Published in Invest Ophthalmol Vis Sci on July 01, 2004
Mechanism of lysine oxidation in human lens crystallins during aging and in diabetes. J Biol Chem (2009) 1.03
Detection and characterization of in vivo nitration and oxidation of tryptophan residues in proteins. Methods Enzymol (2008) 0.84
Peroxynitrite-induced expression of inducible nitric oxide synthase and activated apoptosis via nuclear factor-kappa B pathway in retinal pigment epithelial cells and antagonism of cholecystokinin octapeptide-8 in vitro. Int J Ophthalmol (2011) 0.76
Cholecystokinin octapeptide antagonizes apoptosis in human retinal pigment epithelial cells. Neural Regen Res (2014) 0.75
Simple limbal epithelial transplantation (SLET): a novel surgical technique for the treatment of unilateral limbal stem cell deficiency. Br J Ophthalmol (2012) 1.73
Clinical outcomes of xeno-free autologous cultivated limbal epithelial transplantation: a 10-year study. Br J Ophthalmol (2011) 1.66
Molecular and cellular assessment of ginkgo biloba extract as a possible ophthalmic drug. Exp Eye Res (2002) 1.48
Glucose-mediated phosphorylation converts the transcription factor Rgt1 from a repressor to an activator. J Biol Chem (2003) 1.41
Smoking and its association with cataract: results of the Andhra Pradesh eye disease study from India. Invest Ophthalmol Vis Sci (2005) 1.24
Mutation spectrum of the CYP1B1 gene in Indian primary congenital glaucoma patients. Mol Vis (2004) 1.19
Identification of novel mutations causing familial primary congenital glaucoma in Indian pedigrees. Invest Ophthalmol Vis Sci (2002) 1.18
Mutation spectrum of FOXC1 and clinical genetic heterogeneity of Axenfeld-Rieger anomaly in India. Mol Vis (2003) 1.10
A glaucoma-associated mutant of optineurin selectively induces death of retinal ganglion cells which is inhibited by antioxidants. Invest Ophthalmol Vis Sci (2007) 1.02
In vitro culture and expansion of human limbal epithelial cells. Nat Protoc (2010) 1.02
Mie light scattering calculations for an Indian age-related nuclear cataract with a high density of multilamellar bodies. Mol Vis (2008) 0.99
Identification of R368H as a predominant CYP1B1 allele causing primary congenital glaucoma in Indian patients. Invest Ophthalmol Vis Sci (2003) 0.98
Focus on molecules: optineurin. Exp Eye Res (2007) 0.96
Identification of myo-inositol-3-phosphate synthase isoforms: characterization, expression, and putative role of a 16-kDa gamma(c) isoform. J Biol Chem (2009) 0.95
Disease-causing mutations in proteins: structural analysis of the CYP1B1 mutations causing primary congenital glaucoma in humans. Biophys J (2006) 0.95
Mutation causing self-aggregation in human gammaC-crystallin leading to congenital cataract. Invest Ophthalmol Vis Sci (2006) 0.95
Regulation of endocytic trafficking of transferrin receptor by optineurin and its impairment by a glaucoma-associated mutant. BMC Cell Biol (2010) 0.93
Ultrastructural analysis of damage to nuclear fiber cell membranes in advanced age-related cataracts from India. Exp Eye Res (2008) 0.92
Microsporidial keratitis in India: 16S rRNA gene-based PCR assay for diagnosis and species identification of microsporidia in clinical samples. Invest Ophthalmol Vis Sci (2006) 0.92
Visualization of in situ intracellular aggregation of two cataract-associated human gamma-crystallin mutants: lose a tail, lose transparency. Invest Ophthalmol Vis Sci (2008) 0.90
Optineurin and its mutants: molecules associated with some forms of glaucoma. Ophthalmic Res (2009) 0.89
The mutation V42M distorts the compact packing of the human gamma-S-crystallin molecule, resulting in congenital cataract. PLoS One (2012) 0.87
Multilamellar spherical particles as potential sources of excessive light scattering in human age-related nuclear cataracts. Exp Eye Res (2010) 0.86
Structural integrity of the Greek key motif in βγ-crystallins is vital for central eye lens transparency. PLoS One (2013) 0.86
Novel mutations of the carbohydrate sulfotransferase-6 (CHST6) gene causing macular corneal dystrophy in India. Mol Vis (2003) 0.85
Activation of a cyclic amp-guanine exchange factor in hepatocytes decreases nitric oxide synthase expression. Shock (2013) 0.82
Structural and aggregation behavior of the human γD-crystallin mutant E107A, associated with congenital nuclear cataract. Mol Vis (2010) 0.81
Structural analysis of the mutant protein D26G of human γS-crystallin, associated with Coppock cataract. Mol Vis (2013) 0.80
17β-Estradiol attenuates cytokine-induced nitric oxide production in rat hepatocyte. J Trauma Acute Care Surg (2012) 0.80
Oral epithelial cells transplanted on to corneal surface tend to adapt to the ocular phenotype. Indian J Ophthalmol (2014) 0.79
Gene symbol: CYP1B1. Disease: glaucoma, primary congenital. Hum Genet (2003) 0.76
Functional analysis of optineurin and some of its disease-associated mutants. IUBMB Life (2015) 0.76
Role of xanthurenic acid 8-O-beta-D-glucoside, a novel fluorophore that accumulates in the brunescent human eye lens. Photochem Photobiol (2002) 0.76
Proteomic analysis of rat prefrontal cortex after chronic valproate treatment. J Neurosci Res (2014) 0.75
Corneal chalcosis following blast injury. Br J Ophthalmol (2012) 0.75
Gene symbol: MY0C (GLC1A). Disease: glaucoma 1, open angle. Hum Genet (2003) 0.75