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R J Wanders

Showing results (201-210 of 497) with videos related to

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Prenatal Diagnosis|April 1, 1991
Prenatal diagnosis of inborn errors in peroxisomal beta-oxidationR J Wanders, R B Schutgens, H van den Bosch, et al.
Biochimica Et Biophysica Acta|October 11, 1982
An evaluation of the metabolite indicator method for determining the cytosolic phosphate potential in rat liver cellsA K Groen, R C Vervoorn, R J Wanders, et al.
The Journal of Biological Chemistry|March 25, 1982
Quantification of the contribution of various steps to the control of mitochondrial respirationA K Groen, R J Wanders, H V Westerhoff, et al.
European Journal of Biochemistry|January 1, 1981
Relationship between the rate of citrulline synthesis and bulk changes in the intramitochondrial ATP/ADP ratio in rat-liver mitochondriaR J Wanders, G M Van Woerkom, R F Nooteboom, et al.
Human Molecular Genetics|May 23, 1998
Acyl-CoA:dihydroxyacetonephosphate acyltransferase: cloning of the human cDNA and resolution of the molecular basis in rhizomelic chondrodysplasia punctata type 2R Ofman, E H Hettema, E M Hogenhout, 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.
Journal of Inherited Metabolic Disease|January 1, 1995
Phytanic acid oxidation in man: identification of a new enzyme catalysing the formation of 2-ketophytanic acid from 2-hydroxyphytanic acid and its deficiency in the Zellweger syndromeR J Wanders, C W van Roermund, D S Schor, et al.
Journal of the Neurological Sciences|August 1, 1996
Evidence against increased oxidative stress in fibroblasts from patients with non-superoxide-dismutase-1 mutant familial amyotrophic lateral sclerosisG A Jansen, R J Wanders, G J Jöbsis, et al.
European Journal of Pediatrics|July 1, 1990
Peroxisomal beta-oxidation defect with detectable peroxisomes: a case with neonatal onset and progressive courseP G Barth, R J Wanders, R B Schutgens, et al.
Human Genetics|June 1, 1992
Genetic and biochemical heterogeneity in patients with the rhizomelic form of chondrodysplasia punctata--a complementation studyJ C Heikoop, R J Wanders, A Strijland, et al.
Pageof 50

Showing results (201-210 of 497) with videos related to

Sort By:
Pageof 50
Prenatal Diagnosis|April 1, 1991
Prenatal diagnosis of inborn errors in peroxisomal beta-oxidationR J Wanders, R B Schutgens, H van den Bosch, et al.
Biochimica Et Biophysica Acta|October 11, 1982
An evaluation of the metabolite indicator method for determining the cytosolic phosphate potential in rat liver cellsA K Groen, R C Vervoorn, R J Wanders, et al.
The Journal of Biological Chemistry|March 25, 1982
Quantification of the contribution of various steps to the control of mitochondrial respirationA K Groen, R J Wanders, H V Westerhoff, et al.
European Journal of Biochemistry|January 1, 1981
Relationship between the rate of citrulline synthesis and bulk changes in the intramitochondrial ATP/ADP ratio in rat-liver mitochondriaR J Wanders, G M Van Woerkom, R F Nooteboom, et al.
Human Molecular Genetics|May 23, 1998
Acyl-CoA:dihydroxyacetonephosphate acyltransferase: cloning of the human cDNA and resolution of the molecular basis in rhizomelic chondrodysplasia punctata type 2R Ofman, E H Hettema, E M Hogenhout, 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.
Journal of Inherited Metabolic Disease|January 1, 1995
Phytanic acid oxidation in man: identification of a new enzyme catalysing the formation of 2-ketophytanic acid from 2-hydroxyphytanic acid and its deficiency in the Zellweger syndromeR J Wanders, C W van Roermund, D S Schor, et al.
Journal of the Neurological Sciences|August 1, 1996
Evidence against increased oxidative stress in fibroblasts from patients with non-superoxide-dismutase-1 mutant familial amyotrophic lateral sclerosisG A Jansen, R J Wanders, G J Jöbsis, et al.
European Journal of Pediatrics|July 1, 1990
Peroxisomal beta-oxidation defect with detectable peroxisomes: a case with neonatal onset and progressive courseP G Barth, R J Wanders, R B Schutgens, et al.
Human Genetics|June 1, 1992
Genetic and biochemical heterogeneity in patients with the rhizomelic form of chondrodysplasia punctata--a complementation studyJ C Heikoop, R J Wanders, A Strijland, et al.
Pageof 50