Molecular diversity of the NMDA receptor channel.

Binding of ArgTX-636 in the NMDA receptor ion channel.

channel complex.

Developmental changes in distribution of NMDA receptor channel subunit mRNAs.

Molecular cloning and characterization of the rat NMDA receptor.

Glutamate activation of a single NMDA receptor-channel produces a cluster of channel openings.

The differential contribution of GluN1 and GluN2 to the gating operation of the NMDA receptor channel.

Molecular Basis of Functional Myocardial Potassium Channel Diversity.

Effect of nitric oxide production on the redox modulatory site of the NMDA receptor-channel complex.

Redox modulatory site of the NMDA receptor-channel complex: regulation by oxidized glutathione.

Channel kinetics determine the time course of NMDA receptor-mediated synaptic currents.

From molecular phylogeny towards differentiating pharmacology for NMDA receptor subtypes.

Open-channel block of N-methyl-D-aspartate (NMDA) responses by memantine: therapeutic advantage against NMDA receptor-mediated neurotoxicity.

Ethanol and the NMDA receptor.

Rapid decay of averaged single-channel NMDA receptor activations recorded at low agonist concentration.

Functional characterization of a heteromeric NMDA receptor channel expressed from cloned cDNAs.

Effect of zinc on NMDA receptor-mediated channel currents in cortical neurons.

NMDA channel behavior depends on agonist affinity.

Calcium channel antagonists attenuate NMDA receptor-mediated neurotoxicity of retinal ganglion cells in culture.

Monoamine NMDA receptor channel blockers inhibit and potentiate native and recombinant proton-gated ion channels.

1,10-Diaminodecane and 1,12-diaminododecane block NMDA receptor currents by an open channel mechanism.

Molecular and genetic determinants of the NMDA receptor for superior learning and memory functions.

Block of NMDA receptor channels by endogenous neurosteroids: implications for the agonist induced conformational states of the channel vestibule.

Neramexane: a moderate-affinity NMDA receptor channel blocker: new prospects and indications.

Modulation of the NMDA receptor by polyamines.

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Binding of ArgTX-636 in the NMDA receptor ion channel.

channel complex.

Developmental changes in distribution of NMDA receptor channel subunit mRNAs.

Molecular cloning and characterization of the rat NMDA receptor.

Glutamate activation of a single NMDA receptor-channel produces a cluster of channel openings.

The differential contribution of GluN1 and GluN2 to the gating operation of the NMDA receptor channel.

Molecular Basis of Functional Myocardial Potassium Channel Diversity.

Effect of nitric oxide production on the redox modulatory site of the NMDA receptor-channel complex.

Redox modulatory site of the NMDA receptor-channel complex: regulation by oxidized glutathione.

Channel kinetics determine the time course of NMDA receptor-mediated synaptic currents.

From molecular phylogeny towards differentiating pharmacology for NMDA receptor subtypes.

Open-channel block of N-methyl-D-aspartate (NMDA) responses by memantine: therapeutic advantage against NMDA receptor-mediated neurotoxicity.

Ethanol and the NMDA receptor.

Rapid decay of averaged single-channel NMDA receptor activations recorded at low agonist concentration.

Functional characterization of a heteromeric NMDA receptor channel expressed from cloned cDNAs.

Effect of zinc on NMDA receptor-mediated channel currents in cortical neurons.

NMDA channel behavior depends on agonist affinity.

Calcium channel antagonists attenuate NMDA receptor-mediated neurotoxicity of retinal ganglion cells in culture.

Monoamine NMDA receptor channel blockers inhibit and potentiate native and recombinant proton-gated ion channels.

1,10-Diaminodecane and 1,12-diaminododecane block NMDA receptor currents by an open channel mechanism.

Molecular and genetic determinants of the NMDA receptor for superior learning and memory functions.

Block of NMDA receptor channels by endogenous neurosteroids: implications for the agonist induced conformational states of the channel vestibule.

Neramexane: a moderate-affinity NMDA receptor channel blocker: new prospects and indications.

Modulation of the NMDA receptor by polyamines.

Molecular diversity of the NMDA receptor channel.

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