The DOI matches its Crossref record; 2,576 of the 2,576 references it cites were found in a registry or an index.
Structure, Function, and Pharmacology of Glutamate Receptor Ion Channels
Open accessAbstract
Many physiologic effects of l-glutamate, the major excitatory neurotransmitter in the mammalian central nervous system, are mediated via signaling by ionotropic glutamate receptors (iGluRs). These ligand-gated ion channels are critical to brain function and are centrally implicated in numerous psychiatric and neurologic disorders. There are different classes of iGluRs with a variety of receptor subtypes in each class that play distinct roles in neuronal functions. The diversity in iGluR subtypes, with their unique functional properties and physiologic roles, has motivated a large number of studies. Our understanding of receptor subtypes has advanced considerably since the first iGluR subunit gene was cloned in 1989, and the research focus has expanded to encompass facets of biology that have been recently discovered and to exploit experimental paradigms made possible by technological advances. Here, we review insights from more than 3 decades of iGluR studies with an emphasis on the progress that has occurred in the past decade. We cover structure, function, pharmacology, roles in neurophysiology, and therapeutic implications for all classes of receptors assembled from the subunits encoded by the 18 ionotropic glutamate receptor genes. SIGNIFICANCE STATEMENT: Glutamate receptors play important roles in virtually all aspects of brain function and are either involved in mediating some clinical features of neurological disease or represent a therapeutic target for treatment. Therefore, understanding the structure, function, and pharmacology of this class of receptors will advance our understanding of many aspects of brain function at molecular, cellular, and system levels and provide new opportunities to treat patients.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“NMDARs are heterotetrameric ligand-gated ionotropic receptors”
From Mechanisms of ketamine and its metabolites as antidepressants (2022) · cites this paper as Hansen et al., 2021
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Items 1,401–1,600 of 2,576
Benveniste, M., & Mayer, M. L. (1991) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1991.tb12409.x · Cited by 78
Stegenga, S. L., & Kalb, R. G. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00143-9 · Cited by 78
Mannara, F., Radosevic, M., Planagumà, J., Soto, D., Aguilar, E., García‐Serra, A., Maudes, E., Pedreño, M., Paul, S. M., Doherty, J., et al. (2020) · Brain · doi:10.1093/brain/awaa195 · Cited by 78
Hansen, K. B., & Traynelis, S. F. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.5565-10.2011 · Cited by 77
Self-citationHirai, K., Yoshioka, H., Kihara, M., Hasegawa, K., Sakamoto, T., Sawada, T., & Fushiki, S. (1999) · Developmental Brain Research · doi:10.1016/s0165-3806(99)00019-x · Cited by 77
Neto1 and Neto2: auxiliary subunits that determine key properties of native kainate receptors
Tomita, S., & Castillo, P. E. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2011.221101 · Cited by 77
Interdomain Interactions in AMPA and Kainate Receptors Regulate Affinity for Glutamate
Weston, M. C., Gertler, C., Mayer, M. L., & Rosenmund, C. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1519-06.2006 · Cited by 77
NMDA Receptors Containing the GluN2D Subunit Control Neuronal Function in the Subthalamic Nucleus
Swanger, S. A., Vance, K. M., Paré, J., Sotty, F., Fog, K., Smith, Y., & Traynelis, S. F. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1702-15.2015 · Cited by 77
Self-citationSeparation of Domain Contacts Is Required for Heterotetrameric Assembly of Functional NMDA Receptors
Farina, A. N., Blain, K. Y., Maruo, T., Kwiatkowski, W., Choe, S., & Nakagawa, T. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6041-10.2011 · Cited by 77
Self-citationWATSON, G., & Lanthorn, T. H. (1990) · Neuropharmacology · doi:10.1016/0028-3908(90)90125-b · Cited by 77
Bhattacharya, S., Khatri, A., Swanger, S. A., DiRaddo, J. O., Yi, F., Hansen, K. B., Yuan, H., & Traynelis, S. F. (2018) · Neuron · doi:10.1016/j.neuron.2018.06.010 · Cited by 77
Self-citationEmerging roles for telomerase in neuronal development and apoptosis
Mattson, M. P., & Klapper, W. (2001) · Journal of Neuroscience Research · doi:10.1002/1097-4547(20010101)63:1 · Cited by 76
Sessoms-Sikes, S., Honse, Y., Lovinger, D. M., & Colbran, R. J. (2005) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2005.01.006 · Cited by 76
Voltage and concentration dependence of Ca2+ permeability in recombinant glutamate receptor subtypes
Jatzke, C., Watanabe, J., & Wollmuth, L. P. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2001.012897 · Cited by 76
Self-citationExpression of AMPA Receptor Subunits at Synapses in Laminae I–III of the Rodent Spinal Dorsal Horn
Polgár, E., Watanabe, M., Hartmann, B., Grant, S. G. N., & Todd, A. J. (2008) · Molecular Pain · doi:10.1186/1744-8069-4-5 · Cited by 76
Babiec, W. E., Guglietta, R., Jami, S. A., Morishita, W., Malenka, R. C., & O’Dell, T. J. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.5419-13.2014 · Cited by 76
Weiss, B., Alt, A. J., Ogden, A. M. L., Gates, M. R., Dieckman, D. K., Clemens‐Smith, A., Ho, K. H., Jarvie, K. R., Rizkalla, G., Wright, R. A., et al. (2006) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.106.101428 · Cited by 76
d-Cycloserine Augmentation of Cognitive Behavioral Therapy for Anxiety Disorders: an Update
Hofmann, S. G., Otto, M. W., Pollack, M. H., & Smits, J. A. J. (2014) · Current Psychiatry Reports · doi:10.1007/s11920-014-0532-2 · Cited by 76
Subunit-specific potentiation of recombinant N-methyl-D-aspartate receptors by histamine.
