(Q36438009)

14 August 2017

1 reference

title

The Werner mutation: does it lead to a "public" or "private" mechanism of aging? (English)

1 reference

14 August 2017

G M Martin

1

1 reference

PMCID

2230204

14 August 2017

language of work or name

English

0 references

publication date

1 June 1997

1 reference

14 August 2017

1 reference

14 August 2017

3

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14 August 2017

356-358

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14 August 2017

6

1 reference

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

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2230204

Excess of rare cancers in Werner syndrome (adult progeria)

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2230204

Genetic analysis of ageing: role of oxidative damage and environmental stresses.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2230204

Positional cloning of the Werner's syndrome gene

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2230204

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2230204

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2230204

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2230204

Mutator phenotype of Werner syndrome is characterized by extensive deletions

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2230204

Metal-catalyzed oxidation of proteins. Physiological consequences

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2230204

Impaired S-phase transit of Werner syndrome cells expressed in lymphoblastoid cell lines

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2230204

Hypermutable ligation of plasmid DNA ends in cells from patients with Werner syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2230204

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

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2230204

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

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2230204

Variegated translocation mosaicism in human skin fibroblast cultures

21 October 2018

1 reference

12 December 2020

Cardiovascular features of the Werner syndrome

1 reference

12 December 2020

Regulation of c-fos expression in senescing Werner syndrome fibroblasts differs from that observed in senescing fibroblasts from normal donors

1 reference

12 December 2020

Homozygous and compound heterozygous mutations at the Werner syndrome locus

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

PMCID

2230204

1 reference

14 August 2017

1 reference

PMCID

2230204