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A new colorimetric assay for purine nucleoside phosphorylase

Clinical Biochemistry, 1989
A new colorimetric procedure for the determination of purine nucleoside phosphorylase (PNP, E.C. 2.4.2.1) activity is described. In this procedure, the hydrogen peroxide formed in the PNP-xanthine oxidase reaction is used to oxidize the chromogenic reagents--3,5-dichloro-2-hydroxybenzenesulfonic acid/4-aminophenazone using the enzyme peroxidase.
Peter Cashion, Samuel Y. Chu, Min Jiang
openaire   +3 more sources

Plasma purine nucleoside phosphorylase in cancer patients

Clinica Chimica Acta, 2004
Purine nucleoside phosphorylase (PNP) is the purine salvage enzyme that converts guanosine to guanine and inosine to hypoxanthine.279 samples from patients with differing cancers were collected during treatment at both pre- and post-dose stages for plasma PNP activity and compared with a normal population.Normal plasma PNP activity was found to be 3.2+/
Russell P. Newton   +2 more
openaire   +3 more sources

FISH-MUSCLE PURINE AND PYRIMIDINE NUCLEOSIDE PHOSPHORYLASES

Canadian Journal of Biochemistry, 1967
Three purine nucleoside phosphorylase preparations (isoenzymes) were obtained by ammonium sulfate fractionation and DEAE-cellulose chromatography of aqueous extracts of lingcod muscle. Dialysis, adsorption on alumina Cγ, and elution with 0.4 M phosphate buffer yielded further purification.
Joan E. Roy, H. L. A. Tarr
openaire   +2 more sources

Genetic Variability of Purine Nucleoside Phosphorylase in the Mouse

1984
The inherited human deficiency of purine nucleoside phosphorylase is associated primarily with cellular immune dysfunction1. We have begun to screen for quantitative activity variants of purine nucleoside phosphorylase in Mus musculus in attempts to establish an animal model for the enzyme deficiencies associated with immunodeficiency disease.
Marcia J. Sparling   +3 more
openaire   +3 more sources

Inhibitors of the enzyme purine nucleoside phosphorylase

Expert Opinion on Therapeutic Patents, 1998
The enzyme purine nucleoside phosphorylase (PNP) catalyses the reversible cleavage of purine nucleosides to the purine base and ribose-1-phosphate. Several cases of a rare genetic disorder in which PNP is lacking have been reported in children. These children were found to be T-cell immunodeficient while their B-cell immunity remained normal.
Philip E. Morris, John A. Montgomery
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Combined immunodeficiency due to purine nucleoside phosphorylase deficiency: Outcome of three patients.

European Journal of Medical Genetics, 2022
Basak Torun   +8 more
semanticscholar   +1 more source

Chapter 3. Purine Nucleoside Phosphorylase

2007
Purine nucleoside phosphorylase (PNP) catalyzes the reversible phosphorolysis of purine ribonucleosides and 2′-deoxypurine ribonucleosides to the free base, and ribose 1-phosphate or 2′-deoxyribose 1-phosphate, respectively.1–3 PNPs are found in most prokaryotic and eukaryotic organisms where the en...
Steven E. Ealick, Yang Zhang
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Purine nucleoside phosphorylase polymorphism in sheep erythrocytes

Biochemical Genetics, 1977
A polymorphism of purine nucleoside phosphorylase is described in sheep erythrocytes. Two isozymes were distinguished electrophoretically, one with high activity (NP-1) and one with low activity (NP-2). Breeding data suggest that the two isozymes are the product of two codominant alleles, NP1 and NP2.
P. G. Board, J. E. Smith
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Functional analysis of purine nucleoside phosphorylase as a key enzyme in ribavirin metabolism.

Drug Metabolism and Pharmacokinetics, 2014
Ribavirin is a purine nucleoside analogue that possesses potent anti-hepatitis C virus activity, and it has long been considered likely that ribavirin undergoes a first-pass metabolism at the small intestine. Although purine nucleoside phosphorylase (PNP)
Tomomi Furihata   +5 more
semanticscholar   +1 more source

Purine Nucleoside Phosphorylase Deficiency: A Mutation Update

Nucleosides, Nucleotides and Nucleic Acids, 2011
Purine nucleoside phosphorylase (PNPase) deficiency is an autosomal recessive disorder affecting purine degradation and salvage pathways. Clinically, patients typically present with severe immunodeficiency, neurological dysfunction, and autoimmunity. Biochemically, PNPase deficiency may be suspected in the presence of hypouricemia.
A. Corrigan   +5 more
openaire   +3 more sources

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