Works matching IS 10900535 AND DT 2020 AND VI 26
Results: 71
In vitro generation of primary cultures of human hyalocytes.
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- Molecular Vision, 2020, v. 26, p. 818
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- Article
Osmotic regulation of aquaporin-8 expression in retinal pigment epithelial cells in vitro: Dependence on K<sub>ATP</sub> channel activation.
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- Molecular Vision, 2020, v. 26, p. 797
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A hospital-based five-year prospective study on the prevalence of Leber's hereditary optic neuropathy with genetic confirmation.
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- Molecular Vision, 2020, v. 26, p. 789
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The regulatory role of vasoactive intestinal peptide in lacrimal gland ductal fluid secretion: A new piece of the puzzle in tear production.
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- Molecular Vision, 2020, v. 26, p. 780
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Single-cell transcriptomic profiling provides insights into retinal endothelial barrier properties.
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- Molecular Vision, 2020, v. 26, p. 766
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- Article
A mutation in DOP1B identified as a probable cause for autosomal recessive Peters anomaly in a consanguineous family.
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- Molecular Vision, 2020, v. 26, p. 757
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Role of inhibitor of differentiation 3 gene in cellular differentiation of human corneal stromal fibroblasts.
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- Molecular Vision, 2020, v. 26, p. 742
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Arteriovenous crossing in retinal vessels of mice, rats, and pigs.
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- Molecular Vision, 2020, v. 26, p. 731
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Levels of the oxidative stress biomarker malondialdehyde in tears of patients with central serous chorioretinopathy relate to disease activity.
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- Molecular Vision, 2020, v. 26, p. 722
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Inflammation and diabetic retinopathy.
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- Molecular Vision, 2020, v. 26, p. 718
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An optimized protocol for retina single-cell RNA sequencing.
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- Molecular Vision, 2020, v. 26, p. 705
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- Article
Neuroprotective effects of Acer palmatum thumb. leaf extract (KIOM-2015E) against ischemia/reperfusion-induced injury in the rat retina.
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- Molecular Vision, 2020, v. 26, p. 691
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- Article
Ablation of C3 modulates macrophage reactivity in the outer retina during photo-oxidative damage.
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- Molecular Vision, 2020, v. 26, p. 679
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- Article
A large deletion spanning PITX2 and PANCR in a Chinese family with Axenfeld-Rieger syndrome.
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- Molecular Vision, 2020, v. 26, p. 670
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Genetic and environmental risk factors for extramacular drusen.
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- Molecular Vision, 2020, v. 26, p. 661
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Review: Intraflagellar transport proteins in the retina.
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- Molecular Vision, 2020, v. 26, p. 652
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Tofacitinib inhibits the development of experimental autoimmune uveitis and reduces the proportions of Th1 but not of Th17 cells.
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- Molecular Vision, 2020, v. 26, p. 641
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- Article
Alterations in proteome of human sclera associated with primary open-angle glaucoma involve proteins participating in regulation of the extracellular matrix.
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- Molecular Vision, 2020, v. 26, p. 623
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- Article
The impact of the c.5603A>T hypomorphic variant on founder mutation screening of ABCA4 for Stargardt disease in South Africa.
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- Molecular Vision, 2020, v. 26, p. 613
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CP49 and filensin intermediate filaments are essential for formation of cold cataract.
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- Molecular Vision, 2020, v. 26, p. 603
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Genotypes and phenotypes of genes associated with achromatopsia: A reference for clinical genetic testing.
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- Molecular Vision, 2020, v. 26, p. 588
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TRPV1, TRPA1, and TRPM8 are expressed in axon terminals in the cornea: TRPV1 axons contain CGRP and secretogranin II; TRPA1 axons contain secretogranin 3.
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- Molecular Vision, 2020, v. 26, p. 576
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Full retraction: Sasirekha Krishnan, Shruthi Lakshmanan, Geetha Krishnan Iyer, Krishnan UmaMaheswari, Subramanian Krishnakumar. The role of signaling pathways in the expansion of corneal epithelial cells in serum-free B27 supplemented medium. Mol Vis. 2010; 16:1169-1177
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- Molecular Vision, 2020, v. 26, p. 575
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- Article
Erratum: Inhibitory effects of S100A4 gene silencing on alkali burn-induced corneal neovascularization: an in vivo study.
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- Molecular Vision, 2020, v. 26, p. 574
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- Article
Accumulation of Asn450Tyr mutant myocilin in ER promotes apoptosis of human trabecular meshwork cells.
