Relative abundance of subunit mRNAs determines gating and Ca2+ permeability of AMPA receptors in principal neurons and interneurons in rat CNS

Glutamate neurotoxicity and diseases of the nervous system

Choi, D. W. (1988) · Neuron · doi:10.1016/0896-6273(88)90162-6 · Cited by 8,152 · see citing works

Cloned Glutamate Receptors

Hollmann, M., & Heinemann, S. F. (1994) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.17.030194.000335 · Cited by 4,011 · see citing works

Single-Channel Recording

Sakmann, B. J., & Neher, E. (1995) · Springer eBooks · doi:10.1007/978-1-4419-1229-9 · Cited by 2,543 · see citing works

RNA editing in brain controls a determinant of ion flow in glutamate-gated channels

Sommer, B., Köhler, M., Sprengel, R., & Seeburg, P. H. (1991) · Cell · doi:10.1016/0092-8674(91)90568-j · Cited by 1,517 · see citing works

A Family of AMPA-Selective Glutamate Receptors

Keinänen, K., Wisden, W., Sommer, B., Werner, P., Herb, A., Verdoorn, T. A., Sakmann, B., & Seeburg, P. H. (1990) · Science · doi:10.1126/science.2166337 · Cited by 1,479 · see citing works

Ca2 + Permeability of KA-AMPA—Gated Glutamate Receptor Channels Depends on Subunit Composition

Hollmann, M., Hartley, M., & Heinemann, S. F. (1991) · Science · doi:10.1126/science.1709304 · Cited by 1,450 · see citing works

Amplified RNA synthesized from limited quantities of heterogeneous cDNA.

Gelder, R. N. V., von Zastrow, M., Yool, A., Dement, W. C., Barchas, J. D., & Eberwine, J. H. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.5.1663 · Cited by 1,262 · see citing works

Flip and Flop: A Cell-Specific Functional Switch in Glutamate-Operated Channels of the CNS

Sommer, B., KEINÄNEN, K. P., Verdoorn, T. A., Wisden, W., Burnashev, N., Herb, A., Köhler, M. G., Takagi, T., Sakmann, B. J., & Seeburg, P. H. (1990) · Science · doi:10.1126/science.1699275 · Cited by 1,259 · see citing works

Divalent ion permeability of AMPA receptor channels is dominated by the edited form of a single subunit

Burnashev, N., Monyer, H., Seeburg, P. H., & Sakmann, B. (1992) · Neuron · doi:10.1016/0896-6273(92)90120-3 · Cited by 1,087 · see citing works

Decreased Hippocampal Inhibition and a Selective Loss of Interneurons in Experimental Epilepsy

Sloviter, R. S. (1987) · Science · doi:10.1126/science.2879352 · Cited by 1,082 · see citing works

Permeation and block of N‐methyl‐D‐aspartic acid receptor channels by divalent cations in mouse cultured central neurones.

Mayer, M. L., & Westbrook, G. L. (1987) · The Journal of Physiology · doi:10.1113/jphysiol.1987.sp016883 · Cited by 935 · see citing works

Structural Determinants of Ion Flow Through Recombinant Glutamate Receptor Channels

Verdoorn, T. A., Burnashev, N., Monyer, H., Seeburg, P. H., & Sakmann, B. J. (1991) · Science · doi:10.1126/science.1710829 · Cited by 815 · see citing works

Patch-clamp recordings from the soma and dendrites of neurons in brain slices using infrared video microscopy

Stuart, G. J., Dodt, H., & Sakmann, B. J. (1993) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf00374949 · Cited by 804 · see citing works

Identification of a Site in Glutamate Receptor Subunits That Controls Calcium Permeability

Hume, R. I., Dingledine, R. J., & Heinemann, S. F. (1991) · Science · doi:10.1126/science.1653450 · Cited by 767 · see citing works

Control of Kinetic Properties of AMPA Receptor Channels by Nuclear RNA Editing

Lomeli, H., Mosbacher, J., Melcher, T., Höger, T., Geiger, J. R. P., Kuner, T., Monyer, H., Higuchi, M., Bach, A., & Seeburg, P. H. (1994) · Science · doi:10.1126/science.7992055 · Cited by 746 · see citing works

Differences in Ca2+ permeability of AMPA-type glutamate receptor channels in neocortical neurons caused by differential GluR-B subunit expression

Jonas, P. (1994) · Neuron · doi:10.1016/0896-6273(94)90444-8 · Cited by 666 · see citing works

A Molecular Determinant for Submillisecond Desensitization in Glutamate Receptors

