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Katz A (2022) A century of exercise physiology: key concepts in regulation of glycogen metabolism in skeletal muscle

Therefore, most of the disorders of fatty acid -oxidation metabolism and some of the disorders of abnormal branched-chain amino acid metabolism can be detected by measuring the levels of acyl carnitine in different lengths of carbon chains

It was demonstrated, [16] that muscle cells, that lack AMPD1, stock and consume significantly more glutamate, and produce more alanine in this state, compared to healthy controls, which indicates occurrence of a higher concentration of pyruvate in the cell during exercise

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