Block of kainate receptor desensitization uncovers a key trafficking checkpoint.
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Functional comparison of the effects of TARPs and cornichons on AMPA receptor trafficking and gatingMolecular Basis of Kainate Receptor Modulation by SodiumStability of ligand-binding domain dimer assembly controls kainate receptor desensitizationCorrelating efficacy and desensitization with GluK2 ligand-binding domain movementsGlutamate binding and conformational flexibility of ligand-binding domains are critical early determinants of efficient kainate receptor biogenesis.Glutamate receptor ion channels: structure, regulation, and functionA transmembrane accessory subunit that modulates kainate-type glutamate receptors.Contribution of the global subunit structure and stargazin on the maturation of AMPA receptorsGABA acts as a ligand chaperone in the early secretory pathway to promote cell surface expression of GABAA receptorsControl of assembly and function of glutamate receptors by the amino-terminal domain.The biochemistry, ultrastructure, and subunit assembly mechanism of AMPA receptors.ER to synapse trafficking of NMDA receptorsProbing TARP modulation of AMPA receptor conductance with polyamine toxins.Trafficking of kainate receptors.Key amino acid residues within the third membrane domains of NR1 and NR2 subunits contribute to the regulation of the surface delivery of N-methyl-D-aspartate receptors.Regulation of synaptic transmission by ambient extracellular glutamateAn overview of trafficking and assembly of neurotransmitter receptors and ion channels (Review).Structural rearrangements of NR1/NR2A NMDA receptors during allosteric inhibition.Structure and mechanism of glutamate receptor ion channel assembly, activation and modulation.The multifaceted subunit interfaces of ionotropic glutamate receptors.Assembly of AMPA receptors: mechanisms and regulation.Retour aux sources: defining the structural basis of glutamate receptor activation.Crosslinking the ligand-binding domain dimer interface locks kainate receptors out of the main open state.The integrity of the glycine co-agonist binding site of N-methyl-D-aspartate receptors is a functional quality control checkpoint for cell surface delivery.Gating motions underlie AMPA receptor secretion from the endoplasmic reticulum.The N-terminal domain modulates α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor desensitization.Structural Bases of Desensitization in AMPA Receptor-Auxiliary Subunit Complexes.NMDA receptor activation requires remodelling of intersubunit contacts within ligand-binding heterodimersThe pain receptor TRPV1 displays agonist-dependent activation stoichiometry.Defining the structural relationship between kainate-receptor deactivation and desensitizationA nondesensitizing kainate receptor point mutant.SynDIG4/Prrt1 Is Required for Excitatory Synapse Development and Plasticity Underlying Cognitive Function.
P2860
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P2860
Block of kainate receptor desensitization uncovers a key trafficking checkpoint.
description
2006 nî lūn-bûn
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2006年の論文
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2006年学术文章
@wuu
2006年学术文章
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2006年学术文章
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2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
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2006年學術文章
@zh-hant
name
Block of kainate receptor desensitization uncovers a key trafficking checkpoint.
@en
Block of kainate receptor desensitization uncovers a key trafficking checkpoint.
@nl
type
label
Block of kainate receptor desensitization uncovers a key trafficking checkpoint.
@en
Block of kainate receptor desensitization uncovers a key trafficking checkpoint.
@nl
prefLabel
Block of kainate receptor desensitization uncovers a key trafficking checkpoint.
@en
Block of kainate receptor desensitization uncovers a key trafficking checkpoint.
@nl
P1433
P1476
Block of kainate receptor desensitization uncovers a key trafficking checkpoint
@en
P2093
Sanja Selak
Yael Stern-Bach
P304
P356
10.1016/J.NEURON.2006.12.006
P407
P577
2006-12-01T00:00:00Z