VCAN wt Allele

Known as: CSPG2, Versican wt Allele, WGN1 
Human VCAN wild-type allele is located in the vicinity of 5q14.3 and is approximately 111 kb in length. This allele, which encodes versican core… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1992-2017
02419922017

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Wogonin(WGN) exhibits a number of hepato-protective effects [1]. WGN has a suppressive effect on tumor growth in hepatocellular… (More)
Is this relevant?
2014
2014
Inhibition of high mobility group box 1 (HMGB1) protein and restoration of endothelial integrity is emerging as an attractive… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
2013
2013
OBJECTIVE To assess the association between CSPG2 and HSPG2 gene polymorphisms and intracranial aneurysm (IA) in ethnic Han… (More)
Is this relevant?
2012
2012
Die Integration der neuen Proteasehemmer in die Erstoder Retherapie bei chronischer Hepatitis-C-Infektion mit dem HCV-Genotyp 1… (More)
Is this relevant?
2010
2010
We proposed a novel approach for “Evaluating Web Sites Based on GHAP”, we evaluate websites based on web usage mining and try to… (More)
  • table 3
Is this relevant?
Review
2009
Review
2009
Measurement of the background radio noise is very important process being used in survey of radio noise environment, calculating… (More)
  • table 2
  • figure 4
  • figure 2
  • figure 5
  • figure 6
Is this relevant?
2005
2005
We present in this paper an algorithm of filtering the noisy real ECG signal. The classical wavelet denoising process, based on… (More)
  • figure 1
  • figure 2
  • figure 3
Is this relevant?
2003
2003
PURPOSE To identify the locus responsible for the blind mutation rdd (retinal dysplasia and degeneration) in chickens and to… (More)
  • figure 1
  • figure 2
  • table 1
  • table 2
  • figure 3
Is this relevant?
2001
2001
Background: Autosomal dominant vitreoretinopathies are characterized by genetic heterogeneity. Structural mutations in COL2A1 are… (More)
  • figure 1
  • figure 3
  • table 1
Is this relevant?
1999
1999
Wagner syndrome (WGN1; MIM 143200), an autosomal dominant vitreoretinopathy characterized by chorioretinal atrophy, cataract, and… (More)
Is this relevant?