Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Hypersensitivity and BRCA2[original query] |
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Evidence of haplotype insufficiency in human cells containing a germline mutation in BRCA1 or BRCA2. International journal of cancer 2002 1 97 (5): 557-61. Buchholz Thomas A, Wu Xifeng, Hussain Abu, Tucker Susan L, Mills Gordon B, Haffty Bruce, Bergh Sherry, Story Michael, Geara Fady B, Brock William |
Mutational analysis of FANCL, FANCM and the recently identified FANCI suggests that among the 13 known Fanconi Anemia genes, only FANCD1/BRCA2 plays a major role in high-risk breast cancer predisposition. Carcinogenesis 2009 Nov 30 (11): 1898-902. García María J, Fernández Victoria, Osorio Ana, Barroso Alicia, Fernández Fernando, Urioste Miguel, Benítez Javi |
Molecular contribution of BRCA1 and BRCA2 to genome instability in breast cancer patients: review of radiosensitivity assays. Biological procedures online 2020 10 22 23. Sadeghi Fatemeh, Asgari Marzieh, Matloubi Mojdeh, Ranjbar Maral, Karkhaneh Yousefi Nahid, Azari Tahereh, Zaki-Dizaji Maj |
Incidence of Hypersensitivity Reactions to Carboplatin or Paclitaxel in Patients With Ovarian, Fallopian Tube, or Primary Peritoneal Cancer With or Without BRCA1 or BRCA2 Mutations. Journal of the advanced practitioner in oncology 2021 1 10 (5): 428-439. Garcia Andrew, Frahm Corey, Jeter Joanne M, Abraham Ivo, Chambers Setsuko K, Cragun Janiel M, McBride A |
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