Mosbacher, J., Schoepfer, R., Monyer, H., Burnashev, N., SEEBURG, P. H., & Ruppersberg, J. P. (1994) · Science · doi:10.1126/science.7973663 · Cited by 610 · see citing works

Selective modulation of desensitization at AMPA versus kainate receptors by cyclothiazide and concanavalin A

Partin, K. M., Patneau, D. K., Winters, C. A., Mayer, M. L., & Buonanno, A. (1993) · Neuron · doi:10.1016/0896-6273(93)90220-l · Cited by 583 · see citing works

AMPA receptor subunits expressed by single purkinje cells

Lambolez, B., Audinat, É., Bochet, P., Crépel, F., & Rossier, J. (1992) · Neuron · doi:10.1016/0896-6273(92)90164-9 · Cited by 544 · see citing works

Chapter 1 Chapter Neurons, numbers and the hippocampal network

Amaral, D. G., Ishizuka, N., & Claiborne, B. J. (1990) · Progress in brain research · doi:10.1016/s0079-6123(08)61237-6 · Cited by 523 · see citing works

Immunochemical characterization of the non-NMDA glutamate receptor using subunit-specific antibodies. Evidence for a hetero-oligomeric structure in rat brain.

Wenthold, R. J., Yokotani, N., Doi, K., & Wada, K. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)48523-7 · Cited by 521 · see citing works

Fractional calcium currents through recombinant GluR channels of the NMDA, AMPA and kainate receptor subtypes.

Burnashev, N., Zhou, Z., Neher, E., & Sakmann, B. J. (1995) · The Journal of Physiology · doi:10.1113/jphysiol.1995.sp020738 · Cited by 450 · see citing works

Action of brief pulses of glutamate on AMPA/kainate receptors in patches from different neurones of rat hippocampal slices.

Colquhoun, D., Jónás, P., & Sakmann, B. J. (1992) · The Journal of Physiology · doi:10.1113/jphysiol.1992.sp019417 · Cited by 433 · see citing works

Calcium-Permeable AMPA-Kainate Receptors in Fusiform Cerebellar Glial Cells

Burnashev, N., Khodorova, A. B., Jónás, P., Helm, P. J., Wisden, W., Monyer, H., Seeburg, P. H., & Sakmann, B. J. (1992) · Science · doi:10.1126/science.1317970 · Cited by 430 · see citing works

Ion‐concentration dependence of the reversal potential and the single channel conductance of ion channels at the frog neuromuscular junction.

Lewis, C. A. (1979) · The Journal of Physiology · doi:10.1113/jphysiol.1979.sp012629 · Cited by 404 · see citing works

Subunit composition at the single-cell level explains functional properties of a glutamate-gated channel

Bochet, P., Audinat, É., Lambolez, B., Crépel, F., Rossier, J., Iino, M., Tsuzuki, K., & Ozawa, S. (1994) · Neuron · doi:10.1016/0896-6273(94)90279-8 · Cited by 353 · see citing works

Calcium Entry Through Kainate Receptors and Resulting Potassium-Channel Blockade in Bergmann Glial Cells

Müller, T. H., Möller, T., Berger, T., Schnitzer, J., & Kettenmann, H. (1992) · Science · doi:10.1126/science.1317969 · Cited by 337 · see citing works

Cyclothiazide differentially modulates desensitization of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor splice variants.

Partin, K. M., Patneau, D. K., & Mayer, M. L. (1994) · Molecular Pharmacology · doi:10.1016/s0026-895x(25)08654-7 · Cited by 296 · see citing works

Neural factors regulate AChR subunit mRNAs at rat neuromuscular synapses.

Witzemann, V., Brenner, H. R., & Sakmann, B. J. (1991) · The Journal of Cell Biology · doi:10.1083/jcb.114.1.125 · Cited by 259 · see citing works

Different glutamate receptor channels mediate fast excitatory synaptic currents in inhibitory and excitatory cortical neurons

Hestrin, S. (1993) · Neuron · doi:10.1016/0896-6273(93)90221-c · Cited by 238 · see citing works

Ca(2+)‐permeable AMPA and NMDA receptor channels in basket cells of rat hippocampal dentate gyrus.

