(Q34502476)

2 August 2017

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title

Mechanistic studies of ABCR, the ABC transporter in photoreceptor outer segments responsible for autosomal recessive Stargardt disease (English)

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2 August 2017

main subject

photoreceptor protein

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author name string

Sun H

series ordinal

1

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2 August 2017

Nathans J

series ordinal

2

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2 August 2017

language of work or name

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1 December 2001

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Journal of Bioenergetics and Biomembranes

2 August 2017

published in

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2 August 2017

volume

33

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2 August 2017

issue

6

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2 August 2017

page(s)

523-530

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Mechanisms of opsin activation

2 August 2017

cites work

1 reference

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The lipofuscin fluorophore A2E mediates blue light-induced damage to retinal pigmented epithelial cells.

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12 December 2020

Rod outer segment retinol dehydrogenase: substrate specificity and role in phototransduction

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12 December 2020

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

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12 December 2020

Further evidence for an association of ABCR alleles with age-related macular degeneration. The International ABCR Screening Consortium

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Retinal age pigments generated by self-assembling lysosomotropic detergents

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12 December 2020

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

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12 December 2020

Identification and characterization of all-trans-retinol dehydrogenase from photoreceptor outer segments, the visual cycle enzyme that reduces all-trans-retinal to all-trans-retinol

1 reference

12 December 2020

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

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12 December 2020

Crystal structure of the ATP-binding subunit of an ABC transporter

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12 December 2020

Characterization of the ATPase activity of purified Chinese hamster P-glycoprotein

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12 December 2020

Transducin activation by the bovine opsin apoprotein

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12 December 2020

Spontaneous quantal events induced in toad rods by pigment bleaching.

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12 December 2020

The 2588G-->C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with Stargardt disease

1 reference

12 December 2020

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

1 reference

12 December 2020

In vivo measurement of lipofuscin in Stargardt's disease--Fundus flavimaculatus

1 reference

12 December 2020

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

1 reference

12 December 2020

Fundus flavimaculatus. Clinical, functional and histopathologic observations

1 reference

12 December 2020

Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR

1 reference

12 December 2020

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

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12 December 2020

Partial purification and reconstitution of the human multidrug-resistance pump: characterization of the drug-stimulatable ATP hydrolysis

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12 December 2020

ABCR expression in foveal cone photoreceptors and its role in Stargardt macular dystrophy

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Histopathology of Incipient Fundus Flavimaculatus

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In vivo fluorescence of the ocular fundus exhibits retinal pigment epithelium lipofuscin characteristics

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Rhodopsin kinetics in the human eye

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The 220-kDa rim protein of retinal rod outer segments is a member of the ABC transporter superfamily

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12 December 2020

Biochemical aspects of the visual process. XXVII. Stereospecificity of ocular retinol dehydrogenases and the visual cycle

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12 December 2020

The attenuation of rod signals by bleachings

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12 December 2020

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

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Mechanism of activation and inactivation of opsin: role of Glu113 and Lys296

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12 December 2020

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

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12 December 2020

The effect of lipid environment and retinoids on the ATPase activity of ABCR, the photoreceptor ABC transporter responsible for Stargardt macular dystrophy

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12 December 2020

Biosynthesis of a major lipofuscin fluorophore in mice and humans with ABCR-mediated retinal and macular degeneration

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Dark adaptation in vertebrate photoreceptors.

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Biochemical defects in ABCR protein variants associated with human retinopathies

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12 December 2020

Expression of the human multidrug resistance cDNA in insect cells generates a high activity drug-stimulated membrane ATPase

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Delayed rod dark adaptation in patients with Stargardt's disease

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12 December 2020

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

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12 December 2020

Reduction of all-trans-retinal limits regeneration of visual pigment in mice

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12 December 2020

Mapping of the rod photoreceptor ABC transporter (ABCR) to 1p21-p22.1 and identification of novel mutations in Stargardt's disease

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12 December 2020

Spectrum of ABCR gene mutations in autosomal recessive macular dystrophies

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12 December 2020

Dynamics and function of vitamin A compounds in rat retina after a small bleach of rhodopsin

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12 December 2020

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

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12 December 2020

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

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12 December 2020

ATPase activity of purified and reconstituted P-glycoprotein from Chinese hamster ovary cells.

1 reference

12 December 2020

Mutations of the retinal specific ATP binding transporter gene (ABCR) in a single family segregating both autosomal recessive retinitis pigmentosa RP19 and Stargardt disease: evidence of clinical heterogeneity at this locus

1 reference

12 December 2020

Identifiers

DOI

10.1023/A:1012883306823

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Dimensions Publication ID

2 August 2017

1037260569

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1 reference