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Alcohol and Alcoholism (Oxford, Oxfordshire)|November 1, 1994
Genetic polymorphisms of alcohol metabolizing enzymes related to alcohol sensitivity and alcoholic diseasesA YoshidaHemoglobin|January 1, 1980
A contradiction between in vivo and in vitro activities of normal and variant glucose 6-phosphate dehydrogenaseA YoshidaHuman Genetics|March 1, 1993
Arginase deficiency manifesting delayed clinical sequelae and induction of a kidney arginase isozymeW W Grody, R M Kern, D Klein, 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.Pageof 137