Venkataraman D - Search Results

1

Association of LOXL1 polymorphisms with pseudoexfoliation in the Chinese.

Lee KY, Ho SL, Thalamuthu A, Venkatraman A, Venkataraman D, Pek DC, Aung T, Vithana EN. Lee KY, et al. Among authors: venkataraman d. Mol Vis. 2009 Jun 4;15:1120-6. Mol Vis. 2009. PMID: 19503743 Free PMC article.

2

Analysis of conjunctival fibroblasts from a proband with Schnyder corneal dystrophy.

Mehta JS, Vithana EN, Venkataraman D, Venkatraman A, Poh R, Beuerman RW, Aung T, Tan DT. Mehta JS, et al. Among authors: venkataraman d. Mol Vis. 2008 Jul 9;14:1277-81. Mol Vis. 2008. PMID: 18618004 Free PMC article.

3

Molecular analysis of CHX10 and MFRP in Chinese subjects with primary angle closure glaucoma and short axial length eyes.

Aung T, Lim MC, Wong TT, Thalamuthu A, Yong VH, Venkataraman D, Venkatraman A, Chew PT, Vithana EN. Aung T, et al. Among authors: venkataraman d. Mol Vis. 2008 Jul 17;14:1313-8. Mol Vis. 2008. PMID: 18648522 Free PMC article.

4

Identification of a novel mutation in the NTF4 gene that causes primary open-angle glaucoma in a Chinese population.

Vithana EN, Nongpiur ME, Venkataraman D, Chan SH, Mavinahalli J, Aung T. Vithana EN, et al. Among authors: venkataraman d. Mol Vis. 2010 Aug 15;16:1640-5. Mol Vis. 2010. PMID: 20806036 Free PMC article.

5

Association of TCF4 gene polymorphisms with Fuchs' corneal dystrophy in the Chinese.

Thalamuthu A, Khor CC, Venkataraman D, Koh LW, Tan DT, Aung T, Mehta JS, Vithana EN. Thalamuthu A, et al. Among authors: venkataraman d. Invest Ophthalmol Vis Sci. 2011 Jul 29;52(8):5573-8. doi: 10.1167/iovs.11-7568. Invest Ophthalmol Vis Sci. 2011. PMID: 21659310

6

Surgical management and genetic analysis of a Chinese family with the S171P mutation in the UBIAD1 gene, the gene for Schnyder corneal dystrophy.

Mehta JS, Vithana EN, Venkataraman D, Venkatraman A, Yong VH, Aung T, Tan DT. Mehta JS, et al. Among authors: venkataraman d. Br J Ophthalmol. 2009 Jul;93(7):926-31. doi: 10.1136/bjo.2008.152140. Epub 2009 May 7. Br J Ophthalmol. 2009. PMID: 19429578

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: venkataraman d. 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

Lack of association between the rs2664538 polymorphism in the MMP-9 gene and primary angle closure glaucoma in Singaporean subjects.

Aung T, Yong VH, Lim MC, Venkataraman D, Toh JY, Chew PT, Vithana EN. Aung T, et al. Among authors: venkataraman d. J Glaucoma. 2008 Jun-Jul;17(4):257-8. doi: 10.1097/IJG.0b013e31815c3aa5. J Glaucoma. 2008. PMID: 18552608

9

Toll-like receptor 3 polymorphism rs3775291 is not associated with choroidal neovascularization or polypoidal choroidal vasculopathy in Chinese subjects.

Sng CC, Cackett PD, Yeo IY, Thalamuthu A, Venkatraman A, Venkataraman D, Koh AH, Tai ES, Wong TY, Aung T, Vithana EN. Sng CC, et al. Among authors: venkataraman d. Ophthalmic Res. 2011;45(4):191-6. doi: 10.1159/000321387. Epub 2010 Nov 16. Ophthalmic Res. 2011. PMID: 21079408

10

Depletion of SLC4A11 causes cell death by apoptosis in an immortalized human corneal endothelial cell line.

Liu J, Seet LF, Koh LW, Venkatraman A, Venkataraman D, Mohan RR, Praetorius J, Bonanno JA, Aung T, Vithana EN. Liu J, et al. Among authors: venkataraman d. Invest Ophthalmol Vis Sci. 2012 Jun 5;53(7):3270-9. doi: 10.1167/iovs.11-8724. Invest Ophthalmol Vis Sci. 2012. PMID: 22447871 Free PMC article.

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