Works matching IS 10900535 AND DT 2022 AND VI 28
Results: 44
Safety evaluation and pharmacodynamics of minocycline hydrochloride eye drops.
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- Molecular Vision, 2022, v. 28, p. 460
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Analysis of hemopexin plasma levels in patients with age-related macular degeneration.
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- Molecular Vision, 2022, v. 28, p. 536
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Chronic ocular sequelae in Stevens--Johnson syndrome: a genetic association study.
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- Molecular Vision, 2022, v. 28, p. 526
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PET imaging of retinal inflammation in mice exposed to blue light using [<sup>18</sup>F]-DPA-714.
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- Molecular Vision, 2022, v. 28, p. 507
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Epac1 and PKA agonists inhibit ROS to reduce NLRP3 inflammasome proteins in retinal endothelial cells.
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- Molecular Vision, 2022, v. 28, p. 500
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Novel segmentation algorithm for high-throughput analysis of spectral domain-optical coherence tomography imaging of teleost retinas.
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- Molecular Vision, 2022, v. 28, p. 492
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Whole exome sequencing revealed novel pathogenic variants in Vietnamese patients with FEVR.
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- Molecular Vision, 2022, v. 28, p. 480
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Psychological stress induces moderate pathology in the ganglion cell layer in mice.
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- Molecular Vision, 2022, v. 28, p. 451
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Lipoxin A4 alleviates inflammation in Aspergillus fumigatus--stimulated human corneal epithelial cells by Nrf2/HO-1 signaling pathway.
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- Molecular Vision, 2022, v. 28, p. 441
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In vitro induction and intraocular application in oxygen-induced retinopathy of adipose-derived mesenchymal stem cells.
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- Molecular Vision, 2022, v. 28, p. 432
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Neural differentiation of human retinal pigment epithelial cells on alginate/gelatin substrate.
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- Molecular Vision, 2022, v. 28, p. 412
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Morphological, biochemical, and transcriptomic characterization of iPSC-derived human RPE cells from normal and Smith-Lemli-Opitz syndrome patients.
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- Molecular Vision, 2022, v. 28, p. 394
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Sulforaphane recovers cone function in an Nrf2-dependent manner in middle-aged mice undergoing RPE oxidative stress.
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- Molecular Vision, 2022, v. 28, p. 378
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Association of IGF1 polymorphisms with exotropia in a Pakistani cohort.
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- Molecular Vision, 2022, v. 28, p. 369
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Autosomal dominant retinitis pigmentosa with incomplete penetrance due to an intronic mutation of the PRPF31 gene.
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- Molecular Vision, 2022, v. 28, p. 359
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Clinical and genetic studies of 17 Han Chinese pedigrees and 31 sporadic patients with blepharophimosis-ptosis-epicanthus inversus syndrome.
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- Molecular Vision, 2022, v. 28, p. 352
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Oxidative stress alters transcript localization of disease-associated genes in the retinal pigment epithelium.
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- Molecular Vision, 2022, v. 28, p. 340
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Isolation efficiency of collagenase and EDTA for the culture of corneal endothelial cells.
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- Molecular Vision, 2022, v. 28, p. 331
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Structural and functional analysis of SNP rs76740365 G>A in exon-3 of the alpha A-crystallin gene in lens epithelial cells.
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- Molecular Vision, 2022, v. 28, p. 317
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A five-year follow-up of ABCA4 carriers showing deterioration of retinal function and increased structural changes.
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- Molecular Vision, 2022, v. 28, p. 300
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Nestin contributes to laser choroidal and retinal neovascularization.
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- Molecular Vision, 2022, v. 28, p. 280
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The long noncoding RNA MALAT1/microRNA-598-3p axis regulates the proliferation and apoptosis of retinoblastoma cells through the PI3K/AKT pathway.
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- Molecular Vision, 2022, v. 28, p. 269
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The phenotypic spectrum of ADAMTSL4-associated ectopia lentis: Additional cases, complications, and review of literature.
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- Molecular Vision, 2022, v. 28, p. 257
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Hyposmotic stress causes ATP release in a discrete zone within the outer cortex of rat lens.
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- Molecular Vision, 2022, v. 28, p. 245
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Untargeted metabolomic analysis of aqueous humor in diabetic macular edema.
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- Molecular Vision, 2022, v. 28, p. 230
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Using optical coherence tomography angiography as a biomarker of retinopathy severity and treatment for diabetic retinopathy.
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- Molecular Vision, 2022, v. 28, p. 220
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Identification of numerous novel disease-causing variants in patients with inherited retinal diseases, combining careful clinical-functional phenotyping with systematic, broad NGS panel-based genotyping.
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- Molecular Vision, 2022, v. 28, p. 203
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Dopachrome tautomerase is a retinoblastoma-specific gene, and its proximal promoter is preferentially active in human retinoblastoma cells.
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- Molecular Vision, 2022, v. 28, p. 192
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Hsa-miR-150-5p inhibits Wnt-β-catenin signaling in human corneal epithelial stem cells.
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- Molecular Vision, 2022, v. 28, p. 178
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Oral administration of a dual ET<sub>A</sub>/ET<sub>B</sub> receptor antagonist promotes neuroprotection in a rodent model of glaucoma.
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- Molecular Vision, 2022, v. 28, p. 165
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aA and aB peptides from human cataractous lenses show antichaperone activity and enhance aggregation of lens proteins.
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- Molecular Vision, 2022, v. 28, p. 147
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Review: New horizons in retinoblastoma treatment: an updated review article.
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- Molecular Vision, 2022, v. 28, p. 130
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TNFAIP3 is anti-inflammatory in the retinal vasculature.
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- Molecular Vision, 2022, v. 28, p. 124
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Diquafosol ophthalmic solution enhances mucin expression via ERK activation in human conjunctival epithelial cells with hyperosmotic stress.
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- Molecular Vision, 2022, v. 28, p. 114
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Whole-exome sequencing identified genes known to be responsible for retinitis pigmentosa in 28 Chinese families.
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- Molecular Vision, 2022, v. 28, p. 96
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Comprehensive circular RNA expression profiling with associated ceRNA network in orbital venous malformation.
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- Molecular Vision, 2022, v. 28, p. 83
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Protective effect of Glutaredoxin 1 against oxidative stress in lens epithelial cells of age-related nuclear cataracts.
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- Molecular Vision, 2022, v. 28, p. 70
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Novel SIX6 mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia.
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- Molecular Vision, 2022, v. 28, p. 57
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Novel homozygous mutations in the transcription factor NRL cause non-syndromic retinitis pigmentosa.
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- Molecular Vision, 2022, v. 28, p. 48
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Glial cell line-derived neurotrophic factor (GDNF) in patients with primary open-angle glaucoma and age-related cataract.
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- Molecular Vision, 2022, v. 28, p. 39
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Ocular manifestations of Chinese patients with copy number variants in the NDP gene.
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- Molecular Vision, 2022, v. 28, p. 29
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Relatively mild blue cone monochromacy phenotype caused by various haplotypes in the L- and M-cone opsin genes.
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- Molecular Vision, 2022, v. 28, p. 21
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GPX1 knockout, not catalase knockout, causes accelerated abnormal optical aberrations and cataract in the aging lens.
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- Molecular Vision, 2022, v. 28, p. 11
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Association of ABCA1 (rs2472493) and GAS7 (rs9913911) gene variants with primary open-angle glaucoma in a Brazilian population.
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- Molecular Vision, 2022, v. 28, p. 1
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