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INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, ISSN 0146-0404, 03/2019, Volume 60, Issue 4, pp. 1265 - 1274
PURPOSE. MicroRNA-182 (miR-182) is abundantly expressed in mammalian retinas; however, the association between miR-182 and retinal function remains unclear. In... 
SURVIVAL | retinal dystrophy | photoreceptor | LARGE COHORT | INACTIVATION | IMPACT | DYSTROPHY | ROLES | miR-182 | electroretinogram | MICRORNA GENE-REGULATION | OPHTHALMOLOGY | MUTATIONS | CLUSTER
Journal Article
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 2, pp. e17084 - e17084
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2016, Volume 11, Issue 3, pp. e0149663 - e0149663
Journal Article
Journal of Cellular Biochemistry, ISSN 0730-2312, 08/2019, Volume 120, Issue 8, pp. 13881 - 13892
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 06/2017, Volume 114, Issue 24, pp. 6376 - 6381
MicroRNAs (miRNAs) are known to be essential for retinal maturation and functionality; however, the role of the most abundant miRNAs, the miR-183/96/182... 
Degeneration | Regulation | Mir-183/96/182 cluster | Taurine transporter | Photoreceptor | RETINAL DEGENERATION | MULTIDISCIPLINARY SCIENCES | photoreceptor | taurine transporter | MODEL | MICRORNAS | TAURINE DEFICIENCY | degeneration | INACTIVATION | OVEREXPRESSION | regulation | miR-183/96/182 cluster | DIFFERENTIATION | MIR-96 | RETINITIS-PIGMENTOSA | EXPRESSION | Electroretinography | Membrane Glycoproteins - metabolism | Retinal Degeneration - genetics | Epigenesis, Genetic | Mice, Inbred C57BL | Gene Expression Regulation | Mice, Transgenic | MicroRNAs - metabolism | Gene Knockout Techniques | Retinal Degeneration - metabolism | Membrane Glycoproteins - genetics | Mice, Knockout | Animals | Membrane Transport Proteins - genetics | Color Vision - physiology | Retinal Cone Photoreceptor Cells - pathology | Membrane Transport Proteins - metabolism | Night Vision - physiology | Mice | MicroRNAs - genetics | Photoreceptor Cells, Vertebrate - metabolism | Retinal Degeneration - pathology | Photoreceptor Cells, Vertebrate - pathology | Retinal Cone Photoreceptor Cells - metabolism | Photoreceptors | Health aspects | MicroRNA | Photoreception | Maturation | MiRNA | Retina | Viruses | Maintenance | Nuclei | Ablation | Dislocations | Electroretinograms | Rodents | Clusters | Age | Index Medicus | 182 cluster | Biological Sciences | miR-183
Journal Article
Human Mutation, ISSN 1059-7794, 08/2019, Volume 40, Issue 8, pp. 1039 - 1045
Retinitis pigmentosa (RP) is the most common manifestation of inherited retinal diseases with high degree of genetic, allelic, and phenotypic heterogeneity.... 
nonsyndromic RP | CEP250 | cilia | knockin mice | retinal dysfunction | GENOTYPE-PHENOTYPE CORRELATION | CENTROSOME | DEGENERATION | PROTEIN C-NAP1 | DYSTROPHY | GENETICS | GENETICS & HEREDITY | MUTATIONS | LINKER | CEP78 | Retinal diseases | Animal models | Phenotypes | Retinitis pigmentosa | Retina | Photoreceptors | Retinitis | Mutation | Electroretinograms | Index Medicus
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 1120 - 9
High myopia (HM) is a leading cause of mid-way blindness with a high heritability in East Asia. Although only a few disease genes have been reported, a small... 
REFRACTIVE ERROR | ONSET HIGH MYOPIA | PROTEIN | MULTIDISCIPLINARY SCIENCES | VISUAL IMPAIRMENT | ENVIRONMENT | GENETIC-VARIANTS | SUSCEPTIBILITY LOCUS | PREVALENCE | HIGH-GRADE MYOPIA | GENOME-WIDE ASSOCIATION | Pathogenicity | Heritability | Missense mutation | Mutation | Myopia | Blindness | Index Medicus
Journal Article