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Journal of Lipid Research|November 4, 2000
Subcellular localization and physiological role of alpha-methylacyl-CoA racemaseS Ferdinandusse, S Denis, L IJlst, et al.Molecular Genetics and Metabolism|August 18, 2001
Valproate induces in vitro accumulation of long-chain fatty acylcarnitinesM F Silva, C Jakobs, M Duran, et al.Journal of Lipid Research|November 28, 1997
Phytanic acid alpha-oxidation: decarboxylation of 2-hydroxyphytanoyl-CoA to pristanic acid in human liverN M Verhoeven, R J Wanders, D S Schor, et al.Acta Neuropathologica|July 6, 2004
Optico-cochleo-dentate degeneration associated with severe peripheral neuropathy and caused by peroxisomal D-bifunctional protein deficiencyJ M Schröder, V Hackel, R J A Wanders, et al.Journal of Hepatology|October 27, 2011
The value of pre-operative magnetic resonance spectroscopy in the assessment of steatohepatitis in patients with colorectal liver metastasisJozef Urdzik, Tomas Bjerner, Alkwin Wanders, et al.The Journal of Nutrition|July 15, 2011
A high intake of trans fatty acids has little effect on markers of inflammation and oxidative stress in humansLiesbeth A Smit, Martijn B Katan, Anne J Wanders, et al.The Journal of Clinical Investigation|August 15, 1996
Common missense mutation G1528C in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Characterization and expression of the mutant protein, mutation analysis on genomic DNA and chromosomal localization of the mitochondrial trifunctional protein alpha subunit geneL IJlst, J P Ruiter, J M Hoovers, et al.Journal of Experimental Psychology. Applied|December 18, 2023
Better to bend than to break? Effects of rule behavior on dominance, prestige, and leadership grantingAstrid C Homan, Florian Wanders, Annelies E M van Vianen, et al.Brain & Development|September 18, 2003
Gas chromatography/mass spectrometry analysis of very long chain fatty acids, docosahexaenoic acid, phytanic acid and plasmalogen for the screening of peroxisomal disordersYasuhiko Takemoto, Yasuyuki Suzuki, Ryoko Horibe, et al.Journal of Lipid and Atherosclerosis|October 7, 2020
Mitochondrial Fatty Acid Oxidation Disorders: Laboratory Diagnosis, Pathogenesis, and the Complicated Route to TreatmentRonald J A Wanders, Gepke Visser, Sacha Ferdinandusse, et al.Pageof 132