Showing results (51-60 of 65) with videos related to
Sort By:
Pageof 7
Enzyme|January 1, 1983
Separation of ornithine and lysine activities of the ornithine-transcarbamylase-catalyzed reactionF A Hommes, A G Eller, D F Scott, et al.Acta Paediatrica Scandinavica|March 1, 1976
Two cases of phosphoenolpyruvate carboxykinase deficiencyF A Hommes, K Bendien, J D Elema, et al.Enzyme|January 1, 1984
Further evidence for a separate enzymic entity for the synthesis of homocitrulline, distinct from the regular ornithine transcarbamylaseA L Carter, A G Eller, S Rufo, et al.Biology of the Neonate|January 1, 1979
Effect of cyclic nucleotides on weight of gastrocnemius and creatine kinase activity after denervation of muscle in young ratsH J Kloosterboer, H van Faassen, S A Stoker-de Vries, et al.Biology of the Neonate|January 1, 1979
Effect of hormones on the development of creatine kinase activity in rat skeletal muscleH J Kloosterboer, H van Faassen, S A Stoker-De Vries, et al.Biology of the Neonate|January 1, 1979
Quantitative analysis of morphological changes in skeletal muscle of the rat after hormone administrationH J Kloosterboer, S A Stoker-De Vries, C E Hulstaert, et al.Neuropediatrics|February 1, 1986
Studies on a case of HHH-syndrome (hyperammonemia, hyperornithinemia, homocitrullinuria)F A Hommes, R A Roesel, K Metoki, et al.Journal of Inherited Metabolic Disease|January 1, 1982
Decreased transport of ornithine across the inner mitochondrial membrane as a cause of hyperornithinaemiaF A Hommes, C K Ho, R A Roesel, et al.Journal of Inherited Metabolic Disease|January 1, 1982
Cell genetic studies on propionyl-CoA carboxylase deficient cell linesG H Van Leeuwen, G De Vrieze, J A Gimpel, et al.Journal of Mental Deficiency Research|December 1, 1985
Serum carnosinase deficiency: a non-disabling phenotype?M Cohen, P L Hartlage, N Krawiecki, et al.Pageof 7