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Intravenous administration is more likely to increase plasma carnitine concentration, yet homeostatic mechanisms tightly control blood concentration through metabolism and renal excretion: Up to 90% of 2 g of L-carnitine administered intravenously is excreted into the urine within 12 to 24 hours

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Expression of IGF-I splice variants in young and old human skeletal muscle after high resistance exercise

The K48-TUBEs approach excludes the ability of Ube3C to assemble K29-linked and other ubiquitin chain types, which are also able to mediate protein degradation 37,49