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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.
Journal of Lipid Research|November 4, 2000
Subcellular localization and physiological role of alpha-methylacyl-CoA racemaseS Ferdinandusse, S Denis, L IJlst, 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.
The Journal of Clinical Investigation|August 6, 1998
Molecular basis of hepatic carnitine palmitoyltransferase I deficiencyL IJlst, H Mandel, W Oostheim, et al.
Molecular Genetics and Metabolism|September 24, 2005
Differential inhibitory effect of long-chain acyl-CoA esters on succinate and glutamate transport into rat liver mitochondria and its possible implications for long-chain fatty acid oxidation defectsF V Ventura, J Ruiter, L Ijlst, et al.
Biochimica Et Biophysica Acta|October 13, 1992
A new, simple assay for long-chain acyl-CoA dehydrogenase in cultured skin fibroblasts using stable isotopes and GC-MSK E Niezen-Koning, R J Wanders, G T Nagel, 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.
The Journal of Biological Chemistry|May 30, 1998
Alkyl-dihydroxyacetonephosphate synthase. Fate in peroxisome biogenesis disorders and identification of the point mutation underlying a single enzyme deficiencyE C de Vet, L Ijlst, W Oostheim, et al.
Biochemical and Biophysical Research Communications|September 16, 1999
Molecular cloning and expression of human carnitine octanoyltransferase: evidence for its role in the peroxisomal beta-oxidation of branched-chain fatty acidsS Ferdinandusse, J Mulders, L IJlst, et al.
Molecular Genetics and Metabolism|July 29, 2017
Processing of mutant N-acetyl-α-glucosaminidase in mucopolysaccharidosis type IIIB fibroblasts cultured at low temperatureO L M Meijer, H Te Brinke, R Ofman, et al.
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