WFS1 gene

Known as: WOLFRAMIN, WFS1, WFS 
 
National Institutes of Health

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Topic mentions per year

1979-2018
051019792018

Papers overview

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Highly Cited
2010
Highly Cited
2010
Wolfram syndrome is an autosomal-recessive disorder characterized by insulin-dependent diabetes mellitus, caused by nonautoimmune… (More)
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2009
2009
BACKGROUND Valproate is a standard treatment for bipolar disorder and a first-line mood stabilizer. The molecular mechanisms… (More)
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2008
2008
Recently, variants in WFS1 have been shown to be associated with type 2 diabetes. We aimed to examine metabolic risk phenotypes… (More)
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Highly Cited
2006
Highly Cited
2006
Wolfram syndrome, an autosomal recessive disorder associated with diabetes mellitus and optic atrophy, is caused by mutations in… (More)
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2006
2006
The WFS1 gene, encoding an endoplasmic reticulum (ER) membrane glycoprotein, is mutated in Wolfram syndrome characterized by… (More)
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2006
2006
XBP1 is a key transcription factor in the endoplasmic reticulum (ER) stress response pathway. In a previous study, we suggested a… (More)
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Highly Cited
2005
Highly Cited
2005
In Wolfram syndrome, a rare form of juvenile diabetes, pancreatic beta-cell death is not accompanied by an autoimmune response… (More)
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2005
2005
OBJECTIVE The WFS1 gene encodes an endoplasmic reticulum (ER) membrane-embedded protein. Homozygous WFS1 gene mutations cause… (More)
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2004
2004
Diabetic and psychiatric symptoms often appear in patients with Wolfram syndrome, and obligate carriers of WFS1 have increased… (More)
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2004
2004
Mutations of the WFS1 gene are responsible for two hereditary diseases, Wolfram syndrome and low frequency sensorineural hearing… (More)
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