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Revista Brasileira De Pesquisas Medicas E Biologicas|May 1, 1975
Reappearance of embryonal antigens in planarian regeneratesJ P Guimarães, L B Klaczko, K Hirano, et al.Journal of Inherited Metabolic Disease|December 18, 2019
Slc22a5 haploinsufficiency does not aggravate the phenotype of the long-chain acyl-CoA dehydrogenase KO mousePablo Ranea-Robles, Chunli Yu, Naomi van Vlies, et al.Journal of Lipid and Atherosclerosis|October 7, 2020
Mitochondrial Fatty Acid Oxidation Disorders: Laboratory Diagnosis, Pathogenesis, and the Complicated Route to TreatmentRonald J A Wanders, Gepke Visser, Sacha Ferdinandusse, et al.Biochimica Et Biophysica Acta|August 19, 2007
PPAR alpha-activation results in enhanced carnitine biosynthesis and OCTN2-mediated hepatic carnitine accumulationNaomi van Vlies, Sacha Ferdinandusse, Marjolein Turkenburg, et al.Immunology Letters|December 1, 1995
Anti-gamma delta T cell antibody blocks the induction and maintenance of oral tolerance to ovalbumin in miceJ Mengel, F Cardillo, L S Aroeira, et al.Immunology|January 1, 1993
Decrease in susceptibility to oral tolerance induction and occurrence of oral immunization to ovalbumin in 20-38-week-old mice. The effect of interval between oral exposures and rate of antigen intake in the oral immunizationA M Faria, G Garcia, M J Rios, et al.Proceedings of the National Academy of Sciences of the United States of America|September 1, 1973
Independent segregation of the H-2 locus and the locus for responsiveness to histamine-sensitizing factorZ Ovary, T W Vris, C de Szalay, et al.Journal of Inherited Metabolic Disease|September 15, 2006
Prolonged moderate-intensity exercise without and with L-carnitine supplementation in patients with MCAD deficiencyH H Huidekoper, J Schneider, T Westphal, et al.Disease Models & Mechanisms|September 15, 2022
Stimulating the sir2-spargel axis rescues exercise capacity and mitochondrial respiration in a Drosophila model of Barth syndromeDeena Damschroder, Rubén Zapata-Pérez, Kristin Richardson, et al.Journal of Lipid Research|November 9, 2011
Delineating the role of alterations in lipid metabolism to the pathogenesis of inherited skeletal and cardiac muscle disorders: Thematic Review Series: Genetics of Human Lipid DiseasesHarjot K Saini-Chohan, Ryan W Mitchell, Frédéric M Vaz, et al.Pageof 55