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

由 Mehta, J.S., Vithana, E.N., Venkataraman, D., Venkatraman, A., Yong, V.H.K., Aung, T., Tan, D.T.H.
出版 2011

Biochemical properties and aggregation propensity of transforming growth factor-induced protein (TGFBIp) and the amyloid forming mutants

由 Lakshminarayanan R, Chaurasia S.S, Murugan E, Venkatraman A, Chai S.-M, Vithana E.N, Beuerman R.W, Mehta J.S
出版 2016

Association of LOXL1 gene polymorphisms with pseudoexfoliation in the Japanese

由 Ozaki, M., Lee, K.Y.C., Vithana, E.N., Yong, V.H., Venkatraman, A., Aung, T., Thalamuthu, A., Mizoguchi, T.
出版 2011

Analysis of conjunctival fibroblasts from a proband with Schnyder corneal dystrophy

由 Mehta, J.S., Vithana, E.N., Venkataraman, D., Venkatraman, A., Poh, R., Beuerman, R.W., Aung, T., Tan, D.T.H.
出版 2011

Association of LOXL1 polymorphisms with pseudoexfoliation in the Chinese

由 Lee, K.Y.C., Aung, T., Ho, S.L., Pek, D.C.K., Thalamuthu, A., Venkatraman, A., Venkataraman, D., Vithana, E.N.
出版 2011

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

由 Aung, T., Lim, M.C.C., Wong, T.T.L., Yong, V.H.K., Venkataraman, D., Venkatraman, A., Vithana, E.N., Chew, P.T.K., Thalamuthu, A.
出版 2011

A novel mutation in transforming growth factor-beta induced protein (TGFβIp) reveals secondary structure perturbation in lattice corneal dystrophy

由 Lakshminarayanan, R., Vithana, E.N., Chai, S.-M., Chaurasia, S.S., Saraswathi, P., Venkatraman, A., Rojare, C., Venkataraman, D., Tan, D., Aung, T., Beuerman, R.W., Mehta, J.S.
出版 2014

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

由 Sng, C.C.A., Cackett, P.D., Yeo, I.Y., Thalamuthu, A., Venkatraman, A., Venkataraman, D., Koh, A.H., Tai, E.-S., Wong, T.Y., Aung, T., Vithana, E.N.
出版 2014

PH Induced Conformational Transitions in the Transforming Growth Factor ?-Induced Protein (TGF?IP) Associated Corneal Dystrophy Mutants

由 Murugan, E, Venkatraman, A, Lei, Z, Mouvet, V, Rui Yi Lim, R, Muruganantham, N, Goh, E, Swee Lim Peh, G, Beuerman, R.W, Chaurasia, S.S, Rajamani, L, Mehta, J.S
出版 2020

SLC4A11 mutations in Fuchs endothelial corneal dystrophy

由 Vithana, E.N., Tan, D.T.H., Venkataraman, D., Venkatraman, A., Aung, T., Morgan, P.E., Casey, J.R., Ramprasad, V., Nagasamy, S., Kumaramanickevel, G., Rajagopal, R., Yam, G.H.F., Law, R.W.K., Pang, C.P., Yong, V.H.K
出版 2011