(Q45254555)

11 December 2017

title

Evolution of ABCA4 proteins in vertebrates (English)

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11 December 2017

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5

James R Lupski

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11 December 2017

4

Milan Jamrich

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11 December 2017

Alexander N Yatsenko

1

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11 December 2017

Wojciech Wiszniewski

series ordinal

2

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11 December 2017

Charles M Zaremba

series ordinal

3

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11 December 2017

publication date

1 January 2005

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Journal of Molecular Evolution

11 December 2017

published in

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11 December 2017

volume

60

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11 December 2017

issue

1

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11 December 2017

page(s)

72-80

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An ABCA4 genomic deletion in patients with Stargardt disease

11 December 2017

cites work

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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

1 reference

12 December 2020

The neighbor-joining method: a new method for reconstructing phylogenetic trees

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12 December 2020

Biochemical defects in retina-specific human ATP binding cassette transporter nucleotide binding domain 1 mutants associated with macular degeneration

1 reference

12 December 2020

Photoreceptor membrane proteins, phototransduction, and retinal degenerative diseases. The Friedenwald Lecture

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12 December 2020

Likelihood models for detecting positively selected amino acid sites and applications to the HIV-1 envelope gene

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12 December 2020

Phenotypic spectrum of autosomal recessive cone-rod dystrophies caused by mutations in the ABCA4 (ABCR) gene.

1 reference

12 December 2020

Adaptive Evolution of MRG, a Neuron-Specific Gene Family Implicated in Nociception

1 reference

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

Mutations in ABCA4 result in accumulation of lipofuscin before slowing of the retinoid cycle: a reappraisal of the human disease sequence

1 reference

12 December 2020

The cone visual pigments of an Australian marsupial, the tammar wallaby (Macropus eugenii): sequence, spectral tuning, and evolution

1 reference

12 December 2020

The human ATP-binding cassette (ABC) transporter superfamily

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

New ABCR mutations and clinical phenotype in Italian patients with Stargardt disease

1 reference

12 December 2020

Immunocytochemical localization of a large intrinsic membrane protein to the incisures and margins of frog rod outer segment disks.

1 reference

12 December 2020

A comprehensive survey of sequence variation in the ABCA4 (ABCR) gene in Stargardt disease and age-related macular degeneration.

1 reference

12 December 2020

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

1 reference

12 December 2020

Molecular evolution of proteins involved in vertebrate phototransduction

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12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Late-onset Stargardt disease is associated with missense mutations that map outside known functional regions of ABCR (ABCA4).

1 reference

12 December 2020

Cosegregation and functional analysis of mutant ABCR (ABCA4) alleles in families that manifest both Stargardt disease and age-related macular degeneration.

1 reference

12 December 2020

Delayed dark-adaptation and lipofuscin accumulation in abcr+/- mice: implications for involvement of ABCR in age-related macular degeneration

1 reference

12 December 2020

Functional interaction between the two halves of the photoreceptor-specific ATP binding cassette protein ABCR (ABCA4). Evidence for a non-exchangeable ADP in the first nucleotide binding domain

1 reference

12 December 2020

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

1 reference

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Spectrum ofABCA4(ABCR) gene mutations in Spanish patients with autosomal recessive macular dystrophies

1 reference

12 December 2020

An analysis of ABCR mutations in British patients with recessive retinal dystrophies

1 reference

12 December 2020

The mammalian photoreceptor mosaic-adaptive design

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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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12 December 2020

Biochemical defects in ABCR protein variants associated with human retinopathies

1 reference

12 December 2020

PAML: a program package for phylogenetic analysis by maximum likelihood

1 reference

12 December 2020

The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genes

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Synonymous and nonsynonymous rate variation in nuclear genes of mammals.

1 reference

12 December 2020

Whole-Genome Shotgun Assembly and Analysis of the Genome of Fugu rubripes

1 reference

12 December 2020

Functional analysis of genetic mutations in nucleotide binding domain 2 of the human retina specific ABC transporter.

1 reference

12 December 2020

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

1 reference

12 December 2020

An analysis of allelic variation in the ABCA4 gene

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12 December 2020

Early vertebrate evolution of the TATA-binding protein, TBP

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12 December 2020

The molecular basis for spectral tuning of rod visual pigments in deep-sea fish.

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12 December 2020

10.1007/S00239-004-0118-4

Identifiers

DOI

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Dimensions Publication ID

11 December 2017

1051979330

0 references

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