Aung T - Search Results

1

Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locus.

Hauser MA, Aboobakar IF, Liu Y, Miura S, Whigham BT, Challa P, Wheeler J, Williams A, Santiago-Turla C, Qin X, Rautenbach RM, Ziskind A, Ramsay M, Uebe S, Song L, Safi A, Vithana EN, Mizoguchi T, Nakano S, Kubota T, Hayashi K, Manabe S, Kazama S, Mori Y, Miyata K, Yoshimura N, Reis A, Crawford GE, Pasutto F, Carmichael TR, Williams SE, Ozaki M, Aung T, Khor CC, Stamer WD, Ashley-Koch AE, Allingham RR. Hauser MA, et al. Among authors: aung t. Hum Mol Genet. 2015 Nov 15;24(22):6552-63. doi: 10.1093/hmg/ddv347. Epub 2015 Aug 25. Hum Mol Genet. 2015. PMID: 26307087 Free PMC article.

2

Molecular analysis of the myocilin gene in Chinese subjects with chronic primary-angle closure glaucoma.

Aung T, Yong VH, Chew PT, Seah SK, Gazzard G, Foster PJ, Vithana EN. Aung T, et al. Invest Ophthalmol Vis Sci. 2005 Apr;46(4):1303-6. doi: 10.1167/iovs.04-1163. Invest Ophthalmol Vis Sci. 2005. PMID: 15790895

3

Characterization of Bietti crystalline dystrophy patients with CYP4V2 mutations.

Lee KY, Koh AH, Aung T, Yong VH, Yeung K, Ang CL, Vithana EN. Lee KY, et al. Among authors: aung t. Invest Ophthalmol Vis Sci. 2005 Oct;46(10):3812-6. doi: 10.1167/iovs.05-0378. Invest Ophthalmol Vis Sci. 2005. PMID: 16186368

4

Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2).

Vithana EN, Morgan P, Sundaresan P, Ebenezer ND, Tan DT, Mohamed MD, Anand S, Khine KO, Venkataraman D, Yong VH, Salto-Tellez M, Venkatraman A, Guo K, Hemadevi B, Srinivasan M, Prajna V, Khine M, Casey JR, Inglehearn CF, Aung T. Vithana EN, et al. Among authors: aung t. Nat Genet. 2006 Jul;38(7):755-7. doi: 10.1038/ng1824. Epub 2006 Jun 11. Nat Genet. 2006. PMID: 16767101

5

Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2). Mutation in brief #958. Online.

Ramprasad VL, Ebenezer ND, Aung T, Rajagopal R, Yong VH, Tuft SJ, Viswanathan D, El-Ashry MF, Liskova P, Tan DT, Bhattacharya SS, Kumaramanickavel G, Vithana EN. Ramprasad VL, et al. Among authors: aung t. Hum Mutat. 2007 May;28(5):522-3. doi: 10.1002/humu.9487. Hum Mutat. 2007. PMID: 17397048

6

Lack of association between interleukin-1 gene cluster polymorphisms and glaucoma in Chinese subjects.

How AC, Aung T, Chew X, Yong VH, Lim MC, Lee KY, Toh JY, Li Y, Liu J, Vithana EN. How AC, et al. Among authors: aung t. Invest Ophthalmol Vis Sci. 2007 May;48(5):2123-6. doi: 10.1167/iovs.06-1213. Invest Ophthalmol Vis Sci. 2007. PMID: 17460270

7

SLC4A11 mutations in Fuchs endothelial corneal dystrophy.

Vithana EN, Morgan PE, Ramprasad V, Tan DT, Yong VH, Venkataraman D, Venkatraman A, Yam GH, Nagasamy S, Law RW, Rajagopal R, Pang CP, Kumaramanickevel G, Casey JR, Aung T. Vithana EN, et al. Among authors: aung t. Hum Mol Genet. 2008 Mar 1;17(5):656-66. doi: 10.1093/hmg/ddm337. Epub 2007 Nov 16. Hum Mol Genet. 2008. PMID: 18024964

8

Analysis of the posterior polymorphous corneal dystrophy 3 gene, TCF8, in late-onset Fuchs endothelial corneal dystrophy.

Mehta JS, Vithana EN, Tan DT, Yong VH, Yam GH, Law RW, Chong WG, Pang CP, Aung T. Mehta JS, et al. Among authors: aung t. Invest Ophthalmol Vis Sci. 2008 Jan;49(1):184-8. doi: 10.1167/iovs.07-0847. Invest Ophthalmol Vis Sci. 2008. PMID: 18172091

9

Association of LOXL1 gene polymorphisms with pseudoexfoliation in the Japanese.

Ozaki M, Lee KY, Vithana EN, Yong VH, Thalamuthu A, Mizoguchi T, Venkatraman A, Aung T. Ozaki M, et al. Among authors: aung t. Invest Ophthalmol Vis Sci. 2008 Sep;49(9):3976-80. doi: 10.1167/iovs.08-1805. Epub 2008 Apr 30. Invest Ophthalmol Vis Sci. 2008. PMID: 18450598

10

Association analysis of CFH, C2, BF, and HTRA1 gene polymorphisms in Chinese patients with polypoidal choroidal vasculopathy.

Lee KY, Vithana EN, Mathur R, Yong VH, Yeo IY, Thalamuthu A, Lee MW, Koh AH, Lim MC, How AC, Wong DW, Aung T. Lee KY, et al. Among authors: aung t. Invest Ophthalmol Vis Sci. 2008 Jun;49(6):2613-9. doi: 10.1167/iovs.07-0860. Invest Ophthalmol Vis Sci. 2008. PMID: 18515590

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