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R J Wanders

Showing results (51-60 of 497) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1985
Peroxisomal matrix enzymes in Zellweger syndrome: activity and subcellular localization in liverR J Wanders, R B Schutgens, J M Tager
Biochemical and Biophysical Research Communications|August 16, 1990
Latency of the peroxisomal enzyme acyl-CoA:dihydroxyacetonephosphate acyltransferase in digitonin-permeabilized fibroblasts: the effect of ATP and ATPase inhibitorsE J Wolvetang, J M Tager, R J Wanders
Journal of Neuropathology and Experimental Neurology|September 1, 1995
Peroxisomal disorders: a reviewR J Wanders, R B Schutgens, P G Barth
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
Pediatric Research|July 1, 1994
beta-Oxidation enzymes in fibroblasts from patients with 3-hydroxydicarboxylic aciduriaN Venizelos, L Ijlst, R J Wanders, et al.
American Journal of Medical Genetics|November 1, 1990
VACTERL and hydrocephalusF A Beemer, R J Wanders, R B Schutgens
Journal of Inherited Metabolic Disease|July 1, 1997
Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of two new mutationsL IJlst, W Oostheim, J P Ruiter, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: a new method to identify the G1528C mutation in genomic DNA showing its high frequency (approximately 90%) and identification of a new mutation (T2198C)L Ijlst, J P Ruiter, J Vreijling, et al.
Analytical Biochemistry|September 2, 1991
A fluorimetric assay for acyl-CoA synthetase activitiesW Lageweg, I Steen, J M Tager, et al.
European Journal of Pediatrics|May 2, 2000
Secondary respiratory chain defect in a boy with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: possible diagnostic pitfallsA M Das, R Fingerhut, R J Wanders, et al.
Pageof 50

Showing results (51-60 of 497) with videos related to

Sort By:
Pageof 50
Journal of Inherited Metabolic Disease|January 1, 1985
Peroxisomal matrix enzymes in Zellweger syndrome: activity and subcellular localization in liverR J Wanders, R B Schutgens, J M Tager
Biochemical and Biophysical Research Communications|August 16, 1990
Latency of the peroxisomal enzyme acyl-CoA:dihydroxyacetonephosphate acyltransferase in digitonin-permeabilized fibroblasts: the effect of ATP and ATPase inhibitorsE J Wolvetang, J M Tager, R J Wanders
Journal of Neuropathology and Experimental Neurology|September 1, 1995
Peroxisomal disorders: a reviewR J Wanders, R B Schutgens, P G Barth
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
Pediatric Research|July 1, 1994
beta-Oxidation enzymes in fibroblasts from patients with 3-hydroxydicarboxylic aciduriaN Venizelos, L Ijlst, R J Wanders, et al.
American Journal of Medical Genetics|November 1, 1990
VACTERL and hydrocephalusF A Beemer, R J Wanders, R B Schutgens
Journal of Inherited Metabolic Disease|July 1, 1997
Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of two new mutationsL IJlst, W Oostheim, J P Ruiter, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: a new method to identify the G1528C mutation in genomic DNA showing its high frequency (approximately 90%) and identification of a new mutation (T2198C)L Ijlst, J P Ruiter, J Vreijling, et al.
Analytical Biochemistry|September 2, 1991
A fluorimetric assay for acyl-CoA synthetase activitiesW Lageweg, I Steen, J M Tager, et al.
European Journal of Pediatrics|May 2, 2000
Secondary respiratory chain defect in a boy with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: possible diagnostic pitfallsA M Das, R Fingerhut, R J Wanders, et al.
Pageof 50