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Description
Phase 3 data from Chinese population
We identified lst-1 and sygl-1 as GLP-1 primary transcriptional targets through three genome-wide approaches
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Endogenous GLP-1 is quickly metabolized into the inactive peptide by dipeptidyl peptidase (DPP)-4, whereas GLP-1R agonists (GLP-1RAs) have a substantially longer plasma half-life than GLP-1 because of their resistance to DPP-4
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