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A Wanders

Showing results (51-60 of 480) with videos related to

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Molecular Genetics and Metabolism|January 13, 2009
Toxicity of peroxisomal C27-bile acid intermediatesSacha Ferdinandusse, Simone Denis, Georges Dacremont, et al.
FEBS Letters|June 2, 2006
Brain pyruvate and 2-oxoglutarate dehydrogenase complexes are mitochondrial targets of the CoA ester of the Refsum disease marker phytanic acidVictoria I Bunik, Günter Raddatz, Ronald J A Wanders, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 28, 2002
A new defect of peroxisomal function involving pristanic acid: a case reportB N McLean, J Allen, S Ferdinandusse, et al.
Biochemical and Biophysical Research Communications|December 13, 2006
Inhibition of adenine nucleotide transport in rat liver mitochondria by long-chain acyl-coenzyme A beta-oxidation intermediatesFátima V Ventura, Isabel Tavares de Almeida, Ronald J A Wanders
European Journal of Human Genetics : EJHG|October 23, 2003
Novel mutations in the PEX12 gene of patients with a peroxisome biogenesis disorderJeannette Gootjes, Frank Schmohl, Hans R Waterham, et al.
Journal of Lipid Research|April 10, 2009
Bile acids: the role of peroxisomesSacha Ferdinandusse, Simone Denis, Phyllis L Faust, et al.
Journal of Inherited Metabolic Disease|April 30, 2010
Clinical aspects of short-chain acyl-CoA dehydrogenase deficiencyBianca T van Maldegem, Ronald J A Wanders, Frits A Wijburg
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.
Annual Review of Physiology|October 17, 2015
The Biochemistry and Physiology of Mitochondrial Fatty Acid β-Oxidation and Its Genetic DisordersSander M Houten, Sara Violante, Fatima V Ventura, et al.
Journal of Inherited Metabolic Disease|May 2, 2024
Disorders of fatty acid homeostasisFrédéric M Vaz, Sacha Ferdinandusse, Gajja S Salomons, et al.
Pageof 48

Showing results (51-60 of 480) with videos related to

Sort By:
Pageof 48
Molecular Genetics and Metabolism|January 13, 2009
Toxicity of peroxisomal C27-bile acid intermediatesSacha Ferdinandusse, Simone Denis, Georges Dacremont, et al.
FEBS Letters|June 2, 2006
Brain pyruvate and 2-oxoglutarate dehydrogenase complexes are mitochondrial targets of the CoA ester of the Refsum disease marker phytanic acidVictoria I Bunik, Günter Raddatz, Ronald J A Wanders, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 28, 2002
A new defect of peroxisomal function involving pristanic acid: a case reportB N McLean, J Allen, S Ferdinandusse, et al.
Biochemical and Biophysical Research Communications|December 13, 2006
Inhibition of adenine nucleotide transport in rat liver mitochondria by long-chain acyl-coenzyme A beta-oxidation intermediatesFátima V Ventura, Isabel Tavares de Almeida, Ronald J A Wanders
European Journal of Human Genetics : EJHG|October 23, 2003
Novel mutations in the PEX12 gene of patients with a peroxisome biogenesis disorderJeannette Gootjes, Frank Schmohl, Hans R Waterham, et al.
Journal of Lipid Research|April 10, 2009
Bile acids: the role of peroxisomesSacha Ferdinandusse, Simone Denis, Phyllis L Faust, et al.
Journal of Inherited Metabolic Disease|April 30, 2010
Clinical aspects of short-chain acyl-CoA dehydrogenase deficiencyBianca T van Maldegem, Ronald J A Wanders, Frits A Wijburg
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.
Annual Review of Physiology|October 17, 2015
The Biochemistry and Physiology of Mitochondrial Fatty Acid β-Oxidation and Its Genetic DisordersSander M Houten, Sara Violante, Fatima V Ventura, et al.
Journal of Inherited Metabolic Disease|May 2, 2024
Disorders of fatty acid homeostasisFrédéric M Vaz, Sacha Ferdinandusse, Gajja S Salomons, et al.
Pageof 48