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The Journal of Clinical Investigation|March 1, 1987
Hereditary xanthinuria. Evidence for enhanced hypoxanthine salvageF A Mateos, J G Puig, M L Jiménez, et al.Science (New York, N.Y.)|August 18, 1978
Lymphocyte ecto-5'-nucleotidase deficiency in agammaglobulinemiaN L Edwards, D B Magilavy, J T Cassidy, et al.Metabolism: Clinical and Experimental|March 1, 1980
Purine metabolism during strenuous muscular exercise in manJ R Sutton, C J Toews, G R Ward, et al.Chest|November 1, 1985
Evidence for adenosine triphosphate degradation in critically-ill patientsC M Grum, R H Simon, D R Dantzker, et al.The Journal of Laboratory and Clinical Medicine|March 1, 1991
Adenotin and adenotin-like proteins coexist with adenosine receptors in mammalian tissuesC Work, S Zolnierowicz, K A Hutchinson, et al.Archives of Biochemistry and Biophysics|January 1, 1989
Characteristics of an adenosine A1 binding site in human placental membranesC Work, K Hutchison, M Prasad, et al.The American Journal of Physiology|November 1, 1982
Regulation of purine metabolism by plasma membrane and cytoplasmic 5'-nucleotidasesN L Edwards, D Recker, J Manfredi, et al.Metabolism: Clinical and Experimental|August 1, 1985
Hyperuricemia and hypertriglyceridemia: metabolic basis for the associationI H Fox, D John, S DeBruyne, et al.Neurology|September 1, 1985
ATP degradation products after ischemic exercise: hereditary lack of phosphorylase or carnitine palmityltransferaseT E Bertorini, V Shively, B Taylor, et al.Immunological Communications|January 1, 1975
Inhibition of mitogen mediated lymphocyte blastogenesis by adenosineI H Fox, E C Keystone, D D Gladman, et al.Pageof 10