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Transcriptional activation by the Werner syndrome gene product in yeast
scientific article published on 01 November 1998
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9951624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9951624%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
title
Transcriptional activation by the Werner syndrome gene product in yeast
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9951624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9951624%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
main subject
Werner syndrome
1 reference
based on heuristic
inferred from title
author name string
L Ye
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9951624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9951624%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
J Nakura
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9951624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9951624%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
A Morishima
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9951624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9951624%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
T Miki
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9951624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9951624%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
publication date
1 November 1998
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9951624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9951624%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
published in
Experimental Gerontology
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9951624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9951624%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
volume
33
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9951624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9951624%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
issue
7-8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9951624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9951624%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
page(s)
805-812
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9951624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9951624%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
cites work
Diminished response of Werner's syndrome fibroblasts to growth factors PDGF and FGF.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A retarded rate of DNA replication and normal level of DNA repair in Werner's syndrome fibroblasts in culture
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Elevated spontaneous mutation rate in SV40-transformed Werner syndrome fibroblast cell lines.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutator phenotype of Werner syndrome is characterized by extensive deletions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Increased frequency of 6-thioguanine-resistant peripheral blood lymphocytes in Werner syndrome patients.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Werner syndrome: a molecular genetic hypothesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
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/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Werner syndrome protein is a DNA helicase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Decrease in the average size of replicons in a Werner syndrome cell line by Simian virus 40 infection
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The p21 Cdk-interacting protein Cip1 is a potent inhibitor of G1 cyclin-dependent kinases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Normal level of unscheduled DNA synthesis in Werner's syndrome fibroblasts in culture
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional dissection of a eukaryotic transcriptional activator protein, GCN4 of yeast
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
DNA damage and repair in telomeres: relation to aging
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Differential regulation of plasminogen activator and inhibitor gene transcription by the tumor suppressor p53
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of gene sequences overexpressed in senescent and Werner syndrome human fibroblasts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletion analysis of GAL4 defines two transcriptional activating segments
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The human cut homeodomain protein can repress gene expression by two distinct mechanisms: active repression and competition for binding site occupancy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
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/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Impaired nuclear localization of defective DNA helicases in Werner's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comparative sequence analysis of ribonucleases HII, III, II PH and D
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A putative nucleic acid-binding domain in Bloom's and Werner's syndrome helicases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Diverse gene sequences are overexpressed in werner syndrome fibroblasts undergoing premature replicative senescence
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Werner's syndrome: twenty-four cases with a review of the Japanese medical literature
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Positionally cloned human disease genes: patterns of evolutionary conservation and functional motifs
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygosity mapping of the Werner syndrome locus (WRN)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Narrowing the position of the Werner syndrome locus by homozygosity analysis-extension of homozygosity analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
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/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Systematic growth studies, cocultivation, and cell hybridization studies of Werner syndrome cultured skin fibroblasts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Werner's syndrome: a review of recent research with an analysis of connective tissue metabolism, growth control of cultured cells, and chromosomal aberrations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygosity mapping and Werner's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
DNA helicase activity in Werner's syndrome gene product synthesized in a baculovirus system
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prolongation of S phase and whole cell cycle in Werner's syndrome fibroblasts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Altered frequency of initiation sites of DNA replication in Werner's syndrome cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Increase in DNA synthesis in Werner's syndrome cells by hybridization with normal human diploid and HeLa cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Roles of nuclear and cytoplasmic environments in the retarded DNA synthesis in Werner syndrome cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cell fusion studies in the Werner syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Association of a polymorphic variant of the Werner helicase gene with myocardial infarction in a Japanese population
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0531-5565%2898%2900044-8
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/10.1016%2FS0531-5565%2898%2900044-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0531-5565(98)00044-8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9951624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9951624%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
PubMed publication ID
9951624
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9951624
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9951624%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 December 2019
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