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English
RP11 and RP13: unexpected gene loci
scientific article published on 01 November 2001
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11689314
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11689314%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
title
RP11 and RP13: unexpected gene loci
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11689314
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11689314%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
author name string
W Baehr
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11689314
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11689314%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
C K Chen
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11689314
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11689314%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
publication date
1 November 2001
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11689314
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11689314%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
published in
Trends in Molecular Medicine
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11689314
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11689314%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
volume
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11689314
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11689314%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
issue
11
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11689314
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11689314%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
page(s)
484-486
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11689314
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11689314%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
cites work
A human homolog of yeast pre-mRNA splicing gene, PRP31, underlies autosomal dominant retinitis pigmentosa on chromosome 19q13.4 (RP11)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902177-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902177-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inherited retinal degeneration: exceptional genetic and clinical heterogeneity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902177-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902177-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902177-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902177-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new locus for autosomal dominant retinitis pigmentosa on the short arm of chromosome 17.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902177-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
SMN mutants of spinal muscular atrophy patients are defective in binding to snRNP proteins.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902177-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S1471-4914(01)02177-3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11689314
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11689314%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
PubMed publication ID
11689314
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11689314
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11689314%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 December 2019
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