(Q40981685)

English

Detection by epitope-defined monoclonal antibodies of Werner DNA helicases in the nucleoplasm and their upregulation by cell transformation and immortalization

scientific article published on January 1999

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scholarly article

1 reference

Europe PubMed Central

25 September 2017

Detection by epitope-defined monoclonal antibodies of Werner DNA helicases in the nucleoplasm and their upregulation by cell transformation and immortalization (English)

1 reference

Europe PubMed Central

25 September 2017

1 reference

based on heuristic

inferred from title

author name string

M Shiratori

1

1 reference

Europe PubMed Central

25 September 2017

S Sakamoto

2

1 reference

Europe PubMed Central

25 September 2017

N Suzuki

3

1 reference

Europe PubMed Central

25 September 2017

Y Tokutake

4

1 reference

Europe PubMed Central

25 September 2017

Y Kawabe

5

1 reference

Europe PubMed Central

25 September 2017

T Enomoto

6

1 reference

Europe PubMed Central

25 September 2017

M Sugimoto

7

1 reference

Europe PubMed Central

25 September 2017

M Goto

8

1 reference

Europe PubMed Central

25 September 2017

T Matsumoto

9

1 reference

Europe PubMed Central

25 September 2017

Y Furuichi

10

1 reference

Europe PubMed Central

25 September 2017

language of work or name

0 references

publication date

1 January 1999

1 reference

Europe PubMed Central

25 September 2017

Journal of Cell Biology

1 reference

Europe PubMed Central

25 September 2017

144

1 reference

Europe PubMed Central

25 September 2017

1-9

1 reference

Europe PubMed Central

25 September 2017

1

1 reference

Europe PubMed Central

25 September 2017

Sp1-mediated transcription of the Werner helicase gene is modulated by Rb and p53.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2148112

25 September 2017

Bloom's and Werner's syndrome genes suppress hyperrecombination in yeast sgs1 mutant: implication for genomic instability in human diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2148112

25 September 2017

Nucleolar localization of the Werner syndrome protein in human cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2148112

25 September 2017

The Werner syndrome 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=2148112

25 September 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=2148112

25 September 2017

DNA helicase activity in Werner's syndrome gene product synthesized in a baculovirus system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2148112

25 September 2017

Positionally cloned human disease genes: patterns of evolutionary conservation and functional motifs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2148112

25 September 2017

Excess of rare cancers in Werner syndrome (adult progeria)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2148112

25 September 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=2148112

25 September 2017

Helicase-catalyzed DNA unwinding

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2148112

25 September 2017

When cells stop making sense: effects of nonsense codons on RNA metabolism in vertebrate cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2148112

25 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=2148112

25 September 2017

Genetic syndromes in man with potential relevance to the pathobiology of aging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2148112

25 September 2017

Abnormal telomere dynamics of B-lymphoblastoid cell strains from Werner's syndrome patients transformed by Epstein-Barr virus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2148112

25 September 2017

Cell-cycle-regulated phosphorylation of DNA replication factor A from human and yeast cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2148112

17 June 2018

Characterization of the nuclear localization signal in the DNA helicase involved in Werner's syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2148112

19 August 2018

A Review of its Symptomatology, Natural History, Pathologic Features, Genetics And Relationship to the Natural Aging Process

1 reference

https://api.crossref.org/works/10.1083%2FJCB.144.1.1

21 January 2018

Localization of p53, retinoblastoma and host replication proteins at sites of viral replication in herpes-infected cells

1 reference

https://api.crossref.org/works/10.1083%2FJCB.144.1.1

21 January 2018

Growth characteristics of Werner syndrome cells in vitro

1 reference

https://pubmed.ncbi.nlm.nih.gov/9885239

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of the properties of a human homologue of Escherichia coli RecQ from xeroderma pigmentosum group C and from HeLa cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/9885239

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygous and compound heterozygous mutations at the Werner syndrome locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/9885239

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Down-regulation of the defective transcripts of the Werner's syndrome gene in the cells of patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/9885239

12 December 2020

based on heuristic

inferred from PubMed ID 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

https://pubmed.ncbi.nlm.nih.gov/9885239

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Impaired nuclear localization of defective DNA helicases in Werner's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9885239

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hierarchical deterioration of body systems in Werner's syndrome: implications for normal ageing

1 reference

https://pubmed.ncbi.nlm.nih.gov/9885239

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1083/JCB.144.1.1

1 reference

Europe PubMed Central

25 September 2017

1 reference

Europe PubMed Central

25 September 2017

1 reference

Europe PubMed Central

25 September 2017

ResearchGate publication ID

0 references

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