Congenital stationary night blindness in the dog: common mutation in the RPE65 gene indicates founder effect.
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A frameshift mutation in golden retriever dogs with progressive retinal atrophy endorses SLC4A3 as a candidate gene for human retinal degenerationsThe Finnish lapphund retinal atrophy locus maps to the centromeric region of CFA9RPE65 is the isomerohydrolase in the retinoid visual cycleSafety and efficacy of gene transfer for Leber's congenital amaurosisRecombinant adeno-associated virus type 2-mediated gene delivery into the Rpe65-/- knockout mouse eye results in limited rescueA Naturally Occurring Canine Model of Autosomal Recessive Congenital Stationary Night BlindnessSafety and efficacy of subretinal readministration of a viral vector in large animals to treat congenital blindnessGenetic and phenotypic variations of inherited retinal diseases in dogs: the power of within- and across-breed studiesMolecular origins of rapid and continuous morphological evolutionAssessment of Rod, Cone, and Intrinsically Photosensitive Retinal Ganglion Cell Contributions to the Canine Chromatic Pupillary ResponseEfficient non-viral ocular gene transfer with compacted DNA nanoparticles.Reversal of blindness in animal models of leber congenital amaurosis using optimized AAV2-mediated gene transferEvaluation of a behavioral method for objective vision testing and identification of achromatopsia in dogs.From caveman companion to medical innovator: genomic insights into the origin and evolution of domestic dogs.RPE65: role in the visual cycle, human retinal disease, and gene therapy.Using the NAFX to measure the effectiveness over time of gene therapy in canine LCARod-derived cone viability factor for treating blinding diseases: from clinic to redox signalingMolecular ophthalmology: an update on animal models for retinal degenerations and dystrophiesLeber congenital amaurosis due to RPE65 mutations and its treatment with gene therapyThe retinal pigment epithelium in health and diseaseNaturally occurring rhodopsin mutation in the dog causes retinal dysfunction and degeneration mimicking human dominant retinitis pigmentosaRetinal degeneration in animal models with a defective visual cycle.A novel form of progressive retinal atrophy in Swedish vallhund dogsA naturally occurring mutation of the opsin gene (T4R) in dogs affects glycosylation and stability of the G protein-coupled receptor.The genetics of eye disorders in the dogQLT091001, a 9-cis-retinal analog, is well-tolerated by retinas of mice with impaired visual cycles.Altered expression of retinal molecular markers in the canine RPE65 model of Leber congenital amaurosisThe domestic cat as a large animal model for characterization of disease and therapeutic intervention in hereditary retinal blindness.A CNGB1 frameshift mutation in Papillon and Phalène dogs with progressive retinal atrophy.Therapeutic challenges to retinitis pigmentosa: from neuroprotection to gene therapy.Proof of concept for AAV2/5-mediated gene therapy in iPSC-derived retinal pigment epithelium of a choroideremia patient.Canine tricuspid valve malformation, a model of human Ebstein anomaly, maps to dog chromosome 9.Histopathology and functional correlations in a patient with a mutation in RPE65, the gene for retinol isomerase.Increased expression of MERTK is associated with a unique form of canine retinopathyThe newt (Cynops pyrrhogaster) RPE65 promoter: molecular cloning, characterization and functional analysis.Non-viral therapeutic approaches to ocular diseases: An overview and future directionsFinding cardiovascular disease genes in the dog.Diseases caused by defects in the visual cycle: retinoids as potential therapeutic agentsHuman retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvementClinical light exposure, photoreceptor degeneration, and AP-1 activation: a cell death or cell survival signal in the rhodopsin mutant retina?
P2860
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P2860
Congenital stationary night blindness in the dog: common mutation in the RPE65 gene indicates founder effect.
description
1998 nî lūn-bûn
@nan
1998 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Congenital stationary night bl ...... gene indicates founder effect.
@ast
Congenital stationary night bl ...... gene indicates founder effect.
@en
type
label
Congenital stationary night bl ...... gene indicates founder effect.
@ast
Congenital stationary night bl ...... gene indicates founder effect.
@en
prefLabel
Congenital stationary night bl ...... gene indicates founder effect.
@ast
Congenital stationary night bl ...... gene indicates founder effect.
@en
P2093
P1433
P1476
Congenital stationary night bl ...... gene indicates founder effect
@en
P2093
Aguirre GD
Narfström K
Pearce-Kelling S
P577
1998-10-30T00:00:00Z