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Article

Retinal degeneration in Aipl1-deficient mice: a new genetic model of Leber congenital amaurosis

13 Nov 2004

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Share to Glaucoma and retinal disorders
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 15582159
DOI: 10.1016/j.molbrainres.2004.10.011

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Related research

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Retinal degeneration in Aipl1-deficient mice: a new genetic model of Leber congenital amaurosisPMID 15582159Read ↗

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

Leber congenital amaurosis: Genes, proteins and disease mechanismsSemantic proximity Read ↗

AIPL1, the protein that is defective in Leber congenital amaurosis, is essential for the biosynthesis of retinal rod cGMP phosphodiesterase.Semantic proximity Read ↗

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

Leber congenital amaurosis, from darkness to light: An ode to Irene Maumenee.Semantic proximity Read ↗

Molecular genetics of Leber congenital amaurosis.Semantic proximity Read ↗

The phenotype of Leber congenital amaurosis in patients with AIPL1 mutations.Semantic proximity Read ↗

Clinical and Molecular Characterization of AIPL1-Associated Leber Congenital Amaurosis/Early-Onset Severe Retinal Dystrophy.Semantic proximity Read ↗

Predominant rod photoreceptor degeneration in Leber congenital amaurosis.Semantic proximity Read ↗

Prenatal human ocular degeneration occurs in Leber's Congenital Amaurosis (LCA1 and 2).Semantic proximity Read ↗

Retinal Organoids from an AIPL1 CRISPR/Cas9 Knockout Cell Line Successfully Recapitulate the Molecular Features of LCA4 DiseaseSemantic proximity Read ↗

The Leber congenital amaurosis gene product AIPL1 is localized exclusively in rod photoreceptors of the adult human retinaSemantic proximity Read ↗

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