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Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa
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1 reference
stated in
Europe PubMed Central
PubMed ID
10391211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10391211%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
title
Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
10391211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10391211%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
main subject
photoreceptor protein
0 references
RP1 axonemal microtubule associated
1 reference
stated in
GOA release 2020-03-11
phototransduction, visible light
1 reference
stated in
GOA release 2020-03-11
retinitis pigmentosa
1 reference
based on heuristic
inferred from title
author
Eric A Pierce
series ordinal
1
object named as
E A Pierce
author given names
E A
author last names
Pierce
1 reference
stated in
Europe PubMed Central
PubMed ID
10391211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10391211%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
Terrence F Meehan
series ordinal
3
object named as
T Meehan
author given names
T
author last names
Meehan
1 reference
stated in
Europe PubMed Central
PubMed ID
10391211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10391211%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
author name string
Quinn T
series ordinal
2
author given names
T
author last names
Quinn
1 reference
stated in
Europe PubMed Central
PubMed ID
10391211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10391211%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
McGee TL
series ordinal
4
author given names
T L
author last names
McGee
1 reference
stated in
Europe PubMed Central
PubMed ID
10391211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10391211%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
Berson EL
series ordinal
5
author given names
E L
author last names
Berson
1 reference
stated in
Europe PubMed Central
PubMed ID
10391211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10391211%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
Dryja TP
series ordinal
6
author given names
T P
author last names
Dryja
1 reference
stated in
Europe PubMed Central
PubMed ID
10391211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10391211%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
language of work or name
English
0 references
publication date
1 July 1999
1 reference
stated in
Europe PubMed Central
PubMed ID
10391211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10391211%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
10391211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10391211%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
volume
22
1 reference
stated in
Europe PubMed Central
PubMed ID
10391211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10391211%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
page(s)
248-254
1 reference
stated in
Europe PubMed Central
PubMed ID
10391211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10391211%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed ID
10391211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10391211%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
cites work
Molecular genetics of retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Retinitis pigmentosa: unfolding its mystery
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic mapping of RP1 on 8q11-q21 in an Australian family with autosomal dominant retinitis pigmentosa reduces the critical region to 4 cM between D8S601 and D8S285
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Differential display of eukaryotic messenger RNA by means of the polymerase chain reaction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Doyne Lecture. Rhodopsin and autosomal dominant retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rapid amplification of complementary DNA ends for generation of full-length complementary DNAs: thermal RACE.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Drosophila bifocal gene encodes a novel protein which colocalizes with actin and is necessary for photoreceptor morphogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A radiation hybrid map of the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A randomized trial of vitamin A and vitamin E supplementation for retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A point mutation of the rhodopsin gene in one form of retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation in NRL is associated with autosomal dominant retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Further screening of the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The leucine zipper: a hypothetical structure common to a new class of DNA binding proteins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Distribution and cloning of eukaryotic mRNAs by means of differential display: refinements and optimization
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of multiple genes in bovine retinal pericytes altered by exposure to elevated levels of glucose by using mRNA differential display
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of messenger RNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Large- and small-scale preparation of bacteriophage lambda lysate and DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new bacteriophage P1-derived vector for the propagation of large human DNA fragments
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
36B4 cDNA used as an estradiol-independent mRNA control is the cDNA for human acidic ribosomal phosphoprotein PO
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F10305
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/10305
2 references
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4165136
stated in
Europe PubMed Central
PubMed ID
10391211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10391211%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
Dimensions Publication ID
1000442346
0 references
Fatcat ID
release_4ruk6r7zy5fjfkemujl7uacr7u
1 reference
stated in
Fatcat
reference URL
https://api.fatcat.wiki/v0/release/4ruk6r7zy5fjfkemujl7uacr7u
retrieved
24 November 2022
based on heuristic
mapped directly with Wikidata item
OpenCitations bibliographic resource ID
4165136
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4165136
PubMed ID
10391211
1 reference
stated in
Europe PubMed Central
PubMed ID
10391211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10391211%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
ResearchGate publication ID
31965996
0 references
Springer Nature article ID
10.1038/10305
0 references
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