Works matching IS 10900535 AND DT 2016 AND VI 22
Results: 123
Iris transillumination defect and its gene modulators do not correlate with intraocular pressure in the BXD family of mice.
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- Molecular Vision, 2016, v. 22, p. 1
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IRBP deficiency permits precocious ocular development and myopia.
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- Molecular Vision, 2016, v. 22, p. 1
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Association of primary open-angle glaucoma with mitochondrial variants and haplogroups common in African Americans.
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- Molecular Vision, 2016, v. 22, p. 1
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Mechanism of the anticataract effect of liposomal magnesium taurate in galactose-fed rats.
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- Molecular Vision, 2016, v. 22, p. 1
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Optimizing two-photon multiple fluorophore imaging of the human trabecular meshwork.
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- Molecular Vision, 2016, v. 22, p. 1
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PCR analysis for assessment of bacterial bioburden in orthokeratology lens cases.
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- Molecular Vision, 2016, v. 22, p. 1
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Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes.
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- Molecular Vision, 2016, v. 22, p. 1
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Proinflammatory cytokines decrease the expression of genes critical for RPE function.
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- Molecular Vision, 2016, v. 22, p. 1
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TNF-α mediates choroidal neovascularization by upregulating VEGF expression in RPE through ROS-dependent β-catenin activation.
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- Molecular Vision, 2016, v. 22, p. 1
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Three-dimensional retinal organoids from mouse pluripotent stem cells mimic in vivo development with enhanced stratification and rod photoreceptor differentiation.
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- Molecular Vision, 2016, v. 22, p. 1
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Identification of intraocular inflammatory mediators in patients with endophthalmitis.
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- Molecular Vision, 2016, v. 22, p. 1
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Chondrocyte-derived extracellular matrix suppresses pathogenesis of human pterygium epithelial cells by blocking the NF-κB signaling pathways.
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- Molecular Vision, 2016, v. 22, p. 1
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Mutation spectrum of the Norrie disease pseudoglioma (NDP) gene in Indian patients with FEVR.
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- Molecular Vision, 2016, v. 22, p. 1
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Increased serum level of homocysteine correlates with retinal nerve fiber layer thinning in diabetic retinopathy.
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- Molecular Vision, 2016, v. 22, p. 1
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Non-toxic retention of nanoceria in murine eyes.
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- Molecular Vision, 2016, v. 22, p. 1
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Neutrophil extracellular traps involvement in corneal fungal infection.
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- Molecular Vision, 2016, v. 22, p. 1
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The synthetic progestin norgestrel acts to increase LIF levels in the rd10 mouse model of retinitis pigmentosa.
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- Molecular Vision, 2016, v. 22, p. 1
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Deficient glucose and glutamine metabolism in Aralar/AGC1/Slc25a12 knockout mice contributes to altered visual function.
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- Molecular Vision, 2016, v. 22, p. 1
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Next-generation sequencing-based method shows increased mutation detection sensitivity in an Indian retinoblastoma cohort.
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- Molecular Vision, 2016, v. 22, p. 1
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NGF increases VEGF expression and promotes cell proliferation via ERK1/2 and AKT signaling in Müller cells.
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- Molecular Vision, 2016, v. 22, p. 1
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A novel start codon mutation of the MERTK gene in a patient with retinitis pigmentosa.
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- Molecular Vision, 2016, v. 22, p. 1
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A novel coculture model of porcine central neuroretina explants and retinal pigment epithelium cells.
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- Molecular Vision, 2016, v. 22, p. 1
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Mutation survey and genotype-phenotype analysis of COL2A1 and COL11A1 genes in 16 Chinese patients with Stickler syndrome.
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- Molecular Vision, 2016, v. 22, p. 1
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Xlinked-heterozygous mutations in ARR3 cause female-limited early onset high myopia.
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- Molecular Vision, 2016, v. 22, p. 1
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Evaluation of treatment for dry eye with 2-hydroxyestradiol using a dry eye rat model.
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- Molecular Vision, 2016, v. 22, p. 1
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Effect of human milk as a treatment for dry eye syndrome in a mouse model.
