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Attempts to block inhibitory signals, and potentially trigger effector function through Fc recognition, have been pursued through immune checkpoint inhibitor (ICI) strategies [117,118,119]

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Structurally, iGluRs are transmembrane proteins composed of four subunits that form a central ionic pore comprised of an extracellular amino-terminal domain, an extracellular ligand-binding domain, four transmembrane domains, and an intracellular carboxyl-terminal domain (Traynelis et al., 2010)

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