247 related articles for article (PubMed ID: 15583986)
1. [Single nucleotide polymorphisms and point mutations of ataxia telangiectasia mutated gene in Chinese of Han ethnicity].
Tang HW; Bian JC; Jiang F; Shen Q; Zhu QX; Zhang HW; Wu Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):579-82. PubMed ID: 15583986
[TBL] [Abstract][Full Text] [Related]
2. Exon-scanning mutation analysis of the ATM gene in patients with ataxia-telangiectasia.
Vorechovský I; Luo L; Prudente S; Chessa L; Russo G; Kanariou M; James M; Negrini M; Webster AD; Hammarström L
Eur J Hum Genet; 1996; 4(6):352-5. PubMed ID: 9043869
[TBL] [Abstract][Full Text] [Related]
3. PCR-mediated detection of a polymorphism in the ATM gene.
Maillet P; Vaudan G; Chappuis P; Sappino A
Mol Cell Probes; 1999 Feb; 13(1):67-9. PubMed ID: 10024435
[TBL] [Abstract][Full Text] [Related]
4. ATM haplotypes and associated mutations in Iranian patients with ataxia-telangiectasia: recurring homozygosity without a founder haplotype.
Babaei M; Mitui M; Olson ER; Gatti RA
Hum Genet; 2005 Jul; 117(2-3):101-6. PubMed ID: 15843990
[TBL] [Abstract][Full Text] [Related]
5. Mutation analysis of the ATM gene in two Chinese patients with ataxia telangiectasia.
Jiang H; Tang B; Xia K; Hu Z; Shen L; Tang J; Zhao G; Zhang Y; Cai F; Pan Q; Long Z; Wang G; Dai H
J Neurol Sci; 2006 Feb; 241(1-2):1-6. PubMed ID: 16380133
[TBL] [Abstract][Full Text] [Related]
6. Five haplotypes account for fifty-five percent of ATM mutations in Brazilian patients with ataxia telangiectasia: seven new mutations.
Coutinho G; Mitui M; Campbell C; Costa Carvalho BT; Nahas S; Sun X; Huo Y; Lai CH; Thorstenson Y; Tanouye R; Raskin S; Kim CA; Llerena J; Gatti RA
Am J Med Genet A; 2004 Apr; 126A(1):33-40. PubMed ID: 15039971
[TBL] [Abstract][Full Text] [Related]
7. Sequence analysis of the ATM gene in 20 patients with RTOG grade 3 or 4 acute and/or late tissue radiation side effects.
Oppitz U; Bernthaler U; Schindler D; Sobeck A; Hoehn H; Platzer M; Rosenthal A; Flentje M
Int J Radiat Oncol Biol Phys; 1999 Jul; 44(5):981-8. PubMed ID: 10421529
[TBL] [Abstract][Full Text] [Related]
8. New mutations, polymorphisms, and rare variants in the ATM gene detected by a novel SSCP strategy.
Castellví-Bel S; Sheikhavandi S; Telatar M; Tai LQ; Hwang M; Wang Z; Yang Z; Cheng R; Gatti RA
Hum Mutat; 1999; 14(2):156-62. PubMed ID: 10425038
[TBL] [Abstract][Full Text] [Related]
9. [Association of the exon 8 and intron 8 polymorphisms of the human urate transporter 1 gene with primary hyperuricemia in Chinese Han population].
