233 related articles for article (PubMed ID: 31347298)
21. Current knowledge on the pathophysiology of Fanconi anemia: from genes to phenotypes.
Yamashita T; Nakahata T
Int J Hematol; 2001 Jul; 74(1):33-41. PubMed ID: 11530803
[TBL] [Abstract][Full Text] [Related]
22. The emergence of Fanconi anaemia type S: a phenotypic spectrum of biallelic
Hughes T; Rose AM
Front Oncol; 2023; 13():1278004. PubMed ID: 38146508
[TBL] [Abstract][Full Text] [Related]
23. First description of a sporadic breast cancer in a woman with BRCA1 germline mutation.
Curtit E; Benhamo V; Gruel N; Popova T; Manie E; Cottu P; Mariani O; Stoppa-Lyonnet D; Pivot X; Stern MH; Vincent-Salomon A
Oncotarget; 2015 Nov; 6(34):35616-24. PubMed ID: 26426992
[TBL] [Abstract][Full Text] [Related]
24. Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer.
Reid S; Schindler D; Hanenberg H; Barker K; Hanks S; Kalb R; Neveling K; Kelly P; Seal S; Freund M; Wurm M; Batish SD; Lach FP; Yetgin S; Neitzel H; Ariffin H; Tischkowitz M; Mathew CG; Auerbach AD; Rahman N
Nat Genet; 2007 Feb; 39(2):162-4. PubMed ID: 17200671
[TBL] [Abstract][Full Text] [Related]
25. Chromosome Instability in Fanconi Anemia: From Breaks to Phenotypic Consequences.
García-de-Teresa B; Rodríguez A; Frias S
Genes (Basel); 2020 Dec; 11(12):. PubMed ID: 33371494
[TBL] [Abstract][Full Text] [Related]
26. Lack of impact of the ALDH2 rs671 variant on breast cancer development in Japanese BRCA1/2-mutation carriers.
Mori T; Okamoto Y; Mu A; Ide Y; Yoshimura A; Senda N; Inagaki-Kawata Y; Kawashima M; Kitao H; Tokunaga E; Miyoshi Y; Ohsumi S; Tsugawa K; Ohta T; Katagiri T; Ohtsuru S; Koike K; Ogawa S; Toi M; Iwata H; Nakamura S; Matsuo K; Takata M
Cancer Med; 2023 Mar; 12(6):6594-6602. PubMed ID: 36345163
[TBL] [Abstract][Full Text] [Related]
27. Genetic Predisposition to Breast Cancer Due to Mutations Other Than BRCA1 and BRCA2 Founder Alleles Among Ashkenazi Jewish Women.
Walsh T; Mandell JB; Norquist BM; Casadei S; Gulsuner S; Lee MK; King MC
JAMA Oncol; 2017 Dec; 3(12):1647-1653. PubMed ID: 28727877
[TBL] [Abstract][Full Text] [Related]
28. Male with an apparently normal phenotype carrying a BRCA1 exon 20 duplication in trans to a BRCA1 frameshift variant.
Block I; Mateu-Regué À; Do TTN; Miceikaite I; Sdogati D; Larsen MJ; Hao Q; Nielsen HR; Boonen SE; Skytte AB; Jensen UB; Høffding LK; De Nicolo A; Viel A; Tudini E; Parsons MT; Hansen TVO; Rossing M; Kruse TA; Spurdle AB; Thomassen M
Breast Cancer Res; 2024 Jan; 26(1):6. PubMed ID: 38195559
[TBL] [Abstract][Full Text] [Related]
29. Biallelic inactivation of BRCA2 in Fanconi anemia.
Howlett NG; Taniguchi T; Olson S; Cox B; Waisfisz Q; De Die-Smulders C; Persky N; Grompe M; Joenje H; Pals G; Ikeda H; Fox EA; D'Andrea AD
Science; 2002 Jul; 297(5581):606-9. PubMed ID: 12065746
[TBL] [Abstract][Full Text] [Related]
30. Phenotypic variability in patients with Fanconi anemia and biallelic FANCF mutations.
Tryon R; Zierhut H; MacMillan ML; Wagner JE
Am J Med Genet A; 2017 Jan; 173(1):260-263. PubMed ID: 27714961
[TBL] [Abstract][Full Text] [Related]
31. Novel germline BRCA1 mutations detected in women in singapore who developed breast carcinoma before the age of 36 years.
