150 related articles for article (PubMed ID: 25703136)
21. Fanconi anemia founder mutation in Macedonian patients.
Madjunkova S; Kocheva SA; Plaseska-Karanfilska D
Acta Haematol; 2014; 132(1):15-21. PubMed ID: 24356203
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Fanconi anemia protein complex: mapping protein interactions in the yeast 2- and 3-hybrid systems.
Gordon SM; Buchwald M
Blood; 2003 Jul; 102(1):136-41. PubMed ID: 12649160
[TBL] [Abstract][Full Text] [Related]
24. Spectrum of sequence variation in the FANCG gene: an International Fanconi Anemia Registry (IFAR) study.
Auerbach AD; Greenbaum J; Pujara K; Batish SD; Bitencourt MA; Kokemohr I; Schneider H; Lobitzc S; Pasquini R; Giampietro PF; Hanenberg H; Levran O;
Hum Mutat; 2003 Feb; 21(2):158-68. PubMed ID: 12552564
[TBL] [Abstract][Full Text] [Related]
25. Diagnosis of Fanconi Anaemia by ionising radiation- or mitomycin C-induced micronuclei.
Francies FZ; Wainwright R; Poole J; De Leeneer K; Coene I; Wieme G; Poirel HA; Brichard B; Vermeulen S; Vral A; Slabbert J; Claes K; Baeyens A
DNA Repair (Amst); 2018 Jan; 61():17-24. PubMed ID: 29154021
[TBL] [Abstract][Full Text] [Related]
26. Clinical and Genetic Features of Patients With Fanconi Anemia in Lebanon and Report on Novel Mutations in the FANCA and FANCG Genes.
Farah RA; Nair P; Koueik J; Yammine T; Khalifeh H; Korban R; Collet A; Khayat C; Dubois-Denghien C; Chouery E; Blanluet M; El-Hayek S; Stoppa-Lyonnet D; Megarbane A
J Pediatr Hematol Oncol; 2021 Jul; 43(5):e727-e735. PubMed ID: 32947577
[TBL] [Abstract][Full Text] [Related]
27. Heterogeneous activation of the Fanconi anemia pathway by patient-derived FANCA mutants.
Adachi D; Oda T; Yagasaki H; Nakasato K; Taniguchi T; D'Andrea AD; Asano S; Yamashita T
Hum Mol Genet; 2002 Dec; 11(25):3125-34. PubMed ID: 12444097
[TBL] [Abstract][Full Text] [Related]
28. Fanconi anaemia in black South African patients heterozygous for the FANCG c.637-643delTACCGCC founder mutation.
Wainstein T; Kerr R; Mitchell CL; Madaree S; Essop FB; Vorster E; Wainwright R; Poole J; Krause A
S Afr Med J; 2013 Oct; 103(12 Suppl 1):970-3. PubMed ID: 24300640
[TBL] [Abstract][Full Text] [Related]
29. Hematological consequences of a FANCG founder mutation in Black South African patients with Fanconi anemia.
Feben C; Kromberg J; Wainwright R; Stones D; Poole J; Haw T; Krause A
Blood Cells Mol Dis; 2015 Mar; 54(3):270-4. PubMed ID: 25477267
[TBL] [Abstract][Full Text] [Related]
30. Strong FANCA/FANCG but weak FANCA/FANCC interaction in the yeast 2-hybrid system.
Reuter T; Herterich S; Bernhard O; Hoehn H; Gross HJ
Blood; 2000 Jan; 95(2):719-20. PubMed ID: 10627486
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Resistance to mitomycin C requires direct interaction between the Fanconi anemia proteins FANCA and FANCG in the nucleus through an arginine-rich domain.
Kruyt FA; Abou-Zahr F; Mok H; Youssoufian H
J Biol Chem; 1999 Nov; 274(48):34212-8. PubMed ID: 10567393
[TBL] [Abstract][Full Text] [Related]
33. A physical complex of the Fanconi anemia proteins FANCG/XRCC9 and FANCA.
Waisfisz Q; de Winter JP; Kruyt FA; de Groot J; van der Weel L; Dijkmans LM; Zhi Y; Arwert F; Scheper RJ; Youssoufian H; Hoatlin ME; Joenje H
Proc Natl Acad Sci U S A; 1999 Aug; 96(18):10320-5. PubMed ID: 10468606
[TBL] [Abstract][Full Text] [Related]
34. Investigation of Fanconi anemia protein interactions by yeast two-hybrid analysis.
Huber PA; Medhurst AL; Youssoufian H; Mathew CG
Biochem Biophys Res Commun; 2000 Feb; 268(1):73-7. PubMed ID: 10652215
[TBL] [Abstract][Full Text] [Related]
35. Functional analysis of patient-derived mutations in the Fanconi anemia gene, FANCG/XRCC9.
Nakanishi K; Moran A; Hays T; Kuang Y; Fox E; Garneau D; Montes de Oca R; Grompe M; D'Andrea AD
Exp Hematol; 2001 Jul; 29(7):842-9. PubMed ID: 11438206
[TBL] [Abstract][Full Text] [Related]
36. Direct interaction of the Fanconi anaemia protein FANCG with BRCA2/FANCD1.
Hussain S; Witt E; Huber PA; Medhurst AL; Ashworth A; Mathew CG
Hum Mol Genet; 2003 Oct; 12(19):2503-10. PubMed ID: 12915460
[TBL] [Abstract][Full Text] [Related]
37. Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia.
Chandrasekharappa SC; Lach FP; Kimble DC; Kamat A; Teer JK; Donovan FX; Flynn E; Sen SK; Thongthip S; Sanborn E; Smogorzewska A; Auerbach AD; Ostrander EA;
Blood; 2013 May; 121(22):e138-48. PubMed ID: 23613520
[TBL] [Abstract][Full Text] [Related]
38. Spectrum of sequence variations in the FANCA gene: an International Fanconi Anemia Registry (IFAR) study.
Levran O; Diotti R; Pujara K; Batish SD; Hanenberg H; Auerbach AD
Hum Mutat; 2005 Feb; 25(2):142-9. PubMed ID: 15643609
[TBL] [Abstract][Full Text] [Related]
39. A common Fanconi anemia mutation in black populations of sub-Saharan Africa.
Morgan NV; Essop F; Demuth I; de Ravel T; Jansen S; Tischkowitz M; Lewis CM; Wainwright L; Poole J; Joenje H; Digweed M; Krause A; Mathew CG
Blood; 2005 May; 105(9):3542-4. PubMed ID: 15657175
[TBL] [Abstract][Full Text] [Related]
40. Screening for mutations in two exons of FANCG gene in Pakistani population.
Aymun U; Iram S; Aftab I; Khaliq S; Nadir A; Nisar A; Mohsin S
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub; 2017 Jun; 161(2):158-163. PubMed ID: 28627524
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]