Year |
Citation |
Score |
2009 |
Mitui M, Nahas SA, Du LT, Yang Z, Lai CH, Nakamura K, Arroyo S, Scott S, Purayidom A, Concannon P, Lavin M, Gatti RA. Functional and computational assessment of missense variants in the ataxia-telangiectasia mutated (ATM) gene: mutations with increased cancer risk. Human Mutation. 30: 12-21. PMID 18634022 DOI: 10.1002/Humu.20805 |
0.725 |
|
2008 |
Du L, Lai CH, Concannon P, Gatti RA. Rapid screen for truncating ATM mutations by PTT-ELISA. Mutation Research. 640: 139-44. PMID 18321536 DOI: 10.1016/J.Mrfmmm.2008.01.002 |
0.649 |
|
2005 |
Nahas SA, Lai CH, Gatti RA. Post-irradiation phosphorylation of structural maintenance chromosome 1 (SMC1) is independent of the Fanconi protein pathway. International Journal of Radiation Oncology, Biology, Physics. 61: 1167-72. PMID 15752898 DOI: 10.1016/J.Ijrobp.2004.11.023 |
0.661 |
|
2004 |
Lai CH, Chun HH, Nahas SA, Mitui M, Gamo KM, Du L, Gatti RA. Correction of ATM gene function by aminoglycoside-induced read-through of premature termination codons. Proceedings of the National Academy of Sciences of the United States of America. 101: 15676-81. PMID 15498871 DOI: 10.1073/Pnas.0405155101 |
0.734 |
|
2004 |
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. Five haplotypes account for fifty-five percent of ATM mutations in Brazilian patients with ataxia telangiectasia: seven new mutations. American Journal of Medical Genetics. Part A. 126: 33-40. PMID 15039971 DOI: 10.1002/Ajmg.A.20570 |
0.714 |
|
2003 |
Chun HH, Sun X, Nahas SA, Teraoka S, Lai CH, Concannon P, Gatti RA. Improved diagnostic testing for ataxia-telangiectasia by immunoblotting of nuclear lysates for ATM protein expression. Molecular Genetics and Metabolism. 80: 437-43. PMID 14654357 DOI: 10.1016/J.Ymgme.2003.09.008 |
0.73 |
|
2003 |
Mitui M, Campbell C, Coutinho G, Sun X, Lai CH, Thorstenson Y, Castellvi-Bel S, Fernandez L, Monros E, Carvalho BT, Porras O, Fontan G, Gatti RA. Independent mutational events are rare in the ATM gene: haplotype prescreening enhances mutation detection rate. Human Mutation. 22: 43-50. PMID 12815592 DOI: 10.1002/Humu.10232 |
0.638 |
|
2001 |
Gatti RA, Becker-Catania S, Chun HH, Sun X, Mitui M, Lai CH, Khanlou N, Babaei M, Cheng R, Clark C, Huo Y, Udar NC, Iyer RK. The pathogenesis of ataxia-telangiectasia. Learning from a Rosetta Stone. Clinical Reviews in Allergy & Immunology. 20: 87-108. PMID 11269230 DOI: 10.1385/Criai:20:1:87 |
0.674 |
|
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