These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
228 related articles for article (PubMed ID: 26691948)
61. Positional cloning of a novel Fanconi anemia gene, FANCD2. Timmers C; Taniguchi T; Hejna J; Reifsteck C; Lucas L; Bruun D; Thayer M; Cox B; Olson S; D'Andrea AD; Moses R; Grompe M Mol Cell; 2001 Feb; 7(2):241-8. PubMed ID: 11239453 [TBL] [Abstract][Full Text] [Related]
62. Mutations in Fanconi anemia genes and the risk of esophageal cancer. Akbari MR; Malekzadeh R; Lepage P; Roquis D; Sadjadi AR; Aghcheli K; Yazdanbod A; Shakeri R; Bashiri J; Sotoudeh M; Pourshams A; Ghadirian P; Narod SA Hum Genet; 2011 May; 129(5):573-82. PubMed ID: 21279724 [TBL] [Abstract][Full Text] [Related]
63. Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients. Mori M; Hira A; Yoshida K; Muramatsu H; Okuno Y; Shiraishi Y; Anmae M; Yasuda J; Tadaka S; Kinoshita K; Osumi T; Noguchi Y; Adachi S; Kobayashi R; Kawabata H; Imai K; Morio T; Tamura K; Takaori-Kondo A; Yamamoto M; Miyano S; Kojima S; Ito E; Ogawa S; Matsuo K; Yabe H; Yabe M; Takata M Haematologica; 2019 Oct; 104(10):1962-1973. PubMed ID: 30792206 [TBL] [Abstract][Full Text] [Related]
64. Novel mutations of the FANCG gene causing alternative splicing in Japanese Fanconi anemia. Yamada T; Tachibana A; Shimizu T; Mugishima H; Okubo M; Sasaki MS J Hum Genet; 2000; 45(3):159-66. PubMed ID: 10807541 [TBL] [Abstract][Full Text] [Related]
65. Fanconi anemia is associated with a defect in the BRCA2 partner PALB2. Xia B; Dorsman JC; Ameziane N; de Vries Y; Rooimans MA; Sheng Q; Pals G; Errami A; Gluckman E; Llera J; Wang W; Livingston DM; Joenje H; de Winter JP Nat Genet; 2007 Feb; 39(2):159-61. PubMed ID: 17200672 [TBL] [Abstract][Full Text] [Related]
66. A homozygous nonsense mutation early in exon 5 of BRCA2 is associated with very severe Fanconi anemia. Radulovic I; Kuechler A; Schündeln MM; Paulussen M; von Neuhoff N; Reinhardt D; Hanenberg H Eur J Med Genet; 2021 Aug; 64(8):104260. PubMed ID: 34118472 [TBL] [Abstract][Full Text] [Related]
67. [Molecular study of Fanconi anemia in Tunisia]. Bouchlaka C; Abdelhak S; Dellagi K; Tunis Med; 2004 May; 82(5):402-10. PubMed ID: 15453041 [TBL] [Abstract][Full Text] [Related]
68. A novel cancer risk prediction score for the natural course of FA patients with biallelic BRCA2/FANCD1 mutations. Radulovic I; Schündeln MM; Müller L; Ptok J; Honisch E; Niederacher D; Wiek C; Scheckenbach K; Leblanc T; Larcher L; Soulier J; Reinhardt D; Schaal H; Andreassen PR; Hanenberg H Hum Mol Genet; 2023 May; 32(11):1836-1849. PubMed ID: 36721989 [TBL] [Abstract][Full Text] [Related]
69. Molecular pathogenesis of fanconi anemia. Taniguchi T; Dandrea AD Int J Hematol; 2002 Feb; 75(2):123-8. PubMed ID: 11939257 [TBL] [Abstract][Full Text] [Related]
70. Direct interactions of the five known Fanconi anaemia proteins suggest a common functional pathway. Medhurst AL; Huber PA; Waisfisz Q; de Winter JP; Mathew CG Hum Mol Genet; 2001 Feb; 10(4):423-9. PubMed ID: 11157805 [TBL] [Abstract][Full Text] [Related]
71. Evidence for complete epistasis of null mutations in murine Fanconi anemia genes Fanca and Fancg. van de Vrugt HJ; Koomen M; Bakker S; Berns MA; Cheng NC; van der Valk MA; de Vries Y; Rooimans MA; Oostra AB; Hoatlin ME; Te Riele H; Joenje H; Arwert F DNA Repair (Amst); 2011 Dec; 10(12):1252-61. PubMed ID: 22036606 [TBL] [Abstract][Full Text] [Related]
72. Heterozygosity for p53 (Trp53+/-) accelerates epithelial tumor formation in fanconi anemia complementation group D2 (Fancd2) knockout mice. Houghtaling S; Granville L; Akkari Y; Torimaru Y; Olson S; Finegold M; Grompe M Cancer Res; 2005 Jan; 65(1):85-91. PubMed ID: 15665282 [TBL] [Abstract][Full Text] [Related]
73. Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology. De Rocco D; Bottega R; Cappelli E; Cavani S; Criscuolo M; Nicchia E; Corsolini F; Greco C; Borriello A; Svahn J; Pillon M; Mecucci C; Casazza G; Verzegnassi F; Cugno C; Locasciulli A; Farruggia P; Longoni D; Ramenghi U; Barberi W; Tucci F; Perrotta S; Grammatico P; Hanenberg H; Della Ragione F; Dufour C; Savoia A; Haematologica; 2014 Jun; 99(6):1022-31. PubMed ID: 24584348 [TBL] [Abstract][Full Text] [Related]
78. Germ line Fanconi anemia complementation group C mutations and pancreatic cancer. Couch FJ; Johnson MR; Rabe K; Boardman L; McWilliams R; de Andrade M; Petersen G Cancer Res; 2005 Jan; 65(2):383-6. PubMed ID: 15695377 [TBL] [Abstract][Full Text] [Related]
79. Novel mutations and polymorphisms in the Fanconi anemia group C gene. Gibson RA; Morgan NV; Goldstein LH; Pearson IC; Kesterton IP; Foot NJ; Jansen S; Havenga C; Pearson T; de Ravel TJ; Cohn RJ; Marques IM; Dokal I; Roberts I; Marsh J; Ball S; Milner RD; Llerena JC; Samochatova E; Mohan SP; Vasudevan P; Birjandi F; Hajianpour A; Murer-Orlando M; Mathew CG Hum Mutat; 1996; 8(2):140-8. PubMed ID: 8844212 [TBL] [Abstract][Full Text] [Related]
80. Pediatric acute promyelocytic leukemia and Fanconi anemia: Case report and literature review. Freycon C; Sepulchre E; Lavallée VP; Mitchell D; MacMillan ML; Vezina C; Goudie C Clin Genet; 2024 Aug; 106(2):193-198. PubMed ID: 38658784 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]