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Human Molecular Genetics|October 26, 2013
ACAD9, a complex I assembly factor with a moonlighting function in fatty acid oxidation deficienciesJessica Nouws, Heleen Te Brinke, Leo G Nijtmans, et al.Journal of Inherited Metabolic Disease|January 11, 2024
Glyoxylate reductase: Definitive identification in human liver mitochondria, its importance for the compartment-specific detoxification of glyoxylateSander F Garrelfs, Serhii Chornyi, Heleen Te Brinke, et al.Journal 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.Molecular Genetics and Metabolism|December 14, 2007
Characterization of L-aminocarnitine, an inhibitor of fatty acid oxidationMalika Chegary, Heleen Te Brinke, Mirjam Doolaard, et al.Annals of Neurology|October 13, 2017
Prediction of phenotypic severity in mucopolysaccharidosis type IIIASuzan J G Knottnerus, Stephanie C M Nijmeijer, Lodewijk IJlst, et al.Biochimica Et Biophysica Acta|May 31, 2011
Differential effects of short- and long-term high-fat diet feeding on hepatic fatty acid metabolism in ratsJolita Ciapaite, Nicole M van den Broek, Heleen Te Brinke, 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.Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 9, 2005
Phenotype determination guides swift genotyping of a DFNA2/KCNQ4 family with a hot spot mutation (W276S)Vedat Topsakal, Ronald J E Pennings, Heleen te Brinke, et al.Biochimica Et Biophysica Acta|July 16, 2013
Peroxisomes contribute to the acylcarnitine production when the carnitine shuttle is deficientSara Violante, Lodewijk Ijlst, Heleen Te Brinke, et al.Journal of Inherited Metabolic Disease|August 3, 2020
Increased protein propionylation contributes to mitochondrial dysfunction in liver cells and fibroblasts, but not in myotubesBart Lagerwaard, Olga Pougovkina, Anna F Bekebrede, et al.Pageof 3