Showing results (201-210 of 480) with videos related to
Sort By:
Pageof 48
Molecular Genetics and Metabolism|September 17, 2005
Identification of the human mitochondrial FAD transporter and its potential role in multiple acyl-CoA dehydrogenase deficiencyAndrás N Spaan, Lodewijk Ijlst, Carlo W T van Roermund, et al.Journal of Inherited Metabolic Disease|May 15, 2021
Inborn disorders of the malate aspartate shuttleMelissa H Broeks, Clara D M van Karnebeek, Ronald J A Wanders, et al.Archives of Disease in Childhood|October 23, 2004
High tolerance for oral galactose in classical galactosaemia: dietary implicationsA M Bosch, H D Bakker, L J M de B Wenniger-Prick, et al.Clinical Chemistry|April 8, 2006
Real-time nucleic acid sequence-based amplification assay to quantify changes in mitochondrial DNA concentrations in cell cultures and blood cells from HIV-infected patients receiving antiviral therapyEveline C Timmermans, Pablo Tebas, Jos P N Ruiter, et al.Psychiatry Research|October 17, 2012
Red blood cell polyunsaturated fatty acids measured in red blood cells and schizophrenia: a meta-analysisWendela P Hoen, Jeroen G Lijmer, Marinus Duran, et al.Molecular Genetics and Metabolism|October 25, 2016
A novel UPLC-MS/MS based method to determine the activity of N-acetylglutamate synthase in liver tissueMarli Dercksen, Marinus Duran, Lodewijk IJlst, et al.The New England Journal of Medicine|April 27, 2007
A lethal defect of mitochondrial and peroxisomal fissionHans R Waterham, Janet Koster, Carlo W T van Roermund, et al.Biochimica Et Biophysica Acta|May 7, 2013
Inhibition of N-acetylglutamate synthase by various monocarboxylic and dicarboxylic short-chain coenzyme A esters and the production of alternative glutamate estersM Dercksen, L IJlst, M Duran, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 17, 2013
Carnitine palmitoyltransferase 2 and carnitine/acylcarnitine translocase are involved in the mitochondrial synthesis and export of acylcarnitinesSara Violante, Lodewijk Ijlst, Heleen Te Brinke, et al.Pediatric Research|November 25, 2003
Novel mutations in the PEX2 gene of four unrelated patients with a peroxisome biogenesis disorderJeannette Gootjes, Orly Elpeleg, François Eyskens, et al.Pageof 48