Novel rhodopsin mutations Gly114Val and Gln184Pro in dominant retinitis pigmentosa.
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Safranal, a saffron constituent, attenuates retinal degeneration in P23H ratsPrevalence of disease-causing mutations in families with autosomal dominant retinitis pigmentosa: a screen of known genes in 200 familiesRestoration of visual function in P23H rhodopsin transgenic rats by gene delivery of BiP/Grp78Finding and interpreting genetic variations that are important to ophthalmologists.The biochemistry, ultrastructure, and subunit assembly mechanism of AMPA receptors.Mutations in PRPF31 inhibit pre-mRNA splicing of rhodopsin gene and cause apoptosis of retinal cells.Rhodopsin gene expression determines rod outer segment size and rod cell resistance to a dominant-negative neurodegeneration mutantProbing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutations.Correlation between SD-OCT, immunocytochemistry and functional findings in an animal model of retinal degeneration.Spectrum of rhodopsin mutations in French autosomal dominant rod-cone dystrophy patientsCone photoreceptor mosaic disruption associated with Cys203Arg mutation in the M-cone opsinAAV delivery of wild-type rhodopsin preserves retinal function in a mouse model of autosomal dominant retinitis pigmentosa.Haplotypes of RHO polymorphisms and susceptibility to age-related macular degeneration.Genotypic and phenotypic characterization of P23H line 1 rat model.Mislocalization and degradation of human P23H-rhodopsin-GFP in a knockin mouse model of retinitis pigmentosaErythropoietin Slows Photoreceptor Cell Death in a Mouse Model of Autosomal Dominant Retinitis Pigmentosa.Proinsulin slows retinal degeneration and vision loss in the P23H rat model of retinitis pigmentosaLight and inherited retinal degeneration.Pre-mRNA splicing and retinitis pigmentosaStructure and activation of rhodopsin.Disease course in patients with autosomal recessive retinitis pigmentosa due to the USH2A gene.Search for a correlation between telomere length and severity of retinitis pigmentosa due to the dominant rhodopsin Pro23His mutationMutation screening and haplotype analysis of the rhodopsin gene locus in Japanese patients with retinitis pigmentosa.Molecular genetics of retinal degeneration: A Drosophila perspective.Microglia activation in a model of retinal degeneration and TUDCA neuroprotective effects.Inverse agonism of SQ 29,548 and Ramatroban on Thromboxane A2 receptor.Astrocytes and Müller Cell Alterations During Retinal Degeneration in a Transgenic Rat Model of Retinitis Pigmentosa.The molecular and cellular basis of rhodopsin retinitis pigmentosa reveals potential strategies for therapy.Gene panel sequencing in Brazilian patients with retinitis pigmentosa.Retinal Vascular Degeneration in the Transgenic P23H Rat Model of Retinitis Pigmentosa.
P2860
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P2860
Novel rhodopsin mutations Gly114Val and Gln184Pro in dominant retinitis pigmentosa.
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2000 nî lūn-bûn
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2000 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
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2000 թվականի սեպտեմբերին հրատարակված գիտական հոդված
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name
Novel rhodopsin mutations Gly114Val and Gln184Pro in dominant retinitis pigmentosa.
@ast
Novel rhodopsin mutations Gly114Val and Gln184Pro in dominant retinitis pigmentosa.
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type
label
Novel rhodopsin mutations Gly114Val and Gln184Pro in dominant retinitis pigmentosa.
@ast
Novel rhodopsin mutations Gly114Val and Gln184Pro in dominant retinitis pigmentosa.
@en
prefLabel
Novel rhodopsin mutations Gly114Val and Gln184Pro in dominant retinitis pigmentosa.
@ast
Novel rhodopsin mutations Gly114Val and Gln184Pro in dominant retinitis pigmentosa.
@en
P2093
P1476
Novel rhodopsin mutations Gly114Val and Gln184Pro in dominant retinitis pigmentosa
@en
P2093
P304
P407
P577
2000-09-01T00:00:00Z