HPRT

(redirected from Hypoxanthine phosphoribosyltransferase)
Also found in: Medical.
AcronymDefinition
HPRTHypoxanthine Phosphoribosyltransferase
HPRTHarvard Program in Refugee Trauma (Massachusetts General Hospital; Cambridge, MA)
HPRTHydraulic Power Recovery Turbine
HPRTHypothalamic-Pituitary Radiation Therapy
HPRTHighest-Priority Range Table
References in periodicals archive ?
1982) Isolation of a genomic clone partially encoding human hypoxanthine phosphoribosyltransferase.
Expression was normalized against hypoxanthine phosphoribosyltransferase 1 (.
The primer sequences used for StAR, P450scc, 3[beta]-HSD-1, and hypoxanthine phosphoribosyltransferase (HPRT) (internal control) were based on previously published sequences (Jin et al.
A neurologic disorder, LNS is the result of a single mutated gene that codes for a protein known as hypoxanthine phosphoribosyltransferase (HPRT).
Regulation of hypoxanthine phosphoribosyltransferase, glyceraldehydes-3-phosphate dehydrogenase and beta-actin mRNA expression in porcine immune cells and tissues.
6] Human genes: CDH16, cadherin 16, KSP-cadherin; HIF1A, hypoxia-inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor); HPRT1, hypoxanthine phosphoribosyltransferase 1; PPIA, peptidylprolyl isomerase A (cyclophilin A); KLK3, kallikrein-related peptidase 3; TBP, TATA box binding protein; RN18S1, RNA, 18S ribosomal 1; MIR155HG, MIR155 host gene (nonprotein coding).
2004) reported data on hypoxanthine phosphoribosyltransferase (HPRT) gene mutant frequency (HPR[T.