Williams, K. L. (1994) · Molecular Pharmacology · doi:10.1016/s0026-895x(25)09731-7 · Cited by 76
Glial Cell AMPA Receptors in Nervous System Health, Injury and Disease
Ceprián, M., & Fulton, D. J. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20102450 · Cited by 76
Yamada, J., & Jinno, S. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.107710 · Cited by 76
Antigenic and mechanistic characterization of anti‐ AMPA receptor encephalitis
Gleichman, A. J., Panzer, J. A., Baumann, B. H., Dalmau, J. O., & Lynch, D. R. (2014) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.43 · Cited by 76
Kalbaugh, T. L., Zhang, J., & Diamond, J. S. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4240-08.2009 · Cited by 76
Self-citationMetabolic and microstructural alterations in the SLE brain correlate with cognitive impairment
Mackay, M. C., Vo, A., Tang, C. C., SMALL, M. P., Anderson, E., Ploran, E. J., Storbeck, J., Bascetta, B., Kang, S., Aranow, C. B., et al. (2019) · JCI Insight · doi:10.1172/jci.insight.124002 · Cited by 76
Milojkovic, B. A., Radojicic, M. S., Goldman‐Rakic, P. S., & Antic, S. D. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.061416 · Cited by 75
Guo, S., Huang, K., Shi, Y., Tang, W., Zhou, J. P., Feng, G., Zhu, S., Liu, H., Chen, Y., Sun, X.-D., et al. (2007) · Schizophrenia Research · doi:10.1016/j.schres.2007.03.007 · Cited by 75
Kay, A. R., & Tóth, K. (2008) · Science Signaling · doi:10.1126/stke.119re3 · Cited by 75
Philips, A. K., Sirén, A., Avela, K., Somer, M., Peippo, M. M., Ahvenainen, M., Doagu, F., Arvio, M., Kääriäinen, H., Esch, H. V., et al. (2014) · Orphanet Journal of Rare Diseases · doi:10.1186/1750-1172-9-49 · Cited by 75
Turecek, J., Jackman, S. L., & Regehr, W. G. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.11.081 · Cited by 75
Neuroprotective and cardioprotective conopeptides: an emerging class of drug leads.
Twede, V., Miljanich, G. P., Olivera, B. M., et al. (2009) · PubMed · Cited by 75
Bustos, F. J., Varela‐Nallar, L., Campos, M., Henríquez, B., Phillips, M. A., Opazo, C., Aguayo, L. G., Montecino, M. A., Constantine‐Paton, M., Inestrosa, N. C., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0094037 · Cited by 75
Gating mechanism and a modulatory niche of human GluN1-GluN2A NMDA receptors
Wang, H., Lv, S., Stroebel, D., Zhang, J., Pan, Y., Huang, X., Zhang, X., Paoletti, P., & Zhu, S. (2021) · Neuron · doi:10.1016/j.neuron.2021.05.031 · Cited by 75
Yasumura, M., Yoshida, T., Lee, S., Uemura, T., Joo, J., & Mishina, M. (2011) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2011.07631.x · Cited by 74
Kainate Receptors Exhibit Differential Sensitivities to (S)-5-Iodowillardiine
Swanson, G. T., Green, T., & Heinemann, S. F. (1998) · Molecular Pharmacology · doi:10.1016/s0026-895x(24)13262-2 · Cited by 74
Self-citationWilliams, K. L., Kashiwagi, K., Fukuchi, J., & Igarashi, K. (1995) · Molecular Pharmacology · doi:10.1016/s0026-895x(25)10580-4 · Cited by 74
Medina, I., Filippova, N., Charton, G., Rougeole, S., Ben‐Ari, Y., Khrestchatisky, M., & Bregestovski, P. D. (1995) · The Journal of Physiology · doi:10.1113/jphysiol.1995.sp020540 · Cited by 74
Tyrosine dephosphorylation regulates AMPAR internalisation in mGluR-LTD
Gladding, C. M., Collett, V. J., Jia, Z., Bashir, Z. I., Collingridge, G. L., & Molnár, E. (2009) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2008.10.014 · Cited by 74
Dolman, N. P., More, J. C. A., Alt, A. J., Knauss, J. L., Pentikäinen, O. T., Glasser, C. R., Bleakman, D., Mayer, M., Collingridge, G. L., & Jane, D. E. (2007) · Journal of Medicinal Chemistry · doi:10.1021/jm061041u · Cited by 74
Papadakis, M., Hawkins, L. M., & Stephenson, F. A. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m313446200 · Cited by 74
Kinetic basis of partial agonism at NMDA receptors
Kussius, C. L., & Popescu, G. (2009) · Nature Neuroscience · doi:10.1038/nn.2361 · Cited by 74
Functional and pharmacological properties of triheteromeric GluN1/2B/2D NMDA receptors
Yi, F., Bhattacharya, S., Thompson, C. M., Traynelis, S. F., & Hansen, K. B. (2019) · The Journal of Physiology · doi:10.1113/jp278168 · Cited by 74
Self-citationHillman, B. G., Gupta, S. C., Stairs, D. J., Buonanno, A., & Dravid, S. M. (2011) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2011.01.008 · Cited by 73
External anions and cations distinguish between AMPA and kainate receptor gating mechanisms
Bowie, D. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2001.013407 · Cited by 73
Self-citationMedial prefrontal cortex activation facilitates re-extinction of fear in ratsPreprint
Chang, C., & Maren, S. (2011) · Learning & Memory · doi:10.1101/lm.2070111 · Cited by 73
Glutamate and Glycine Binding to the NMDA Receptor
Yu, A., & Lau, A. Y. (2018) · Structure · doi:10.1016/j.str.2018.05.004 · Cited by 73
Talukder, I., Borker, P., & Wollmuth, L. P. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5382-09.2010 · Cited by 73
