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Description
Modern advances in long-acting peptide design, biased agonism, receptor de-orphanization, and systems pharmacology fundamentally alter the riskbenefit calculus of these targets
This can be particularly useful for patients who experience side effects at standard escalation rates and benefit from a slower, more gradual titration
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Exendin-4, a new peptide from Heloderma suspectum venom, potentiates cholecystokinin-induced amylase release from rat pancreatic acini
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