(Q33618324)

28 July 2017

Werner syndrome gene variants in human sarcomas (English)

1 reference

28 July 2017

1 reference

Jessica J Hsu

1

1 reference

28 July 2017

Ashwini S Kamath-Loeb

2

1 reference

28 July 2017

Eitan Glick

3

1 reference

28 July 2017

Brett Wallden

4

1 reference

28 July 2017

Karen Swisshelm

5

1 reference

28 July 2017

Brian P Rubin

6

1 reference

28 July 2017

Lawrence A Loeb

7

1 reference

28 July 2017

1 February 2010

1 reference

28 July 2017

Molecular Carcinogenesis

1 reference

28 July 2017

49

1 reference

28 July 2017

166-174

1 reference

28 July 2017

2

1 reference

describes a project that uses

28 July 2017

ImageQuant

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2813347/fullTextXML

inferred from PubMed Central ID database lookup

cites work

Rising from the RecQ-age: the role of human RecQ helicases in genome maintenance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813347

The spectrum of WRN mutations in Werner syndrome patients

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813347

The enzymatic activities of the Werner syndrome protein are disabled by the amino acid polymorphism R834C.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813347

RecQ helicases: suppressors of tumorigenesis and premature aging.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813347

Werner syndrome and the function of the Werner protein; what they can teach us about the molecular aging process.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813347

Unwinding the 'Gordian knot' of helicase action.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813347

Characterization of the human and mouse WRN 3'-->5' exonuclease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813347

WRN mutations in Werner syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813347

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813347

The proofreading domain of Escherichia coli DNA polymerase I and other DNA and/or RNA exonuclease domains

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813347

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813347

Excess of rare cancers in Werner syndrome (adult progeria)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813347

Positional cloning of the Werner's syndrome gene

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813347

Cytogenetics of Werner's syndrome cultured skin fibroblasts: variegated translocation mosaicism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813347

Replicative life-span of cultivated human cells. Effects of donor's age, tissue, and genotype

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813347

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813347

Mutator phenotype of Werner syndrome is characterized by extensive deletions

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813347

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

21 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FMC.20586

A polymorphism in Werner syndrome gene is associated with breast cancer susceptibility in Chinese women

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813347

WRN gene 1367 Arg allele protects against development of type 2 diabetes mellitus

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813347

The three faces of the WS helicase.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813347

Genetic instability and hematologic disease risk in Werner syndrome patients and heterozygotes

30 October 2018

1 reference

12 December 2020

A polymorphic variant at the Werner helicase (WRN) gene is associated with bone density, but not spondylosis, in postmenopausal women

1 reference

12 December 2020

Homozygous and compound heterozygous mutations at the Werner syndrome locus

1 reference

12 December 2020

Mutation and haplotype analyses of the Werner's syndrome gene based on its genomic structure: genetic epidemiology in the Japanese population

1 reference

12 December 2020

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

1 reference

12 December 2020

Impact of genetic variations in the WRN gene on age related pathologies and mortality

1 reference

12 December 2020

Case of Werner's syndrome with pancreatic carcinoma

1 reference

12 December 2020

Identifiers

DOI

10.1002/MC.20586

1 reference

28 July 2017

1 reference

28 July 2017

1 reference