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Article

New views on RPE65 deficiency: the rod system is the source of vision in a mouse model of Leber congenital amaurosis

20 Aug 2001

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Share to Photoreceptor and optogenetics research
Share to Retinal Development and Disorders
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 11528395
DOI: 10.1038/ng712

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Related research

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New views on RPE65 deficiency: the rod system is the source of vision in a mouse model of Leber congenital amaurosisPMID 11528395Read ↗

Gene Therapy Restores Vision-Dependent Behavior as Well as Retinal Structure and Function in a Mouse Model of RPE65 Leber Congenital AmaurosisSemantic proximity Read ↗

An overview of leber congenital amaurosis: a model to understand human retinal developmentSemantic proximity Read ↗

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Protection of Rpe65-deficient mice identifies rhodopsin as a mediator of light-induced retinal degenerationSemantic proximity Read ↗

Mouse Models as Tools to Identify Genetic Pathways for Retinal Degeneration, as Exemplified by Leber's Congenital Amaurosis.Semantic proximity Read ↗

<i>RPE65</i> knockout <i>Xenopus laevis</i> have a compromised but detectable electroretinogram and altered visual responses, without retinal degeneration or altered melanophore dispersionSemantic proximity Read ↗

Retinal degeneration in Aipl1-deficient mice: a new genetic model of Leber congenital amaurosisSemantic proximity Read ↗

Human cone photoreceptor dependence on RPE65 isomeraseSemantic proximity Read ↗

Leber congenital amaurosis due to RPE65 mutations and its treatment with gene therapy.Semantic proximity Read ↗

In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell death.Semantic proximity Read ↗

Retinal degeneration in the mouse is rodless retina.Semantic proximity Read ↗

Inverse correlation between fatty acid transport protein 4 and vision in Leber congenital amaurosis associated with RPE65 mutation.Semantic proximity Read ↗

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