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This strategic design allows researchers to fully engage the GIP pathway for enhanced metabolic effects while minimizing the dose-limiting gastrointestinal tolerability issues common with high-dose GLP-1 agonism, making it uniquely valuable for studying synergistic incretin mechanisms

doi: 10.3389/fimmu.2022.816282 26 ScIndia PhDYLeeds MdJSwaminathan MdS

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