Koh, D., Geiger, J. R. P., Jónás, P., & Sakmann, B. J. (1995) · The Journal of Physiology · doi:10.1113/jphysiol.1995.sp020737 · Cited by 226 · see citing works

Pathway-specific variants of AMPA receptors and their contribution to neuronal signaling

Raman, I., Zhang, S., & Trussell, L. O. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-08-04998.1994 · Cited by 194 · see citing works

Mechanisms shaping glutamate-mediated excitatory postsynaptic currents in the CNS

Jónás, P., & Spruston, N. (1994) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(94)90098-1 · Cited by 154 · see citing works

The binaural auditory pathway: excitatory amino acid receptors mediate dual timecourse excitatory postsynaptic currents in the rat medial nucleus of the trapezoid body

Forsythe, I. D., & Barnes‐Davies, M. (1993) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1993.0022 · Cited by 152 · see citing works

Proportion of parvalbumin‐positive basket cells in the GABAergic innervation of pyramidal and granule cells of the rat hippocampal formation

Ribak, C. E., Nitsch, R., & Seress, L. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.903000402 · Cited by 147 · see citing works

The propagation of transient potentials in some linear cable structures

Jack, J., & Redman, S. (1971) · The Journal of Physiology · doi:10.1113/jphysiol.1971.sp009472 · Cited by 141 · see citing works

AMPA receptors with high Ca2+ permeability mediate synaptic transmission in the avian auditory pathway.

Otis, T. S., Raman, I. M., & Trussell, L. O. (1995) · The Journal of Physiology · doi:10.1113/jphysiol.1995.sp020519 · Cited by 136 · see citing works

Fast Application of Agonists to Isolated Membrane Patches

Jónás, P. (1995) · Springer eBooks · doi:10.1007/978-1-4419-1229-9_10 · Cited by 122 · see citing works

Glutamate-activated currents in outside-out patches from spiny versus aspiny hilar neurons of rat hippocampal slices

Livsey, C. T., Costa, E., & Vicini, S. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-12-05324.1993 · Cited by 88 · see citing works

Kainate-induced inactivation of NMDA currents via an elevation of intracellular Ca2+ in hippocampal neurons

Medina, I., Filippova, N., Barbin, G., Ben‐Ari, Y., & Bregestovski, P. D. (1994) · Journal of Neurophysiology · doi:10.1152/jn.1994.72.1.456 · Cited by 58 · see citing works

Polymerase Chain Reaction Analysis of Ion Channel Expression in Single Neurons of Brain Slices

Monyer, H., & Jónás, P. (1995) · Springer eBooks · doi:10.1007/978-1-4419-1229-9_16 · Cited by 45 · see citing works

Recombinant lonotropic Glutamate Receptors: Functional Distinctions Imparted by Different Subunits

Burnashev, N. (1993) · Cellular Physiology and Biochemistry · doi:10.1159/000154696 · Cited by 38 · see citing works

GABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits

Tremblay, R., Lee, S., & Rudy, B. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.033 · Cited by 2,033 · see citing works

Synaptic mechanisms of synchronized gamma oscillations in inhibitory interneuron networks

Bartos, M., Vida, I., & Jonas, P. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2044 · Cited by 2,070 · see citing works

Fast-spiking, parvalbumin ⁺ GABAergic interneurons: From cellular design to microcircuit function

Hu, H., Gan, J., & Jonas, P. (2014) · Science · doi:10.1126/science.1255263 · Cited by 1,197 · see citing works

Point mutation in an AMPA receptor gene rescues lethality in mice deficient in the RNA-editing enzyme ADAR2

Higuchi, M., Maas, S., Single, F. N., Hartner, J., Rozov, A., Burnashev, N., Feldmeyer, D., Sprengel, R., & Seeburg, P. H. (2000) · Nature · doi:10.1038/35017558 · Cited by 967 · see citing works

Hippocampal GABAergic Inhibitory Interneurons

Pelkey, K. A., Chittajallu, R., Craig, M. T., Tricoire, L., Wester, J. C., & McBain, C. J. (2017) · Physiological Reviews · doi:10.1152/physrev.00007.2017 · Cited by 889 · see citing works

Synaptic basis of cortical persistent activity: the importance of NMDA receptors to working memory

Wang, X.-J. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-21-09587.1999 · Cited by 859 · see citing works

The role of the GluR2 subunit in AMPA receptor function and synaptic plasticity

Isaac, J. T. R., Ashby, M. C., & McBain, C. J. (2007) · Neuron · doi:10.1016/j.neuron.2007.06.001 · Cited by 802 · see citing works

Structure, Function, and Pharmacology of Glutamate Receptor Ion Channels

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., et al. (2021) · Pharmacological Reviews · doi:10.1124/pharmrev.120.000131 · Cited by 686 · see citing works

Regulatory mechanisms of AMPA receptors in synaptic plasticity

Derkach, V. A., Oh, M. C., Guire, E. S., & Soderling, T. R. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2055 · Cited by 708 · see citing works

