Naturally occurring rhodopsin mutation in the dog causes retinal dysfunction and degeneration mimicking human dominant retinitis pigmentosa
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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 CFA9Screening of the arrestin gene in dogs afflicted with generalized progressive retinal atrophyGenetic and phenotypic variations of inherited retinal diseases in dogs: the power of within- and across-breed studiesMan's best friend becomes biology's best in show: genome analyses in the domestic dogCone degeneration following rod ablation in a reversible model of retinal degeneration.In vivo dynamics of retinal injury and repair in the rhodopsin mutant dog model of human retinitis pigmentosaCytochrome P450 2C epoxygenases mediate photochemical stress-induced death of photoreceptors.Progressive retinal atrophy in the Border Collie: a new XLPRA.Operating in the dark: a night-vision system for surgery in retinas susceptible to light damage.CREB1/ATF1 activation in photoreceptor degeneration and protection.From caveman companion to medical innovator: genomic insights into the origin and evolution of domestic dogs.Acute and Protracted Cell Death in Light-Induced Retinal Degeneration in the Canine Model of Rhodopsin Autosomal Dominant Retinitis Pigmentosa.Mutations of the opsin gene (Y102H and I307N) lead to light-induced degeneration of photoreceptors and constitutive activation of phototransduction in mice.A Coding Variant in the Gene Bardet-Biedl Syndrome 4 (BBS4) Is Associated with a Novel Form of Canine Progressive Retinal Atrophy.Chaperoning G protein-coupled receptors: from cell biology to therapeuticsMutation discovered in a feline model of human congenital retinal blinding disease.Leber congenital amaurosis due to RPE65 mutations and its treatment with gene therapyGene augmentation for adRP mutations in RHO.Real-time imaging of rabbit retina with retinal degeneration by using spectral-domain optical coherence tomographyA 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 dogEvaluation of lateral spread of transgene expression following subretinal AAV-mediated gene delivery in dogsRadiation hybrid mapping of cataract genes in the dog.The 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.Exclusion of the unfolded protein response in light-induced retinal degeneration in the canine T4R RHO model of autosomal dominant retinitis pigmentosa.Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutationsIncreased expression of MERTK is associated with a unique form of canine retinopathyGenetically engineered pig models for human diseases.DNA testing and domestic dogsAssessment of hereditary retinal degeneration in the English springer spaniel dog and disease relationship to an RPGRIP1 mutation.Bestrophin gene mutations cause canine multifocal retinopathy: a novel animal model for best diseaseDog star rising: the canine genetic system.Development of lead hammerhead ribozyme candidates against human rod opsin mRNA for retinal degeneration therapy.Light and inherited retinal degeneration.Diseases caused by defects in the visual cycle: retinoids as potential therapeutic agentsClinical light exposure, photoreceptor degeneration, and AP-1 activation: a cell death or cell survival signal in the rhodopsin mutant retina?From vivarium to bedside: lessons learned from animal models.Determining consequences of retinal membrane guanylyl cyclase (RetGC1) deficiency in human Leber congenital amaurosis en route to therapy: residual cone-photoreceptor vision correlates with biochemical properties of the mutants
P2860
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P2860
Naturally occurring rhodopsin mutation in the dog causes retinal dysfunction and degeneration mimicking human dominant retinitis pigmentosa
description
2002 nî lūn-bûn
@nan
2002 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Naturally occurring rhodopsin ...... dominant retinitis pigmentosa
@ast
Naturally occurring rhodopsin ...... dominant retinitis pigmentosa
@en
Naturally occurring rhodopsin ...... dominant retinitis pigmentosa
@nl
type
label
Naturally occurring rhodopsin ...... dominant retinitis pigmentosa
@ast
Naturally occurring rhodopsin ...... dominant retinitis pigmentosa
@en
Naturally occurring rhodopsin ...... dominant retinitis pigmentosa
@nl
prefLabel
Naturally occurring rhodopsin ...... dominant retinitis pigmentosa
@ast
Naturally occurring rhodopsin ...... dominant retinitis pigmentosa
@en
Naturally occurring rhodopsin ...... dominant retinitis pigmentosa
@nl
P2093
P2860
P356
P1476
Naturally occurring rhodopsin ...... dominant retinitis pigmentosa
@en
P2093
Artur V Cideciyan
Brian J Miller
Gregory M Acland
Gustavo D Aguirre
James W Kijas
Susan E Pearce-Kelling
Tomas S Aleman
P2860
P304
P356
10.1073/PNAS.082714499
P407
P577
2002-04-23T00:00:00Z