(Q71955051)

English

Polygenic disease and retinitis pigmentosa: albinism exacerbates photoreceptor degeneration induced by the expression of a mutant opsin in transgenic mice

scientific article published on 01 December 1996

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8987813%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

Polygenic disease and retinitis pigmentosa: albinism exacerbates photoreceptor degeneration induced by the expression of a mutant opsin in transgenic mice (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8987813%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

retinitis pigmentosa

1 reference

based on heuristic

inferred from title

polygenic disease

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

M I Naash

1

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6579236&resulttype=core&format=json

15 May 2020

H Ripps

2

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6579236&resulttype=core&format=json

15 May 2020

S Li

3

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6579236&resulttype=core&format=json

15 May 2020

Y Goto

4

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6579236&resulttype=core&format=json

15 May 2020

N S Peachey

5

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6579236&resulttype=core&format=json

15 May 2020

publication date

1 December 1996

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8987813%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

Journal of Neuroscience

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6579236&resulttype=core&format=json

15 May 2020

16

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6579236&resulttype=core&format=json

15 May 2020

24

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6579236&resulttype=core&format=json

15 May 2020

7853-7858

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6579236&resulttype=core&format=json

15 May 2020

Rod phototransduction in transgenic mice expressing a mutant opsin gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extracellular glucose dependence of rhodopsin regeneration in the excised mouse eye

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ganglion cell distribution in the albino rabbit's retina

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Visual adaptation in the retina of the skate

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (Pro-23-His).

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Light-induced acceleration of photoreceptor degeneration in transgenic mice expressing mutant rhodopsin

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Origins of crossed and uncrossed retinal projections in pigmented and albino mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional Distribution of Retinal Degeneration in Patients with the Proline to Histidine Mutation in Codon 23 of the Rhodopsion Gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic regulation of light damage to photoreceptors.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and analysis of the mouse opsin gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Constitutive activation of phototransduction by K296E opsin is not a cause of photoreceptor degeneration

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional abnormalities in transgenic mice expressing a mutant rhodopsin gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mouse opsin. Gene structure and molecular basis of multiple transcripts.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Night blindness revisited: from man to molecules. Proctor lecture

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of ocular pigmentation in protecting against retinal light damage

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Computer analysis of photochemical changes in the human retina

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Simulation of human autosomal dominant retinitis pigmentosa in transgenic mice expressing a mutated murine opsin gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant sectoral retinitis pigmentosa. Two families with transversion mutation in codon 23 of rhodopsin

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variations in retinal degenerations

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Retinal abnormalities in the Siamese cat

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A rhodopsin gene mutation responsible for autosomal dominant retinitis pigmentosa results in a protein that is defective in localization to the photoreceptor outer segment

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Calcium binding in pigmented and albino eyes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal rod dark adaptation in autosomal dominant retinitis pigmentosa with proline-23-histidine rhodopsin mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Retinitis pigmentosa. The Friedenwald Lecture

1 reference

https://pubmed.ncbi.nlm.nih.gov/8987813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1523/JNEUROSCI.16-24-07853.1996

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6579236&resulttype=core&format=json

15 May 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6579236&resulttype=core&format=json

15 May 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6579236&resulttype=core&format=json

15 May 2020

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=Q71955051&oldid=1945017469"