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Clinical Nutrition (Edinburgh, Scotland)|September 19, 2020
Exploring the metabolic fate of medium-chain triglycerides in healthy individuals using a stable isotope tracerSuzan J G Knottnerus, Dewi van Harskamp, Henk Schierbeek, et al.Thrombosis and Haemostasis|July 19, 2022
The Platelet Lipidome Is Altered in Patients with COVID-19 and Correlates with Platelet ReactivityAlex R Schuurman, Valentine Léopold, Liza Pereverzeva, et al.Virology Journal|November 28, 2018
Virome analyses of Hevea brasiliensis using small RNA deep sequencing and PCR techniques reveal the presence of a potential new virusPaula L C Fonseca, Fernanda Badotti, Tatiana F P de Oliveira, et al.Journal of Lipid Research|May 10, 2022
Adaptations of the 3T3-L1 adipocyte lipidome to defective ether lipid catabolism upon Agmo knockdownSabrina Sailer, Katharina Lackner, Mia L Pras-Raves, et al.European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|December 6, 2024
Challenges in the identification and quantification of an unknown impurity in chenodeoxycholic acid drug substanceNatalja Bouwhuis, Yasmin Polak, Anneliene M Schimmel, et al.Circulation. Heart Failure|June 15, 2021
Cardiolipin Remodeling Defects Impair Mitochondrial Architecture and Function in a Murine Model of Barth Syndrome CardiomyopathySiting Zhu, Ze'e Chen, Mason Zhu, et al.Molecular Genetics and Metabolism Reports|December 20, 2021
Mitochondrial neurogastrointestinal encephalomyopathy: Clinical and biochemical impact of allogeneic stem cell transplantation in a Greek patient with one novel <i>TYMP</i> mutationA Paisiou, M Rogalidou, R Pons, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|May 12, 2021
Circadian misalignment disturbs the skeletal muscle lipidome in healthy young menJan-Frieder Harmsen, Nynke van Polanen, Michel van Weeghel, et al.Molecular Genetics and Metabolism|May 24, 2018
Deoxysphingolipid precursors indicate abnormal sphingolipid metabolism in individuals with primary and secondary disturbances of serine availabilityC R Ferreira, S M I Goorden, A Soldatos, et al.JIMD Reports|July 21, 2020
A newborn screening approach to diagnose 3-hydroxy-3-methylglutaryl-CoA lyase deficiencyJan Václavík, Lucie Mádrová, Štěpán Kouřil, et al.Pageof 55