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… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1985-2018
0246819852018

Papers overview

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2017
2017
OBJECTIVE To investigate the risk and genetic association of oxcarbazepine-induced cutaneous adverse reactions (OXC-cADRs… (More)
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2016
2016
PURPOSE Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are very serious forms of drug-induced cutaneous… (More)
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2008
2008
Schwartz-Jampel syndrome (SJS) is a recessive neuromyotonia with chondrodysplasia. It results from hypomorphic mutations of the… (More)
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2007
2007
Perlecan knock-in mice were developed to model Schwartz-Jampel syndrome (SJS), a skeletal disease resulting from decreased… (More)
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2000
2000
Xenopus laevis has three distinctive olfactory neuroepithelia. We examined the axonal projection from each of these epithelia to… (More)
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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… (More)
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1994
1994
Lectin-binding patterns of the three olfactory receptors, olfactory epithelium (OE), vomeronasal organ (VNO) and septal olfactory… (More)
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1993
1993
The complete intron-exon organization of the gene encoding human perlecan (HSPG2), the major heparan sulfate proteoglycan of… (More)
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1993
1993
Lectin-binding patterns in the accessory olfactory bulb (AOB) of the golden hamster were investigated histochemically with 21… (More)
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1985
1985
The expression of receptors for N-acetylgalactosamine-recognizing lectins, namely Helix pomatia agglutinin (HPA), Sophora… (More)
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