Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q73040760)
Watch
English
Insights from a lost visual pigment
scientific article published on 01 February 1997
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9020830
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020830%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
title
Insights from a lost visual pigment
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9020830
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020830%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
author name string
G H Travis
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9020830
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020830%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
publication date
1 February 1997
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9020830
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020830%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9020830
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020830%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
volume
15
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9020830
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020830%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9020830
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020830%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
page(s)
115-117
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9020830
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020830%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/ng0297-115
0 references
cites work
Retinopathy induced in mice by targeted disruption of the rhodopsin gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Development and degeneration of retina in rds mutant mice: electron microscopy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning of the human and murine ROM1 genes: genomic organization and sequence conservation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Retinal degeneration slow (rds) in mouse results from simple insertion of a t haplotype-specific element into protein-coding exon II.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Development and degeneration of retina in rds mutant mice: photoreceptor abnormalities in the heterozygotes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescens
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Altered cAMP levels in retinas from transgenic mice expressing a rhodopsin mutant
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transgenic mice carrying the dominant rhodopsin mutation P347S: evidence for defective vectorial transport of rhodopsin to the outer segments
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI 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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
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/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Role of the intradiscal domain in rhodopsin assembly and function
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cyclophilin-related protein RanBP2 acts as chaperone for red/green opsin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structure and function in rhodopsin: the role of asparagine-linked glycosylation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Determinants of visual pigment absorbance: identification of the retinylidene Schiff's base counterion in bovine rhodopsin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Constitutive activation of opsin: influence of charge at position 134 and size at position 296.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Constitutively active mutants of rhodopsin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal dominant retinitis pigmentosa: Four new mutations in rhodopsin, one of them in the retinal attachment site
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Constitutive activation of opsin: interaction of mutants with rhodopsin kinase and arrestin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
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/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Three cytoplasmic loops of rhodopsin interact with transducin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two adjacent cysteine residues in the C-terminal cytoplasmic fragment of bovine rhodopsin are palmitylated
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phosphorylation sites in bovine rhodopsin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0297-115
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0297-115
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9020830
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020830%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
PubMed publication ID
9020830
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9020830
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9020830%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit