Similarly, sensitivity analysis was performed after excluding patients who took DPP-4 inhibitors and results were consistent (Supplementary Table 2)
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In addition, chimeric GLP-2 whose C-terminal fragment (residues 2033) was replaced with that of GLP-1 displayed a 17-fold potency reduction in GLP-2R signaling but successfully elicited GLP-1R-mediated cAMP accumulation (Fig