Self-citationFleming, T. M., Scott, V., Naskar, K., Joe, N., Brown, C. H., & Stern, J. E. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2011.207340 · Cited by 73
Matt, L., Kirk, L. M., Chenaux, G., Speca, D. J., Puhger, K. R., Pride, M. C., Qneibi, M., Haham, T., Plambeck, K. E., Stern-Bach, Y., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.02.026 · Cited by 73
Ravikrishnan, A., Gandhi, P. J., Shelkar, G. P., Liu, J., Pavuluri, R., & Dravid, S. M. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.03.011 · Cited by 73
Vesicular glutamate release from central axons contributes to myelin damage
Doyle, S., Hansen, D. B., Vella, J., Bond, P., Harper, G. M., Zammit, C., Valentino, M., & Fern, R. F. (2018) · Nature Communications · doi:10.1038/s41467-018-03427-1 · Cited by 73
Distinct gating modes determine the biphasic relaxation of NMDA receptor currents
Zhang, W., Howe, J. R., & Popescu, G. (2008) · Nature Neuroscience · doi:10.1038/nn.2214 · Cited by 72
Awobuluyi, M., Yang, J. Y., Ye, Y., Chatterton, J. E., Godzik, A., Lipton, S. A., & Zhang, D. (2006) · Molecular Pharmacology · doi:10.1124/mol.106.030700 · Cited by 72
D-Cycloserine Effects on Extinction of Conditioned Responses to Drug-Related Cues
Myers, K. M., & Carlezon, W. A. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.02.030 · Cited by 72
An analysis of philanthotoxin block for recombinant rat GluR6(Q) glutamate receptor channels
Bähring, R., & Mayer, M. L. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.635bm.x · Cited by 72
Novel NMDA receptor modulators: an update
Santangelo, R., Acker, T. M., Zimmerman, S. S., Katzman, B. M., Strong, K. L., Traynelis, S. F., & Liotta, D. C. (2012) · Expert Opinion on Therapeutic Patents · doi:10.1517/13543776.2012.728587 · Cited by 72
Self-citationRen, Z., Riley, N. J., Needleman, L. A., Sanders, J. M., Swanson, G. T., & Marshall, J. J. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m309585200 · Cited by 72
Self-citationDistinct Spatio‐temporal Distributions of the NMDA Receptor Channel Subunit mRNAs in the Brain
Watanabe, M., Inoue, Y., Sakimura, K., & Mishina, M. (1993) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1993.tb38099.x · Cited by 72
Banerjee, A., González-Rueda, A., Sampaio‐Baptista, C., Paulsen, O., & Moreno, A. R. (2014) · Physiological Reports · doi:10.1002/phy2.271 · Cited by 72
Different Mechanisms of Ca2+ Transport in NMDA and Ca2+-permeable AMPA Glutamate Receptor Channels
Wollmuth, L. P., & Sakmann, B. J. (1998) · The Journal of General Physiology · doi:10.1085/jgp.112.5.623 · Cited by 72
Self-citationKhlestova, E., Johnson, J. W., Krystal, J. H., & Lisman, J. E. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1203-16.2016 · Cited by 72
Wild, A. R., Sinnen, B. L., Dittmer, P. J., Kennedy, M. J., Sather, W. A., & Dell’Acqua, M. L. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.03.005 · Cited by 72
Self-citationEsketamine is approved in Europe for treating resistant major depressive disorder
Mahase, E. (2019) · BMJ · doi:10.1136/bmj.l7069 · Cited by 72
Yuan, H.-J., Myers, S. J., Wells, G., Nicholson, K., Swanger, S., Lyuboslavsky, P., Tahirovic, Y., Menaldino, D., Ganesh, T., Wilson, L., et al. (2015) · Neuron · doi:10.1016/j.neuron.2015.02.008 · Cited by 72
Self-citationA Homozygous Deletion in GRID2 Causes a Human Phenotype With Cerebellar Ataxia and Atrophy
Ütine, G. E., Haliloğlu, G., Salancı, B. V., Çetinkaya, A., Şimşek‐Kiper, P. Ö., Alanay, Y., Aktaş, D., Boduroğlu, K., & Alikaşifoğlu, M. (2013) · Journal of Child Neurology · doi:10.1177/0883073813484967 · Cited by 72
A Novel Conus Snail Polypeptide Causes Excitotoxicity by Blocking Desensitization of AMPA Receptors
Walker, C. S., Jensen, S., Ellison, M., Matta, J. A., Lee, W. Y., Imperial, J. S., Duclos, N., Brockie, P. J., Madsen, D. M., Isaac, J. T. R., et al. (2009) · Current Biology · doi:10.1016/j.cub.2009.05.017 · Cited by 72
Mutations of N-Methyl-D-Aspartate Receptor Subunits in Epilepsy
Xu, X., & Luo, J. (2017) · Neuroscience Bulletin · doi:10.1007/s12264-017-0191-5 · Cited by 72
Burnell, E. S., Irvine, M. W., Fang, G., Sapkota, K., Jane, D. E., & Monaghan, D. T. (2018) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.7b01640 · Cited by 72
Glutamate receptors of the delta family are widely expressed in the adult brain
Hepp, R., Hay, Y. A., Aguado, C., Lujan, R., Dauphinot, L., Potier, M. C., Nomura, S., Poirel, O., El Mestikawy, S., Lambolez, B., et al. (2015) · Brain Structure and Function · doi:10.1007/s00429-014-0827-4 · Cited by 71
Hansen, K. B., Naur, P., Kurtkaya, N. L., Kristensen, A. S., Gajhede, M., Kastrup, J. S., & Traynelis, S. F. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4081-08.2009 · Cited by 71
Self-citationKuner, T., Beck, C., Sakmann, B. J., & Seeburg, P. H. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-12-04162.2001 · Cited by 71
Cloning and functional characterization of human heteromeric N-methyl-D-aspartate receptors.
