A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity (Q28589633)

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English	A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity	scientific journal article

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scholarly article

1 reference

PubMed publication ID

31 January 2017

A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity (English)

1 reference

PubMed publication ID

31 January 2017

Werner syndrome RecQ like helicase

1 reference

GOA release 2020-03-11

Werner syndrome

1 reference

based on heuristic

inferred from title

author name string

M. Lebel

1

1 reference

PubMed publication ID

31 January 2017

P. Leder

2

1 reference

PubMed publication ID

31 January 2017

language of work or name

0 references

publication date

27 October 1998

1 reference

PubMed publication ID

31 January 2017

Proceedings of the National Academy of Sciences of the United States of America

1 reference

PubMed publication ID

31 January 2017

95

1 reference

PubMed publication ID

31 January 2017

22

1 reference

PubMed publication ID

31 January 2017

13097–13102

1 reference

PubMed publication ID

31 January 2017

Accelerated aging and nucleolar fragmentation in yeast sgs1 mutants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

17 March 2017

Targeted disruption of the mouse topoisomerase I gene by camptothecin selection

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

17 March 2017

The yeast type I topoisomerase Top3 interacts with Sgs1, a DNA helicase homolog: a potential eukaryotic reverse gyrase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

17 March 2017

Sgs1: a eukaryotic homolog of E. coli RecQ that interacts with topoisomerase II in vivo and is required for faithful chromosome segregation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

17 March 2017

Mutator phenotype of Werner syndrome is characterized by extensive deletions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

17 March 2017

Mice Lacking p21CIP1/WAF1 undergo normal development, but are defective in G1 checkpoint control

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

7 April 2017

Positional cloning of the Werner's syndrome gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

7 April 2017

Differential effects of cytotoxic drugs on mortal and immortalized B-lymphoblastoid cell lines from normal and Werner's syndrome patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

29 September 2017

Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

29 September 2017

The expression of poly(ADP-ribose) polymerase during differentiation-linked DNA replication reveals that it is a component of the multiprotein DNA replication complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

29 September 2017

Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

29 September 2017

Effects of topoisomerase II inhibition in lymphoblasts from patients with progeroid and "chromosome instability" syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

29 September 2017

The gene responsible for Werner syndrome may be a cell division "counting" gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

29 September 2017

Identification of human DNA topoisomerase I as a cofactor for activator-dependent transcription by RNA polymerase II.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

29 September 2017

A genetic linkage map of the mouse: current applications and future prospects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

29 September 2017

Maps from two interspecific backcross DNA panels available as a community genetic mapping resource

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

29 September 2017

Correlation between senescence and DNA repair in cells from young and old individuals and in premature aging syndromes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

29 September 2017

Werner's syndrome: proliferation in vitro of clones of cells bearing chromosome translocations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

29 September 2017

Werner's syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

29 September 2017

Werner's syndrome associated with malignancies: five case reports with a survey of case histories in Japan

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

29 September 2017

Involvement of DNA topoisomerase I in transcription of human ribosomal RNA genes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

29 September 2017

Escherichia coli RecQ protein is a DNA helicase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

29 September 2017

Camptothecin cytotoxicity in mammalian cells is associated with the induction of persistent double strand breaks in replicating DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

29 September 2017

Genetic linkage of Werner's syndrome to five markers on chromosome 8

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

29 September 2017

Production of homozygous mutant ES cells with a single targeting construct

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

29 September 2017

Cloning of a mouse homologue of the human Werner syndrome gene and assignment to 8A4 by fluorescence in situ hybridization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

3 June 2018

SGS1, a homologue of the Bloom's and Werner's syndrome genes, is required for maintenance of genome stability in Saccharomyces cerevisiae

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

3 June 2018

A 17S multiprotein form of murine cell DNA polymerase mediates polyomavirus DNA replication in vitro

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

3 June 2018

Establishment and characterization of testicular cell lines from MT-PVLT-10 transgenic mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

3 June 2018

Elevated spontaneous mutation rate in SV40-transformed Werner syndrome fibroblast cell lines.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

3 June 2018

Effects of incorporation of 6-thioguanine into SV40 DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

3 June 2018

Clonal structural chromosomal rearrangements in lymphocytes of four patients with Werner's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

3 June 2018

Immortalization of Werner syndrome and progeria fibroblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

3 June 2018

Mutagenic consequences of the incorporation of 6-thioguanine into DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

27 November 2018

Accelerated loss of telomeric repeats may not explain accelerated replicative decline of Werner syndrome cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

27 November 2018

Increased frequency of 6-thioguanine-resistant peripheral blood lymphocytes in Werner syndrome patients.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23722

27 November 2018

Narrowing the position of the Werner syndrome locus by homozygosity analysis-extension of homozygosity analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9789047

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragmentation of centromeric DNA and prevention of homologous chromosome separation in male mouse meiosis in vivo by the topoisomerase II inhibitor etoposide

1 reference

https://pubmed.ncbi.nlm.nih.gov/9789047

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Systematic growth studies, cocultivation, and cell hybridization studies of Werner syndrome cultured skin fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/9789047

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA topoisomerases

1 reference

https://pubmed.ncbi.nlm.nih.gov/9789047

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and structure of a covalent cross-link adduct between mitomycin C and DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/9789047

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome instability in lymphocytes from a patient with Werner's syndrome is not associated with DNA repair defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/9789047

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA topoisomerase I--targeted chemotherapy of human colon cancer in xenografts

1 reference

https://pubmed.ncbi.nlm.nih.gov/9789047

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygosity mapping and Werner's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9789047

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.95.22.13097

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1998PNAS...9513097L

0 references

release_n57djwgxtfg7hmvd27xr6rqqlm

1 reference

https://api.fatcat.wiki/v0/release/n57djwgxtfg7hmvd27xr6rqqlm

24 November 2022

based on heuristic

mapped directly with Wikidata item

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

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