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Here, plasma membrane mini-G s recruitment was somewhat reduced for exendin-4-C16 compared to exendin-4, which is compatible with results from our nanoBiT complementation assay demonstrating reduced global mini-G s recruitment efficacy to GLP-1R for this ligand

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N-terminal domain of androgen receptor is a major therapeutic barrier and potential pharmacological target for treating castration resistant prostate cancer: a comprehensive review