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J P Ruiter

Showing results (1-10 of 17) with videos related to

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Biochimica Et Biophysica Acta|June 19, 1993
Studies on mitochondrial oxidative phosphorylation in permeabilized human skin fibroblasts: application to mitochondrial encephalomyopathiesR J Wanders, J P Ruiter, F A Wijburg
Biochimica Et Biophysica Acta|August 26, 1998
2,6-Dimethylheptanoyl-CoA is a specific substrate for long-chain acyl-CoA dehydrogenase (LCAD): evidence for a major role of LCAD in branched-chain fatty acid oxidationR J Wanders, S Denis, J P Ruiter, et al.
Biochimica Et Biophysica Acta|August 15, 1995
Inhibition of oxidative phosphorylation by palmitoyl-CoA in digitonin permeabilized fibroblasts: implications for long-chain fatty acid beta-oxidation disordersF V Ventura, J P Ruiter, L Ijlst, et al.
The Journal of Clinical Investigation|August 6, 1998
Molecular basis of hepatic carnitine palmitoyltransferase I deficiencyL IJlst, H Mandel, W Oostheim, et al.
The Journal of Clinical Investigation|August 15, 1996
Common missense mutation G1528C in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Characterization and expression of the mutant protein, mutation analysis on genomic DNA and chromosomal localization of the mitochondrial trifunctional protein alpha subunit geneL IJlst, J P Ruiter, J M Hoovers, et al.
Journal of Inherited Metabolic Disease|October 8, 1998
Lactic acidosis in long-chain fatty acid beta-oxidation disordersF V Ventura, J P Ruiter, L IJlst, et al.
Pediatric Research|December 5, 2000
Progressive infantile neurodegeneration caused by 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency: a novel inborn error of branched-chain fatty acid and isoleucine metabolismJ Zschocke, J P Ruiter, J Brand, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Measurement of peroxisomal fatty acid beta-oxidation in cultured human skin fibroblastsR J Wanders, S Denis, J P Ruiter, et al.
Chemico-Biological Interactions|September 22, 2001
Differential effect of valproate and its Delta2- and Delta4-unsaturated metabolites, on the beta-oxidation rate of long-chain and medium-chain fatty acidsM F Silva, J P Ruiter, L IJlst, et al.
Saudi Medical Journal|December 18, 2001
Carnitine palmityl transferase I deficiencyA I Al-Aqeel, M S Rashed, J P Ruiter, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Biochimica Et Biophysica Acta|June 19, 1993
Studies on mitochondrial oxidative phosphorylation in permeabilized human skin fibroblasts: application to mitochondrial encephalomyopathiesR J Wanders, J P Ruiter, F A Wijburg
Biochimica Et Biophysica Acta|August 26, 1998
2,6-Dimethylheptanoyl-CoA is a specific substrate for long-chain acyl-CoA dehydrogenase (LCAD): evidence for a major role of LCAD in branched-chain fatty acid oxidationR J Wanders, S Denis, J P Ruiter, et al.
Biochimica Et Biophysica Acta|August 15, 1995
Inhibition of oxidative phosphorylation by palmitoyl-CoA in digitonin permeabilized fibroblasts: implications for long-chain fatty acid beta-oxidation disordersF V Ventura, J P Ruiter, L Ijlst, et al.
The Journal of Clinical Investigation|August 6, 1998
Molecular basis of hepatic carnitine palmitoyltransferase I deficiencyL IJlst, H Mandel, W Oostheim, et al.
The Journal of Clinical Investigation|August 15, 1996
Common missense mutation G1528C in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Characterization and expression of the mutant protein, mutation analysis on genomic DNA and chromosomal localization of the mitochondrial trifunctional protein alpha subunit geneL IJlst, J P Ruiter, J M Hoovers, et al.
Journal of Inherited Metabolic Disease|October 8, 1998
Lactic acidosis in long-chain fatty acid beta-oxidation disordersF V Ventura, J P Ruiter, L IJlst, et al.
Pediatric Research|December 5, 2000
Progressive infantile neurodegeneration caused by 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency: a novel inborn error of branched-chain fatty acid and isoleucine metabolismJ Zschocke, J P Ruiter, J Brand, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Measurement of peroxisomal fatty acid beta-oxidation in cultured human skin fibroblastsR J Wanders, S Denis, J P Ruiter, et al.
Chemico-Biological Interactions|September 22, 2001
Differential effect of valproate and its Delta2- and Delta4-unsaturated metabolites, on the beta-oxidation rate of long-chain and medium-chain fatty acidsM F Silva, J P Ruiter, L IJlst, et al.
Saudi Medical Journal|December 18, 2001
Carnitine palmityl transferase I deficiencyA I Al-Aqeel, M S Rashed, J P Ruiter, et al.
Pageof 2