Ho GH; Phang BH; Ng IS; Law HY; Soo KC; Ng EH
Cancer; 2000 Aug; 89(4):811-6. PubMed ID: 10951344
[TBL] [Abstract][Full Text] [Related]
32. Attenuation of the formation of DNA-repair foci containing RAD51 in Fanconi anaemia.
Digweed M; Rothe S; Demuth I; Scholz R; Schindler D; Stumm M; Grompe M; Jordan A; Sperling K
Carcinogenesis; 2002 Jul; 23(7):1121-6. PubMed ID: 12117768
[TBL] [Abstract][Full Text] [Related]
33. Recent discoveries in the molecular pathogenesis of the inherited bone marrow failure syndrome Fanconi anemia.
Mamrak NE; Shimamura A; Howlett NG
Blood Rev; 2017 May; 31(3):93-99. PubMed ID: 27760710
[TBL] [Abstract][Full Text] [Related]
34. Spectrum and clinical relevance of PALB2 germline mutations in 7657 Chinese BRCA1/2-negative breast cancer patients.
Wu Y; Ouyang T; Li J; Wang T; Fan Z; Fan T; Lin B; Xu Y; Xie Y
Breast Cancer Res Treat; 2020 Feb; 179(3):605-614. PubMed ID: 31768816
[TBL] [Abstract][Full Text] [Related]
35. Chromosome fragility in patients with Fanconi anaemia: diagnostic implications and clinical impact.
Castella M; Pujol R; Callén E; Ramírez MJ; Casado JA; Talavera M; Ferro T; Muñoz A; Sevilla J; Madero L; Cela E; Beléndez C; de Heredia CD; Olivé T; de Toledo JS; Badell I; Estella J; Dasí Á; Rodríguez-Villa A; Gómez P; Tapia M; Molinés A; Figuera Á; Bueren JA; Surrallés J
J Med Genet; 2011 Apr; 48(4):242-50. PubMed ID: 21217111
[TBL] [Abstract][Full Text] [Related]
36. Mutation analysis of BRIP1/BACH1 in BRCA1/BRCA2 negative Chinese women with early onset breast cancer or affected relatives.
Cao AY; Huang J; Hu Z; Li WF; Ma ZL; Tang LL; Zhang B; Su FX; Zhou J; Di GH; Shen KW; Wu J; Lu JS; Luo JM; Yuan WT; Shen ZZ; Huang W; Shao ZM
Breast Cancer Res Treat; 2009 May; 115(1):51-5. PubMed ID: 18483852
[TBL] [Abstract][Full Text] [Related]
37. BRCA1 Mutational Complementation Induces Synthetic Viability.
Nacson J; Di Marcantonio D; Wang Y; Bernhardy AJ; Clausen E; Hua X; Cai KQ; Martinez E; Feng W; Callén E; Wu W; Gupta GP; Testa JR; Nussenzweig A; Sykes SM; Johnson N
Mol Cell; 2020 Jun; 78(5):951-959.e6. PubMed ID: 32359443
[TBL] [Abstract][Full Text] [Related]
38. Mutation of the RAD51C gene in a Fanconi anemia-like disorder.
Vaz F; Hanenberg H; Schuster B; Barker K; Wiek C; Erven V; Neveling K; Endt D; Kesterton I; Autore F; Fraternali F; Freund M; Hartmann L; Grimwade D; Roberts RG; Schaal H; Mohammed S; Rahman N; Schindler D; Mathew CG
Nat Genet; 2010 May; 42(5):406-9. PubMed ID: 20400963
[TBL] [Abstract][Full Text] [Related]
39. Fanconi anaemia and cancer: an intricate relationship.
Nalepa G; Clapp DW
Nat Rev Cancer; 2018 Mar; 18(3):168-185. PubMed ID: 29376519
[TBL] [Abstract][Full Text] [Related]
40. Germline RAD51C mutations in ovarian cancer susceptibility.
Coulet F; Fajac A; Colas C; Eyries M; Dion-Minière A; Rouzier R; Uzan S; Lefranc JP; Carbonnel M; Cornelis F; Cortez A; Soubrier F
Clin Genet; 2013 Apr; 83(4):332-6. PubMed ID: 22725699
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
