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Chemically-diverse ligands at the glycine B site coupled to (NMDA) receptors selectively block the late phase of formalin-induced pain in mice

BiochemistryFunctional SelectivityPain MedicineMedicineMolecular PainNeuropharmacologyChemically-diverse LigandsPain MechanismPharmacologyGlycine B SiteDrug DiscoveryFormalin-induced PainPain Research