Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q24310486)
Watch
English
The Werner syndrome protein is a DNA helicase
scientific article
In more languages
edit
Statements
instance of
scholarly article
0 references
title
The Werner syndrome protein is a DNA helicase
(English)
0 references
main subject
Werner syndrome RecQ like helicase
1 reference
stated in
GOA release 2020-03-11
human ageing
1 reference
stated in
GOA release 2020-03-11
Werner syndrome
1 reference
based on heuristic
inferred from title
author name string
M D Gray
series ordinal
1
0 references
J C Shen
series ordinal
2
0 references
A S Kamath-Loeb
series ordinal
3
0 references
A Blank
series ordinal
4
0 references
B L Sopher
series ordinal
5
0 references
G M Martin
series ordinal
6
0 references
J Oshima
series ordinal
7
0 references
L A Loeb
series ordinal
8
0 references
language of work or name
English
0 references
publication date
September 1997
0 references
published in
Nature Genetics
0 references
volume
17
0 references
page(s)
100-3
0 references
issue
1
0 references
exact match
https://scigraph.springernature.com/pub.10.1038/ng0997-100
0 references
cites work
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/NG0997-100
retrieved
20 April 2017
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%2FNG0997-100
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytogenetics of Werner's syndrome cultured skin fibroblasts: variegated translocation mosaicism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0997-100
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/10.1038%2FNG0997-100
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%2FNG0997-100
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structure and function of transcription-repair coupling factor. I. Structural domains and binding properties.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0997-100
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of simian virus 40 T antigen in insect cells using a baculovirus expression vector
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0997-100
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A dominant negative allele of the Escherichia coli uvrD gene encoding DNA helicase II. A biochemical and genetic characterization.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0997-100
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human homologues of yeast helicase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0997-100
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Escherichia coli RecQ protein is a DNA helicase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0997-100
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human xeroderma pigmentosum group D gene encodes a DNA helicase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0997-100
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
RecQ DNA helicase of Escherichia coli. Characterization of the helix-unwinding activity with emphasis on the effect of single-stranded DNA-binding protein.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0997-100
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation and genetic characterization of a thymineless death-resistant mutant of Escherichia coli K12: identification of a new mutation (recQ1) that blocks the RecF recombination pathway.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0997-100
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sgs1: a eukaryotic homolog of E. coli RecQ that interacts with topoisomerase II in vivo and is required for faithful chromosome segregation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0997-100
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Spontaneous and induced chromosomal instability in Werner syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0997-100
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%2FNG0997-100
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
recF and recR are required for the resumption of replication at DNA replication forks in Escherichia coli
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0997-100
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Impaired S-phase transit of Werner syndrome cells expressed in lymphoblastoid cell lines
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0997-100
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An improved method for the colorimetric determination of phosphate
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0997-100
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Werner's syndrome 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%2FNG0997-100
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0997-100
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3595778
Dimensions Publication ID
1014232098
0 references
OpenCitations bibliographic resource ID
3595778
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3595778
PubMed ID
9288107
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3595778
ResearchGate publication ID
13933111
0 references
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit