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This synthetic peptide based on a natural compound in stomach juice is stable in the stomach acid and can be effective when taken orally in studies
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Collectively, our data suggest that T3 might also be able to increase the production of non-12-OH FXR-antagonistic BA species in human likely consequent to the increased synthesis of non-12-OH BAs, thereby potentiating the GLP-1 and insulin production by suppressing the intestinal FXR signaling (Fig
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