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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.
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.
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