Gene therapy restores vision in rd1 mice after removal of a confounding mutation in Gpr179 - Wikidata - wikimedia - TriplyDB

Gene therapy restores vision in rd1 mice after removal of a confounding mutation in Gpr179

Gene therapy restores vision in rd1 mice after removal of a confounding mutation in Gpr179

http://www.wikidata.org/entity/Q30626026

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Axial Spondylometaphyseal Dysplasia Is Caused by C21orf2 Mutations Rebuilding the Missing Part-A Review on Photoreceptor Transplantation Donor and host photoreceptors engage in material transfer following transplantation of post-mitotic photoreceptor precursors.A novel immunodeficient NOD.SCID-rd1 mouse model of retinitis pigmentosa to investigate potential therapeutics and pathogenesis of retinal degeneration Spatially and Temporally Regulated NRF2 Gene Therapy Using Mcp-1 Promoter in Retinal Ganglion Cell Injury.CLINICAL PROGRESS IN INHERITED RETINAL DEGENERATIONS: GENE THERAPY CLINICAL TRIALS AND ADVANCES IN GENETIC SEQUENCING.Variable phenotypic expressivity in inbred retinal degeneration mouse lines: A comparative study of C3H/HeOu and FVB/N rd1 mice Survey of the nob5 mutation in C3H substrains.Circadian and light-driven regulation of rod dark adaptation.Advances in Gene Therapy for Diseases of the Eye.Insights from Genetic Model Systems of Retinal Degeneration: Role of Epsins in Retinal Angiogenesis and VEGFR2 Signaling.In vivo cellular imaging of various stress/response pathways using AAV following axonal injury in mice.AAV-mediated Gene Therapy Halts Retinal Degeneration in PDE6β-deficient Dogs.Emerging therapies for inherited retinal degeneration.Tropism of engineered and evolved recombinant AAV serotypes in the rd1 mouse and ex vivo primate retina.Gene Therapy in a Large Animal Model of PDE6A-Retinitis Pigmentosa.Development of an optimized AAV2/5 gene therapy vector for Leber congenital amaurosis owing to defects in RPE65.The neuroprotective effect of hesperidin in NMDA-induced retinal injury acts by suppressing oxidative stress and excessive calpain activation.Prefrontal cortical control of a brainstem social behavior circuit.Evaluation of micro Electroretinograms Recorded with Multiple Electrode Array to Assess Focal Retinal Function.Genetic rescue models refute nonautonomous rod cell death in retinitis pigmentosa.Light and the laboratory mouse.Tissue inhibitor of metalloproteinases 1 enhances rod survival in the rd1 mouse retina.Prevention of Photoreceptor Cell Loss in a Cln6 Mouse Model of Batten Disease Requires CLN6 Gene Transfer to Bipolar Cells Retained Plasticity and Substantial Recovery of Rod-Mediated Visual Acuity at the Visual Cortex in Blind Adult Mice with Retinal Dystrophy Reliable detection of low visual acuity in mice with pattern visually evoked potentials

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Gene therapy restores vision in rd1 mice after removal of a confounding mutation in Gpr179

http://www.wikidata.org/entity/Q30626026

description

2015 nî lūn-bûn

@nan

2015 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի հունվարին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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name

Gene therapy restores vision i ...... confounding mutation in Gpr179

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Gene therapy restores vision i ...... confounding mutation in Gpr179

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type

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Gene therapy restores vision i ...... confounding mutation in Gpr179

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Gene therapy restores vision i ...... confounding mutation in Gpr179

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prefLabel

Gene therapy restores vision i ...... confounding mutation in Gpr179

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Gene therapy restores vision i ...... confounding mutation in Gpr179

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Nature Communications

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Gene therapy restores vision i ...... confounding mutation in Gpr179

@en

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Alexander J Smith

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Joana Ribeiro

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Kate Powell

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Koji M Nishiguchi

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Matteo Rizzi

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Robin R Ali

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Selina A Azam

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Sophia-Martha kleine Holthaus

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Ulrich F O Luhmann

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Yanai Duran

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P2860

GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness

Differential modulation of retinal degeneration by Ccl2 and Cx3cr1 chemokine signalling

Assessment and in vivo scoring of murine experimental autoimmune uveoretinitis using optical coherence tomography

Fiji: an open-source platform for biological-image analysis.

Identification of the gene and the mutation responsible for the mouse nob phenotype

Restoration of vision in the pde6β-deficient dog, a large animal model of rod-cone dystrophy

Photoreceptor cell rescue in retinal degeneration (rd) mice by in vivo gene therapy

Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod cGMP-phosphodiesterase.

Gene therapy with a promoter targeting both rods and cones rescues retinal degeneration caused by AIPL1 mutations

The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses

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10.1038/NCOMMS7006

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6

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Livia S. Carvalho

James W. Bainbridge

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2015-01-23T00:00:00Z

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271331115

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