AAV-mediated gene therapy in mouse models of recessive retinal degeneration - Wikidata - wikimedia - TriplyDB

AAV-mediated gene therapy in mouse models of recessive retinal degeneration

AAV-mediated gene therapy in mouse models of recessive retinal degeneration

http://www.wikidata.org/entity/Q27009291

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AAV-mediated cone rescue in a naturally occurring mouse model of CNGA3-achromatopsia Translational models of ocular disease.A Novel, Real-Time, In Vivo Mouse Retinal Imaging System Photoreceptor rescue by an abbreviated human RPGR gene in a murine model of X-linked retinitis pigmentosa.Gene therapy approaches for the treatment of retinal disorders AAV-mediated lysophosphatidylcholine acyltransferase 1 (Lpcat1) gene replacement therapy rescues retinal degeneration in rd11 mice.MicroRNAs in the Neural Retina.Long-term retinal cone rescue using a capsid mutant AAV8 vector in a mouse model of CNGA3-achromatopsia.

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AAV-mediated gene therapy in mouse models of recessive retinal degeneration

http://www.wikidata.org/entity/Q27009291

description

2012 nî lūn-bûn

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2012 թուականի Մարտին հրատարակուած գիտական յօդուած

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2012 թվականի մարտին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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name

AAV-mediated gene therapy in mouse models of recessive retinal degeneration

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AAV-mediated gene therapy in mouse models of recessive retinal degeneration

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AAV-mediated gene therapy in mouse models of recessive retinal degeneration

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type

label

AAV-mediated gene therapy in mouse models of recessive retinal degeneration

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AAV-mediated gene therapy in mouse models of recessive retinal degeneration

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AAV-mediated gene therapy in mouse models of recessive retinal degeneration

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prefLabel

AAV-mediated gene therapy in mouse models of recessive retinal degeneration

@ast

AAV-mediated gene therapy in mouse models of recessive retinal degeneration

@en

AAV-mediated gene therapy in mouse models of recessive retinal degeneration

@nl

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Current Molecular Medicine

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AAV-mediated gene therapy in mouse models of recessive retinal degeneration

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Dai X

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Dinculescu A

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Lei L

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Liu X

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McDowell JH

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Pang JJ

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Shi W

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P2860

Genetic basis of total colourblindness among the Pingelapese islanders

Mutations in the cone photoreceptor G-protein alpha-subunit gene GNAT2 in patients with achromatopsia

Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with retinitis pigmentosa

A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy

Two rhodopsins mediate phototaxis to low- and high-intensity light in Chlamydomonas reinhardtii

CNGA3 mutations in hereditary cone photoreceptor disorders

Null RPGRIP1 alleles in patients with Leber congenital amaurosis.

Retinal dehydrogenase 12 (RDH12) mutations in leber congenital amaurosis

Ectopic expression of a microbial-type rhodopsin restores visual responses in mice with photoreceptor degeneration

Vision 1 year after gene therapy for Leber's congenital amaurosis

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316-30

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10.2174/156652412799218877

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221801028

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22300136

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