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Structural basis for partial agonist action at ionotropic glutamate receptorsOpen probability of homomeric murine 5-HT3A serotonin receptors depends on subunit occupancyCitrate modulates the regulation by Zn2+ of N-methyl-D-aspartate receptor-mediated channel current and neurotransmitter releaseFunctional properties of glycine receptors expressed in primary cultures of mouse cerebellar granule cells.Dysregulated NMDA-Receptor Signaling Inhibits Long-Term Depression in a Mouse Model of Fragile X Syndrome.The dilated TRPA1 channel pore state is blocked by amiloride and analogues.Subunit-specific gating controls rat NR1/NR2A and NR1/NR2B NMDA channel kinetics and synaptic signalling profiles.Protons trap NR1/NR2B NMDA receptors in a nonconducting state.Allosteric interaction between the amino terminal domain and the ligand binding domain of NR2A.Agonist discrimination between AMPA receptor subtypes.Pharmacological properties of homomeric and heteromeric GluR1o and GluR3o receptors.Activation of NR1/NR2B NMDA receptors.Identification of amino acid residues in GluR1 responsible for ligand binding and desensitization.Tonic activation of group I mGluRs modulates inhibitory synaptic strength by regulating KCC2 activity.STEP inhibition reverses behavioral, electrophysiologic, and synaptic abnormalities in Fmr1 KO mice.Hyperactivity and lack of social discrimination in the adolescent Fmr1 knockout mouse.Novel potent AMPA analogues differentially affect desensitisation of AMPA receptors in cultured hippocampal neurons.GABAergic input onto CA3 hippocampal interneurons remains shunting throughout development.Inhibition of TRPV1 channels enables long-term potentiation in the entorhinal cortex.Intracellular zinc irritates TRPA1.Inhibition of GluN2A NMDA receptors ameliorates synaptic plasticity deficits in the Fmr1-/y mouse model
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