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Neuropsychology|April 28, 2001
Deficits in memory strategy use related to prefrontal dysfunction during early development: evidence from children with phenylketonuriaD A White, M J Nortz, T Mandernach, 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.American Journal of Medical Genetics|August 22, 2000
Cholesterol supplementation with egg yolk increases plasma cholesterol and decreases plasma 7-dehydrocholesterol in Smith-Lemli-Opitz syndromeL M Linck, D S Lin, D Flavell, 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.Journal of Lipid Research|September 7, 2000
Sterol balance in the Smith-Lemli-Opitz syndrome. Reduction in whole body cholesterol synthesis and normal bile acid productionR D Steiner, L M Linck, D P Flavell, et al.Molecular Genetics and Metabolism|February 13, 2001
Carrier frequency of the common mutation IVS8-1G>C in DHCR7 and estimate of the expected incidence of Smith-Lemli-Opitz syndromeK P Battaile, B C Battaile, L S Merkens, et al.The Journal of Pediatrics|June 1, 1997
Black children deficient in galactose 1-phosphate uridyltransferase: correlation of activity and immunoreactive protein in erythrocytes and leukocytesM Landt, D Ritter, K Lai, 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.Pageof 10