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- Molecular Vision, 2020, v. 26, p. 563
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Thrombin alters the synthesis and processing of CYR61/CCN1 in human corneal stromal fibroblasts and myofibroblasts through multiple distinct mechanisms.
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- Molecular Vision, 2020, v. 26, p. 540
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Changes in melatonin receptor expression in a murine model of glaucoma.
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- Molecular Vision, 2020, v. 26, p. 530
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Interleukin-6 promotes proliferative vitreoretinopathy by inducing epithelial-mesenchymal transition via the JAK1/STAT3 signaling pathway.
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- Molecular Vision, 2020, v. 26, p. 517
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Immunohistochemical study of STAT3, HIF-1a and VEGF in pterygium and normal conjunctiva: Experimental research and literature review.
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- Molecular Vision, 2020, v. 26, p. 510
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Genetic factors associated with treatment response to reducedfluence photodynamic therapy for chronic central serous chorioretinopathy.
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- Molecular Vision, 2020, v. 26, p. 505
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Tetramethylpyrazine protects mice retinas against sodium iodate-induced oxidative injury.
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- Molecular Vision, 2020, v. 26, p. 494
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Differential DNA methylation patterns in human Schlemm's canal endothelial cells with glaucoma.
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- Molecular Vision, 2020, v. 26, p. 483
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Correlations between vitreous cytokine levels and inflammatory cells in fibrovascular membranes of patients with proliferative diabetic retinopathy.
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- Molecular Vision, 2020, v. 26, p. 472
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The use of Matrigel combined with encapsulated cell technology to deliver a complement inhibitor in a mouse model of choroidal neovascularization.
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- Molecular Vision, 2020, v. 26, p. 370
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The correlation of cytokines and sensory hypersensitivity in mild dry eye patients characterized by symptoms outweighing signs.
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- Molecular Vision, 2020, v. 26, p. 359
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A systems genetics approach to revealing the Pdgfb molecular network of the retina.
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- Molecular Vision, 2020, v. 26, p. 459
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Review: Role of cAMP signaling in diabetic retinopathy.
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- Molecular Vision, 2020, v. 26, p. 355
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Clinical heterogeneity in retinitis pigmentosa caused by variants in RP1 and RLBP1 in five extended consanguineous pedigrees.
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- Molecular Vision, 2020, v. 26, p. 445
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Analysis of variants in Chinese individuals with primary openangle glaucoma using molecular inversion probe (MIP)-based panel sequencing.
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- Molecular Vision, 2020, v. 26, p. 378
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Clinical, histopathological, and in silico pathogenicity analyses in a pedigree with familial amyloidosis of the Finnish type (Meretoja syndrome) caused by a novel gelsolin mutation.
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- Molecular Vision, 2020, v. 26, p. 345
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Technical brief: Direct, real-time electrochemical measurement of nitric oxide in ex vivo cultured human corneoscleral segments.
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- Molecular Vision, 2020, v. 26, p. 434
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Biallelic RP1-associated retinal dystrophies: Expanding the mutational and clinical spectrum.
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- Molecular Vision, 2020, v. 26, p. 423
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Tyrosine triple mutated AAV2-BDNF gene therapy in an inner retinal injury model induced by intravitreal injection of N-methyl-D-aspartate (NMDA).
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- Molecular Vision, 2020, v. 26, p. 409
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Mutations in FYCO1 identified in families with congenital cataracts.
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- Molecular Vision, 2020, v. 26, p. 334
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A pilot study to assess the effect of a three-month vitamin supplementation containing L-methylfolate on systemic homocysteine plasma concentrations and retinal blood flow in patients with diabetes.
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- Molecular Vision, 2020, v. 26, p. 326
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Effect of vitamin B<sub>12</sub> supplementation on retinal lesions in diabetic rats.
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- Molecular Vision, 2020, v. 26, p. 311
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A unique PRDM13-associated variant in a Georgian Jewish family with probable North Carolina macular dystrophy and the possible contribution of a unique CFH variant.
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- Molecular Vision, 2020, v. 26, p. 299
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Clinical findings and RS1 genotype in 90 Chinese families with X-linked retinoschisis.
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- Molecular Vision, 2020, v. 26, p. 291
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Proinflammatory cytokines trigger biochemical and neurochemical changes in mouse retinal explants exposed to hyperglycemic conditions.
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- Molecular Vision, 2020, v. 26, p. 277
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Long-term evaluation of retinal morphology and function in a mouse model of oxygen-induced retinopathy.
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- Molecular Vision, 2020, v. 26, p. 257
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