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- Molecular Vision, 2016, v. 22, p. 1
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Retinal safety of intravitreal rtPA in healthy rats and under excitotoxic conditions.
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- Molecular Vision, 2016, v. 22, p. 1
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The regulatory role of hepatoma-derived growth factor as an angiogenic factor in the eye.
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- Molecular Vision, 2016, v. 22, p. 1
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Genetic and immunohistochemical analysis of HSPA5 in mouse and human retinas.
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- Molecular Vision, 2016, v. 22, p. 1
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Multiplex MALDI-TOF MS detection of mitochondrial variants in Brazilian patients with hereditary optic neuropathy.
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- Molecular Vision, 2016, v. 22, p. 1
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Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosis.
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- Molecular Vision, 2016, v. 22, p. 1
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Characterization of macular structure and function in two Swedish families with genetically identified autosomal dominant retinitis pigmentosa.
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- Molecular Vision, 2016, v. 22, p. 1
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Heat shock protein concentration and clarity of porcine lenses incubated at elevated temperatures.
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- Molecular Vision, 2016, v. 22, p. 1
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Association of a NOS3 gene polymorphism with Behçet's disease but not with Vogt-Koyanagi-Harada syndrome in Han Chinese.
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- Molecular Vision, 2016, v. 22, p. 1
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GLUT1 activity contributes to the impairment of PEDF secretion by the RPE.
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- Molecular Vision, 2016, v. 22, p. 1
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Regulatory effect of chrysin on expression of lenticular calcium transporters, calpains, and apoptotic-cascade components in selenite-induced cataract.
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- Molecular Vision, 2016, v. 22, p. 1
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Loss of Nrf2 exacerbates the visual deficits and optic neuritis elicited by experimental autoimmune encephalomyelitis.
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- Molecular Vision, 2016, v. 22, p. 1
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Changes in posterior scleral collagen microstructure in canine eyes with an ADAMTS10 mutation.
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- Molecular Vision, 2016, v. 22, p. 1
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Stage-specific differentiation of iPSCs toward retinal ganglion cell lineage.
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- Molecular Vision, 2016, v. 22, p. 1
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North Carolina macular dystrophy (MCDR1) caused by a novel tandem duplication of the PRDM13 gene.
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- Molecular Vision, 2016, v. 22, p. 1
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Gene expression changes in the retina following subretinal injection of human neural progenitor cells into a rodent model for retinal degeneration.
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- Molecular Vision, 2016, v. 22, p. 1
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Targeting of exon VI-skipping human RGR-opsin to the plasma membrane of pigment epithelium and co-localization with terminal complement complex C5b-9.
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- Molecular Vision, 2016, v. 22, p. 1
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p27<sup>KIP1</sup> loss promotes proliferation and phagocytosis but prevents epithelial-mesenchymal transition in RPE cells after photoreceptor damage.
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- Molecular Vision, 2016, v. 22, p. 1
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Citrullination of glial intermediate filaments is an early response in retinal injury.
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- Molecular Vision, 2016, v. 22, p. 1
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Next-generation sequencing-based comprehensive molecular analysis of 43 Japanese patients with cone and cone-rod dystrophies.
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- Molecular Vision, 2016, v. 22, p. 1
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Serum molecular signature for proliferative diabetic retinopathy in Saudi patients with type 2 diabetes.
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- Molecular Vision, 2016, v. 22, p. 1
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Involvement of TonEBP/NFAT5 in osmoadaptative response of human retinal pigmented epithelial cells to hyperosmolar stress.
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- Molecular Vision, 2016, v. 22, p. 1
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Variation in PTCHD2, CRISP3, NAP1L4, FSCB, and AP3B2 associated with spherical equivalent.
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- Molecular Vision, 2016, v. 22, p. 1
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A unique lineage gives rise to the meibomian gland.
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- Molecular Vision, 2016, v. 22, p. 1
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Contact-mediated control of radial migration of corneal epithelial cells.
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- Molecular Vision, 2016, v. 22, p. 1
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