Hess, S. D., Daggett, L. P., Crona, J. H., Deal, C., Lu, C., Urrutia, A., Chavez-Noriega, L. E., Ellis, S. B., Johnson, E. C., & Veliçelebi, G. (1996) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)20667-x · Cited by 71
Chen, W., Tankovic, A., Burger, P. B., Kusumoto, H., Traynelis, S. F., & Yuan, H. (2017) · Molecular Pharmacology · doi:10.1124/mol.116.106781 · Cited by 71
Self-citationJaafari, N., Henley, J. M., & Hanley, J. G. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.5068-11.2012 · Cited by 71
Tethered ligands reveal glutamate receptor desensitization depends on subunit occupancy
Reiner, A., & Isacoff, E. Y. (2014) · Nature Chemical Biology · doi:10.1038/nchembio.1458 · Cited by 71
Bath, C. P., Farrell, L. N., Gilmore, J., et al. (1996) · European Journal of Pharmacology · doi:10.1016/0014-2999(95)00846-2 · Cited by 71
Arvola, M., & KEINÄNEN, K. P. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.26.15527 · Cited by 71
d-Serine, the Shape-Shifting NMDA Receptor Co-agonist
Coyle, J. T., Balu, D. T., & Wolosker, H. (2020) · Neurochemical Research · doi:10.1007/s11064-020-03014-1 · Cited by 71
Enhancement of psychosocial treatment with D-cycloserine: Models, moderators, and future directions
Otto, M. W., Kredlow, M. A., Smits, J. A. J., Hofmann, S. G., Tolin, D. F., de Kleine, R. A., van Minnen, A., Evins, A. E., & Pollack, M. H. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.09.007 · Cited by 70
Short-term plasticity as a neural mechanism supporting memory and attentional functions
Jääskeläinen, I. P., Ahveninen, J., Andermann, M. L., Belliveau, J. W., Raij, T., & Sams, M. E. (2011) · Brain Research · doi:10.1016/j.brainres.2011.09.031 · Cited by 70
Stargazin controls the pharmacology of AMPA receptor potentiators
Tomita, S., Sekiguchi, M., Wada, K., Nicoll, R. A., & Bredt, D. S. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0603128103 · Cited by 70
Veran, J., Kumar, J., Pinheiro, P. S., Athané, A., Mayer, M. L., Perrais, D., & Mulle, C. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.027 · Cited by 70
Activation of extrasynaptic NMDA receptors induces LTD in rat hippocampal CA1 neurons
Liu, D.-D., Yang, Q., & Li, S. (2012) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2012.12.003 · Cited by 70
BDNF upregulation rescues synaptic plasticity in middle-aged ovariectomized rats
Kramár, E. A., Chen, L. Y., Lauterborn, J. C., Simmons, D. A., Gall, C. M., & LYNCH, G. S. (2010) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2010.06.008 · Cited by 70
Gupta, S. C., Yadav, R., Pavuluri, R., Morley, B. J., Stairs, D. J., & Dravid, S. M. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.02.013 · Cited by 70
Chen, X., Lee, G., Maher, B. S., Fanous, A. H., Chen, J., Zhao, Z., Guo, A., van den Oord, E. J. C. G., Sullivan, P. F., Shi, J., et al. (2010) · Molecular Psychiatry · doi:10.1038/mp.2010.96 · Cited by 70
GluN1 splice variant control of GluN1/GluN2D NMDA receptors
Vance, K. M., Hansen, K. B., & Traynelis, S. F. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.234062 · Cited by 69
Self-citationErreger, K., & Traynelis, S. F. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2005.095497 · Cited by 69
Self-citationAllosteric signaling and dynamics of the clamshell-like NMDA receptor GluN1 N-terminal domain
Zhu, S., Stroebel, D., Yao, C. A., Taly, A., & Paoletti, P. (2013) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.2522 · Cited by 69
Ayalon, G., Segev, E., Elgavish, S., & Stern-Bach, Y. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m408413200 · Cited by 69
Lodge, D., Bond, A., O’Neill, M. J., Hicks, C. A., & Jones, M. G. (1996) · Neuropharmacology · doi:10.1016/s0028-3908(96)00155-4 · Cited by 69
Mechanism of Partial Agonism at NMDA Receptors for a Conformationally Restricted Glutamate Analog
Erreger, K., Geballe, M. T., Dravid, S. M., Snyder, J. P., Wyllie, D. J. A., & Traynelis, S. F. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1613-05.2005 · Cited by 69
Self-citationStefani, A., Chen, Q., Flores‐Hernández, J., Jiao, Y., Reiner, A. J., & Surmeier, D. J. (1998) · Developmental Neuroscience · doi:10.1159/000017318 · Cited by 69
Synaptic activation of kainate receptors gates presynaptic CB1 signaling at GABAergic synapses
Lourenço, J., Cannich, A., Carta, M., Coussen, F., Mulle, C., & Marsicano, G. (2010) · Nature Neuroscience · doi:10.1038/nn.2481 · Cited by 69
Braga, M. F. M., Aroniadou‐Anderjaska, V., Li, H., & Rogawski, M. A. (2009) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.109.153908 · Cited by 69
Liu, S., Zhou, L., Yuan, H., Vieira, M., Sanz-Clemente, A., Badger, J. D., Lu, W., Traynelis, S. F., & Roche, K. W. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.0827-16.2017 · Cited by 69
Self-citationKrall, R. F., Moutal, A., Phillips, M. B., Asraf, H., Johnson, J. W., Khanna, R., Hershfinkel, M., Aizenman, E., & Tzounopoulos, T. (2020) · Science Advances · doi:10.1126/sciadv.abb1515 · Cited by 69
Zwart, R., Sher, E., Ping, X., et al. (2014) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.114.212779 · Cited by 69
Distinct Structural Pathways Coordinate the Activation of AMPA Receptor-Auxiliary Subunit Complexes
Dawe, G. B., Musgaard, M., Aurousseau, M. R. P., Nayeem, N., Green, T., Biggin, P. C., & Bowie, D. (2016) · Neuron · doi:10.1016/j.neuron.2016.01.038 · Cited by 69
Self-citationAvenet, P., Léonardon, J., Besnard, F., Graham, D., Depoortere, H., & Scatton, B. (1997) · Neuroscience Letters · doi:10.1016/s0304-3940(97)13422-x · Cited by 68
D,L-(Tetrazol-5-yl) glycine: a novel and highly potent NMDA receptor agonist
Schoepp, D. D., Smith, C., Lodge, D., Millar, J. D., Leander, J. D., Sacaan, A. I., & Lunn, W. H. W. (1991) · European Journal of Pharmacology · doi:10.1016/0014-2999(91)90719-7 · Cited by 68
