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Description
While newly approved pharmacotherapies such as glucagon-like peptide-1 receptor agonists (GLP-1 RAs) show efficacy, their clinical utility remains constrained by dose-dependent gastrointestinal complications, underscoring the urgent need for safer alternatives

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These features enable stable receptor engagement in biochemical assays and make GLP-RTuseful for studying coordinated incretin signaling mechanisms within controlled experimental environments

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