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GIP (glucose-dependent insulinotropic polypeptide) receptors are expressed in adipose tissue and the liver, and their activation appears to improve lipid partitioning
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We study the effect of GSH and sexual dimorphism on acetaminophen toxicity by using a previously constructed model of acetaminophen metabolism [10]
This multi-receptor approach produces more powerful metabolic effects than current dual agonists like tirzepatide (Mounjaro/Zepbound)
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