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We also confirmed that treatment with aMsD4-C6, which is incapable of binding to Met (Supplementary Table 2 and Supplementary Fig

107 Dipeptidyl peptidase-IV (DPP-IV) is the enzyme responsible for the majority of the rapid GLP-1 degradation, by cleaving the first two N-terminal residues from GLP-1 (736 amide) and GLP-1 (737) to form GLP-1 (936 amide) and GLP-1 (937), respectively

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