(Q44597001)

English

Macular appearance by means of OCT and electrophysiology in members of two families with different mutations in RDS (the peripherin/RDS gene).

scientific article published in October 2003

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

Macular appearance by means of OCT and electrophysiology in members of two families with different mutations in RDS (the peripherin/RDS gene). (English)

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

electrophysiology

1 reference

based on heuristic

inferred from title

1

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

author name string

Magnus Abrahamson

2

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

Louise Eksandh

3

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

Vesna Ponjavic

4

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

Sten Andréasson

5

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 October 2003

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

Acta Ophthalmologica

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

81

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

500-507

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

X-linked recessive atrophic macular degeneration from RPGR mutation

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

21 January 2018

Peripherin/rds fusogenic function correlates with subunit assembly

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

21 January 2018

A peptide analogue to a fusion domain within photoreceptor peripherin/rds promotes membrane adhesion and depolarization

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

21 January 2018

Newfoundland rod-cone dystrophy, an early-onset retinal dystrophy, is caused by splice-junction mutations in RLBP1

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

21 January 2018

Adult vitelliform macular dystrophy is frequently associated with mutations in the peripherin/RDS gene

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

21 January 2018

Guidelines for basic multifocal electroretinography (mfERG).

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

21 January 2018

Standard for clinical electro-oculography. International Society for Clinical Electrophysiology of Vision.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

21 January 2018

Standard for clinical electroretinography (1999 update). International Society for Clinical Electrophysiology of Vision.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

21 January 2018

Peptides and membrane fusion: towards an understanding of the molecular mechanism of protein-induced fusion

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

21 January 2018

Optical coherence tomography findings in adult-onset foveomacular vitelliform dystrophy

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

21 January 2018

The field topography of ERG components in man—I. The photopic luminance response

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

21 January 2018

Narrow-band filtering for monitoring low-amplitude cone electroretinograms in retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Imaging localized retinal dysfunction with the multifocal electroretinogram

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Fusion between disk membranes and plasma membrane of bovine photoreceptor cells is calcium dependent

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Purification and light-dependent phosphorylation of a candidate fusion protein, the photoreceptor cell peripherin/rds

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Adult vitelliform macular dystrophy is frequently associated with mutations in the peripherin/RDS gene

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

7 January 2021

based on heuristic

inferred from DOI database lookup

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Autosomal dominant cone-rod dystrophy associated with mutations in codon 244 (Asn244His) and codon 184 (Tyr184Ser) of the peripherin/RDS gene

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Macular dystrophy associated with monogenic Arg172Trp mutation of the peripherin/RDS gene in a Japanese family

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Full-field electroretinograms in patients with central areolar choroidal dystrophy

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical expression of Best's vitelliform macular dystrophy in Swedish families with mutations in the bestrophin gene

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

7 January 2021

based on heuristic

inferred from DOI database lookup

A point mutation in the RDS-peripherin gene in a Spanish family with central areolar choroidal dystrophy

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

7 January 2021

based on heuristic

inferred from DOI database lookup

The retinal degeneration slow (rds) gene product is a photoreceptor disc membrane-associated glycoprotein.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0420.2003.00134.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1034/J.1600-0420.2003.00134.X

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q44597001&oldid=1645345010"