Two dynamically distinct inhibitory networks in layer 4 of the neocortex

Beierlein, M., Gibson, J. R., & Connors, B. W. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00283.2003 · Cited by 591 · see citing works

Synaptic basis for intense thalamocortical activation of feedforward inhibitory cells in neocortex

Cruikshank, S. J., Lewis, T. J., & Connors, B. W. (2007) · Nature Neuroscience · doi:10.1038/nn1861 · Cited by 558 · see citing works

Interneurons unbound

McBain, C. J., & Fisahn, A. (2001) · Nature Reviews Neuroscience · doi:10.1038/35049047 · Cited by 581 · see citing works

Recruitment of Parvalbumin-Positive Interneurons Determines Hippocampal Function and Associated Behavior

Fuchs, E. C., Zivkovic, A. R., Cunningham, M. O., Middleton, S., LeBeau, F. E. N., Bannerman, D. M., Rozov, A., Whittington, M. A., Traub, R. D., Rawlins, J. N. P., et al. (2007) · Neuron · doi:10.1016/j.neuron.2007.01.031 · Cited by 532 · see citing works

Molecular Mechanisms of Glutamate Receptor-Mediated Excitotoxic Neuronal Cell Death

Sattler, R., & Tymianski, M. (2001) · Molecular Neurobiology · doi:10.1385/mn:24:1-3:107 · Cited by 537 · see citing works

Stargazin modulates AMPA receptor gating and trafficking by distinct domains

Tomita, S., Adesnik, H., Sekiguchi, M., Zhang, W., Wada, K., Howe, J. R., Nicoll, R. A., & Bredt, D. S. (2005) · Nature · doi:10.1038/nature03624 · Cited by 486 · see citing works

Submillisecond AMPA receptor-mediated signaling at a principal neuron-interneuron synapse

Geiger, J. R. P., Lübke, J., Roth, A., Frotscher, M., & Jonas, P. (1997) · Neuron · doi:10.1016/s0896-6273(00)80339-6 · Cited by 407 · see citing works

Functional and Molecular Differences between Voltage-Gated K⁺Channels of Fast-Spiking Interneurons and Pyramidal Neurons of Rat Hippocampus

Martina, M., Schultz, J. H., Ehmke, H., Monyer, H., & Jonas, P. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-20-08111.1998 · Cited by 396 · see citing works

Presynaptic and Postsynaptic Amplifications of Neuropathic Pain in the Anterior Cingulate Cortex

Xu, H., Wu, L.-J., Wang, H., Zhang, X., Vadakkan, K. I., Kim, S. S., Steenland, H. W., & Zhuo, M. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1812-08.2008 · Cited by 370 · see citing works

Long-term synaptic plasticity in hippocampal interneurons

Kullmann, D. M., & Lamsa, K. P. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2207 · Cited by 340 · see citing works

Narp regulates homeostatic scaling of excitatory synapses on parvalbumin-expressing interneurons

Chang, M. C., Park, J. M., Pelkey, K. A., Grabenstatter, H. L., Xu, D., Linden, D. J., Sutula, T. P., McBain, C. J., & Worley, P. F. (2010) · Nature Neuroscience · doi:10.1038/nn.2621 · Cited by 316 · see citing works

Classification of fusiform neocortical interneurons based on unsupervised clustering

Cauli, B., Porter, J. T., Tsuzuki, K., Lambolez, B., Rossier, J., Quenet, B., & Audinat, E. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.11.6144 · Cited by 316 · see citing works

NPTX2 and cognitive dysfunction in Alzheimer’s Disease

Xiao, M.-F., Xu, D., Craig, M. T., Pelkey, K. A., Chien, C.-C., Shi, Y., Zhang, J., Resnick, S., Pletnikova, O., Salmon, D., et al. (2017) · eLife · doi:10.7554/elife.23798 · Cited by 316 · see citing works

Highly energized inhibitory interneurons are a central element for information processing in cortical networks.

Kann, O., Papageorgiou, I. E., & Draguhn, A. (2014) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2014.104 · Cited by 295 · see citing works

Postsynaptic expression of homeostatic plasticity at neocortical synapses

Wierenga, C. J., Ibata, K., & Turrigiano, G. G. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.5217-04.2005 · Cited by 306 · see citing works

Connexin expression in electrically coupled postnatal rat brain neurons

Venance, L., Rozov, A., Blatow, M., Burnashev, N., Feldmeyer, D., & Monyer, H. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.160037097 · Cited by 273 · see citing works

Electrical synapses define networks of neocortical GABAergic neurons

Hestrin, S., & Galarreta, M. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.04.001 · Cited by 258 · see citing works

