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S D Cederbaum

Showing results (51-60 of 93) with videos related to

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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.
Journal of Inherited Metabolic Disease|January 14, 1998
Spontaneous pneumothorax in association with pyridoxine-responsive homocystinuriaH N Bass, D LaGrave, R Mardach, 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.
Nucleic Acids Research|December 9, 1986
A PvuII RFLP for the human liver arginase (ARG1) geneJ R Kidd, G J Dizikes, W W Grody, 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.
Molecular Genetics and Metabolism|January 16, 1999
Isolated isobutyryl-CoA dehydrogenase deficiency: an unrecognized defect in human valine metabolismC R Roe, S D Cederbaum, D S Roe, et al.
The Journal of Pediatrics|March 1, 1986
Arginase deficiency in a 12-year-old boy with mild impairment of intellectual functionJ Bernar, R A Hanson, R Kern, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Genetic linkage group (ARG1-D6S33-MYB) on chromosome 6q containing the arginase-1 and MYB genesJ Nguyen, P Charmley, W W Grody, et al.
The Journal of Pediatrics|October 1, 1974
Combined immunodeficiency presenting as the Letterer-Siwe syndromeS D Cederbaum, G Niwayama, E R Stiehm, et al.
Molecular and Cellular Biochemistry|January 1, 1983
Regulation of expression of genes for enzymes of the mammalian urea cycle in permanent cell-culture lines of hepatic and non-hepatic originD F Haggerty, E B Spector, M Lynch, et al.
Pageof 10

Showing results (51-60 of 93) with videos related to

Sort By:
Pageof 10
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.
Journal of Inherited Metabolic Disease|January 14, 1998
Spontaneous pneumothorax in association with pyridoxine-responsive homocystinuriaH N Bass, D LaGrave, R Mardach, 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.
Nucleic Acids Research|December 9, 1986
A PvuII RFLP for the human liver arginase (ARG1) geneJ R Kidd, G J Dizikes, W W Grody, 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.
Molecular Genetics and Metabolism|January 16, 1999
Isolated isobutyryl-CoA dehydrogenase deficiency: an unrecognized defect in human valine metabolismC R Roe, S D Cederbaum, D S Roe, et al.
The Journal of Pediatrics|March 1, 1986
Arginase deficiency in a 12-year-old boy with mild impairment of intellectual functionJ Bernar, R A Hanson, R Kern, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Genetic linkage group (ARG1-D6S33-MYB) on chromosome 6q containing the arginase-1 and MYB genesJ Nguyen, P Charmley, W W Grody, et al.
The Journal of Pediatrics|October 1, 1974
Combined immunodeficiency presenting as the Letterer-Siwe syndromeS D Cederbaum, G Niwayama, E R Stiehm, et al.
Molecular and Cellular Biochemistry|January 1, 1983
Regulation of expression of genes for enzymes of the mammalian urea cycle in permanent cell-culture lines of hepatic and non-hepatic originD F Haggerty, E B Spector, M Lynch, et al.
Pageof 10