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63−65 It was found that the C-terminal residues Ala 24 and Gly 35 in the peptide were docked in a close proximity to Glu 133 and Glu 125 of the extracellular domain (ECD) of the receptor, respectively
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Although their mechanisms suggest potential advantages, particularly for patients with a cardiometabolic phenotype, clinical evidence supporting improvements in major clinical outcomes is lacking
