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Relating NMDA receptor function to receptor subunit composition: limitations of the pharmacological approach

The Journal of neuroscience, 2006-02, Vol.26 (5), p.1331-1333

2006

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Zinc alleviates pain through high-affinity binding to the NMDA receptor NR2A subunit

Nature neuroscience, 2011-07, Vol.14 (8), p.1017-1022

2011

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The micromolar zinc-binding domain on the NMDA receptor subunit NR2B

The Journal of neuroscience, 2005-01, Vol.25 (2), p.308-317

2005

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Structural Rearrangements of NR1/NR2A NMDA Receptors during Allosteric Inhibition

Neuron (Cambridge, Mass.), 2008-01, Vol.57 (1), p.80-93

2008

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High-Affinity Zinc Inhibition of NMDA NR1-NR2A Receptors

The Journal of neuroscience, 1997-08, Vol.17 (15), p.5711-5725

1997

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Mapping the Binding Site of the Neuroprotectant Ifenprodil on NMDA Receptors

The Journal of neuroscience, 2002-07, Vol.22 (14), p.5955-5965

2002

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Molecular Organization of a Zinc Binding N-Terminal Modulatory Domain in a NMDA Receptor Subunit

Neuron (Cambridge, Mass.), 2000-12, Vol.28 (3), p.911-925

2000

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NMDA receptor subunits: function and pharmacology

Current opinion in pharmacology, 2007-02, Vol.7 (1), p.39-47

2007

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Structural Basis of NR2B-Selective Antagonist Recognition by N-Methyl-d-aspartate Receptors

Molecular pharmacology, 2009-01, Vol.75 (1), p.60-74

2009

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Conformational transitions of the serotonin 5-HT3 receptor

Nature (London), 2018-11, Vol.563 (7730), p.275-279

2018

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The Binding of Palonosetron and Other Antiemetic Drugs to the Serotonin 5-HT3 Receptor

Structure (London), 2020-10, Vol.28 (10), p.1131-1140.e4

2020

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Identification of critical residues in the amino terminal domain of the human NR2B subunit involved in the RO 25-6981 binding pocket

The Journal of pharmacology and experimental therapeutics, 2003-12, Vol.307 (3), p.897-905

2003

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Author Correction: Structural determinants for activity of the antidepressant vortioxetine at human and rodent 5-HT3 receptors

Nature structural & molecular biology, 2024-07, Vol.31 (7), p.1145-1145

2024

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Structural determinants for activity of the antidepressant vortioxetine at human and rodent 5-HT3 receptors

Nature structural & molecular biology, 2024-08, Vol.31 (8), p.1232-1242

2024

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A prokaryotic proton-gated ion channel from the nicotinic acetylcholine receptor family

Nature, 2007-01, Vol.445 (7123), p.116-119

2007

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Conformational transitions of the serotonin 5-HT^sub 3^ receptor

Nature (London), 2018-11, Vol.563 (7730), p.275-279S

2018

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Internal Mg2+ block of recombinant NMDA channels mutated within the selectivity filter and expressed in Xenopus oocytes

The Journal of physiology, 1998-02, Vol.507 (1), p.1-12

1998

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Structural determinants for activity of the antidepressant vortioxetine at human and rodent 5-HT 3 receptors

Nature structural & molecular biology, 2024-08, Vol.31 (8), p.1232

2024

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Four residues of the extracellular N-terminal domain of the NR2A subunit control high-affinity Zn2+ binding to NMDA receptors

Neuron (Cambridge, Mass.), 2000-03, Vol.25 (3), p.683-694

2000

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Conformational transitions of the serotonin 5-HT 3 receptor

Nature (London), 2018-11, Vol.563 (7730), p.275

2018

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A Startling Role for Synaptic Zinc

Neuron (Cambridge, Mass.), 2006-11, Vol.52 (4), p.572-574

2006

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Synthesis and Biological Evaluation of 1-Amino-2-Phosphonomethylcyclopropanecarboxylic Acids, New Group III Metabotropic Glutamate Receptor Agonists

Journal of medicinal chemistry, 2007-07, Vol.50 (15), p.3585-3595

2007

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Reactive derivatives for affinity labeling in the ifenprodil site of NMDA receptors

Bioorganic & medicinal chemistry, 2008-05, Vol.18 (9), p.2765-2770

2008

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Glycine-independent and subunit-specific potentiation of NMDA responses by extracellular Mg2

Neuron (Cambridge, Mass.), 1995-11, Vol.15 (5), p.1109-1120

1995

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Article: Structural Rearrangements of NR1/NR2A NMDA Receptors during Allosteric Inhibition

Neuron (Cambridge, Mass.), 2008-01, Vol.57 (1), p.80-93

2008

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Relating NMDA receptor function to receptor subunit composition: limitations of the pharmacological approach

Zinc alleviates pain through high-affinity binding to the NMDA receptor NR2A subunit

The micromolar zinc-binding domain on the NMDA receptor subunit NR2B

Structural Rearrangements of NR1/NR2A NMDA Receptors during Allosteric Inhibition

High-Affinity Zinc Inhibition of NMDA NR1-NR2A Receptors

Mapping the Binding Site of the Neuroprotectant Ifenprodil on NMDA Receptors

Molecular Organization of a Zinc Binding N-Terminal Modulatory Domain in a NMDA Receptor Subunit

NMDA receptor subunits: function and pharmacology

Structural Basis of NR2B-Selective Antagonist Recognition by N-Methyl-d-aspartate Receptors

Conformational transitions of the serotonin 5-HT3 receptor

The Binding of Palonosetron and Other Antiemetic Drugs to the Serotonin 5-HT3 Receptor

Identification of critical residues in the amino terminal domain of the human NR2B subunit involved in the RO 25-6981 binding pocket

Author Correction: Structural determinants for activity of the antidepressant vortioxetine at human and rodent 5-HT3 receptors

Structural determinants for activity of the antidepressant vortioxetine at human and rodent 5-HT3 receptors

A prokaryotic proton-gated ion channel from the nicotinic acetylcholine receptor family

Conformational transitions of the serotonin 5-HT^sub 3^ receptor

Internal Mg2+ block of recombinant NMDA channels mutated within the selectivity filter and expressed in Xenopus oocytes

Structural determinants for activity of the antidepressant vortioxetine at human and rodent 5-HT 3 receptors

Four residues of the extracellular N-terminal domain of the NR2A subunit control high-affinity Zn2+ binding to NMDA receptors

Conformational transitions of the serotonin 5-HT 3 receptor

A Startling Role for Synaptic Zinc

Synthesis and Biological Evaluation of 1-Amino-2-Phosphonomethylcyclopropanecarboxylic Acids, New Group III Metabotropic Glutamate Receptor Agonists

Reactive derivatives for affinity labeling in the ifenprodil site of NMDA receptors

Glycine-independent and subunit-specific potentiation of NMDA responses by extracellular Mg2

Article: Structural Rearrangements of NR1/NR2A NMDA Receptors during Allosteric Inhibition

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