Lipofuscin accumulation, abnormal electrophysiology, and photoreceptor degeneration in mutant ELOVL4 transgenic mice: a model for macular degeneration (Q33932466)

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

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scholarly article

1 reference

Europe PubMed Central

30 July 2017

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

1 reference

Europe PubMed Central

30 July 2017

photoreceptor protein

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electrophysiology

1 reference

based on heuristic

inferred from title

author name string

G Karan

1

1 reference

Europe PubMed Central

30 July 2017

C Lillo

2

1 reference

Europe PubMed Central

30 July 2017

Z Yang

3

1 reference

Europe PubMed Central

30 July 2017

D J Cameron

4

1 reference

Europe PubMed Central

30 July 2017

K G Locke

5

1 reference

Europe PubMed Central

30 July 2017

Y Zhao

6

1 reference

Europe PubMed Central

30 July 2017

S Thirumalaichary

7

1 reference

Europe PubMed Central

30 July 2017

C Li

8

1 reference

Europe PubMed Central

30 July 2017

D G Birch

9

1 reference

Europe PubMed Central

30 July 2017

H R Vollmer-Snarr

10

1 reference

Europe PubMed Central

30 July 2017

D S Williams

11

1 reference

Europe PubMed Central

30 July 2017

K Zhang

12

1 reference

Europe PubMed Central

30 July 2017

language of work or name

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publication date

4 March 2005

1 reference

Europe PubMed Central

30 July 2017

Proceedings of the National Academy of Sciences of the United States of America

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Europe PubMed Central

30 July 2017

102

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Europe PubMed Central

30 July 2017

11

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Europe PubMed Central

30 July 2017

4164-4169

1 reference

Europe PubMed Central

30 July 2017

Prevalence of age-related macular degeneration in the United States

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554798

28 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554798

28 July 2018

Treatment with isotretinoin inhibits lipofuscin accumulation in a mouse model of recessive Stargardt's macular degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554798

28 July 2018

A novel gene for autosomal dominant Stargardt-like macular dystrophy with homology to the SUR4 protein family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554798

28 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554798

28 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554798

28 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554798

28 July 2018

Light adaptation of human rod receptors: the leading edge of the human a-wave and models of rod receptor activity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554798

28 July 2018

Docosahexaenoic acid in red blood cells of patients with X-linked retinitis pigmentosa.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554798

28 July 2018

Chemistry and metabolism of lipids in the vertebrate retina

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554798

28 July 2018

Fluorophores of the human retinal pigment epithelium: Separation and spectral characterization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554798

28 July 2018

An international standard for electroretinography

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554798

28 July 2018

The fatty acid chain elongation system of mammalian endoplasmic reticulum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554798

28 July 2018

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

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0407698102

21 January 2018

Effect of docosahexaenoic acid supplementation on retinal function in a patient with autosomal dominant Stargardt-like retinal dystrophy

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0407698102

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0407698102

21 January 2018

Elovl4 mRNA distribution in the developing mouse retina and phylogenetic conservation of Elovl4 genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554798

29 October 2018

Low docosahexaenoic acid levels in rod outer segments of rats with P23H and S334ter rhodopsin mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554798

29 October 2018

Plasma lipid abnormalities in retinitis pigmentosa and related conditions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554798

29 October 2018

Tissue-specific expression in transgenic mice directed by the 5'-flanking sequences of the human gene encoding interphotoreceptor retinoid-binding protein.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554798

29 October 2018

Retinal age pigments generated by self-assembling lysosomotropic detergents

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0407698102

21 January 2018

Diverse macular dystrophy phenotype caused by a novel complex mutation in the ELOVL4 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/15749821

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The fate of the phagosome: conversion to 'age pigment' and impact in human retinal pigment epithelium

1 reference

https://pubmed.ncbi.nlm.nih.gov/15749821

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Age-related macular degeneration

1 reference

https://pubmed.ncbi.nlm.nih.gov/15749821

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal activation and inactivation mechanisms of rod transduction in patients with autosomal dominant retinitis pigmentosa and the pro-23-his mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/15749821

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.0407698102

1 reference

Europe PubMed Central

30 July 2017

2005PNAS..102.4164K

0 references

1 reference

Europe PubMed Central

30 July 2017

1 reference

Europe PubMed Central

30 July 2017

ResearchGate publication ID

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