Inner retina remodeling in a mouse model of stargardt-like macular dystrophy (STGD3). - Wikidata - wikimedia - TriplyDB

Inner retina remodeling in a mouse model of stargardt-like macular dystrophy (STGD3).

Inner retina remodeling in a mouse model of stargardt-like macular dystrophy (STGD3).

http://www.wikidata.org/entity/Q33844987

about

Early alteration of retinal neurons in Aipl1-/- animals.Role of ELOVL4 and very long-chain polyunsaturated fatty acids in mouse models of Stargardt type 3 retinal degeneration.Mouse Models of Stargardt 3 Dominant Macular Degeneration Retinal degeneration increases susceptibility to myopia in mice.Elovl4 5-bp deletion does not accelerate cone photoreceptor degeneration in an all-cone mouse.Early impairment of the full-field photopic negative response in patients with Stargardt disease and pathogenic variants of the ABCA4 gene.A Third-Generation Lipid Emulsion that Contains n-3 Long-Chain PUFAs Preserves Retinal Function in Parenterally Fed Neonatal Piglets.Photoreceptor-induced RPE phagolysosomal maturation defects in Stargardt-like Maculopathy (STGD3).

P2860

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P2860

Inner retina remodeling in a mouse model of stargardt-like macular dystrophy (STGD3).

http://www.wikidata.org/entity/Q33844987

description

2009 nî lūn-bûn

@nan

2009 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年論文

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2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

@wuu

name

Inner retina remodeling in a mouse model of stargardt-like macular dystrophy (STGD3).

@ast

Inner retina remodeling in a mouse model of stargardt-like macular dystrophy (STGD3).

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type

label

Inner retina remodeling in a mouse model of stargardt-like macular dystrophy (STGD3).

@ast

Inner retina remodeling in a mouse model of stargardt-like macular dystrophy (STGD3).

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prefLabel

Inner retina remodeling in a mouse model of stargardt-like macular dystrophy (STGD3).

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Inner retina remodeling in a mouse model of stargardt-like macular dystrophy (STGD3).

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Investigative Ophthalmology & Visual Science

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Inner retina remodeling in a mouse model of stargardt-like macular dystrophy (STGD3).

@en

P2093

Frédéric Gaillard

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Janet R Sparrow

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Kang Zhang

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Paul R Freund

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Sharee Kuny

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Yves Sauvé

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P2860

A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy

Dominant negative mechanism underlies autosomal dominant Stargardt-like macular dystrophy linked to mutations in ELOVL4

Retinal pathology and skin barrier defect in mice carrying a Stargardt disease-3 mutation in elongase of very long chain fatty acids-4

Structural homeostasis: compensatory adjustments of dendritic arbor geometry in response to variations of synaptic input

Syntaxin 3 and SNAP-25 pairing, regulated by omega-3 docosahexaenoic acid, controls the delivery of rhodopsin for the biogenesis of cilia-derived sensory organelles, the rod outer segments

Autosomal dominant Stargardt-like macular dystrophy: I. Clinical characterization, longitudinal follow-up, and evidence for a common ancestry in families linked to chromosome 6q14

Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q

Atrophic macular degeneration mutations in ELOVL4 result in the intracellular misrouting of the protein

Association of adipose and red blood cell lipids with severity of dominant Stargardt macular dystrophy (STGD3) secondary to an ELOVL4 mutation

Role of Stargardt-3 macular dystrophy protein (ELOVL4) in the biosynthesis of very long chain fatty acids

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2248-2262

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scholarly article

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10.1167/IOVS.09-4718

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4

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51

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Silvina C. Mema

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2009-11-20T00:00:00Z

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40026558

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19933199

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2868397

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