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Journal of Inherited Metabolic Disease|October 22, 2008
Biochemical characterization of mutant phenylalanine hydroxylase enzymes and correlation with clinical presentation in hyperphenylalaninaemic patientsS F Dobrowolski, A L Pey, R Koch, et al.
Biochemical and Molecular Medicine|October 1, 1996
Loss of function mutations in conserved regions of the human arginase I geneJ G Vockley, B K Goodman, D E Tabor, et al.
The American Journal of Physiology|November 1, 1996
Arginase activity in endothelial cells: inhibition by NG-hydroxy-L-arginine during high-output NO productionG M Buga, R Singh, S Pervin, et al.
Gene Therapy|December 5, 2014
Minimal ureagenesis is necessary for survival in the murine model of hyperargininemia treated by AAV-based gene therapyC Hu, D S Tai, H Park, et al.
The Journal of Clinical Investigation|February 1, 1989
Differential expression of the two human arginase genes in hyperargininemia. Enzymatic, pathologic, and molecular analysisW W Grody, C Argyle, R M Kern, et al.
Biochemical Genetics|December 1, 1988
Effects of deletions in mouse chromosome 7 on expression of genes encoding the urea-cycle enzymes and phosphoenolpyruvate carboxykinase (GTP) in liver, kidney, and intestineS M Morris, C L Moncman, D M Kepka, et al.
The Journal of Pediatrics|August 1, 1989
Parenteral nutrition in propionic and methylmalonic acidemiaS G Kahler, D S Millington, S D Cederbaum, et al.
American Journal of Human Genetics|August 1, 1986
The gene for human liver arginase (ARG1) is assigned to chromosome band 6q23R S Sparkes, G J Dizikes, I Klisak, et al.
Pediatric Research|May 1, 1995
Medium chain acyl-CoA dehydrogenase deficiency in Pennsylvania: neonatal screening shows high incidence and unexpected mutation frequenciesR Ziadeh, E P Hoffman, D N Finegold, et al.
Biochemical and Biophysical Research Communications|May 25, 1995
Co-induction of arginase and nitric oxide synthase in murine macrophages activated by lipopolysaccharideW W Wang, C P Jenkinson, J M Griscavage, et al.
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