(Q24309305)

Journal of Biological Chemistry

GOA release 2020-03-11

author name string

Celene Grayson

series ordinal

1

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Robert S Molday

series ordinal

2

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language of work or name

English

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publication date

16 September 2005

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published in

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volume

280

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issue

37

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page(s)

32521-30

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cites work

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

N-retinylidene-phosphatidylethanolamine is the preferred retinoid substrate for the photoreceptor-specific ABC transporter ABCA4 (ABCR).

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

Mutations in the ABCA4 (ABCR) gene are the major cause of autosomal recessive cone-rod dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

Characterization of mouse orthologue of ELOVL4: genomic organization and spatial and temporal expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

A novel mutation in the ELOVL4 gene causes autosomal dominant Stargardt-like macular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

ELO2 and ELO3, homologues of the Saccharomyces cerevisiae ELO1 gene, function in fatty acid elongation and are required for sphingolipid formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

Role of a new mammalian gene family in the biosynthesis of very long chain fatty acids and sphingolipids

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

Role for ELOVL3 and fatty acid chain length in development of hair and skin function

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

Eight histidine residues are catalytically essential in a membrane-associated iron enzyme, stearoyl-CoA desaturase, and are conserved in alkane hydroxylase and xylene monooxygenase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

The gene responsible for adrenoleukodystrophy encodes a peroxisomal membrane protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

Evidence that the trans-10,cis-12 isomer of conjugated linoleic acid induces body composition changes in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

Chemistry and metabolism of lipids in the vertebrate retina

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

High-efficiency transformation of mammalian cells by plasmid DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

Membrane topology of the ATP binding cassette transporter ABCR and its relationship to ABC1 and related ABCA transporters: identification of N-linked glycosylation sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

Intracellular functions of N-linked glycans

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

Transport between ER and Golgi

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

Quality control in the endoplasmic reticulum

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

Aggresomes: a cellular response to misfolded proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

Aggresomes, inclusion bodies and protein aggregation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

Characterization and dynamics of aggresome formation by a cytosolic GFP-chimera

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

A rhodopsin mutant linked to autosomal dominant retinitis pigmentosa is prone to aggregate and interacts with the ubiquitin proteasome system

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

Deficiency of rds/peripherin causes photoreceptor death in mouse models of digenic and dominant retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

The role of subunit assembly in peripherin-2 targeting to rod photoreceptor disk membranes and retinitis pigmentosa.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

Evolutionarily conserved ELOVL4 gene expression in the vertebrate retina

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

Autosomal dominant Stargardt-like macular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

Partial purification of the acyl-CoA elongase of Allium porrum leaves

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

The fatty acid chain elongation system of mammalian endoplasmic reticulum

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

Dietary 20:4n-6 and 22:6n-3 modulates the profile of long- and very-long-chain fatty acids, rhodopsin content, and kinetics in developing photoreceptor cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

Lipofuscin accumulation, abnormal electrophysiology, and photoreceptor degeneration in mutant ELOVL4 transgenic mice: a model for macular degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

Abnormal plasma lipids of patients with Retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

inferred from DOI database lookup

7 January 2021

based on heuristic

Purification of the acyl-CoA elongase complex from developing rapeseed and characterization of the 3-ketoacyl-CoA synthase and the 3-hydroxyacyl-CoA dehydratase

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200

inferred from DOI database lookup

7 January 2021

based on heuristic

Solubilization and partial purification of constituents of acyl-CoA elongase from Lunaria annua

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M503411200