The subtype of GluN2 C-terminal domain determines the response to excitotoxic insults.
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Antagonist properties of Conus parius peptides on N-methyl-D-aspartate receptors and their effects on CREB signalingMolecular bases of NMDA receptor subtype-dependent propertiesMolecular and genetic determinants of the NMDA receptor for superior learning and memory functionsLate Arc/Arg3.1 expression in the basolateral amygdala is essential for persistence of newly-acquired and reactivated contextual fear memories.Role of NMDA Receptor-Mediated Glutamatergic Signaling in Chronic and Acute NeuropathologiesInhibition of N-Methyl-D-aspartate-induced Retinal Neuronal Death by Polyarginine Peptides Is Linked to the Attenuation of Stress-induced Hyperpolarization of the Inner Mitochondrial Membrane PotentialMicroRNA-223 is neuroprotective by targeting glutamate receptors.Phosphorylation of tau at Y18, but not tau-fyn binding, is required for tau to modulate NMDA receptor-dependent excitotoxicity in primary neuronal culture.GLYX-13, a NMDA Receptor Glycine-Site Functional Partial Agonist, Attenuates Cerebral Ischemia Injury In Vivo and Vitro by Differential Modulations of NMDA Receptors Subunit Components at Different Post-Ischemia Stage in MiceActivation of mGluR5 attenuates NMDA-induced neurotoxicity through disruption of the NMDAR-PSD-95 complex and preservation of mitochondrial function in differentiated PC12 cells.Organization, control and function of extrasynaptic NMDA receptors.NR2B phosphorylation at tyrosine 1472 contributes to brain injury in a rodent model of neonatal hypoxia-ischemiaDifferential Tiam1/Rac1 activation in hippocampal and cortical neurons mediates differential spine shrinkage in response to oxygen/glucose deprivation.NADPH oxidase-2: linking glucose, acidosis, and excitotoxicity in stroke.Astrocytes increase the activity of synaptic GluN2B NMDA receptorsSelective dendritic susceptibility to bioenergetic, excitotoxic and redox perturbations in cortical neurons.TCN 201 selectively blocks GluN2A-containing NMDARs in a GluN1 co-agonist dependent but non-competitive mannerThe transcription factor calcium-response factor limits NMDA receptor-dependent transcription in the developing brain.Phosphoinositide 3-kinase couples NMDA receptors to superoxide release in excitotoxic neuronal death.NMDA receptor subunit composition determines beta-amyloid-induced neurodegeneration and synaptic loss.A Novel Binding Mode Reveals Two Distinct Classes of NMDA Receptor GluN2B-selective AntagonistsNMDA receptor-dependent glutamate excitotoxicity in human embryonic stem cell-derived neuronsInvolvement of the GluN2A and GluN2B subunits in synaptic and extrasynaptic N-methyl-D-aspartate receptor function and neuronal excitotoxicity.Recovery of NMDA receptor currents from MK-801 blockade is accelerated by Mg2+ and memantine under conditions of agonist exposureHuman immunodeficiency virus-1 Tat protein increases the number of inhibitory synapses between hippocampal neurons in cultureGlycine triggers a non-ionotropic activity of GluN2A-containing NMDA receptors to confer neuroprotection.Evidence for evolutionary divergence of activity-dependent gene expression in developing neuronsNeuroprotection Mediated through GluN2C-Containing N-methyl-D-aspartate (NMDA) Receptors Following IschemiaNMDARs Adapt to Neurotoxic HIV Protein Tat Downstream of a GluN2A-Ubiquitin Ligase Signaling Pathway.Influence of GluN2 subunit identity on NMDA receptor function.Pannexin channels and ischaemia.The interplay of microRNAs and post-ischemic glutamate excitotoxicity: an emergent research field in stroke medicine.The Role of GluN2A in Cerebral Ischemia: Promoting Neuron Death and Survival in the Early Stage and Thereafter.Location- and Subunit-Specific NMDA Receptors Determine the Developmental Sevoflurane Neurotoxicity Through ERK1/2 Signaling.Neurodegeneration and the Brain Tumor Microenvironment. [corrected]Identification and characterization of a small-molecule inhibitor of death-associated protein kinase 1.Pro-death NMDA receptor signaling is promoted by the GluN2B C-terminus independently of Dapk1.Involvement of protein phosphatases in the destabilization of methamphetamine-associated contextual memoryAllosteric Interactions between NMDA Receptor Subunits Shape the Developmental Shift in Channel Properties.Activity-dependent regulation of NMDA receptors in substantia nigra dopaminergic neurones.
P2860
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P2860
The subtype of GluN2 C-terminal domain determines the response to excitotoxic insults.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
The subtype of GluN2 C-terminal domain determines the response to excitotoxic insults.
@ast
The subtype of GluN2 C-terminal domain determines the response to excitotoxic insults.
@en
type
label
The subtype of GluN2 C-terminal domain determines the response to excitotoxic insults.
@ast
The subtype of GluN2 C-terminal domain determines the response to excitotoxic insults.
@en
prefLabel
The subtype of GluN2 C-terminal domain determines the response to excitotoxic insults.
@ast
The subtype of GluN2 C-terminal domain determines the response to excitotoxic insults.
@en
P2093
P2860
P50
P1433
P1476
The subtype of GluN2 C-terminal domain determines the response to excitotoxic insults.
@en
P2093
Bashayer Al-Mubarak
Jill H Fowler
Karen F S Bell
Marc-André Martel
Noboru H Komiyama
Seth G N Grant
P2860
P304
P356
10.1016/J.NEURON.2012.03.021
P407
P577
2012-05-01T00:00:00Z