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Disconnect between signalling potency and in vivo efficacy of pharmacokinetically optimised biased glucagon-like peptide-1 receptor agonists
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Genetically encoded photocross-linkers determine the biological binding site of exendin-4 peptide in the N-terminal domain of the intact human glucagon-like peptide-1 receptor (GLP-1R)
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Exendin-4 gene modification and microscaffold encapsulation promote self-persistence and antidiabetic activity of MSCs
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Acylation of the incretin peptide exendin-4 directly impacts GLP-1 receptor signalling and trafficking
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Immunogenicity Analysis of Exendin-4: High-Sensitivity ELISA Detection Protocols
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