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N-terminally and C-terminally truncated forms of glucose-dependent insulinotropic polypeptide are high-affinity competitive antagonists of the human GIP receptor
FIGURE 1 FIGURE 2 FIGURE 3 TABLE 1 Parameter estimates of the final model and 95% confidential interval
Future research directions include direct comparative trials between various GLP-1 RAs and multi-agonists in MASLD populations to identify optimal therapeutic choices for specific patient subgroups
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