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2. Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles. Seal S; Thompson D; Renwick A; Elliott A; Kelly P; Barfoot R; Chagtai T; Jayatilake H; Ahmed M; Spanova K; North B; McGuffog L; Evans DG; Eccles D; ; Easton DF; Stratton MR; Rahman N Nat Genet; 2006 Nov; 38(11):1239-41. PubMed ID: 17033622 [TBL] [Abstract][Full Text] [Related]
3. The BRIP1 helicase functions independently of BRCA1 in the Fanconi anemia pathway for DNA crosslink repair. Bridge WL; Vandenberg CJ; Franklin RJ; Hiom K Nat Genet; 2005 Sep; 37(9):953-7. PubMed ID: 16116421 [TBL] [Abstract][Full Text] [Related]
4. The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia. Levran O; Attwooll C; Henry RT; Milton KL; Neveling K; Rio P; Batish SD; Kalb R; Velleuer E; Barral S; Ott J; Petrini J; Schindler D; Hanenberg H; Auerbach AD Nat Genet; 2005 Sep; 37(9):931-3. PubMed ID: 16116424 [TBL] [Abstract][Full Text] [Related]
5. Analysis of BRIP1 Variants among Korean Patients with BRCA1/2 Mutation-Negative High-Risk Breast Cancer. Kim H; Cho DY; Choi DH; Jung GH; Shin I; Park W; Huh SJ; Nam SJ; Lee JE; Gil WH; Kim SW Cancer Res Treat; 2016 Jul; 48(3):955-61. PubMed ID: 26790966 [TBL] [Abstract][Full Text] [Related]
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8. A minimal threshold of FANCJ helicase activity is required for its response to replication stress or double-strand break repair. Bharti SK; Sommers JA; Awate S; Bellani MA; Khan I; Bradley L; King GA; Seol Y; Vidhyasagar V; Wu Y; Abe T; Kobayashi K; Shin-Ya K; Kitao H; Wold MS; Branzei D; Neuman KC; Brosh RM Nucleic Acids Res; 2018 Jul; 46(12):6238-6256. PubMed ID: 29788478 [TBL] [Abstract][Full Text] [Related]
9. Unraveling the molecular effect of a rare missense mutation in BRIP1 associated with inherited breast cancer. Velázquez C; Esteban-Cardeñosa EM; Lastra E; Abella LE; de la Cruz V; Lobatón CD; Durán M; Infante M Mol Carcinog; 2019 Jan; 58(1):156-160. PubMed ID: 30230034 [TBL] [Abstract][Full Text] [Related]
10. Mutation status of RAD51C, PALB2 and BRIP1 in 100 Japanese familial breast cancer cases without BRCA1 and BRCA2 mutations. Sato K; Koyasu M; Nomura S; Sato Y; Kita M; Ashihara Y; Adachi Y; Ohno S; Iwase T; Kitagawa D; Nakashima E; Yoshida R; Miki Y; Arai M Cancer Sci; 2017 Nov; 108(11):2287-2294. PubMed ID: 28796317 [TBL] [Abstract][Full Text] [Related]
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13. No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing. Easton DF; Lesueur F; Decker B; Michailidou K; Li J; Allen J; Luccarini C; Pooley KA; Shah M; Bolla MK; Wang Q; Dennis J; Ahmad J; Thompson ER; Damiola F; Pertesi M; Voegele C; Mebirouk N; Robinot N; Durand G; Forey N; Luben RN; Ahmed S; Aittomäki K; Anton-Culver H; Arndt V; ; Baynes C; Beckman MW; Benitez J; Van Den Berg D; Blot WJ; Bogdanova NV; Bojesen SE; Brenner H; Chang-Claude J; Chia KS; Choi JY; Conroy DM; Cox A; Cross SS; Czene K; Darabi H; Devilee P; Eriksson M; Fasching PA; Figueroa J; Flyger H; Fostira F; García-Closas M; Giles GG; Glendon G; González-Neira A; Guénel P; Haiman CA; Hall P; Hart SN; Hartman M; Hooning MJ; Hsiung CN; Ito H; Jakubowska A; James PA; John EM; Johnson N; Jones M; Kabisch M; Kang D; ; Kosma VM; Kristensen V; Lambrechts D; Li N; ; Lindblom A; Long J; Lophatananon A; Lubinski J; Mannermaa A; Manoukian S; Margolin S; Matsuo K; Meindl A; Mitchell G; Muir K; ; Nevelsteen I; van den Ouweland A; Peterlongo P; Phuah SY; Pylkäs K; Rowley SM; Sangrajrang S; Schmutzler RK; Shen CY; Shu XO; Southey MC; Surowy H; Swerdlow A; Teo SH; Tollenaar RA; Tomlinson I; Torres D; Truong T; Vachon C; Verhoef S; Wong-Brown M; Zheng W; Zheng Y; Nevanlinna H; Scott RJ; Andrulis IL; Wu AH; Hopper JL; Couch FJ; Winqvist R; Burwinkel B; Sawyer EJ; Schmidt MK; Rudolph A; Dörk T; Brauch H; Hamann U; Neuhausen SL; Milne RL; Fletcher O; Pharoah PD; Campbell IG; Dunning AM; Le Calvez-Kelm F; Goldgar DE; Tavtigian SV; Chenevix-Trench G J Med Genet; 2016 May; 53(5):298-309. PubMed ID: 26921362 [TBL] [Abstract][Full Text] [Related]
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15. Loss of heterozygosity in FANCG, FANCF and BRIP1 from head and neck squamous cell carcinoma of the oral cavity. Türke C; Horn S; Petto C; Labudde D; Lauer G; Wittenburg G Int J Oncol; 2017 Jun; 50(6):2207-2220. PubMed ID: 28440438 [TBL] [Abstract][Full Text] [Related]
16. Evaluation of Fanconi Anemia genes in familial breast cancer predisposition. Seal S; Barfoot R; Jayatilake H; Smith P; Renwick A; Bascombe L; McGuffog L; Evans DG; Eccles D; Easton DF; Stratton MR; Rahman N; Cancer Res; 2003 Dec; 63(24):8596-9. PubMed ID: 14695169 [TBL] [Abstract][Full Text] [Related]
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20. Landscape of BRIP1 molecular lesions in gastrointestinal cancers from published genomic studies. Voutsadakis IA World J Gastroenterol; 2020 Mar; 26(11):1197-1207. PubMed ID: 32231423 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]