Lai CH - Search Results

1

Correction of ATM gene function by aminoglycoside-induced read-through of premature termination codons.

Lai CH, Chun HH, Nahas SA, Mitui M, Gamo KM, Du L, Gatti RA. Lai CH, et al. Proc Natl Acad Sci U S A. 2004 Nov 2;101(44):15676-81. doi: 10.1073/pnas.0405155101. Epub 2004 Oct 21. Proc Natl Acad Sci U S A. 2004. PMID: 15498871 Free PMC article.

2

Improved diagnostic testing for ataxia-telangiectasia by immunoblotting of nuclear lysates for ATM protein expression.

Chun HH, Sun X, Nahas SA, Teraoka S, Lai CH, Concannon P, Gatti RA. Chun HH, et al. Among authors: lai ch. Mol Genet Metab. 2003 Dec;80(4):437-43. doi: 10.1016/j.ymgme.2003.09.008. Mol Genet Metab. 2003. PMID: 14654357

3

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 Jr, Gatti RA. Coutinho G, et al. Among authors: lai ch. Am J Med Genet A. 2004 Apr 1;126A(1):33-40. doi: 10.1002/ajmg.a.20570. Am J Med Genet A. 2004. PMID: 15039971

4

Post-irradiation phosphorylation of structural maintenance chromosome 1 (SMC1) is independent of the Fanconi protein pathway.

Nahas SA, Lai CH, Gatti RA. Nahas SA, et al. Among authors: lai ch. Int J Radiat Oncol Biol Phys. 2005 Mar 15;61(4):1167-72. doi: 10.1016/j.ijrobp.2004.11.023. Int J Radiat Oncol Biol Phys. 2005. PMID: 15752898

5

Rapid screen for truncating ATM mutations by PTT-ELISA.

Du L, Lai CH, Concannon P, Gatti RA. Du L, et al. Among authors: lai ch. Mutat Res. 2008 Apr 2;640(1-2):139-44. doi: 10.1016/j.mrfmmm.2008.01.002. Epub 2008 Jan 31. Mutat Res. 2008. PMID: 18321536

6

Functional and computational assessment of missense variants in the ataxia-telangiectasia mutated (ATM) gene: mutations with increased cancer risk.

Mitui M, Nahas SA, Du LT, Yang Z, Lai CH, Nakamura K, Arroyo S, Scott S, Purayidom A, Concannon P, Lavin M, Gatti RA. Mitui M, et al. Among authors: lai ch. Hum Mutat. 2009 Jan;30(1):12-21. doi: 10.1002/humu.20805. Hum Mutat. 2009. PMID: 18634022 Free PMC article.

7

Independent mutational events are rare in the ATM gene: haplotype prescreening enhances mutation detection rate.

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. Mitui M, et al. Among authors: lai ch. Hum Mutat. 2003 Jul;22(1):43-50. doi: 10.1002/humu.10232. Hum Mutat. 2003. PMID: 12815592

8

The pathogenesis of ataxia-telangiectasia. Learning from a Rosetta Stone.

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. Gatti RA, et al. Among authors: lai ch. Clin Rev Allergy Immunol. 2001 Feb;20(1):87-108. doi: 10.1385/CRIAI:20:1:87. Clin Rev Allergy Immunol. 2001. PMID: 11269230 Review. No abstract available.

9

Neuroprotection effects of kynurenic acid-loaded micelles for the Parkinson's disease models.

Chen CM, Huang CY, Lai CH, Chen YC, Hwang YT, Lin CY. Chen CM, et al. Among authors: lai ch. J Liposome Res. 2024 May 23:1-12. doi: 10.1080/08982104.2024.2346986. Online ahead of print. J Liposome Res. 2024. PMID: 38779944

10

New tetrahydroisoquinoline-4-carbonitrile derivatives as potent agents against cyclin-dependent kinases, crystal structures, and computational studies.

El Bakri Y, Karthikeyan S, Lai CH, Bakhite EA, Ahmad I, Abdel-Rahman AE, Abuelhassan S, Marae IS, Mohamed SK, Mague JT. El Bakri Y, et al. Among authors: lai ch. J Biomol Struct Dyn. 2024 Jul;42(10):5053-5071. doi: 10.1080/07391102.2023.2224899. Epub 2023 Jun 26. J Biomol Struct Dyn. 2024. PMID: 38764131

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