181 related articles for article (PubMed ID: 29193904)
21. Fanconi anemia: causes and consequences of genetic instability.
Kalb R; Neveling K; Nanda I; Schindler D; Hoehn H
Genome Dyn; 2006; 1():218-242. PubMed ID: 18724063
[TBL] [Abstract][Full Text] [Related]
22. Assessing the spectrum of germline variation in Fanconi anemia genes among patients with head and neck carcinoma before age 50.
Chandrasekharappa SC; Chinn SB; Donovan FX; Chowdhury NI; Kamat A; Adeyemo AA; Thomas JW; Vemulapalli M; Hussey CS; Reid HH; Mullikin JC; Wei Q; Sturgis EM
Cancer; 2017 Oct; 123(20):3943-3954. PubMed ID: 28678401
[TBL] [Abstract][Full Text] [Related]
23. Detection of somatic mosaicism and classification of Fanconi anemia patients by analysis of the FA/BRCA pathway.
Soulier J; Leblanc T; Larghero J; Dastot H; Shimamura A; Guardiola P; Esperou H; Ferry C; Jubert C; Feugeas JP; Henri A; Toubert A; Socié G; Baruchel A; Sigaux F; D'Andrea AD; Gluckman E
Blood; 2005 Feb; 105(3):1329-36. PubMed ID: 15383454
[TBL] [Abstract][Full Text] [Related]
24. Intermediate DNA repair activity associated with the 322delG allele of the fanconi anemia complementation group C gene.
Donahue SL; Lundberg R; Campbell C
J Mol Biol; 2004 Oct; 342(5):1443-55. PubMed ID: 15364573
[TBL] [Abstract][Full Text] [Related]
25. Somatic mosaicism in Fanconi anemia: molecular basis and clinical significance.
Lo Ten Foe JR; Kwee ML; Rooimans MA; Oostra AB; Veerman AJ; van Weel M; Pauli RM; Shahidi NT; Dokal I; Roberts I; Altay C; Gluckman E; Gibson RA; Mathew CG; Arwert F; Joenje H
Eur J Hum Genet; 1997; 5(3):137-48. PubMed ID: 9272737
[TBL] [Abstract][Full Text] [Related]
26. Thinking of VACTERL-H? Rule out Fanconi Anemia according to PHENOS.
Alter BP; Giri N
Am J Med Genet A; 2016 Jun; 170(6):1520-4. PubMed ID: 27028275
[TBL] [Abstract][Full Text] [Related]
27. Multiplexed CRISPR/Cas9-mediated knockout of 19 Fanconi anemia pathway genes in zebrafish revealed their roles in growth, sexual development and fertility.
Ramanagoudr-Bhojappa R; Carrington B; Ramaswami M; Bishop K; Robbins GM; Jones M; Harper U; Frederickson SC; Kimble DC; Sood R; Chandrasekharappa SC
PLoS Genet; 2018 Dec; 14(12):e1007821. PubMed ID: 30540754
[TBL] [Abstract][Full Text] [Related]
28. FANCI is a second monoubiquitinated member of the Fanconi anemia pathway.
Sims AE; Spiteri E; Sims RJ; Arita AG; Lach FP; Landers T; Wurm M; Freund M; Neveling K; Hanenberg H; Auerbach AD; Huang TT
Nat Struct Mol Biol; 2007 Jun; 14(6):564-7. PubMed ID: 17460694
[TBL] [Abstract][Full Text] [Related]
29. The Fanconi anemia pathway of genomic maintenance.
Levitus M; Joenje H; de Winter JP
Cell Oncol; 2006; 28(1-2):3-29. PubMed ID: 16675878
[TBL] [Abstract][Full Text] [Related]
30. A defined role for multiple Fanconi anemia gene products in DNA-damage-associated ubiquitination.
Tan W; Deans AJ
Exp Hematol; 2017 Jun; 50():27-32. PubMed ID: 28315701
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations.
