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R J Wanders

Showing results (101-110 of 497) with videos related to

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Human Molecular Genetics|July 13, 1999
Enoyl-CoA hydratase deficiency: identification of a new type of D-bifunctional protein deficiencyE G van Grunsven, P A Mooijer, P Aubourg, et al.
European Journal of Biochemistry|April 24, 1999
Alkyl-dihydroxyacetone phosphate synthase and dihydroxyacetone phosphate acyltransferase form a protein complex in peroxisomesJ Biermann, W W Just, R J Wanders, et al.
European Journal of Biochemistry|June 1, 1983
Bicarbonate and the pathway of glutamate oxidation in isolated rat-liver mitochondriaR J Wanders, A J Meijer, A K Groen, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Immunoblot analysis of peroxisomal proteins in liver and fibroblasts from patientsR J Wanders, C Dekker, R Ofman, et al.
Nature Cell Biology|January 6, 2000
Peroxisomes in human fibroblasts have a basic pHT B Dansen, K W Wirtz, R J Wanders, et al.
Journal of Lipid Research|March 8, 2000
Peroxisomal fatty acid oxidation disorders and 58 kDa sterol carrier protein X (SCPx). Activity measurements in liver and fibroblasts using a newly developed methodS Ferdinandusse, S Denis, E van Berkel, et al.
Biochemistry International|October 1, 1990
Menadione partially restores NADH-oxidation and ATP-synthesis in complex I deficient fibroblastsF A Wijburg, N Feller, C J de Groot, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Restoration of NADH-oxidation in complex I and complex III deficient fibroblasts by menadioneF A Wijburg, C J de Groot, N Feller, et al.
The EMBO Journal|July 17, 1995
Peroxisomal and mitochondrial carnitine acetyltransferases of Saccharomyces cerevisiae are encoded by a single geneY Elgersma, C W van Roermund, R J Wanders, et al.
Biochemical and Biophysical Research Communications|April 7, 1997
Studies on the intracellular localization of acetyl-CoA carboxylaseM J Geelen, C Bijleveld, G Velasco, et al.
Pageof 50

Showing results (101-110 of 497) with videos related to

Sort By:
Pageof 50
Human Molecular Genetics|July 13, 1999
Enoyl-CoA hydratase deficiency: identification of a new type of D-bifunctional protein deficiencyE G van Grunsven, P A Mooijer, P Aubourg, et al.
European Journal of Biochemistry|April 24, 1999
Alkyl-dihydroxyacetone phosphate synthase and dihydroxyacetone phosphate acyltransferase form a protein complex in peroxisomesJ Biermann, W W Just, R J Wanders, et al.
European Journal of Biochemistry|June 1, 1983
Bicarbonate and the pathway of glutamate oxidation in isolated rat-liver mitochondriaR J Wanders, A J Meijer, A K Groen, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Immunoblot analysis of peroxisomal proteins in liver and fibroblasts from patientsR J Wanders, C Dekker, R Ofman, et al.
Nature Cell Biology|January 6, 2000
Peroxisomes in human fibroblasts have a basic pHT B Dansen, K W Wirtz, R J Wanders, et al.
Journal of Lipid Research|March 8, 2000
Peroxisomal fatty acid oxidation disorders and 58 kDa sterol carrier protein X (SCPx). Activity measurements in liver and fibroblasts using a newly developed methodS Ferdinandusse, S Denis, E van Berkel, et al.
Biochemistry International|October 1, 1990
Menadione partially restores NADH-oxidation and ATP-synthesis in complex I deficient fibroblastsF A Wijburg, N Feller, C J de Groot, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Restoration of NADH-oxidation in complex I and complex III deficient fibroblasts by menadioneF A Wijburg, C J de Groot, N Feller, et al.
The EMBO Journal|July 17, 1995
Peroxisomal and mitochondrial carnitine acetyltransferases of Saccharomyces cerevisiae are encoded by a single geneY Elgersma, C W van Roermund, R J Wanders, et al.
Biochemical and Biophysical Research Communications|April 7, 1997
Studies on the intracellular localization of acetyl-CoA carboxylaseM J Geelen, C Bijleveld, G Velasco, et al.
Pageof 50