(Q30326779)

18 June 2017

title

Expression and characterization of peripherin/rds-rom-1 complexes and mutants implicated in retinal degenerative diseases. (English)

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18 June 2017

Goldberg AF

1

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18 June 2017

Molday RS

series ordinal

2

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18 June 2017

language of work or name

English

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publication date

1 January 2000

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18 June 2017

published in

Methods in Enzymology

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18 June 2017

volume

316

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18 June 2017

page(s)

671-687

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Phenotypic Variation Including Retinitis Pigmentosa, Pattern Dystrophy, and Fundus Flavimaculatus in a Single Family With a Deletion of Codon 153 or 154 of the Peripherin/RDS Gene

18 June 2017

cites work

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7 January 2021

Extensive intrafamilial and interfamilial phenotypic variation among patients with autosomal dominant retinal dystrophy and mutations in the human RDS/peripherin gene

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https://api.crossref.org/works/10.1016%2FS0076-6879%2800%2916756-4

7 January 2021

Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy

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https://api.crossref.org/works/10.1016%2FS0076-6879%2800%2916756-4

7 January 2021

Retinitis pigmentosa and related disorders: phenotypes of rhodopsin and peripherin/RDS mutations

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7 January 2021

Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds)

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7 January 2021

Complete rescue of photoreceptor dysplasia and degeneration in transgenic retinal degeneration slow (rds) mice

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7 January 2021

Absence of receptor outer segments in the retina of rds mutant mice

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7 January 2021

Development and degeneration of retina in rds mutant mice: photoreceptor abnormalities in the heterozygotes

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7 January 2021

Opsin synthesis and mRNA levels in dystrophic retinas devoid of outer segments in retinal degeneration slow (rds) mice

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7 January 2021

Molecular cloning, primary structure, and orientation of the vertebrate photoreceptor cell protein peripherin in the rod outer segment disk membrane

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7 January 2021

The human retinal degeneration slow (RDS) gene: Chromosome assignment and structure of the mRNA

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7 January 2021

The cat RDS transcript: candidate gene analysis and phylogenetic sequence analysis

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7 January 2021

Canine homolog and exclusion of retinal degeneration slow (rds) as the gene for early retinal degeneration (erd) in the dog.

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7 January 2021

Cloning of the CDNA for a novel photoreceptor membrane protein (rom-1) identifies a disk rim protein family implicated in human retinopathies

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7 January 2021

Cloning of the human and murine ROM1 genes: genomic organization and sequence conservation

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7 January 2021

The ins and outs of the transmembrane 4 superfamily

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7 January 2021

Subunit composition of the peripherin/rds-rom-1 disk rim complex from rod photoreceptors: hydrodynamic evidence for a tetrameric quaternary structure

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7 January 2021

Localization of peripherin/rds in the disk membranes of cone and rod photoreceptors: relationship to disk membrane morphogenesis and retinal degeneration

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7 January 2021

Fusion between retinal rod outer segment membranes and model membranes: a role for photoreceptor peripherin/rds

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7 January 2021

Heterologous expression of photoreceptor peripherin/rds and Rom-1 in COS-1 cells: assembly, interactions, and localization of multisubunit complexes.

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7 January 2021

SV40-transformed simian cells support the replication of early SV40 mutants

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7 January 2021

A general method of site-specific mutagenesis using a modification of the Thermus aquaticus polymerase chain reaction

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7 January 2021

Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci

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7 January 2021

High-efficiency transformation of mammalian cells by plasmid DNA

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7 January 2021

Size and shape of membrane protein-detergent complexes: hydrodynamic studies

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https://api.crossref.org/works/10.1016%2FS0076-6879%2800%2916756-4

7 January 2021

Characterization of antibody against the N-terminus of RDS/peripherin

1 reference

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7 January 2021

Cysteine residues of photoreceptor peripherin/rds: role in subunit assembly and autosomal dominant retinitis pigmentosa

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7 January 2021

Preferential Rod and Cone Photoreceptor Abnormalities in Heterozygotes with Point Mutations in theRDSGene

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https://api.crossref.org/works/10.1016%2FS0076-6879%2800%2916756-4

7 January 2021

10.1016/S0076-6879(00)16756-4

Identifiers

DOI

1 reference

18 June 2017

1 reference