Bouchlaka C; Abdelhak S; Amouri A; Ben Abid H; Hadiji S; Frikha M; Ben Othman T; Amri F; Ayadi H; Hachicha M; Rebaï A; Saad A; Dellagi K;
J Hum Genet; 2003; 48(7):352-61. PubMed ID: 12827451
[TBL] [Abstract][Full Text] [Related]
33. Fanconi anemia and DNA repair.
Grompe M; D'Andrea A
Hum Mol Genet; 2001 Oct; 10(20):2253-9. PubMed ID: 11673408
[TBL] [Abstract][Full Text] [Related]
34. Deficiency of the Fanconi anemia E2 ubiqitin conjugase UBE2T only partially abrogates Alu-mediated recombination in a new model of homology dependent recombination.
Lewis TW; Barthelemy JR; Virts EL; Kennedy FM; Gadgil RY; Wiek C; Linka RM; Zhang F; Andreassen PR; Hanenberg H; Leffak M
Nucleic Acids Res; 2019 Apr; 47(7):3503-3520. PubMed ID: 30715513
[TBL] [Abstract][Full Text] [Related]
35. Functional analysis of Fanconi anemia mutations in China.
Li N; Ding L; Li B; Wang J; D'Andrea AD; Chen J
Exp Hematol; 2018 Oct; 66():32-41.e8. PubMed ID: 30031030
[TBL] [Abstract][Full Text] [Related]
36. The genetic and biochemical basis of FANCD2 monoubiquitination.
Rajendra E; Oestergaard VH; Langevin F; Wang M; Dornan GL; Patel KJ; Passmore LA
Mol Cell; 2014 Jun; 54(5):858-69. PubMed ID: 24905007
[TBL] [Abstract][Full Text] [Related]
37. Somatic mosaicism in Fanconi anemia: evidence of genotypic reversion in lymphohematopoietic stem cells.
Gregory JJ; Wagner JE; Verlander PC; Levran O; Batish SD; Eide CR; Steffenhagen A; Hirsch B; Auerbach AD
Proc Natl Acad Sci U S A; 2001 Feb; 98(5):2532-7. PubMed ID: 11226273
[TBL] [Abstract][Full Text] [Related]
38. Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research Group.
Faivre L; Guardiola P; Lewis C; Dokal I; Ebell W; Zatterale A; Altay C; Poole J; Stones D; Kwee ML; van Weel-Sipman M; Havenga C; Morgan N; de Winter J; Digweed M; Savoia A; Pronk J; de Ravel T; Jansen S; Joenje H; Gluckman E; Mathew CG
Blood; 2000 Dec; 96(13):4064-70. PubMed ID: 11110674
[TBL] [Abstract][Full Text] [Related]
39. Genetic analysis of a Fanconi anemia case revealed the presence of FANCF mutation (exon 1;469>C-T) with implications to develop acute myeloid leukemia.
Behera CK; Gyandeep G; Mishra R; Mohanty RP; Pal A; Behera J; Samal S; Das B
Mol Biol Rep; 2023 Jan; 50(1):931-936. PubMed ID: 36369330
[TBL] [Abstract][Full Text] [Related]
40. A comprehensive strategy for the subtyping of patients with Fanconi anaemia: conclusions from the Spanish Fanconi Anemia Research Network.
Antonio Casado J; Callén E; Jacome A; Río P; Castella M; Lobitz S; Ferro T; Muñoz A; Sevilla J; Cantalejo A; Cela E; Cervera J; Sánchez-Calero J; Badell I; Estella J; Dasí A; Olivé T; José Ortega J; Rodriguez-Villa A; Tapia M; Molinés A; Madero L; Segovia JC; Neveling K; Kalb R; Schindler D; Hanenberg H; Surrallés J; Bueren JA
J Med Genet; 2007 Apr; 44(4):241-9. PubMed ID: 17105750
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]