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Impaired nuclear localization of defective DNA helicases in Werner's syndrome
scientific article published on 01 August 1997
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9241267
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9241267%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
title
Impaired nuclear localization of defective DNA helicases in Werner's syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9241267
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9241267%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
author name string
Matsumoto T
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9241267
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9241267%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
Shimamoto A
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9241267
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9241267%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
Goto M
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9241267
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9241267%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
Furuichi Y
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9241267
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9241267%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
publication date
1 August 1997
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9241267
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9241267%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9241267
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9241267%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
volume
16
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9241267
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9241267%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9241267
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9241267%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
page(s)
335-336
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9241267
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9241267%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
cites work
A Review of its Symptomatology, Natural History, Pathologic Features, Genetics And Relationship to the Natural Aging Process
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0897-335
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Positional cloning of the Werner's syndrome gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0897-335
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Bloom's syndrome gene product is homologous to RecQ helicases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0897-335
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation-causing mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0897-335
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygous and compound heterozygous mutations at the Werner syndrome locus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0897-335
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of helicase gene mutations in Japanese Werner's syndrome patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0897-335
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation and haplotype analyses of the Werner's syndrome gene based on its genomic structure: genetic epidemiology in the Japanese population
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0897-335
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Optimized codon usage and chromophore mutations provide enhanced sensitivity with the green fluorescent protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0897-335
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nuclear protein localization
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0897-335
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0897-335
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9241267
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9241267%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
PubMed publication ID
9241267
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9241267
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9241267%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
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