Results 21 to 30 of about 4,359,350 (361)
Enzymological determination of free carnitine concentrations in rat tissues
Journal of Lipid Research, 1964 Purified carnitine acetyltransferase was employed to catalyze the reaction:Carnitine+acetylCoA⇌acetylcarnitine+CoA. In the presence of a known excess of acetyl CoA, free CoA released was determined simultaneously in a coupled spectrophotometric assay ...
Norman R. Marquis, Irving B. Fritz
doaj +3 more sources
Iranian Journal of Public Health, 2013 Diabetes is a major health problem worldwide. Type II diabetic patients are reported to have higher ferritin and lower vitamin C concentrations. Considering the role of ascorbic acid in carnitine biosynthesis and the limited information on free carnitine
Ahmad Pourabbas +3 more
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Screening of Free Carnitine and Acylcarnitine Status in Children With Familial Mediterranean Fever. [PDF]
Arch Rheumatol, 2016 Kiykim E +6 more
europepmc +3 more sources
Hypoglycemia, Hepatic Dysfunction, Muscle Weakness, Cardiomyopathy, Free Carnitine Deficiency and Long-Chain Acylcarnitine Excess Responsive to Medium Chain Triglyceride Diet [PDF]
Pediatric Research, 1983 Allen M. Glasgow +7 more
openalex +2 more sources
Molecules, 2021 Carnitine insufficiency is reported in type 1 diabetes mellitus. To determine whether this is accompanied by defects in biosynthesis and/or renal uptake, liver and kidney were obtained from male Sprague-Dawley rats with streptozotocin-induced diabetes ...
Aman Upadhyay +2 more
doaj +1 more source
Levels of L-carnitine in human seminal plasma are associated with sperm fatty acid composition
Asian Journal of Andrology, 2022 The fatty acid composition of spermatozoa has been shown to be important for their function, and L-carnitine is crucial for fatty acid metabolism. Its levels in the seminal plasma positively correlate with semen quality, whereas high body mass index (BMI)
Mario Iliceto +4 more
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Frontiers in Medicine, 2021 Background: Carnitine supplementation improves various dialysis-related symptoms including erythropoietin-resistant anemia in patients who are undergoing hemodialysis.
Shohei Kaneko +6 more
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Frontiers in Genetics, 2021 Primary carnitine deficiency (PCD) is an autosomal recessive disorder that could result in sudden death. It is caused by a defect in the carnitine transporter encoded by SLC22A5 (Solute Carrier Family 22 Member 5, MIM:603377).
Xiangchun Yang +7 more
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American Journal of Physiology - Gastrointestinal and Liver Physiology, 2023 Medium-chain fatty acid (MCFA) consumption confers a wide range of health benefits that are highly distinct from long-chain fatty acids (LCFA). A major difference between the metabolism of LCFAs compared to MCFAs is that mitochondrial LCFA oxidation ...
Andrea S. Pereyra +3 more
semanticscholar +1 more source