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HSPG2 wt Allele

Known as: Perlecan Proteoglycan Gene, Schwartz-Jampel Syndrome 1 (Chondrodystrophic Myotonia) Gene, PLC 
Human HSPG2 wild-type allele is located within 1p36.1-p34 and is approximately 115 kb in length. This allele, which encodes basement membrane… 
National Institutes of Health

Papers overview

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Highly Cited
2018
Highly Cited
2018
Abstract. A 1200×1200 km2 area of the tropical South Atlantic Ocean near Ascension Island is studied with the HadGEM climate… 
2015
2015
Purpose Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are very serious forms of drug-induced cutaneous… 
Highly Cited
2014
Highly Cited
2014
Objective To evaluate a multistrain, high-dose probiotic in the prevention of eczema. Design A randomised, double-blind, placebo… 
Highly Cited
2001
Highly Cited
2001
Propionyl- l -carnitine (PLC) is a naturally occurring compound that has been considered for the treatment of many forms of… 
Highly Cited
2000
Highly Cited
2000
Schwartz-Jampel syndrome (SJS1) is a rare autosomal recessive disorder characterized by permanent myotonia (prolonged failure of… 
Highly Cited
1996
Highly Cited
1996
In LTK− cells stably transfected with rat D1A receptor cDNA, fenoldopam, a D1 agonist, increased phosphatidylinositol 4,5…