630 related articles for article (PubMed ID: 15059067)
1. Molecular characterization of three novel Fanconi anemia mutations in Israeli Arabs.
Tamary H; Dgany O; Toledano H; Shalev Z; Krasnov T; Shalmon L; Schechter T; Bercovich D; Attias D; Laor R; Koren A; Yaniv I
Eur J Haematol; 2004 May; 72(5):330-5. PubMed ID: 15059067
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Identification of Alu-mediated deletions in the Fanconi anemia gene FAA.
Levran O; Doggett NA; Auerbach AD
Hum Mutat; 1998; 12(3):145-52. PubMed ID: 9711872
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9.
Demuth I; Wlodarski M; Tipping AJ; Morgan NV; de Winter JP; Thiel M; Gräsl S; Schindler D; D'Andrea AD; Altay C; Kayserili H; Zatterale A; Kunze J; Ebell W; Mathew CG; Joenje H; Sperling K; Digweed M
Eur J Hum Genet; 2000 Nov; 8(11):861-8. PubMed ID: 11093276
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Quantitative PCR analysis reveals a high incidence of large intragenic deletions in the FANCA gene in Spanish Fanconi anemia patients.
Callén E; Tischkowitz MD; Creus A; Marcos R; Bueren JA; Casado JA; Mathew CG; Surrallés J
Cytogenet Genome Res; 2004; 104(1-4):341-5. PubMed ID: 15162062
[TBL] [Abstract][Full Text] [Related]
9. [Construction of FANCA mutant protein from Fanconi anemia patient and analysis of its function].
Chen F; Zhang KJ; Zuo XL; Zeng XC
Zhonghua Xue Ye Xue Za Zhi; 2007 Nov; 28(11):741-4. PubMed ID: 18457264
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. The molecular biology of Fanconi anemia.
Tamary H; Bar-Yam R; Zemach M; Dgany O; Shalmon L; Yaniv I
Isr Med Assoc J; 2002 Oct; 4(10):819-23. PubMed ID: 12389351
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Cloning and analysis of the mouse Fanconi anemia group A cDNA and an overlapping penta zinc finger cDNA.
Wong JC; Alon N; Norga K; Kruyt FA; Youssoufian H; Buchwald M
Genomics; 2000 Aug; 67(3):273-83. PubMed ID: 10936049
[TBL] [Abstract][Full Text] [Related]
14. Four novel mutations of the Fanconi anemia group A gene (FAA) in Japanese patients.
Nakamura A; Matsuura S; Tauchi H; Hanada R; Ohashi H; Hasegawa T; Honda K; Masuno M; Imaizumi K; Sugita K; Ide T; Komatsu K
J Hum Genet; 1999; 44(1):48-51. PubMed ID: 9929978
[TBL] [Abstract][Full Text] [Related]
15. The Fanconi anaemia group G gene FANCG is identical with XRCC9.
de Winter JP; Waisfisz Q; Rooimans MA; van Berkel CG; Bosnoyan-Collins L; Alon N; Carreau M; Bender O; Demuth I; Schindler D; Pronk JC; Arwert F; Hoehn H; Digweed M; Buchwald M; Joenje H
Nat Genet; 1998 Nov; 20(3):281-3. PubMed ID: 9806548
[TBL] [Abstract][Full Text] [Related]
16. The FANCA gene in Japanese Fanconi anemia: reports of eight novel mutations and analysis of sequence variability.
Tachibana A; Kato T; Ejima Y; Yamada T; Shimizu T; Yang L; Tsunematsu Y; Sasaki MS
Hum Mutat; 1999; 13(3):237-44. PubMed ID: 10090479
[TBL] [Abstract][Full Text] [Related]
17. Two common founder mutations of the fanconi anemia group G gene FANCG/XRCC9 in the Japanese population.
Yagasaki H; Oda T; Adachi D; Nakajima T; Nakahata T; Asano S; Yamashita T
Hum Mutat; 2003 May; 21(5):555. PubMed ID: 12673805
[TBL] [Abstract][Full Text] [Related]
18. [FANCA gene mutation analysis in Fanconi anemia patients].
Chen F; Peng GJ; Zhang K; Hu Q; Zhang LQ; Liu AG
Zhonghua Xue Ye Xue Za Zhi; 2005 Oct; 26(10):616-8. PubMed ID: 16532972
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Spectrum of FANCA mutations in Italian Fanconi anemia patients: identification of six novel alleles and phenotypic characterization of the S858R variant.
Savino M; Borriello A; D'Apolito M; Criscuolo M; Del Vecchio M; Bianco AM; Di Perna M; Calzone R; Nobili B; Zatterale A; Zelante L; Joenje H; Della Ragione F; Savoia A
Hum Mutat; 2003 Oct; 22(4):338-9. PubMed ID: 12955722
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
