Related Experiment Videos

Erythrocyte nucleotide variations in hypoxanthine phosphoribosyltransferase deficiency

R A Harkness¹, G M McCreanor

¹Division of Inherited Metabolic Diseases, MRC Clinical Research Centre, Harrow, UK.

Journal of Inherited Metabolic Disease

|January 1, 1991

Abstract

No abstract available in PubMed .

Related Concept Videos

Articles linked to this work by shared authors, journal, and citation graph.

The importance of the measurement of ATP depletion and subsequent cell damage with an estimate of size and nature of the market for a practicable method: a review designed for technology transfer.

Scandinavian journal of clinical and laboratory investigation·1998

Is post-hypoxic-ischemic cell damage associated with excessive ATP consumption rather than a failure of ATP production?

Acta paediatrica (Oslo, Norway : 1992)·1997

Lesch-Nyhan syndrome and its pathogenesis: normal nicotinamide-adenine dinucleotide but reduced ATP concentrations that correlate with reduced poly(ADP-ribose) synthetase activity in HPRT-deficient lymphoblasts.

Journal of inherited metabolic disease·1995

Introduction to the age-related diagnosis (ARD) index: an age at presentation related index for diagnostic use.

Journal of inherited metabolic disease·1993

Muscle ATP loss and lactate accumulation at different work intensities in the exercising Thoroughbred horse.

European journal of applied physiology and occupational physiology·1991

The pathogenesis of the Lesch-Nyhan syndrome: ATP use is positively related to hypoxanthine supply to hypoxanthine guanine phosphoribosyltransferase.

Journal of inherited metabolic disease·1991

See all related articles