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In vitro , GIP(17-30) and GIP(4-42) did not increase cellular cAMP production and had only weak insulin releasing activity compared with the native GIP ( Simultaneously, the most abundant circulating GIP fragment GIP(3-42) was identified as a GIP receptor antagonist with the ability to moderate GIP-induced cAMP production and insulin secretion in vitro ( Table 1 )

So that was how we actually started looking at a hypothesis for Alzheimer's and Parkinsons

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