G. McCreanor

发表

The role of catabolism in controlling tissue concentrations of nicotinamide nucleotide coenzymes.

D. Bender, G. McCreanor, 1983, Biochimica et biophysica acta.

The preferred route of kynurenine metabolism in the rat.

D. Bender, G. McCreanor, David A. Bender, 1982, Biochimica et biophysica acta.

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

G. McCreanor, R. Harkness, R. Greenwood, 1991, Journal of Inherited Metabolic Disease.

The metabolism of high intakes of tryptophan, nicotinamide and nicotinic acid in the rat

D. Bender, G. McCreanor, David A. Bender, 1986, British Journal of Nutrition.

The pathology of cornea in Tangier disease (familial high density lipoprotein deficiency).

A. Garner, J. Frohlich, R. Alexander, 1996, Journal of clinical pathology.

Hypoxanthine phosphoribosyltransferase activity in tissues and hypoxanthine concentrations in plasma and CSF of the horse in comparison with other species.

R. Harris, G. McCreanor, R. Harkness, 1990, Comparative biochemistry and physiology. B, Comparative biochemistry.

Kynurenine hydroxylase: a potential rate-limiting enzyme in tryptophan metabolism.

D. Bender, G. McCreanor, 1985, Biochemical Society transactions.

Lethal familial pellagra-like skin lesion associated with neurologic and developmental impairment and the development of cataracts.

D. Bender, M. Salih, G. McCreanor, 1985, Pediatrics.

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

G. McCreanor, R. Harkness, 1995, Journal of Inherited Metabolic Disease.

Reduced concentrations of purine nucleotides in hypoxanthine phosphoribosyltransferase-deficient human lymphoblasts

R. Watts, G. McCreanor, R. Harkness, 1987 .

CEREBROSPINAL FLUID NUCLEOTIDE METABOLITES FOLLOWING SHORT FEBRILE CONVULSIONS

G. McCreanor, J. Livingston, R. A. Harkness, 1989, Developmental medicine and child neurology.

Hypoxanthine output is increased by ATP use in man

G. McCreanor, R. Harkness, 1987 .

Pregnancy in and incidence of xanthine oxidase deficiency

G. McCreanor, R. Harkness, D. Simpson, 1986, Journal of Inherited Metabolic Disease.

Lesch-Nyhan syndrome and its pathogenesis: Purine concentrations in plasma and urine with metabolite profiles in CSF

G. McCreanor, R. Harkness, R. Watts, 1988, Journal of Inherited Metabolic Disease.