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R J Wanders

Showing results (21-30 of 497) with videos related to

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Biochimica Et Biophysica Acta|November 25, 1993
L-2-hydroxyglutarate dehydrogenase: identification of a novel enzyme activity in rat and human liver. Implications for L-2-hydroxyglutaric acidemiaG A Jansen, R J Wanders
Biochemical and Biophysical Research Communications|August 15, 1991
Conclusive evidence that very-long-chain fatty acids are oxidized exclusively in peroxisomes in human skin fibroblastsB S Jakobs, R J Wanders
Molecular Aspects of Medicine|November 25, 1998
Lipid metabolism in peroxisomes in relation to human diseaseR J Wanders, J M Tager
Annals of Clinical Biochemistry|July 1, 1994
Re-evaluation of conditions required for measurement of true alanine:glyoxylate aminotransferase activity in human liver: implications for the diagnosis of hyperoxaluria type IV A Horváth, R J Wanders
Journal of Inherited Metabolic Disease|January 1, 1994
Rapid identification of primary hyperoxaluria type I patients using a novel, fully automated method for measurement of hepatic alanine: glyoxylate aminotransferaseV A Horváth, R J Wanders
Developmental Neuroscience|January 1, 1991
Peroxisomal fatty acid beta-oxidation in relation to adrenoleukodystrophyR J Wanders, J M Tager
Biochemistry|October 4, 1988
Sigmoidal relation between mitochondrial respiration and log ([ATP]/[ADP])out under conditions of extramitochondrial ATP utilization. Implications for the control and thermodynamics of oxidative phosphorylationR J Wanders, H V Westerhoff
Biochemical and Biophysical Research Communications|August 24, 1995
Fatty acid beta-oxidation in peroxisomes and mitochondria: the first, unequivocal evidence for the involvement of carnitine in shuttling propionyl-CoA from peroxisomes to mitochondriaB S Jakobs, R J Wanders
Journal of Inherited Metabolic Disease|January 1, 1996
Impaired peroxisomal fatty acid oxidation in human skin fibroblasts with a mitochondrial acylcarnitine/carnitine translocase deficiencyB S Jakobs, R J Wanders
Journal of Inherited Metabolic Disease|January 1, 1996
Cholesterol biosynthesis in Zellweger syndrome: normal activity of mevalonate kinase, mevalonate-5'-pyrophosphate decarboxylase and IPP-isomerase in patients' fibroblasts but deficient mevalonate kinase activity in liverR J Wanders, G J Romeijn
Pageof 50

Showing results (21-30 of 497) with videos related to

Sort By:
Pageof 50
Biochimica Et Biophysica Acta|November 25, 1993
L-2-hydroxyglutarate dehydrogenase: identification of a novel enzyme activity in rat and human liver. Implications for L-2-hydroxyglutaric acidemiaG A Jansen, R J Wanders
Biochemical and Biophysical Research Communications|August 15, 1991
Conclusive evidence that very-long-chain fatty acids are oxidized exclusively in peroxisomes in human skin fibroblastsB S Jakobs, R J Wanders
Molecular Aspects of Medicine|November 25, 1998
Lipid metabolism in peroxisomes in relation to human diseaseR J Wanders, J M Tager
Annals of Clinical Biochemistry|July 1, 1994
Re-evaluation of conditions required for measurement of true alanine:glyoxylate aminotransferase activity in human liver: implications for the diagnosis of hyperoxaluria type IV A Horváth, R J Wanders
Journal of Inherited Metabolic Disease|January 1, 1994
Rapid identification of primary hyperoxaluria type I patients using a novel, fully automated method for measurement of hepatic alanine: glyoxylate aminotransferaseV A Horváth, R J Wanders
Developmental Neuroscience|January 1, 1991
Peroxisomal fatty acid beta-oxidation in relation to adrenoleukodystrophyR J Wanders, J M Tager
Biochemistry|October 4, 1988
Sigmoidal relation between mitochondrial respiration and log ([ATP]/[ADP])out under conditions of extramitochondrial ATP utilization. Implications for the control and thermodynamics of oxidative phosphorylationR J Wanders, H V Westerhoff
Biochemical and Biophysical Research Communications|August 24, 1995
Fatty acid beta-oxidation in peroxisomes and mitochondria: the first, unequivocal evidence for the involvement of carnitine in shuttling propionyl-CoA from peroxisomes to mitochondriaB S Jakobs, R J Wanders
Journal of Inherited Metabolic Disease|January 1, 1996
Impaired peroxisomal fatty acid oxidation in human skin fibroblasts with a mitochondrial acylcarnitine/carnitine translocase deficiencyB S Jakobs, R J Wanders
Journal of Inherited Metabolic Disease|January 1, 1996
Cholesterol biosynthesis in Zellweger syndrome: normal activity of mevalonate kinase, mevalonate-5'-pyrophosphate decarboxylase and IPP-isomerase in patients' fibroblasts but deficient mevalonate kinase activity in liverR J Wanders, G J Romeijn
Pageof 50