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R J Wanders

Showing results (151-160 of 497) with videos related to

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Molecular Genetics and Metabolism|August 18, 2001
Valproate induces in vitro accumulation of long-chain fatty acylcarnitinesM F Silva, C Jakobs, M Duran, et al.
Journal of Lipid Research|November 28, 1997
Phytanic acid alpha-oxidation: decarboxylation of 2-hydroxyphytanoyl-CoA to pristanic acid in human liverN M Verhoeven, R J Wanders, D S Schor, 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.
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|April 1, 1994
Mitochondrial trifunctional protein deficiency. Catalytic heterogeneity of the mutant enzyme in two patientsT Kamijo, R J Wanders, J M Saudubray, et al.
FEBS Letters|September 20, 1982
Quantification of the role of the adenine nucleotide translocator in the control of mitochondrial respiration in isolated rat-liver cellsJ Duszynski, A K Groen, R J Wanders, et al.
Lancet (London, England)|December 8, 1984
Prenatal detection of Zellweger syndromeR B Schutgens, H S Heymans, R J Wanders, et al.
Neurology|November 14, 2008
A novel Refsum-like disorder that maps to chromosome 20T Fiskerstrand, P Knappskog, J Majewski, et al.
Advances in Experimental Medicine and Biology|May 23, 1998
Subcellular localization of dihydropyrimidine dehydrogenaseA B Van Kuilenburg, H Van Lenthe, R J Wanders, et al.
Journal of Inherited Metabolic Disease|August 7, 2001
Mevalonate kinase deficiency in a child with periodic fever and without hyperimmunoglobulinaemia DM Di Rocco, U Caruso, H R Waterham, et al.
Pageof 50

Showing results (151-160 of 497) with videos related to

Sort By:
Pageof 50
Molecular Genetics and Metabolism|August 18, 2001
Valproate induces in vitro accumulation of long-chain fatty acylcarnitinesM F Silva, C Jakobs, M Duran, et al.
Journal of Lipid Research|November 28, 1997
Phytanic acid alpha-oxidation: decarboxylation of 2-hydroxyphytanoyl-CoA to pristanic acid in human liverN M Verhoeven, R J Wanders, D S Schor, 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.
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|April 1, 1994
Mitochondrial trifunctional protein deficiency. Catalytic heterogeneity of the mutant enzyme in two patientsT Kamijo, R J Wanders, J M Saudubray, et al.
FEBS Letters|September 20, 1982
Quantification of the role of the adenine nucleotide translocator in the control of mitochondrial respiration in isolated rat-liver cellsJ Duszynski, A K Groen, R J Wanders, et al.
Lancet (London, England)|December 8, 1984
Prenatal detection of Zellweger syndromeR B Schutgens, H S Heymans, R J Wanders, et al.
Neurology|November 14, 2008
A novel Refsum-like disorder that maps to chromosome 20T Fiskerstrand, P Knappskog, J Majewski, et al.
Advances in Experimental Medicine and Biology|May 23, 1998
Subcellular localization of dihydropyrimidine dehydrogenaseA B Van Kuilenburg, H Van Lenthe, R J Wanders, et al.
Journal of Inherited Metabolic Disease|August 7, 2001
Mevalonate kinase deficiency in a child with periodic fever and without hyperimmunoglobulinaemia DM Di Rocco, U Caruso, H R Waterham, et al.
Pageof 50