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HPRT1 wt Allele

Known as: HGPRT, HPRT, Hypoxanthine Phosphoribosyltransferase 1 (Lesch-Nyhan Syndrome) wt Allele 
Human HPRT1 wild-type allele is located in the vicinity of Xq26.1 and is approximately 40 kb in length. This allele, which encodes hypoxanthine… 
National Institutes of Health

Related topics

Related topics

7 relations
GoutHPRT1 geneHomo sapiensHypoxanthine Phosphoribosyltransferase

Papers overview

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2017
2017
Expression of genes responsible for cell morphogenesis involved in differentiation in porcine buccal pouch mucosal cells during long-term primary culture and real-time proliferation in vitro.
Recently, using experimental animal model, we demonstrated that porcine buccal pouch mucosal cells reflect increased… 
2006
2006
Transgenic Mouse Models and Human Psychiatric Disease
Genetic susceptibility to common psychiatric disease arises from the complex interactions between a multitude of genes and an… 
2003
2003
HPRT targeting: "Ets" a powerful tool for investigating endothelial-cell specific gene expression.
Elucidating the role of genes that are important for the development of the vascular endothelium and their time course of… 
1993
1993
Facto rs Affecti ng HPRT M utant Freq uency in T- Lym p hocytes of Smokers and Nonsmokers1
The frequency of thioguanine-resistant, hypoxanthine phosphoribosyltransferase-deficient lymphocytes in the peripheral blood of… 
1990
1990
HPRT developments improve payout
Hydraulic power recovery turbines (HPRTs) have been in service throughout the petroleum industry for over 30 years. They capture… 
1989
1989
Linkage localization of Börjeson-Forssman-Lehmann syndrome.
Börjeson-Forssman-Lehmann syndrome (BFLS) is a form of X-linked mental retardation (XLMR) with characteristic minor physical… 
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