(Q24313598)

Gene Ontology release 2020-05-02

Gene Ontology ID

GO:0097050

Wolframin ER transmembrane glycoprotein

1 reference

negative regulation of type B pancreatic cell apoptotic process

GOA release 2020-03-11

1 reference

Wolframin ER transmembrane glycoprotein

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1 reference

Christine Philbrook

1

0 references

Eberhard Fritz

series ordinal

2

0 references

Hans Weiher

series ordinal

3

0 references

language of work or name

English

0 references

publication date

2005

1 reference

Mutations in the Wolfram Syndrome Type 1 Gene (WFS1) Define a Clinical Entity of Dominant Low-Frequency Sensorineural Hearing Loss

PubMed

published in

Experimental Gerontology

0 references

volume

40

0 references

issue

8-9

0 references

page(s)

671-8

0 references

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.EXGER.2005.06.008

7 January 2021

Mutational analysis of the Wolfram syndrome gene in two families with chromosome 4p-linked bipolar affective disorder

1 reference

https://api.crossref.org/works/10.1016%2FJ.EXGER.2005.06.008

7 January 2021

The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells

1 reference

https://api.crossref.org/works/10.1016%2FJ.EXGER.2005.06.008

7 January 2021

Functional effects of expression of wolframin-antisense transcripts in BRIN-BD11 β-cells

1 reference

https://api.crossref.org/works/10.1016%2FJ.EXGER.2005.06.008

7 January 2021

Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FJ.EXGER.2005.06.008

7 January 2021

Endoplasmic reticulum stress-mediated apoptosis in pancreatic beta-cells

1 reference

https://api.crossref.org/works/10.1016%2FJ.EXGER.2005.06.008

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.EXGER.2005.06.008

7 January 2021

Membrane glycoprotein PC-1 and insulin resistance in non-insulin-dependent diabetes mellitus

1 reference

https://api.crossref.org/works/10.1016%2FJ.EXGER.2005.06.008

7 January 2021

Wolframin expression induces novel ion channel activity in endoplasmic reticulum membranes and increases intracellular calcium

1 reference

https://api.crossref.org/works/10.1016%2FJ.EXGER.2005.06.008

7 January 2021

Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss

1 reference

https://api.crossref.org/works/10.1016%2FJ.EXGER.2005.06.008

7 January 2021

WFS1 (Wolfram syndrome 1) gene product: predominant subcellular localization to endoplasmic reticulum in cultured cells and neuronal expression in rat brain

1 reference

https://api.crossref.org/works/10.1016%2FJ.EXGER.2005.06.008

7 January 2021

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://api.crossref.org/works/10.1016%2FJ.EXGER.2005.06.008

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.EXGER.2005.06.008

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.EXGER.2005.06.008

7 January 2021

Stress signaling from the lumen of the endoplasmic reticulum: coordination of gene transcriptional and translational controls

1 reference

https://api.crossref.org/works/10.1016%2FJ.EXGER.2005.06.008

7 January 2021

An overexpressed gene transcript in senescent and quiescent human fibroblasts encoding a novel protein in the epidermal growth factor-like repeat family stimulates DNA synthesis

1 reference

https://api.crossref.org/works/10.1016%2FJ.EXGER.2005.06.008

7 January 2021

Diabetes insipidus, diabetes mellitus, optic atrophy, and deafness. 3 cases of 'DIDMOAD' syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.EXGER.2005.06.008

7 January 2021

Wolfram (DIDMOAD) syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FJ.EXGER.2005.06.008

7 January 2021

Membrane glycoprotein PC-1 inhibition of insulin receptor function occurs via direct interaction with the receptor alpha-subunit

1 reference

https://api.crossref.org/works/10.1016%2FJ.EXGER.2005.06.008

7 January 2021