The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis (Q36101183)

12 August 2017

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title

The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis (English)

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12 August 2017

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6

Vilhelm A Bohr

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12 August 2017

Meltem Muftuoglu

1

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12 August 2017

Junko Oshima

2

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12 August 2017

Cayetano von Kobbe

3

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12 August 2017

Wen-Hsing Cheng

4

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12 August 2017

Dru F Leistritz

5

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12 August 2017

23 September 2008

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12 August 2017

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12 August 2017

124

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12 August 2017

4

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12 August 2017

369-377

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Role of Werner syndrome gene product helicase in carcinogenesis and in resistance to genotoxins by cancer cells

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

Epigenetic gene silencing in cancer: the DNA hypermethylome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

WRN exonuclease activity is blocked by DNA termini harboring 3' obstructive groups

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

Nuclear lamins: laminopathies and their role in premature ageing.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

2 October 2017

WRN's tenth anniversary

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

Epigenetic inactivation of the premature aging Werner syndrome gene in human cancer

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

The spectrum of WRN mutations in Werner syndrome patients

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

Modulation of Werner syndrome protein function by a single mutation in the conserved RecQ domain

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

Deficient DNA repair in the human progeroid disorder, Werner syndrome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

LMNA mutations in atypical Werner's syndrome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

Premature aging in RecQ helicase-deficient human syndromes

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

Diverged nuclear localization of Werner helicase in human and mouse cells

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

WRN helicase expression in Werner syndrome cell lines

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

Werner helicase is localized to transcriptionally active nucleoli of cycling cells

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

Excess of rare cancers in Werner syndrome (adult progeria)

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

Association of a missense single nucleotide polymorphism, Cys1367Arg of the WRN gene, with the risk of bone and soft tissue sarcomas in Japan

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

Interaction of Werner and Bloom syndrome genes with p53 in familial breast cancer

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

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

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

Metabolic improvement and abdominal fat redistribution in Werner syndrome by pioglitazone

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

Werner syndrome protein 1367 variants and disposition towards coronary artery disease in Caucasian patients

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

Lack of amyloid plaque formation in the central nervous system of a patient with Werner syndrome

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

Atypical osteosarcomas in Werner Syndrome (adult progeria).

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

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

23 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00439-008-0562-0

Polymorphisms in DNA repair genes and risk of non-Hodgkin lymphoma among women in Connecticut

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4586253

Down-Regulation of the Defective Transcripts of the Werner's Syndrome Gene in the Cells of Patients

21 October 2018

1 reference

12 December 2020

Prevalence of Werner's syndrome heterozygotes in Japan

1 reference

12 December 2020

Analysis of helicase gene mutations in Japanese Werner's syndrome patients

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12 December 2020

Premature aging in Werner's syndrome spares the central nervous system

1 reference

12 December 2020

Genetic variation in the premature aging gene WRN: a case-control study on breast cancer susceptibility

1 reference

12 December 2020

Homozygous and compound heterozygous mutations at the Werner syndrome locus

1 reference

12 December 2020

Chronic leg ulcers in Werner's syndrome

1 reference

12 December 2020

Characterization of osteoporosis in a patient with Werner's syndrome

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12 December 2020

Werner syndrome and mutations of the WRN and LMNA genes in France

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

Homozygosity mapping of the Werner syndrome locus (WRN)

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12 December 2020

Werner helicase expression in human fetal and adult aortas

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S00439-008-0562-0

Identifiers

DOI

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12 August 2017

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12 August 2017

PubMed publication ID

18810497

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