(Q50965566)

English

A missense single nucleotide polymorphism, V114I of the Werner syndrome gene, is associated with risk of osteoporosis and femoral fracture in the Japanese population.

scientific article published on 31 January 2015

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/25637295

A missense single nucleotide polymorphism, V114I of the Werner syndrome gene, is associated with risk of osteoporosis and femoral fracture in the Japanese population. (English)

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/25637295

0 references

single-nucleotide polymorphism

1 reference

based on heuristic

inferred from title

Werner syndrome

1 reference

based on heuristic

inferred from title

Motohiko Miyachi

10

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25637295%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

12

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25637295%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Haruka Murakami

11

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25637295%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

author name string

Heying Zhou

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25637295%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Seijiro Mori

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25637295%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Masashi Tanaka

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25637295%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Motoji Sawabe

4

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25637295%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Tomio Arai

5

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25637295%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Masaaki Muramatsu

6

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25637295%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Makiko Naka Mieno

7

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25637295%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Shoji Shinkai

8

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25637295%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Yoshiji Yamada

9

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25637295%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Hideki Ito

13

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25637295%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

publication date

31 January 2015

1 reference

Europe PubMed Central

26 March 2018

http://europepmc.org/abstract/MED/25637295

Journal of Bone and Mineral Metabolism

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25637295%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

33

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25637295%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

6

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25637295%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

694-700

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25637295%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

https://scigraph.springernature.com/pub.10.1007/s00774-014-0636-0

0 references

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

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

Diagnostic criteria for Werner syndrome based on Japanese nationwide epidemiological survey

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

Positional cloning of the Werner's syndrome gene

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

Roles of Werner syndrome protein in protection of genome integrity

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

Telomere dysfunction as a cause of genomic instability in Werner syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

Risk of non-Hodgkin lymphoma (NHL) in relation to germline variation in DNA repair and related genes

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

Association of candidate gene polymorphisms with chronic kidney disease in Japanese individuals with hypertension

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

Large-scale evaluation of candidate genes identifies associations between DNA repair and genomic maintenance and development of benzene hematotoxicity

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

Diagnostic criteria for primary osteoporosis: year 2000 revision

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

Association of 29C>T polymorphism in the transforming growth factor-β1 gene with lean body mass in community-dwelling Japanese population.

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

Cooperative effect of serum 25-hydroxyvitamin D concentration and a polymorphism of transforming growth factor-beta1 gene on the prevalence of vertebral fractures in postmenopausal osteoporosis.

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

SNPStats: a web tool for the analysis of association studies.

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

Werner's syndrome: twenty-four cases with a review of the Japanese medical literature

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

Bone and calcium metabolism in Werner's syndrome.

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

Defects in telomere maintenance molecules impair osteoblast differentiation and promote osteoporosis

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

Impairment of osteoblast differentiation due to proliferation-independent telomere dysfunction in mouse models of accelerated aging

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

Functional deficit associated with a missense Werner syndrome mutation

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00774-014-0636-0

21 January 2018

The musculoskeletal manifestations of Werner's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/25637295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/25637295

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/25637295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of osteoporosis in a patient with Werner's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/25637295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Werner's syndrome: a clinical-roentgen entity

1 reference

https://pubmed.ncbi.nlm.nih.gov/25637295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/25637295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bone and joint involvement in adults with Werner's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/25637295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/25637295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A polymorphic variant C1367R of the Werner helicase gene and atherosclerotic diseases in the Japanese population

1 reference

https://pubmed.ncbi.nlm.nih.gov/25637295

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00774-014-0636-0

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25637295%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25637295%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q50965566&oldid=1506929379"