(Q30428986)

English

A correlation between computer-predicted changes in secondary structure and the phenotype of retinal degeneration associated with mutations in peripherin/RDS.

scientific article published in November 1997

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9395773%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

A correlation between computer-predicted changes in secondary structure and the phenotype of retinal degeneration associated with mutations in peripherin/RDS (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9395773%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

retinal degeneration

1 reference

based on heuristic

inferred from title

Mitsuru Nakazawa

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9395773%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

author name string

Y Wada

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9395773%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Y Chida

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9395773%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

M Tamai

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9395773%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

publication date

1 November 1997

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9395773%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Current Eye Research

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9395773%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

16

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9395773%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

11

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9395773%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

1134-1141

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9395773%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

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/10.1076%2FCEYR.16.11.1134.5099

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.11.1134.5099

21 January 2018

Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouse

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.11.1134.5099

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.11.1134.5099

21 January 2018

A novel mutation (Asn244Lys) in the peripherin/RDS gene causing autosomal dominant retinitis pigmentosa associated with bull's-eye maculopathy detected by nonradioisotopic SSCP

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.11.1134.5099

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.11.1134.5099

21 January 2018

Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.11.1134.5099

21 January 2018

Polymorphic variation within "conserved" sequences at the 3' end of the human RDS gene which results in amino acid substitutions

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.11.1134.5099

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.11.1134.5099

21 January 2018

Analysis of the accuracy and implications of simple methods for predicting the secondary structure of globular proteins

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.11.1134.5099

21 January 2018

Standardized full-field electroretinography. Normal values and their variation with age

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.11.1134.5099

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/10.1076%2FCEYR.16.11.1134.5099

21 January 2018

Ocular findings in patients with autosomal dominant retinitis pigmentosa and transversion mutation in codon 244 (Asn244Lys) of the peripherin/RDS gene

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.11.1134.5099

21 January 2018

A novel Cys-214-Ser mutation in the peripherin/RDS gene in a Japanese family with autosomal dominant retinitis pigmentosa

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.11.1134.5099

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.11.1134.5099

21 January 2018

A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescens

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.11.1134.5099

21 January 2018

Pattern dystrophy and retinitis pigmentosa caused by a peripherin/RDS mutation

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.11.1134.5099

21 January 2018

Autosomal dominant pattern dystrophy of the retina associated with a 4-base pair insertion at codon 140 in the peripherin/RDS gene

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.11.1134.5099

21 January 2018

Autosomal dominant cone-rod dystrophy associated with a Val200Glu mutation of the peripherin/RDS gene

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.11.1134.5099

21 January 2018

Standard for clinical electroretinography (1994 update)

1 reference

https://api.crossref.org/works/10.1076%2FCEYR.16.11.1134.5099

21 January 2018

Identifiers

10.1076/CEYR.16.11.1134.5099

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9395773%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9395773%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

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=Q30428986&oldid=1549508196"