PDZ binding of TARPγ-8 controls synaptic transmission but not synaptic plasticity
Sumioka, A., Brown, T. E., Kato, A. S., Bredt, D. S., Kauer, J. A., & Tomita, S. (2011) · Nature Neuroscience · doi:10.1038/nn.2952 · Cited by 68
Chang, P., Zuckermann, A. M. E., Williams, S., Close, A. J., Cano‐Jaimez, M., McEvoy, J. P., Spencer, J., Walker, M. C., & Williams, R. S. B. (2014) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.114.218768 · Cited by 68
Gating Reaction Mechanisms for NMDA Receptor Channels
Auerbach, A. L., & Zhou, Y. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1471-05.2005 · Cited by 68
Martin, S., Chamberlin, A. C., Shinde, D. N., Hempel, M., Strom, T. M., Schreiber, A., Johannsen, J., Ousager, L. B., Larsen, M. J., Hansen, L. K., et al. (2017) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2017.11.004 · Cited by 68
Editing of Neurotransmitter Receptor and Ion Channel RNAs in the Nervous System
Hood, J. L., & Emeson, R. B. (2011) · Current topics in microbiology and immunology · doi:10.1007/82_2011_157 · Cited by 68
Isoform-Specific Early Trafficking of AMPA Receptor Flip and Flop Variants
Coleman, S. K., Möykkynen, T. P., Cai, C., von Ossowski, L., Kuismanen, E., Korpi, E. R., & KEINÄNEN, K. P. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2301-06.2006 · Cited by 68
Löscher, W., & Hönack, D. (1994) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1994.tb17146.x · Cited by 68
NR2 to NR3B subunit switchover of NMDA receptors in early postnatal motoneurons
Fukaya, M., Hayashi, Y., & Watanabe, M. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.03957.x · Cited by 68
Potential for therapeutic targeting of AKAP signaling complexes in nervous system disorders
Wild, A. R., & Dell’Acqua, M. L. (2017) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2017.12.004 · Cited by 68
Self-citationA mouse model of seizures in anti– N ‐methyl‐ d ‐aspartate receptor encephalitis
Taraschenko, O. D., Fox, H. S., Pittock, S. J., Ζεκερίδου, Α., Gafurova, M., Eldridge, E., Liu, J., Dravid, S. M., & Dingledine, R. J. (2019) · Epilepsia · doi:10.1111/epi.14662 · Cited by 68
Redefining the classification of AMPA‐selective ionotropic glutamate receptors
Bowie, D. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2011.221689 · Cited by 67
Self-citationGating Modes in AMPA Receptors
Prieto, M. L., & Wollmuth, L. P. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5613-09.2010 · Cited by 67
Self-citationHiyoshi, T., Kambe, D., Karasawa, J.-I., & Chaki, S. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.05.037 · Cited by 67
Intersubunit Cooperativity in the NMDA Receptor
Regalado, M. P., Villarroel, Á., & Lerma, J. (2001) · Neuron · doi:10.1016/s0896-6273(01)00539-6 · Cited by 67
Flip and Flop: A Molecular Determinant for AMPA Receptor Channel Opening
Pei, W., Huang, Z., Wang, C., Han, Y., Park, J. S., & Niu, L. (2009) · Biochemistry · doi:10.1021/bi8015907 · Cited by 67
Gating and permeation of kainate receptors: differences unveiled
Perrais, D., Veran, J., & Mulle, C. (2010) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2010.08.004 · Cited by 67
Nuclear and Mitochondrial Genome Defects in Autisms
Smith, M., Spence, M. A., & Flodman, P. L. (2008) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2008.03571.x · Cited by 67
Volkmann, R. A., Fanger, C. M., Anderson, D. R., Sirivolu, V. R., Paschetto, K. A., Gordon, E., Virginio, C., Gleyzes, M., Buisson, B., Steidl, E., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0148129 · Cited by 67
Self-citationSoumier, A., Carter, R. M., Schoenfeld, T. J., & Cameron, H. A. (2016) · eNeuro · doi:10.1523/eneuro.0116-15.2016 · Cited by 67
Cais, O., Herguedas, B., Krol, K., Cull-Candy, S. G., Farrant, M., & Greger, I. H. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.09.029 · Cited by 67
Self-citationAssessing the Role of GLUK5and GLUK6at Hippocampal Mossy Fiber Synapses
Breustedt, J., & Schmitz, D. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3078-04.2004 · Cited by 67
Hu, X.-D., Huang, Q., Yang, X., & Xia, H.-H. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.5365-06.2007 · Cited by 67
Structural mechanisms of activation and desensitization in neurotransmitter-gated ion channels
Plested, A. J. R. (2016) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.3214 · Cited by 67
Xie, J., 谢, 敬., Chen, S., 陈, 少., Chen, H., 陈, 红., Zeng, W., 曾, 维., Pan, H., & 潘, 惠. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.732347 · Cited by 67
Purkey, A., Woolfrey, K. M., Crosby, K. C., Stich, D., Chick, W. S. H., Aoto, J. N., & Dell’Acqua, M. L. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.09.085 · Cited by 67
Self-citationThe contribution of rare and common variants in 30 genes to risk nicotine dependence
Yang, J., Wang, S., Yang, Z., Hodgkinson, C. A., Iarikova, P., Ma, J. Z., Payne, T. J., Goldman, D. A., & Li, M. D. (2014) · Molecular Psychiatry · doi:10.1038/mp.2014.156 · Cited by 66
20-Oxo-5β-Pregnan-3α-yl Sulfate Is a Use-Dependent NMDA Receptor Inhibitor
Petrovic, M., Sedlacek, M., Hořák, M., Chodounská, H., & Vyklický, L. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1407-05.2005 · Cited by 66
Expression and novel subunit isoforms of glutamate receptor genes GluR5 and GluR6
Gregor, P., O’Hara, B. F., Yang, X., & Uhl, G. R. (1993) · Neuroreport · doi:10.1097/00001756-199309150-00014 · Cited by 66
Yadav, R., Hillman, B. G., Gupta, S. C., Suryavanshi, P. S., Bhatt, J. M., Pavuluri, R., Stairs, D. J., & Dravid, S. M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0060785 · Cited by 66
Functional characterization of CP-465,022, a selective, noncompetitive AMPA receptor antagonist
