(Q33613095)

28 July 2017

title

WRN helicase expression in Werner syndrome cell lines (English)

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28 July 2017

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M J Moser

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28 July 2017

A S Kamath-Loeb

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28 July 2017

J E Jacob

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28 July 2017

S E Bennett

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28 July 2017

J Oshima

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28 July 2017

R J Monnat

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28 July 2017

language of work or name

English

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publication date

1 January 2000

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28 July 2017

published in

Nucleic Acids Research

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28 July 2017

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28 July 2017

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28 July 2017

page(s)

648-654

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describes a project that uses

28 July 2017

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Immunological diagnosis of Werner syndrome by down-regulated and truncated gene products

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

Defending genome integrity during DNA replication: a proposed role for RecQ family helicases

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

WRN mutations in Werner syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

RNA surveillance. Unforeseen consequences for gene expression, inherited genetic disorders and cancer

14 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

Werner syndrome lymphoblastoid cells are sensitive to camptothecin-induced apoptosis in S-phase

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

A perfect message: RNA surveillance and nonsense-mediated decay

14 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

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

14 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

Cloning of two new human helicase genes of the RecQ family: biological significance of multiple species in higher eukaryotes

14 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

Werner syndrome protein. I. DNA helicase and dna exonuclease reside on the same polypeptide.

14 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

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

14 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

The premature ageing syndrome protein, WRN, is a 3'-->5' exonuclease

14 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

Replication focus-forming activity 1 and the Werner syndrome gene product

14 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

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

14 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

An apoptosis-inducing genotoxin differentiates heterozygotic carriers for Werner helicase mutations from wild-type and homozygous mutants

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

The Werner syndrome protein is a DNA helicase

14 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

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

14 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

Cell cycle-coupled relocation of types I and II topoisomerases and modulation of catalytic enzyme activities

14 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

Excess of rare cancers in Werner syndrome (adult progeria)

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

Positional cloning of the Werner's syndrome gene

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

The Bloom's syndrome gene product is homologous to RecQ helicases

14 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

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

14 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

Isolation of monoclonal antibodies specific for human c-myc proto-oncogene product

14 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

Mutator phenotype of Werner syndrome is characterized by extensive deletions

14 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

Werner syndrome: molecular genetics and mechanistic hypotheses

14 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

Recommendations for a nomenclature system for human gene mutations. Nomenclature Working Group

14 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102521

Spontaneous and induced chromosomal instability in Werner syndrome

30 October 2018

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12 December 2020

Xenopus embryos regulate the nuclear localization of XMyoD

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12 December 2020

Homozygous and compound heterozygous mutations at the Werner syndrome locus

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12 December 2020

Association of a polymorphic variant of the Werner helicase gene with myocardial infarction in a Japanese population

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

The Bloom's syndrome helicase unwinds G4 DNA

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12 December 2020

Polymorphisms at the Werner locus: I. Newly identified polymorphisms, ethnic variability of 1367Cys/Arg, and its stability in a population of Finnish centenarians

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12 December 2020

Determination of copy number of c-Myc protein per cell by quantitative Western blotting

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12 December 2020

Unusual features of thyroid carcinomas in Japanese patients with Werner syndrome and possible genotype-phenotype relations to cell type and race

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12 December 2020

Human werner syndrome DNA helicase unwinds tetrahelical structures of the fragile X syndrome repeat sequence d(CGG)n

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12 December 2020

Identifiers

DOI

10.1093/NAR/28.2.648

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28 July 2017

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28 July 2017

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