(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

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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

https://scigraph.springernature.com/pub.10.1007/s00125-008-1064-2

0 references

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

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