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Cell|July 5, 2014
A mitochondrial expatriate: nuclear pyruvate dehydrogenaseVincent C J de Boer, Sander M HoutenJournal of Inherited Metabolic Disease|February 18, 2014
Aberrant protein acylation is a common observation in inborn errors of acyl-CoA metabolismOlga Pougovkina, Heleen Te Brinke, Ronald J A Wanders, et al.Human Molecular Genetics|February 12, 2014
Mitochondrial protein acetylation is driven by acetyl-CoA from fatty acid oxidationOlga Pougovkina, Heleen te Brinke, Rob Ofman, et al.Annals of Medicine|February 5, 2009
Metabolomics: unraveling the chemical individuality of common human diseasesSander M HoutenAnnals of Medicine|October 30, 2004
The enterohepatic nuclear receptors are major regulators of the enterohepatic circulation of bile saltsSander M Houten, Johan AuwerxThe Journal of Cell Biology|January 18, 2019
Saccharopine, a lysine degradation intermediate, is a mitochondrial toxinJoão Leandro, Sander M HoutenMolecular Genetics and Metabolism|August 10, 2020
The lysine degradation pathway: Subcellular compartmentalization and enzyme deficienciesJoão Leandro, Sander M HoutenBiochimica Et Biophysica Acta|October 13, 2006
Peroxisomes and bile acid biosynthesisSacha Ferdinandusse, Sander M HoutenPageof 19