Lazzaro, J. T., Paternain, A. V., Lerma, J., Chenard, B. L., Ewing, F. E., HUANG, J., WELCH, W. M., Ganong, A. H., & Menniti, F. S. (2002) · Neuropharmacology · doi:10.1016/s0028-3908(01)00170-8 · Cited by 66
Self-citationOrphan Glutamate Receptor δ1 Subunit Required for High-Frequency Hearing
Gao, J., Maison, S. F., Wu, X., Hirose, K., Jones, S. M., Bayazitov, I. T., Tian, Y., Mittleman, G., Matthews, D. B., Zakharenko, S. S., et al. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.02051-06 · Cited by 66
Reconstitution of invertebrate glutamate receptor function depends on stargazin-like proteins
Walker, C. S., Brockie, P. J., Madsen, D. M., Francis, M. M., Zheng, Y., Koduri, S., Mellem, J. E., Strutz‐Seebohm, N., & Maricq, A. V. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604482103 · Cited by 66
Schmidt, J. T. (2004) · Journal of Neurobiology · doi:10.1002/neu.10343 · Cited by 66
Penn, A. C., Balík, A., Wozny, C., Cais, O., & Greger, I. H. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.010 · Cited by 66
Self-citationPresynaptic NMDA Receptor Mechanisms for Enhancing Spontaneous Neurotransmitter Release
Kunz, P. A., Roberts, A. C., & Philpot, B. D. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2482-12.2013 · Cited by 66
Contribution of the Global Subunit Structure and Stargazin on the Maturation of AMPA Receptors
Shanks, N. F., Maruo, T., Farina, A. N., Ellisman, M. H., & Nakagawa, T. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5146-09.2010 · Cited by 66
Self-citationTay, S. H., Fairhurst, A., & Mak, A. (2016) · Autoimmunity Reviews · doi:10.1016/j.autrev.2016.12.002 · Cited by 66
AMPA receptor nanoscale dynamic organization and synaptic plasticities
Choquet, D., & Hosy, E. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.04.003 · Cited by 66
Zinc inhibition of rat NR1/NR2AN‐methyl‐ d ‐aspartate receptors
Erreger, K., & Traynelis, S. F. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.143941 · Cited by 65
Self-citationLee, S. Y., Földy, C., Szabadics, J., & Soltész, I. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.1970-11.2011 · Cited by 65
Mullier, B., Wolff, C., Sands, Z. A., Ghisdal, P., Muglia, P., Kaminski, R. M., & André, V. M. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.05.017 · Cited by 65
Sheng, N., Bemben, M. A., Díaz-Alonso, J., Tao, W., Shi, Y. S., & Nicoll, R. A. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1800719115 · Cited by 65
Shin, W., Kim, K., Serraz, B., Cho, Y. S., Kim, D., Kang, M., Lee, E., Lee, H., Bae, Y. C., Paoletti, P., et al. (2020) · PLoS Biology · doi:10.1371/journal.pbio.3000717 · Cited by 65
Lauvsnes, M. B., Beyer, M. K., Kvaløy, J. T., Greve, O. J., Appenzeller, S., Kvivik, I., Harboe, E., Tjensvoll, A. B., Gøransson, L. G., & Omdal, R. (2014) · Arthritis & Rheumatology · doi:10.1002/art.38852 · Cited by 65
Safieddine, S., & Wenthold, R. J. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-19-07523.1997 · Cited by 65
Probing the Allosteric Modulator Binding Site of GluR2 with Thiazide Derivatives
Ptak, C. P., Ahmed, A. H., & Oswald, R. E. (2009) · Biochemistry · doi:10.1021/bi901127s · Cited by 65
Lanore, F., Labrousse, V. F., Szabó, Z. M., Normand, E., Blanchet, C., & Mulle, C. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2049-12.2012 · Cited by 65
Nasu‐Nishimura, Y., Hurtado, D. E., Braud, S., Tang, T. T.-T., Isaac, J. T. R., & Roche, K. W. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0573-06.2006 · Cited by 65
Characterization of Disease-Associated Mutations in Human Transmembrane Proteins
Molnár, J., Szakács, G., & Tusnády, G. (2016) · PLoS ONE · doi:10.1371/journal.pone.0151760 · Cited by 65
Kitayama, T., Yoneyama, M., & Yoneda, Y. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.01567.x · Cited by 64
Access of inhibitory neurosteroids to the NMDA receptor
Borovská, J., Vyklický, V., Kudová, E., Kapras, V., Slavı́ková, B., Hořák, M., Chodounská, H., & Vyklický, L. (2011) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2011.01816.x · Cited by 64
Control of kinetic properties of GluR2 flop AMPA‐type channels: impact of R/G nuclear editing
Krampfl, K., Schlesinger, F., Zoerner, A., Kappler, M., Dengler, R., & Bufler, J. (2002) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01841.x · Cited by 64
Addy, C., Assaid, C., Hreniuk, D., Stroh, M., Xu, Y., Herring, W. J., Ellenbogen, A. L., Jinnah, H. A., Kirby, L. C., Leibowitz, M. T., et al. (2009) · The Journal of Clinical Pharmacology · doi:10.1177/0091270009336735 · Cited by 64
Ito, A., Miyazaki, T., Miura, E., Matsuda, K., Watanabe, M., Yuzaki, M., & Okabe, S. (2012) · Neuron · doi:10.1016/j.neuron.2012.07.027 · Cited by 64
Kinetic properties of human AMPA‐type glutamate receptors expressed in HEK293 cells
Großkreutz, J., Zoerner, A., Schlesinger, F., Krampfl, K., Dengler, R., & Bufler, J. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02531.x · Cited by 64
Chao, J., Seiler, N., Renault, J., Kashiwagi, K., Masuko, T., Igarashi, K., & Williams, K. L. (1997) · Molecular Pharmacology · doi:10.1124/mol.51.5.861 · Cited by 64
Endogenous 24S-hydroxycholesterol modulates NMDAR-mediated function in hippocampal slices
Sun, M., Izumi, Y., Benz, A. M., Zorumski, C. F., & Mennerick, S. J. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00890.2015 · Cited by 64
Getting a Handle on Neuropharmacology by Targeting Receptor-Associated Proteins
Maher, M. P., Matta, J. A., Gu, S., Seierstad, M., & Bredt, D. S. (2017) · Neuron · doi:10.1016/j.neuron.2017.10.001 · Cited by 64
Li, J., Zhang, J., Tang, W., Mizu, R. K., Kusumoto, H., XiangWei, W., Xu, Y., Chen, W., Amin, J. B., Hu, C., et al. (2019) · Human Mutation · doi:10.1002/humu.23895 · Cited by 64
Self-citationNew mechanisms of excitatory transmitter neurotoxicity.
