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Sacha Ferdinandusse

Showing results (11-20 of 153) with videos related to

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Advances in Experimental Medicine and Biology|January 10, 2004
Regulation of peroxisomal genes by DHEA and vitamin DMarianne Depreter, Jo Vandesompele, Sacha Ferdinandusse, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 2004
Analysis of cysteinyl leukotrienes and their metabolites in bile of patients with peroxisomal or mitochondrial beta-oxidation defectsErtan Mayatepek, Sacha Ferdinandusse, Thomas Meissner, et al.
Molecular Genetics and Metabolism|January 13, 2009
Toxicity of peroxisomal C27-bile acid intermediatesSacha Ferdinandusse, Simone Denis, Georges Dacremont, et al.
Histochemistry and Cell Biology|December 26, 2016
Peroxisomal abnormalities in the immortalized human hepatocyte (IHH) cell lineFemke C C Klouwer, Janet Koster, Sacha Ferdinandusse, et al.
Journal of Medical Case Reports|August 9, 2017
Identification of a novel mutation in PEX10 in a patient with attenuated Zellweger spectrum disorder: a case reportMaria Blomqvist, Karin Ahlberg, Julia Lindgren, et al.
Journal of Lipid Research|April 10, 2009
Bile acids: the role of peroxisomesSacha Ferdinandusse, Simone Denis, Phyllis L Faust, et al.
Orphanet Journal of Rare Diseases|March 12, 2011
Autosomal recessive cerebellar ataxia caused by mutations in the PEX2 geneCaroline Sevin, Sacha Ferdinandusse, Hans R Waterham, et al.
Advances in Experimental Medicine and Biology|January 8, 2021
Fatty Acid Oxidation in Peroxisomes: Enzymology, Metabolic Crosstalk with Other Organelles and Peroxisomal DisordersRonald J A Wanders, Frédéric M Vaz, Hans R Waterham, et al.
Journal of Inherited Metabolic Disease|May 2, 2024
Disorders of fatty acid homeostasisFrédéric M Vaz, Sacha Ferdinandusse, Gajja S Salomons, et al.
JIMD Reports|June 21, 2018
Extrapolation of Variant Phase in Mitochondrial Short-Chain Enoyl-CoA Hydratase (ECHS1) DeficiencyColleen M Carlston, Sacha Ferdinandusse, Judith A Hobert, et al.
Pageof 16

Showing results (11-20 of 153) with videos related to

Sort By:
Pageof 16
Advances in Experimental Medicine and Biology|January 10, 2004
Regulation of peroxisomal genes by DHEA and vitamin DMarianne Depreter, Jo Vandesompele, Sacha Ferdinandusse, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 2004
Analysis of cysteinyl leukotrienes and their metabolites in bile of patients with peroxisomal or mitochondrial beta-oxidation defectsErtan Mayatepek, Sacha Ferdinandusse, Thomas Meissner, et al.
Molecular Genetics and Metabolism|January 13, 2009
Toxicity of peroxisomal C27-bile acid intermediatesSacha Ferdinandusse, Simone Denis, Georges Dacremont, et al.
Histochemistry and Cell Biology|December 26, 2016
Peroxisomal abnormalities in the immortalized human hepatocyte (IHH) cell lineFemke C C Klouwer, Janet Koster, Sacha Ferdinandusse, et al.
Journal of Medical Case Reports|August 9, 2017
Identification of a novel mutation in PEX10 in a patient with attenuated Zellweger spectrum disorder: a case reportMaria Blomqvist, Karin Ahlberg, Julia Lindgren, et al.
Journal of Lipid Research|April 10, 2009
Bile acids: the role of peroxisomesSacha Ferdinandusse, Simone Denis, Phyllis L Faust, et al.
Orphanet Journal of Rare Diseases|March 12, 2011
Autosomal recessive cerebellar ataxia caused by mutations in the PEX2 geneCaroline Sevin, Sacha Ferdinandusse, Hans R Waterham, et al.
Advances in Experimental Medicine and Biology|January 8, 2021
Fatty Acid Oxidation in Peroxisomes: Enzymology, Metabolic Crosstalk with Other Organelles and Peroxisomal DisordersRonald J A Wanders, Frédéric M Vaz, Hans R Waterham, et al.
Journal of Inherited Metabolic Disease|May 2, 2024
Disorders of fatty acid homeostasisFrédéric M Vaz, Sacha Ferdinandusse, Gajja S Salomons, et al.
JIMD Reports|June 21, 2018
Extrapolation of Variant Phase in Mitochondrial Short-Chain Enoyl-CoA Hydratase (ECHS1) DeficiencyColleen M Carlston, Sacha Ferdinandusse, Judith A Hobert, et al.
Pageof 16