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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.Clinica Chimica Acta; International Journal of Clinical Chemistry|May 21, 1980
Enzymatic studies of urinary isomeric chondroitin sulfates from patients with mucopolysaccharidoses. The application of high performance liquid chromatographyG J Lee, J E Evans, H Tieckelmann, 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.Somatic Cell and Molecular Genetics|November 1, 1996
Delivery of cytosolic liver arginase into the mitochondrial matrix space: a possible novel site for gene replacement therapyP B Wissmann, B K Goodman, J G Vockley, et al.Pediatrics|November 1, 1976
Ketonic diet in the management of pyruvate dehydrogenase deficiencyR E Falk, S D Cederbaum, J P Blass, et al.Pediatric Research|June 11, 1992
Deletion in blood mitochondrial DNA in Kearns-Sayre syndromeN Fischel-Ghodsian, M C Bohlman, T R Prezant, et al.Pageof 11