Olney, J. W. (1994) · PubMed · Cited by 63
Church, J., Fletcher, E. J., Baxter, K., & MacDonald, J. F. (1994) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1994.tb17017.x · Cited by 63
Auxiliary Subunits: Shepherding AMPA Receptors to the Plasma Membrane
Haering, S., Tapken, D., Pahl, S., & Hollmann, M. (2014) · Membranes · doi:10.3390/membranes4030469 · Cited by 63
Design of antagonists for NMDA and AMPA receptors
Bolshakov, K. V., Kim, K., Potapjeva, N. N., Гмиро, В. Е., Tikhonov, D. B., Usherwood, P. N. R., Mellor, I. R., & Magazanik, L. G. (2005) · Neuropharmacology · doi:10.1016/j.neuropharm.2005.02.007 · Cited by 63
Neto2 Modulation of Kainate Receptors with Different Subunit Compositions
Straub, C., Zhang, W., & Howe, J. R. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0024-11.2011 · Cited by 63
Enhanced Visual Activity In Vivo Forms Nascent Synapses in the Developing Retinotectal Projection
Aizenman, C. D., & Cline, H. T. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00452.2006 · Cited by 63
Kakegawa, W., Kohda, K., & Yuzaki, M. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.141291 · Cited by 63
Auxiliary subunits of the CKAMP family differentially modulate AMPA receptor properties
Farrow, P., Khodosevich, K. V., Sapir, Y., Schulmann, A., Aslam, M., Stern-Bach, Y., Monyer, H., & von Engelhardt, J. (2015) · eLife · doi:10.7554/elife.09693 · Cited by 63
Novel Functional Properties of Drosophila CNS Glutamate Receptors
Li, Y., Dharkar, P., Han, T.-H., Serpe, M., Lee, C., & Mayer, M. L. (2016) · Neuron · doi:10.1016/j.neuron.2016.10.058 · Cited by 63
Structural Proof of a Dimeric Positive Modulator Bridging Two Identical AMPA Receptor-Binding Sites
Kaae, B. H., Harpsøe, K., Kastrup, J. S., Sanz, A. C., Pickering, D. S., Metzler, B., Clausen, R. P., Gajhede, M., Sauerberg, P., Liljefors, T., et al. (2007) · Chemistry & Biology · doi:10.1016/j.chembiol.2007.10.012 · Cited by 63
Post-Translational Modification Biology of Glutamate Receptors and Drug Addiction
Mao, L., Guo, M., Jin, D.-Z., Fibuch, E. E., Choe, E. S., & Wang, J. Q. (2011) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2011.00019 · Cited by 63
Ravindranathan, A., Donevan, S. D., Sugden, S. G., Greig, A., Rao, M. S., & Parks, T. N. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.00667.x · Cited by 63
Clinical trials in head injury
Reinert, M., & Bullock, R. M. (1999) · Neurological Research · doi:10.1080/01616412.1999.11740940 · Cited by 63
Salimando, G. J., Hyun, M., Boyt, K. M., & Winder, D. G. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0270-20.2020 · Cited by 63
Wyeth, M. S., Pelkey, K. A., Petralia, R. S., Salter, M. W., McInnes, R. R., & McBain, C. J. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.3098-13.2014 · Cited by 62
Self-citationPovysheva, N. V., & Johnson, J. W. (2012) · Journal of Neurophysiology · doi:10.1152/jn.01017.2011 · Cited by 62
Pickard, B. S., Knight, H. M., Hamilton, R. S., Soares, D. C., WALKER, R. E., Boyd, J. K. F., Machell, J., Maclean, A. W., McGhee, K. A., Condie, A., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0800643105 · Cited by 62
Allosteric Regulation and Spatial Distribution of Kainate Receptors Bound to Ancillary Proteins
Bowie, D., Garcia, E. P., Marshall, J. J., Traynelis, S. F., & Lange, G. D. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2002.033076 · Cited by 62
Self-citationGao, K., Tankovic, A., Zhang, Y., Kusumoto, H., Zhang, J., Chen, W., XiangWei, W., Shaulsky, G. H., Hu, C., Traynelis, S. F., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0170818 · Cited by 62
Self-citationAndreae, L. C., & Burrone, J. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.01.032 · Cited by 62
Luque, J. M., Bleuel, Z., Malherbe, P., & Richards, J. G. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90510-x · Cited by 62
Kainate induces rapid redistribution of the actin cytoskeleton in ameboid microglia
Christensen, R. N., Ha, B. K., Sun, F., Bresnahan, J. C., & Beattie, M. S. (2006) · Journal of Neuroscience Research · doi:10.1002/jnr.20865 · Cited by 62
Oh, S. J., Han, K. S., Park, H., Woo, D. H., Kim, H. Y., Traynelis, S. F., & Lee, C. J. (2012) · Molecular Brain · doi:10.1186/1756-6606-5-38 · Cited by 62
Self-citationBowie, D. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.tm118.003794 · Cited by 62
Self-citationDesensitization of NMDA Receptor Channels Is Modulated by Glutamate Agonists
Nahum-Levy, R., Lipinsky, D., Shavit, S., & Benveniste, M. (2001) · Biophysical Journal · doi:10.1016/s0006-3495(01)76188-7 · Cited by 61
Copy number variation in Han Chinese individuals with autism spectrum disorder
Gazzellone, M. J., Zhou, X., Lionel, A. C., Uddin, M. J., Thiruvahindrapuram, B., Liang, S., Sun, C., Wang, J., Zou, M., Tammimies, K., et al. (2014) · Journal of Neurodevelopmental Disorders · doi:10.1186/1866-1955-6-34 · Cited by 61
Shaffer, C. L., Hurst, R. S., Scialis, R. J., Osgood, S. M., Bryce, D. K., Hoffmann, W. E., Lazzaro, J. T., Hanks, A. N., Lotarski, S. M., Weber, M. L., et al. (2013) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.113.204735 · Cited by 61
Self-citationChronic Ampakine Treatments Stimulate Dendritic Growth and Promote Learning in Middle-Aged Rats
Lauterborn, J. C., Palmer, L. C., Jia, Y., Pham, D. T., Hou, B., Wang, W., Trieu, B. H., Cox, C. D., Kantorovich, S., Gall, C. M., et al. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3157-15.2016 · Cited by 61
Sengar, A. S., Li, H., Zhang, W., Leung, C., Ramani, A. K., Saw, N. M. N., Wang, Y., Tu, Y., Ross, P. J., Scherer, S. W., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.11.087 · Cited by 61
