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For example, AuNC-Pt could be fabricated by conjugating the Pt(IV) prodrug to the amine group on the surface of AuNCs and proved to be effective in limiting Pt toxicity while effectively maximizing chemotherapeutic efficacy via depleting intracellular GSH (Yang et al., 2020) (Figure 2C)
High-resolution structural images of retatrutide bound to each of the three receptors, published in 2024, confirmed that one peptide can dock into three different receptor sites, providing the physical basis for the triple-receptor approach [3]
Glucose-dependent insulinotropic polypeptide prevents the progression of macrophage-driven atherosclerosis in diabetic apolipoprotein E-null mice
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Moving forward This research marks a significant step towards understanding weight loss medications' real-world use and outcomes
Keller, K
