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Description
Soontornmalai, A., Vlaming, M
By using a reducible disulfide linker, we built in a redox-sensitive release mechanism to facilitate intracellular release of the unmodified NMDA receptor antagonist, enabling the combined cellular actions of GLP-1 receptor agonism and NMDA receptor antagonism
An outline of the crystallisation of DAP BII in the absence and presence of the peptides is provided in Table S1
10.1016/S1360-1385(02)02312-9 103 MortonA
doi: 10.1001/jamaneurol.2024.3733, 5 AytonS.FauxN
