Insights into the function of Rim protein in photoreceptors and etiology of Stargardt's disease from the phenotype in abcr knockout mice (Q28140171)

Gene Ontology release 2020-05-02

Gene Ontology ID

GO:0140347

ATP-binding cassette, sub-family A (ABC1), member 4

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GOA release 2020-03-11

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J Weng

1

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N L Mata

2

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S M Azarian

3

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R T Tzekov

4

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D G Birch

5

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G H Travis

Prolonged rod dark adaptation in retinitis pigmentosa

6

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language of work or name

English

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publication date

9 July 1999

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published in

Cell

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volume

98

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issue

1

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page(s)

13-23

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cites work

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

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Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration

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Phospholipids of bovine outer segments

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The photoreceptor rim protein is an ABC transporter encoded by the gene for recessive Stargardt's disease (ABCR)

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The human photoreceptor rim protein gene (ABCR): genomic structure and primer set information for mutation analysis

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A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION

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Quantitation of phenacyl esters of retinal fatty acids by high-performance liquid chromatography

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Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR

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Hyperlipofuscinosis and subretinal fibrosis in Stargardt's disease.

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Retinal pigment epithelial abnormalities in fundus flavimaculatus: a light and electron microscopic study

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Delayed rod dark adaptation in patients with Stargardt's disease

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Prolonged rod dark adaptation in patients with cone-rod dystrophy

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Opsin/all-trans-retinal complex activates transducin by different mechanisms than photolyzed rhodopsin

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Count and density of human retinal photoreceptors

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Transgenic analysis of rds/peripherin N-glycosylation: effect on dimerization, interaction with rom1, and rescue of the rds null phenotype

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Molecular basis of dark adaptation in rod photoreceptors

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Genotype/Phenotype analysis of a photoreceptor-specific ATP-binding cassette transporter gene, ABCR, in Stargardt disease

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Recovery phase of the murine rod photoresponse reconstructed from electroretinographic recordings

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Isolation and one-step preparation of A2E and iso-A2E, fluorophores from human retinal pigment epithelium

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Lipofuscin in the retina: quantitative assay for an unprecedented autofluorescent compound (pyridinium bis-retinoid, A2-E) of ocular age pigment

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Histopathology of Incipient Fundus Flavimaculatus

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Symptomatic abnormalities of dark adaptation in patients with age-related Bruch's membrane change

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Allelic variation in ABCR associated with Stargardt disease but not age-related macular degeneration

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Stargardt's ABCR is localized to the disc membrane of retinal rod outer segments

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Retinal stimulates ATP hydrolysis by purified and reconstituted ABCR, the photoreceptor-specific ATP-binding cassette transporter responsible for Stargardt disease

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Transducin activation by the bovine opsin apoprotein

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A simple procedure for the extraction of the native chromophore of visual pigments: the formaldehyde method

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Role for the target enzyme in deactivation of photoreceptor G protein in vivo

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Phospholipid asymmetry and transmembrane diffusion in photoreceptor disc membranes

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Function of Escherichia coli MsbA, an essential ABC family transporter, in lipid A and phospholipid biosynthesis

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Identifiers

DOI

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Consolidated OpenCitations Corpus – April 2017

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Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

10412977

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Consolidated OpenCitations Corpus – April 2017