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Multi-agonist therapy altered respiratory quotient, promoting greater fat oxidation (Fig
Missed signatures and incorrect information entries are examples of mistakes that should be avoided
The oxidative metabolism of glutamine
There is a large body of preclinical studies that provide compelling evidence of a functional BTR signaling system in enteroendocrine cells, the effects of non-nutritive BTR agonists on enteroendocrine hormone secretion, and the potential for stimulating intestinal BTRs to suppress energy intake and reduce postprandial glycemic excursions (59, 66)
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