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English
The power of point mutations
scientific article published on 01 January 2001
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11137984
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11137984%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
title
The power of point mutations
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11137984
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11137984%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
author name string
Maquat LE
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11137984
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11137984%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
publication date
1 January 2001
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11137984
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11137984%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11137984
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11137984%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
volume
27
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11137984
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11137984%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11137984
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11137984%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
page(s)
5-6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11137984
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11137984%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
cites work
A mechanism for exon skipping caused by nonsense or missense mutations in BRCA1 and other genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83759
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A BRCA1 nonsense mutation causes exon skipping
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83759
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A perfect message: RNA surveillance and nonsense-mediated decay
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83759
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nonsense surveillance in lymphocytes?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83759
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The association of nonsense codons with exon skipping
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83759
retrieved
7 January 2021
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inferred from DOI database lookup
Maintenance of an open reading frame as an additional level of scrutiny during splice site selection
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83759
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A premature termination codon in either exon of minute virus of mice P4 promoter-generated pre-mRNA can inhibit nuclear splicing of the intervening intron in an open reading frame-dependent manner
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83759
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83759
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7 January 2021
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inferred from DOI database lookup
Characterization of the 415G>A (E139K) PMM2 mutation in carbohydrate-deficient glycoprotein syndrome type Ia disrupting a splicing enhancer resulting in exon 5 skipping
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83759
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Exonic splicing enhancers: mechanism of action, diversity and role in human genetic diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83759
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human genomic sequences that inhibit splicing
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83759
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The regulation of splice-site selection, and its role in human disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83759
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pre-mRNA splicing of IgM exons M1 and M2 is directed by a juxtaposed splicing enhancer and inhibitor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83759
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/83759
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11137984
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11137984%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
PubMed publication ID
11137984
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11137984
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11137984%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
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