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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… Expand
National Institutes of Health

Papers overview

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Highly Cited
2011
Highly Cited
2011
BackgroundStevens-Johnson syndrome (SJS) and Toxic Epidermal Necrolysis (TEN) are rare but extremely severe cutaneous adverse… Expand
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Highly Cited
2008
Highly Cited
2008
Background Schistosomiasis japonica remains a major public health problem in China. Its pathogen, Schistosoma japonicum has a… Expand
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Highly Cited
2007
Highly Cited
2007
Deletion of 3p is one of the most frequent chromosomal alterations in many solid tumors, including esophageal squamous cell… Expand
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Highly Cited
2006
Highly Cited
2006
Although it is known that an arm swing can enhance the performance in vertical jumping, the mechanisms through which this… Expand
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2001
2001
Propionyl- l -carnitine (PLC) is a naturally occurring compound that has been considered for the treatment of many forms of… Expand
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Highly Cited
2000
Highly Cited
2000
Abstract An optic fibre method was used to measure in humans in vivo Achilles (ATF) and patellar tendon forces (PTF) during… Expand
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Highly Cited
2000
Highly Cited
2000
Schwartz-Jampel syndrome (SJS1) is a rare autosomal recessive disorder characterized by permanent myotonia (prolonged failure of… Expand
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Highly Cited
1999
Highly Cited
1999
Perlecan is a heparan sulfate proteoglycan that is expressed in all basement membranes (BMs), in cartilage, and several other… Expand
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1996
1996
In LTK− cells stably transfected with rat D1A receptor cDNA, fenoldopam, a D1 agonist, increased phosphatidylinositol 4,5… Expand
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1992
1992
We demonstrated previously tyrosine phosphorylation-dependent modulation of phospholipase C-gamma 1 (PLC-gamma 1) catalytic… Expand
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