The intracellular domain of homomeric glycine receptors modulates agonist efficacy.

5 C ) confirm this finding is robust as they gave maximum P open values that were indistinguishable, at 0.98, 0.88, 0.89, and 0.73, for the chimera and 0.99, 0.92, 0.90, and 0.70 for the α 1 GlyR ΔICD for glycine, β -alanine, taurine, and GABA, respectively (differences did not reach statistical significance).

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