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Neurology|July 1, 1975
Familial poliodystrophy, mitochondrial myopathy, and lactate acidemiaY Shapira, S D Cederbaum, P A Cancilla, et al.The Journal of Pediatrics|August 1, 1979
Hyperlysinemia with saccharopinuria due to combined lysine-ketoglutarate reductase and saccharopine dehydrogenase deficiencies presenting as cystinuriaS D Cederbaum, K N Shaw, J Dancis, et al.The Journal of Pediatrics|January 10, 2001
Psychosocial issues and coping strategies in families affected by urea cycle disordersJ A Cederbaum, C LeMons, M Rosen, et al.Biochimica Et Biophysica Acta|July 20, 1981
Microinjection of arginase into enzyme-deficient cells with the isolated glycoproteins of Sendai virus as fusogenC A Kruse, E B Spector, S D Cederbaum, et al.Somatic Cell and Molecular Genetics|July 1, 1991
Effect of an adjacent base on detection of a point mutation by restriction enzyme digestionD Klein, A E Dodson, D E Tabor, et al.Journal of Inherited Metabolic Disease|January 1, 1994
Menstrual cycle and gonadal steroid effects on symptomatic hyperammonaemia of urea-cycle-based and idiopathic aetiologiesW W Grody, R J Chang, N M Panagiotis, et al.Archives of Biochemistry and Biophysics|February 10, 2000
Induction of arginase II in human Caco-2 tumor cells by cyclic AMPL H Wei, S M Morris, S D Cederbaum, et al.American Journal of Human Genetics|November 1, 1985
Comparison of arginase activity in red blood cells of lower mammals, primates, and man: evolution to high activity in primatesE B Spector, S C Rice, R M Kern, et al.International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|June 1, 1994
Subcellular location and differential antibody specificity of arginase in tissue culture and whole animalsE B Spector, C P Jenkinson, M R Grigor, et al.Journal of Inherited Metabolic Disease|January 1, 1982
Treatment of hyperargininaemia due to arginase deficiency with a chemically defined dietS D Cederbaum, S J Moedjono, K N Shaw, et al.Pageof 137