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doi: 10.1016/j.jdiacomp.2006.08.002 33 JaiswalMDiversJDabeleaDIsomSBellRAMartinCLet al
By modifying the OXM peptide sequence with an amino acid-peptide substitution at position 2 to prevent DPP-4 action, in addition to a cholesterol-peptide conjugate, Pocai and colleagues were the first group to show that synthetic dual-agonists were an effective treatment strategy in an animal model
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