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Apart from the -helical domain of G s and the extracellular domain (ECD) of GIPR, the presence of retatrutide, each individual receptor and heterotrimeric G s in the respective complexes were clearly visible in all three cryo-EM maps, thereby allowing unambiguous modeling of the secondary structure and side-chain orientation of all major components (Supplementary Fig

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PGC-1alpha, SIRT1 and AMPK, an energy sensing network that controls energy expenditure

detected GLP-1R protein expression by immunohistochemistry in mouse coronary endothelial and smooth muscle cells [35]

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