Molecular ophthalmology: an update on animal models for retinal degenerations and dystrophies - Wikidata - awgldk - TriplyDB

Molecular ophthalmology: an update on animal models for retinal degenerations and dystrophies

Molecular ophthalmology: an update on animal models for retinal degenerations and dystrophies

http://www.wikidata.org/entity/Q33975506

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Neuroprotection in a novel mouse model of multiple sclerosis Visual electrophysiological features of two naturally occurring mouse models with retinal dysfunction Retinal ultrastructure of murine models of dry age-related macular degeneration (AMD).Constitutive overexpression of human erythropoietin protects the mouse retina against induced but not inherited retinal degeneration Absence of functional and structural abnormalities associated with expression of EGFP in the retina.Recombinant AAV-mediated gene transfer to the retina: gene therapy perspectives.Neural prostheses for vision: designing a functional interface with retinal neurons.Classical complement activation and acquired immune response pathways are not essential for retinal degeneration in the rd1 mouse Optical coherence tomography: future trends for imaging in glaucoma A model for transport of membrane-associated phototransduction polypeptides in rod and cone photoreceptor inner segments From vivarium to bedside: lessons learned from animal models.A review of in vivo animal studies in retinal prosthesis research.Photoelectric Dye Used for Okayama University-Type Retinal Prosthesis Reduces the Apoptosis of Photoreceptor Cells.Prosthetic vision: devices, patient outcomes and retinal research.Hereditary Retinal Dystrophy.Phenotypic stability of Pro347Leu rhodopsin transgenic pigs as indicated by photoreceptor cell degeneration.Stanniocalcin-1 rescued photoreceptor degeneration in two rat models of inherited retinal degeneration.The Complement Regulatory Protein CD46 Deficient Mouse Spontaneously Develops Dry-Type Age-Related Macular Degeneration-Like Phenotype.IRD1 and IRD2 mice, naturally occurring models of hereditary retinal dysfunction, show late-onset and progressive retinal degeneration.A functional rhodopsin-green fluorescent protein fusion protein localizes correctly in transgenic Xenopus laevis retinal rods and is expressed in a time-dependent pattern.Phenotypic characterization of P23H and S334ter rhodopsin transgenic rat models of inherited retinal degeneration.Characterization of a novel form of progressive retinal atrophy in Whippet dogs: a clinical, electroretinographic, and breeding study.

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P2860

Molecular ophthalmology: an update on animal models for retinal degenerations and dystrophies

http://www.wikidata.org/entity/Q33975506

description

2000 nî lūn-bûn

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2000 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2000 թվականի օգոստոսին հրատարակված գիտական հոդված

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2000年の論文

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2000年論文

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2000年論文

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2000年論文

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2000年論文

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2000年論文

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2000年论文

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name

Molecular ophthalmology: an up ...... degenerations and dystrophies

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Molecular ophthalmology: an up ...... degenerations and dystrophies

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Molecular ophthalmology: an up ...... degenerations and dystrophies

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Molecular ophthalmology: an up ...... degenerations and dystrophies

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Molecular ophthalmology: an up ...... degenerations and dystrophies

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British Journal of Ophthalmology

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Molecular ophthalmology: an up ...... degenerations and dystrophies

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Grimm C

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Hafezi F

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Remé CE

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Simmen BC

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Wenzel A

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P2860

Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy

Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis

Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa

Insights into the function of Rim protein in photoreceptors and etiology of Stargardt's disease from the phenotype in abcr knockout mice

Mutations in RPE65 cause Leber's congenital amaurosis

Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

Action spectrum of retinal light-damage in albino rats

Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds)

Cochlear and retinal degeneration in the tubby mouse

Suppression of developmental retinal cell death but not of photoreceptor degeneration in Bax-deficient mice

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10.1136/BJO.84.8.922

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8

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