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English
Expression of a mutant opsin gene increases the susceptibility of the retina to light damage
scientific article published on 01 January 1997
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
9057268
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9057268%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
title
Expression of a mutant opsin gene increases the susceptibility of the retina to light damage
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
9057268
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9057268%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
author name string
M Wang
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
9057268
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9057268%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
T T Lam
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
9057268
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9057268%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
M O Tso
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
9057268
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9057268%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
M I Naash
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
9057268
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9057268%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
publication date
1 January 1997
1 reference
stated in
Europe PubMed Central
PubMed ID
9057268
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9057268%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
published in
Visual neuroscience
1 reference
stated in
Europe PubMed Central
PubMed ID
9057268
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9057268%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
volume
14
1 reference
stated in
Europe PubMed Central
PubMed ID
9057268
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9057268%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed ID
9057268
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9057268%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
page(s)
55-62
1 reference
stated in
Europe PubMed Central
PubMed ID
9057268
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9057268%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
cites work
Light deprivation and retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0952523800008750
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Strain differences in sensitivity to light-induced photoreceptor degeneration in albino mice.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0952523800008750
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation and analysis of the mouse opsin gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0952523800008750
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (Pro-23-His).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0952523800008750
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effects of dark-rearing on the retinal degeneration of the C57BL/6-mivit/mivit mouse.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0952523800008750
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0952523800008750
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular basis of visual excitation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0952523800008750
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0952523800008750
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0952523800008750
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Regional Distribution of Retinal Degeneration in Patients with the Proline to Histidine Mutation in Codon 23 of the Rhodopsion Gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0952523800008750
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Light deprivation for early retinitis pigmentosa. A hypothesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0952523800008750
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal dominant sectoral retinitis pigmentosa. Two families with transversion mutation in codon 23 of rhodopsin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0952523800008750
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Retinal degeneration in the nervous mutant mouse. I. Light microscopic cytopathology and changes in the interphotoreceptor matrix
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0952523800008750
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Alligator rhodopsin: sequence and biochemical properties.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0952523800008750
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal Dominant Retinitis Pigmentosa Caused by the Threonine-17-Methionine Rhodopsin Mutation: Retinal Histopathology and Immunocytochemistry
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0952523800008750
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Simulation of human autosomal dominant retinitis pigmentosa in transgenic mice expressing a mutated murine opsin gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0952523800008750
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rod phototransduction in transgenic mice expressing a mutant opsin gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0952523800008750
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Development and degeneration of retina in rds mutant mice: effects of light on the rate of degeneration in albino and pigmented homozygous and heterozygous mutant and normal mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0952523800008750
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormal rod dark adaptation in autosomal dominant retinitis pigmentosa with proline-23-histidine rhodopsin mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0952523800008750
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Constitutive activation of phototransduction by K296E opsin is not a cause of photoreceptor degeneration
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0952523800008750
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Light deprivation and retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1017%2FS0952523800008750
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1017/S0952523800008750
1 reference
stated in
Europe PubMed Central
PubMed ID
9057268
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9057268%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
PubMed ID
9057268
1 reference
stated in
Europe PubMed Central
PubMed ID
9057268
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9057268%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
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