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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 15, 2022
Time-restricted feeding during the inactive phase abolishes the daily rhythm in mitochondrial respiration in rat skeletal musclePaul de Goede, Rob C I Wüst, Bauke V Schomakers, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 17, 2026
Reduced Versus Oxidized NAD<sup>+</sup> Precursors Drive Distinct Transcriptomic, Proteomic, and Metabolic Profiles in HepatocytesKasper T Vinten, Bauke V Schomakers, Simone Denis, et al.Mitochondrion|September 4, 2017
Mitochondrial disruption in peroxisome deficient cells is hepatocyte selective but is not mediated by common hepatic peroxisomal metabolitesAbhijit Babaji Shinde, Ritesh Kumar Baboota, Simone Denis, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 16, 2021
Reduced nicotinamide mononucleotide is a new and potent NAD<sup>+</sup> precursor in mammalian cells and miceRubén Zapata-Pérez, Alessandra Tammaro, Bauke V Schomakers, et al.Human Molecular Genetics|August 13, 2013
Impaired amino acid metabolism contributes to fasting-induced hypoglycemia in fatty acid oxidation defectsSander M Houten, Hilde Herrema, Heleen Te Brinke, et al.Annals of Neurology|November 10, 2005
Clinical and biochemical spectrum of D-bifunctional protein deficiencySacha Ferdinandusse, Simone Denis, Petra A W Mooyer, et al.Human Molecular Genetics|August 30, 2014
A novel bile acid biosynthesis defect due to a deficiency of peroxisomal ABCD3Sacha Ferdinandusse, Gerardo Jimenez-Sanchez, Janet Koster, et al.Human Molecular Genetics|May 22, 2014
Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemiaSander M Houten, Simone Denis, Heleen Te Brinke, et al.Journal of Medical Genetics|July 22, 2010
Identification of an unusual variant peroxisome biogenesis disorder caused by mutations in the PEX16 geneMerel S Ebberink, Barbara Csanyi, Wui K Chong, et al.Orphanet Journal of Rare Diseases|April 11, 2013
Genetic basis of hyperlysinemiaSander M Houten, Heleen Te Brinke, Simone Denis, et al.Pageof 4