(Q46528428)

English

Impact of polymorphisms in WFS1 on prediabetic phenotypes in a population-based sample of middle-aged people with normal and abnormal glucose regulation

scientific article published on 21 June 2008

In more languages

default values for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18568334

Impact of polymorphisms in WFS1 on prediabetic phenotypes in a population-based sample of middle-aged people with normal and abnormal glucose regulation (English)

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18568334

Anders Albrechtsen

3

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18568334

Torben Jørgensen

4

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18568334

11

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18568334

Benjamin Glaser

object named as

B Glaser

10

0 references

object named as

T Hansen

13

0 references

Oluf Borbye Pedersen

object named as

O Pedersen

12

0 references

Torsten Lauritzen

7

object named as

T Lauritzen

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18568334

Knut Borch-Johnsen

5

object named as

K Borch-Johnsen

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18568334

author name string

T Sparsø

1

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18568334

G Andersen

2

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18568334

A Sandbaek

6

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18568334

J Wasson

8

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18568334

M A Permutt

9

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18568334

publication date

21 June 2008

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18568334

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18568334

51

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18568334

9

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18568334

1646-1652

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18568334

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

1 reference

https://pubmed.ncbi.nlm.nih.gov/18568334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)

1 reference

https://pubmed.ncbi.nlm.nih.gov/18568334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/18568334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A randomized non-pharmacological intervention study for prevention of ischaemic heart disease: baseline results Inter99.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18568334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/18568334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

WFS1-deficiency increases endoplasmic reticulum stress, impairs cell cycle progression and triggers the apoptotic pathway specifically in pancreatic beta-cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/18568334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetically programmed selective islet beta-cell loss in diabetic subjects with Wolfram's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18568334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/18568334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association Studies of Genetic Variation in the WFS1 Gene and Type 2 Diabetes in U.K. Populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/18568334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mice conditionally lacking the Wolfram gene in pancreatic islet beta cells exhibit diabetes as a result of enhanced endoplasmic reticulum stress and apoptosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18568334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disruption of the WFS1 gene in mice causes progressive beta-cell loss and impaired stimulus-secretion coupling in insulin secretion

1 reference

https://pubmed.ncbi.nlm.nih.gov/18568334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Missense variations of the gene responsible for Wolfram syndrome (WFS1/wolframin) in Japanese: possible contribution of the Arg456His mutation to type 1 diabetes as a nonautoimmune genetic basis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18568334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Testing of diabetes-associated WFS1 polymorphisms in the Diabetes Prevention Program

1 reference

https://pubmed.ncbi.nlm.nih.gov/18568334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The ADDITION study: proposed trial of the cost-effectiveness of an intensive multifactorial intervention on morbidity and mortality among people with Type 2 diabetes detected by screening

1 reference

https://pubmed.ncbi.nlm.nih.gov/18568334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

WFS1 mutations in Spanish patients with diabetes mellitus and deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/18568334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common variants in WFS1 confer risk of type 2 diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/18568334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Wolfram syndrome: structural and functional analyses of mutant and wild-type wolframin, the WFS1 gene product

1 reference

https://pubmed.ncbi.nlm.nih.gov/18568334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homeostasis model assessment: insulin resistance and ?-cell function from fasting plasma glucose and insulin concentrations in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/18568334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00125-008-1064-2

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18568334

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18568334

ResearchGate publication ID

0 references

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=Q46528428&oldid=2207931715"