97 articles.
1. Biron-Shental T, Drucker L, Altaras M, Bernheim J, Fishman A . High incidence of BRCA1-2 germline mutations, previous breast cancer and familial cancer history in Jewish patients with uterine serous papillary carcinoma. Eur J Surg Oncol 2006; 32: 1097–1100.
2. Levine DA, Argenta PA, Yee CJ, Marshall DS, Olvera N, Bogomolniy F et al. Fallopian tube and primary peritoneal carcinomas associated with BRCA mutations. J Clin Oncol 2003; 21: 4222–4227.
3. Hennessy BT, Timms KM, Carey MS, Gutin A, Meyer LA, Flake DD et al. Somatic mutations in BRCA1 and BRCA2 could expand the number of patients that benefit from poly (ADP ribose) polymerase inhibitors in ovarian cancer. J Clin Oncol 2010; 28: 3570–3576.
4. Rebbeck TR, Mitra N, Wan F . Association of type and location of brca1 and brca2 mutations with risk of breast and ovarian cancer. JAMA 2015; 313: 1347–1361.
5. Yoshida K, Miki Y . Role of BRCA1 and BRCA2 as regulators of DNA repair, transcription, and cell cycle in response to DNA damage. Cancer Sci 2004; 95: 866–871.
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2. Identification of the most common BRCA alterations through analysis of germline mutation databases: Is droplet digital PCR an additional strategy for the assessment of such alterations in breast and ovarian cancer families?;International Journal of Oncology;2022-04-06
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4. Feasibility of targeted cascade genetic testing in the family members of BRCA1/2 gene pathogenic variant/likely pathogenic variant carriers;Scientific Reports;2022-02-03
5. Universal probe-based intermediate primer-triggered qPCR (UPIP-qPCR) for SNP genotyping;BMC Genomics;2021-11-24
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