about
Three rare diseases in one Sib pair: RAI1, PCK1, GRIN2B mutations associated with Smith–Magenis Syndrome, cytosolic PEPCK deficiency and NMDA receptor glutamate insensitivityGRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel BlockersControl of neuronal ion channel function by glycogen synthase kinase-3: new prospective for an old kinase.GRIN2A mutation and early-onset epileptic encephalopathy: personalized therapy with memantine.Functional assessment of the NMDA receptor variant GluN2A R586K.ER to synapse trafficking of NMDA receptorsBidirectional Effect of Pregnenolone Sulfate on GluN1/GluN2A N-Methyl-D-Aspartate Receptor Gating Depending on Extracellular Calcium and Intracellular MilieuMolecular Mechanism of Disease-Associated Mutations in the Pre-M1 Helix of NMDA Receptors and Potential Rescue Pharmacology.A family of photoswitchable NMDA receptors.Target- and mechanism-based therapeutics for neurodegenerative diseases: strength in numbersMechanistic Insight into NMDA Receptor Dysregulation by Rare Variants in the GluN2A and GluN2B Agonist Binding Domains.The Role of GluN2C-Containing NMDA Receptors in Ketamine's Psychotogenic Action and in Schizophrenia Models.Functional analysis of a de novo GRIN2A missense mutation associated with early-onset epileptic encephalopathy.Influence of GluN2 subunit identity on NMDA receptor function.24(S)-Hydroxycholesterol as a Modulator of Neuronal Signaling and Survival.NMDA Receptor Internalization by Autoantibodies: A Reversible Mechanism Underlying Psychosis?GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects.Augmentation of Anticancer Drug Efficacy in Murine Hepatocellular Carcinoma Cells by a Peripherally Acting Competitive N-Methyl-d-aspartate (NMDA) Receptor Antagonist.De novo mutations in GRIN1 cause extensive bilateral polymicrogyria.Structural basis of subunit selectivity for competitive NMDA receptor antagonists with preference for GluN2A over GluN2B subunits.Functional Evaluation of a De Novo GRIN2A Mutation Identified in a Patient with Profound Global Developmental Delay and Refractory Epilepsy.Developmental Changes of Synaptic and Extrasynaptic NMDA Receptor Expression in Rat Cerebellar Neurons In Vitro.Surface Expression, Function, and Pharmacology of Disease-Associated Mutations in the Membrane Domain of the Human GluN2B Subunit.
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Molecular pharmacology of human NMDA receptors
@ast
Molecular pharmacology of human NMDA receptors
@en
type
label
Molecular pharmacology of human NMDA receptors
@ast
Molecular pharmacology of human NMDA receptors
@en
prefLabel
Molecular pharmacology of human NMDA receptors
@ast
Molecular pharmacology of human NMDA receptors
@en
P2093
P2860
P1476
Molecular pharmacology of human NMDA receptors
@en
P2093
Hans Bräuner-Osborne
Karen T Andersen
Kasper B Hansen
Maiken Hedegaard
Stephen F Traynelis
P2860
P304
P356
10.1016/J.NEUINT.2011.11.016
P577
2011-12-17T00:00:00Z