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Here, GIP(3-30)NH 2 and GIP(5-30)NH 2 were characterized as potent, competitive and high-affinity antagonists of the human GIP receptor (14) ( Table 1 )
Its selective biochemical profile and favorable safety characteristics make it suitable for advanced studies on NAD+ metabolism, mitochondrial function, and metabolic health
Data were collected and analyzed using customized LabView software
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