Structural basis of subunit selectivity for competitive NMDA receptor antagonists with preference for GluN2A over GluN2B subunits.

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Physiological activation of mGlu5 receptors supports the ion channel function of NMDA receptors in hippocampal LTD induction in vivo.

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Structural basis of subunit selectivity for competitive NMDA receptor antagonists with preference for GluN2A over GluN2B subunits.

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http://www.wikidata.org/entity/Q48317933

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2017 nî lūn-bûn

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Structural basis of subunit se ...... r GluN2A over GluN2B subunits.

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Structural basis of subunit se ...... r GluN2A over GluN2B subunits.

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type

Item

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Structural basis of subunit se ...... r GluN2A over GluN2B subunits.

@en

Structural basis of subunit se ...... r GluN2A over GluN2B subunits.

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Structural basis of subunit se ...... r GluN2A over GluN2B subunits.

@en

Structural basis of subunit se ...... r GluN2A over GluN2B subunits.

@nl

P1476

Structural basis of subunit se ...... r GluN2A over GluN2B subunits.

@en

P2093

Carlo De Micheli

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Genevieve E Lind

http://www.w3.org/2001/XMLSchema#string

Lucia Tamborini

http://www.w3.org/2001/XMLSchema#string

Martin G Pomper

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Paola Conti

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Tung-Chung Mou

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P2860

MolProbity: all-atom structure validation for macromolecular crystallography

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Taking the time to study competitive antagonism

Processing of X-ray diffraction data collected in oscillation mode

NMDA receptor modulators: an updated patent review (2013-2014)

Mechanisms of activation, inhibition and specificity: crystal structures of the NMDA receptor NR1 ligand-binding core

Substituted pyrazoles as hepatoselective HMG-CoA reductase inhibitors: discovery of (3R,5R)-7-[2-(4-fluoro-phenyl)-4-isopropyl-5-(4-methyl-benzylcarbamoyl)-2H-pyrazol-3-yl]-3,5-dihydroxyheptanoic acid (PF-3052334) as a candidate for the treatment of

Structural Determinants of Agonist Efficacy at the Glutamate Binding Site of N-Methyl-D-Aspartate Receptors

Crystal Structure and Pharmacological Characterization of a Novel N-Methyl-D-aspartate (NMDA) Receptor Antagonist at the GluN1 Glycine Binding Site

Structural Insights into Competitive Antagonism in NMDA Receptors

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E6942-E6951

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scholarly article

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10.1073/PNAS.1707752114

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English

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114

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Kasper B. Hansen

Andrea Pinto

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2017-07-31T00:00:00Z

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28760974

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P932

5565460

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Structural basis of subunit selectivity for competitive NMDA receptor antagonists with preference for GluN2A over GluN2B subunits.

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P2860

P2860

Structural basis of subunit selectivity for competitive NMDA receptor antagonists with preference for GluN2A over GluN2B subunits.

description

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type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932

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P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932