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Journal of Lipid Research|January 18, 2005
A phytol-enriched diet induces changes in fatty acid metabolism in mice both via PPARalpha-dependent and -independent pathwaysJ Gloerich, N van Vlies, G A Jansen, et al.Journal of Lipid Research|June 11, 2016
Lipidomic analysis of fibroblasts from Zellweger spectrum disorder patients identifies disease-specific phospholipid ratiosKatharina Herzog, Mia L Pras-Raves, Martin A T Vervaart, et al.Mitochondrion|February 26, 2019
Overexpression of carbamoyl-phosphate synthase 1 significantly improves ureagenesis of human liver HepaRG cells only when cultured under shaking conditionsAziza A A Adam, Vincent A van der Mark, Jos P N Ruiter, et al.Journal of Medical Genetics|May 15, 2012
A novel defect of peroxisome division due to a homozygous non-sense mutation in the PEX11β geneMerel S Ebberink, Janet Koster, Gepke Visser, et al.The Biochemical Journal|March 7, 2002
Complete beta-oxidation of valproate: cleavage of 3-oxovalproyl-CoA by a mitochondrial 3-oxoacyl-CoA thiolaseMargarida F B Silva, Jos P N Ruiter, Henk Overmars, et al.American Journal of Human Genetics|April 16, 2003
2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency is caused by mutations in the HADH2 geneRob Ofman, Jos P N Ruiter, Marike Feenstra, et al.Drug Metabolism and Disposition: the Biological Fate of Chemicals|March 25, 2011
Role of isovaleryl-CoA dehydrogenase and short branched-chain acyl-CoA dehydrogenase in the metabolism of valproic acid: implications for the branched-chain amino acid oxidation pathwayPaula B M Luís, Jos P N Ruiter, Lodewijk Ijlst, et al.Endocrinology|April 18, 2012
The inflammatory response in acyl-CoA oxidase 1 deficiency (pseudoneonatal adrenoleukodystrophy)H I El Hajj, A Vluggens, P Andreoletti, et al.Proceedings of the National Academy of Sciences of the United States of America|January 5, 2013
Intrinsic acyl-CoA thioesterase activity of a peroxisomal ATP binding cassette transporter is required for transport and metabolism of fatty acidsCarine De Marcos Lousa, Carlo W T van Roermund, Vincent L G Postis, et al.The FEBS Journal|March 12, 2020
Fibroblast-specific genome-scale modelling predicts an imbalance in amino acid metabolism in Refsum diseaseAgnieszka B Wegrzyn, Katharina Herzog, Albert Gerding, et al.Pageof 48