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WFS1 gene

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

Papers overview

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Review
2017
Review
2017
This paper provides a review on some of the significant research work done on wearable flexible sensors (WFSs). Sensors… Expand
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Highly Cited
2015
Highly Cited
2015
Person re-identification in a non-overlapping multicamera scenario is an open challenge in computer vision because of the large… Expand
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Highly Cited
2013
Highly Cited
2013
Abstract The adoption of more sustainable behaviors, particularly in what concerns to the reduction of energy consumption and the… Expand
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Highly Cited
2007
Highly Cited
2007
We present a novel weighted Fourier series (WFS) representation for cortical surfaces. The WFS representation is a data smoothing… Expand
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Highly Cited
2007
Highly Cited
2007
AIMS/HYPOTHESIS Mutations at the gene encoding wolframin (WFS1) cause Wolfram syndrome, a rare neurological condition… Expand
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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… Expand
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Highly Cited
2006
Highly Cited
2006
Analysis of drifter trajectories in the Gulf of Mexico has revealed the existence of a region on the southern portion of the West… Expand
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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… Expand
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Highly Cited
2003
Highly Cited
2003
Mutations of the WFS1 gene are responsible for Wolfram syndrome, a rare, recessive disorder characterized by early-onset, non… Expand
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Highly Cited
1997
Highly Cited
1997
Mitochondrial (mt)DNA haplogroups in a German control group (n = 67) were characterized by screening mitochondrial coding regions… Expand
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