Alasdair J Gibb, Kevin K Ogden, Miranda J McDaniel, Katie M Vance, Steven A Kell, Chris Butch, Pieter Burger, Dennis C Liotta, Stephen F Traynelis. J Physiol 2018
Times Cited: 22
Times Cited: 22
Times Cited
Times Co-cited
Similarity
Glutamate receptor ion channels: structure, regulation, and function.
Stephen F Traynelis, Lonnie P Wollmuth, Chris J McBain, Frank S Menniti, Katie M Vance, Kevin K Ogden, Kasper B Hansen, Hongjie Yuan, Scott J Myers, Ray Dingledine. Pharmacol Rev 2010
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X-ray structure, symmetry and mechanism of an AMPA-subtype glutamate receptor.
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Wenshu XiangWei, Yuwu Jiang, Hongjie Yuan. Curr Opin Physiol 2018
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Specific sites within the ligand-binding domain and ion channel linkers modulate NMDA receptor gating.
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Functional analysis of a de novo GRIN2A missense mutation associated with early-onset epileptic encephalopathy.
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Mechanistic Insight into NMDA Receptor Dysregulation by Rare Variants in the GluN2A and GluN2B Agonist Binding Domains.
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Subunit arrangement and function in NMDA receptors.
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Channel opening and gating mechanism in AMPA-subtype glutamate receptors.
Edward C Twomey, Maria V Yelshanskaya, Robert A Grassucci, Joachim Frank, Alexander I Sobolevsky. Nature 2017
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An NMDAR positive and negative allosteric modulator series share a binding site and are interconverted by methyl groups.
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Subunit-specific agonist activity at NR2A-, NR2B-, NR2C-, and NR2D-containing N-methyl-D-aspartate glutamate receptors.
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Contribution of the M1 transmembrane helix and pre-M1 region to positive allosteric modulation and gating of N-methyl-D-aspartate receptors.
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Functional Evaluation of a De Novo GRIN2A Mutation Identified in a Patient with Profound Global Developmental Delay and Refractory Epilepsy.
Wenjuan Chen, Anel Tankovic, Pieter B Burger, Hirofumi Kusumoto, Stephen F Traynelis, Hongjie Yuan. Mol Pharmacol 2017
Wenjuan Chen, Anel Tankovic, Pieter B Burger, Hirofumi Kusumoto, Stephen F Traynelis, Hongjie Yuan. Mol Pharmacol 2017
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Subunit-specific gating controls rat NR1/NR2A and NR1/NR2B NMDA channel kinetics and synaptic signalling profiles.
Kevin Erreger, Shashank M Dravid, Tue G Banke, David J A Wyllie, Stephen F Traynelis. J Physiol 2005
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DRPEER: a motif in the extracellular vestibule conferring high Ca2+ flux rates in NMDA receptor channels.
Junryo Watanabe, Christine Beck, Thomas Kuner, Louis S Premkumar, Lonnie P Wollmuth. J Neurosci 2002
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Human GRIN2B variants in neurodevelopmental disorders.
Chun Hu, Wenjuan Chen, Scott J Myers, Hongjie Yuan, Stephen F Traynelis. J Pharmacol Sci 2016
Chun Hu, Wenjuan Chen, Scott J Myers, Hongjie Yuan, Stephen F Traynelis. J Pharmacol Sci 2016
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De novo GRIN variants in NMDA receptor M2 channel pore-forming loop are associated with neurological diseases.
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A conserved glycine harboring disease-associated mutations permits NMDA receptor slow deactivation and high Ca2+ permeability.
Johansen B Amin, Xiaoling Leng, Aaron Gochman, Huan-Xiang Zhou, Lonnie P Wollmuth. Nat Commun 2018
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NMDA receptor channel gating control by the pre-M1 helix.
Miranda J McDaniel, Kevin K Ogden, Steven A Kell, Pieter B Burger, Dennis C Liotta, Stephen F Traynelis. J Gen Physiol 2020
Miranda J McDaniel, Kevin K Ogden, Steven A Kell, Pieter B Burger, Dennis C Liotta, Stephen F Traynelis. J Gen Physiol 2020
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From bedside-to-bench: What disease-associated variants are teaching us about the NMDA receptor.
Johansen B Amin, Gabrielle R Moody, Lonnie P Wollmuth. J Physiol 2021
Johansen B Amin, Gabrielle R Moody, Lonnie P Wollmuth. J Physiol 2021
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Conserved structural and functional control of N-methyl-D-aspartate receptor gating by transmembrane domain M3.
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Structural determinants of agonist efficacy at the glutamate binding site of N-methyl-D-aspartate receptors.
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Ion permeation in ionotropic glutamate receptors: Still dynamic after all these years.
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Asynchronous movements prior to pore opening in NMDA receptors.
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Control of NMDA receptor function by the NR2 subunit amino-terminal domain.
Hongjie Yuan, Kasper B Hansen, Katie M Vance, Kevin K Ogden, Stephen F Traynelis. J Neurosci 2009
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Altered zinc sensitivity of NMDA receptors harboring clinically-relevant mutations.
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