Meng DM; Han L; Miao ZM; Li CG
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Dec; 27(6):659-63. PubMed ID: 21154327
[TBL] [Abstract][Full Text] [Related]
10. Splicing defects in the ataxia-telangiectasia gene, ATM: underlying mutations and consequences.
Teraoka SN; Telatar M; Becker-Catania S; Liang T; Onengüt S; Tolun A; Chessa L; Sanal O; Bernatowska E; Gatti RA; Concannon P
Am J Hum Genet; 1999 Jun; 64(6):1617-31. PubMed ID: 10330348
[TBL] [Abstract][Full Text] [Related]
11. DHPLC screening of ATM gene in Italian patients affected by ataxia-telangiectasia: fourteen novel ATM mutations.
Magliozzi M; Piane M; Torrente I; Sinibaldi L; Rizzo G; Savio C; Lulli P; De Luca A; Dallapiccola B; Chessa L
Dis Markers; 2006; 22(4):257-64. PubMed ID: 17124347
[TBL] [Abstract][Full Text] [Related]
12. Underexpression and abnormal localization of ATM products in ataxia telangiectasia patients bearing ATM missense mutations.
Jacquemin V; Rieunier G; Jacob S; Bellanger D; d'Enghien CD; Laugé A; Stoppa-Lyonnet D; Stern MH
Eur J Hum Genet; 2012 Mar; 20(3):305-12. PubMed ID: 22071889
[TBL] [Abstract][Full Text] [Related]
13. Ataxia-telangiectasia locus: sequence analysis of 184 kb of human genomic DNA containing the entire ATM gene.
Platzer M; Rotman G; Bauer D; Uziel T; Savitsky K; Bar-Shira A; Gilad S; Shiloh Y; Rosenthal A
Genome Res; 1997 Jun; 7(6):592-605. PubMed ID: 9199932
[TBL] [Abstract][Full Text] [Related]
14. [Research on clinical characteristics and ATM gene mutations in Chinese patients with ataxia-telangiectasia].
Jiang H; Tang BS; Hu ZM; Xia K; Xu B; Tang JG
Zhonghua Yi Xue Za Zhi; 2005 Apr; 85(16):1117-20. PubMed ID: 16029571
[TBL] [Abstract][Full Text] [Related]
15. Functional characterization and targeted correction of ATM mutations identified in Japanese patients with ataxia-telangiectasia.
Nakamura K; Du L; Tunuguntla R; Fike F; Cavalieri S; Morio T; Mizutani S; Brusco A; Gatti RA
Hum Mutat; 2012 Jan; 33(1):198-208. PubMed ID: 22006793
[TBL] [Abstract][Full Text] [Related]
16. Global analysis of ATM polymorphism reveals significant functional constraint.
Thorstenson YR; Shen P; Tusher VG; Wayne TL; Davis RW; Chu G; Oefner PJ
Am J Hum Genet; 2001 Aug; 69(2):396-412. PubMed ID: 11443540
[TBL] [Abstract][Full Text] [Related]
17. ATM gene founder haplotypes and associated mutations in Polish families with ataxia-telangiectasia.
Mitui M; Bernatowska E; Pietrucha B; Piotrowska-Jastrzebska J; Eng L; Nahas S; Teraoka S; Sholty G; Purayidom A; Concannon P; Gatti RA
Ann Hum Genet; 2005 Nov; 69(Pt 6):657-64. PubMed ID: 16266405
[TBL] [Abstract][Full Text] [Related]
18. Characterisation of ATM mutations in Slavic Ataxia telangiectasia patients.
Soukupova J; Pohlreich P; Seemanova E
Neuromolecular Med; 2011 Sep; 13(3):204-11. PubMed ID: 21833744
[TBL] [Abstract][Full Text] [Related]
19. Common ataxia telangiectasia mutated haplotypes and risk of breast cancer: a nested case-control study.
Tamimi RM; Hankinson SE; Spiegelman D; Kraft P; Colditz GA; Hunter DJ
Breast Cancer Res; 2004; 6(4):R416-22. PubMed ID: 15217510
[TBL] [Abstract][Full Text] [Related]
20. Functional significance of a deep intronic mutation in the ATM gene and evidence for an alternative exon 28a.
Coutinho G; Xie J; Du L; Brusco A; Krainer AR; Gatti RA
Hum Mutat; 2005 Feb; 25(2):118-24. PubMed ID: 15643608
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
