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

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

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

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

Association of LOXL1 gene polymorphisms with pseudoexfoliation in the Japanese

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

Analysis of conjunctival fibroblasts from a proband with Schnyder corneal dystrophy

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

Association of LOXL1 polymorphisms with pseudoexfoliation in the Chinese

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

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

بواسطة 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.
منشور في 2011

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

بواسطة 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.
منشور في 2014

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

بواسطة 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.
منشور في 2014

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

بواسطة 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
منشور في 2020

SLC4A11 mutations in Fuchs endothelial corneal dystrophy

بواسطة 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
منشور في 2011