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Presented for research literature review only Anderer S (2026)
Of the three, GIP(6-30)NH 2 was the most potent antagonist followed by GIP(7-30) and finally GIP(10-30), ranked by their potencies as inhibitors of GIP-stimulated cAMP production ( In 2001, several synthetic peptide GIP fragments were tested to identify the molecules bioactive domain
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