Drosophila Neto is essential for clustering glutamate receptors at the neuromuscular junctionPreprint
Kim, Y.-J., Bao, H., Bonanno, L. N., Zhang, B., & Serpe, M. (2012) · Genes & Development · doi:10.1101/gad.185165.111 · Cited by 61
Tao, W., Díaz-Alonso, J., Sheng, N., & Nicoll, R. A. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1802737115 · Cited by 61
Dissecting diverse functions of NMDA receptors by structural biology
Wang, J. X., & Furukawa, H. (2019) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2018.12.009 · Cited by 61
Self-citationRycroft, B. K., & Gibb, A. J. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2003.059212 · Cited by 60
Aroniadou‐Anderjaska, V., Pidoplichko, V. I., Figueiredo, T. H., Almeida-Suhett, C. P., Prager, E. M., & Braga, M. F. M. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.07.006 · Cited by 60
Jackson, A. C., & Nicoll, R. A. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.5134-10.2011 · Cited by 60
Probing TARP Modulation of AMPA Receptor Conductance with Polyamine Toxins
Jackson, A. C., Milstein, A. D., Soto, D., Farrant, M., Cull-Candy, S. G., & Nicoll, R. A. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.6688-10.2011 · Cited by 60
Staggering of Subunits in NMDAR Channels
Sobolevsky, A. I., Rooney, L. A., & Wollmuth, L. P. (2002) · Biophysical Journal · doi:10.1016/s0006-3495(02)75331-9 · Cited by 60
Self-citationRen, H., Honse, Y., Karp, B. J., Lipsky, R. H., & Peoples, R. W. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m209486200 · Cited by 60
A Role for Extracellular Na+in the Channel Gating of Native and Recombinant Kainate Receptors
Paternain, A. V., Cohen, A., Stern-Bach, Y., & Lerma, J. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-25-08641.2003 · Cited by 60
The trapping block of NMDA receptor channels in acutely isolated rat hippocampal neurones
Sobolevsky, A. I., & Yelshansky, M. V. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.t01-2-00493.x · Cited by 60
Self-citationAltered hippocampal short‐term plasticity and associative memory in synaptotagmin IV (−/−) mice
Ferguson, G. D., Wang, H., Herschman, H. R., & Storm, D. R. (2004) · Hippocampus · doi:10.1002/hipo.20013 · Cited by 60
Cited by
Sorted by citations
Mechanisms of ketamine and its metabolites as antidepressants
Hess, E. M., Riggs, L. M., Michaelides, M., & Gould, T. D. (2022) · Biochemical Pharmacology · doi:10.1016/j.bcp.2021.114892 · Cited by 175
Coombs, I. D., Ziobro, J., Krotov, V., Surtees, T., Cull‐Candy, S. G., & Farrant, M. (2022) · Epilepsia · doi:10.1111/epi.17419 · Cited by 32
Cryo-EM structure of the human Asc-1 transporter complex
Li, Y., Guo, Y., Bröer, A., Dai, L., Brӧer, S., & Yan, R. (2024) · Nature Communications · doi:10.1038/s41467-024-47468-1 · Cited by 12
Glutamate receptor 4 as a fluid biomarker for the diagnosis of psychiatric disorders
Gómez de San José, N., Goossens, J., Al Shweiki, M. R., Halbgebauer, S., Oeckl, P., Steinacker, P., Danzer, K. M., Graf, H., Schönfeldt-Lecuona, C., Belbin, O., et al. (2022) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2022.10.010 · Cited by 9
Metadata
- Authors
- Hansen, K. B., Wollmuth, L. P., Bowie, D., Furukawa, H., Menniti, F. S., Sobolevsky, A. I., Swanson, G. T., Swanger, S. A., Greger, I. H., Nakagawa, T., McBain, C. J., Jayaraman, V., Low, C.-M., Dell’Acqua, M. L., Diamond, J. S., Camp, C. R., Perszyk, R. E., Yuan, H., & Traynelis, S. F.
- Affiliations
- Northwestern University (US)
- Corresponding author
- Traynelis, Stephen F.
- ORCID
- Hansen, Kasper B.
- Wollmuth, Lonnie P.
- Bowie, Derek
- Furukawa, Hiro
- Menniti, Frank S.
- Sobolevsky, Alexander I.
- Swanson, Geoffrey T.
- Swanger, Sharon A.
- Greger, Ingo H.
- Nakagawa, Terunaga
- McBain, Chris J.
- Jayaraman, Vasanthi
- Low, Chian-Ming
- Dell’Acqua, Mark L.
- Diamond, Jeffrey S.
- Camp, Chad R.
- Perszyk, Riley E.
- Yuan, Hongjie
- Traynelis, Stephen F.
- Venue
- Pharmacological Reviews
- Publisher
- Elsevier BV
- Published
- 2021-10
- Volume
- 73
- Issue
- 4
- Pages
- 1469-1658
- ISSN
- 0031-6997 (ISSN-L)
- PMC
- PMC8626789
- OpenAlex
- W3214054678
- Cited by
- 686
- References
- 2,576
- Citations by year
- 2026: 123 · 2025: 198 · 2024: 160 · 2023: 115 · 2022: 81 · 2021: 9
- FWCI
- 13.86
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Pharmacological Reviews (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory) (acceptedVersion)
- Funders
- National Institutes of Health (5f31ns113530-02)
- Biotechnology and Biological Sciences Research Council (BB/N002113/1)
- National Institute of Mental Health (R56MH123474, R21MH127404, R01MH085926, R01MH123474)
- National Cancer Institute (R01CA206573)
- National Institute of General Medical Sciences (P20GM103546, R35GM122528)
- National Institute of Neurological Disorders and Stroke (F31‐NS113530, R01NS105804, R56NS040701, R01NS083660, R01NS040701, R01NS088479, R01NS111745, RF1NS113632, R01NS105502, R01NS107253, R35NS111619, R37NS083660, R01NS116055, R01NS097536)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (R01HD082373)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nicotinic Acetylcholine Receptors Study
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
- Keywords
- ionotropic glutamate receptors, ligand-gated ion channels, glutamate, receptor subtypes, receptor structure, receptor pharmacology, excitatory neurotransmission, neurophysiology, neurological disorders, mental illness, therapeutic target
- MeSH terms
- Animals, Central Nervous System, Humans, Receptors, Glutamate, Neurotransmitter Agents, Glutamic Acid, Receptors, Ionotropic Glutamate
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review