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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.The Journal of Biological Chemistry|March 10, 1982
Regulation of glucocorticoids of arginase and argininosuccinate synthetase in cultured rat hepatoma cellsD F Haggerty, E B Spector, M Lynch, et al.Genomics|December 1, 1996
Cloning and characterization of the human type II arginase geneJ G Vockley, C P Jenkinson, H Shukla, et al.Molecular Genetics and Metabolism|August 29, 2006
Arginase induction by sodium phenylbutyrate in mouse tissues and human cell linesR M Kern, Z Yang, P S Kim, et al.Pediatrics|January 1, 1975
T-cell reconstitution by thymus transplantation and transfer factor in severe combined immunodeficiencyG S Rachelefsky, E R Stiehm, A J Ammann, et al.Journal of Neuroscience Research|December 18, 2001
Expression of arginase isozymes in mouse brainH Yu, R K Iyer, R M Kern, et al.Somatic Cell and Molecular Genetics|July 1, 1994
Functional and molecular analysis of liver arginase promoter sequences from man and Macaca fascicularisB K Goodman, D Klein, D E Tabor, et al.Pediatric Research|August 1, 1976
Sensitivity to carbohydrate in a patient with familial intermittent lactic acidosis and pyruvate dehydrogenase deficiencyS D Cederbaum, J P Blass, N Minkoff, et al.The New England Journal of Medicine|December 11, 1980
Systemic carnitine deficiency--a treatable inherited lipid-storage disease presenting as Reye's syndromeP R Chapoy, C Angelini, W J Brown, et al.Pageof 10