Afferent-specific innervation of two distinct AMPA receptor subtypes on single hippocampal interneurons

Tóth, K., & McBain, C. J. (1998) · Nature Neuroscience · doi:10.1038/2807 · Cited by 250 · see citing works

A role for AMPA receptors in mood disorders

Alt, A., Nisenbaum, E. S., Bleakman, D., & Witkin, J. M. (2006) · Biochemical Pharmacology · doi:10.1016/j.bcp.2005.12.022 · Cited by 238 · see citing works

Interneuron Diversity series: Containing the detonation – feedforward inhibition in the CA3 hippocampus

Lawrence, J. J., & McBain, C. J. (2003) · Trends in Neurosciences · doi:10.1016/j.tins.2003.09.007 · Cited by 214 · see citing works

Calcium Microdomains in Aspiny Dendrites

Goldberg, J. H., Tamas, G., Aronov, D., & Yuste, R. (2003) · Neuron · doi:10.1016/s0896-6273(03)00714-1 · Cited by 212 · see citing works

Interaction of the N-Terminal Domain of the AMPA Receptor GluR4 Subunit with the Neuronal Pentraxin NP1 Mediates GluR4 Synaptic Recruitment

Sia, G.-M., Béïque, J.-C., Rumbaugh, G., Cho, R., Worley, P. F., & Huganir, R. L. (2007) · Neuron · doi:10.1016/j.neuron.2007.06.020 · Cited by 201 · see citing works

Single-cell RNAseq reveals cell adhesion molecule profiles in electrophysiologically defined neurons

Földy, C., Darmanis, S., Aoto, J., Malenka, R. C., Quake, S. R., & Südhof, T. C. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1610155113 · Cited by 179 · see citing works

The role of metaplasticity mechanisms in regulating memory destabilization and reconsolidation

Finnie, P. S. B., & Nader, K. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.03.008 · Cited by 189 · see citing works

The absence of a major Ca ²⁺ signaling pathway in GABAergic neurons of the hippocampus

Sík, A., Hájos, N., Gulácsi, A., Mody, I., & Freund, T. F. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.6.3245 · Cited by 186 · see citing works

Properties of bipolar VIPergic interneurons and their excitation by pyramidal neurons in the rat neocortex

Porter, J. T., Cauli, B., Staiger, J. F., Lambolez, B., Rossier, J., & Audinat, E. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00367.x · Cited by 173 · see citing works

Long-term potentiation of exogenous glutamate responses at single dendritic spines

Bagal, A. A., Kao, J. P. Y., Tang, C.-M., & Thompson, S. M. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0501956102 · Cited by 169 · see citing works

Glutamate Receptor Subtypes Mediating Synaptic Activation of Prefrontal Cortex Neurons: Relevance for Schizophrenia

Rotaru, D. C., Yoshino, H., Lewis, D. A., Ermentrout, G. B., & Gonzalez-Burgos, G. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.1970-10.2011 · Cited by 151 · see citing works

Correlation between kinetics and RNA splicing of alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid receptors in neocortical neurons.

Lambolez, B., Ropert, N., Perrais, D., Rossier, J., & Hestrin, S. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.5.1797 · Cited by 147 · see citing works

Postsynaptic mechanisms govern the differential excitation of cortical neurons by thalamic inputs

Hull, C., Isaacson, J. S., & Scanziani, M. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5971-08.2009 · Cited by 147 · see citing works

Functional characteristics of parvalbumin‐ and cholecystokinin‐expressing basket cells

Bartos, M., & Elgueta, C. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2011.226175 · Cited by 127 · see citing works

Genetically altered AMPA-type glutamate receptor kinetics in interneurons disrupt long-range synchrony of gamma oscillation

Fuchs, E. C., Doheny, H., Faulkner, H., Caputi, A., Traub, R. D., Bibbig, A., Kopell, N., Whittington, M. A., & Monyer, H. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.051631898 · Cited by 132 · see citing works

Synaptic memory and CaMKII

Nicoll, R. A., & Schulman, H. (2023) · Physiological Reviews · doi:10.1152/physrev.00034.2022 · Cited by 126 · see citing works

Zn ²⁺ currents are mediated by calcium‐permeable AMPA/Kainate channels in cultured murine hippocampal neurones

Jia, Y., Jeng, J., Sensi, S. L., & Weiss, J. H. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2002.020172 · Cited by 118 · see citing works

Glutamatergic synapses onto hippocampal interneurons: precision timing without lasting plasticity

McBain, C. J., Freund, T. F., & Mody, I. (1999) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01347-2 · Cited by 113 · see citing works

Short-Term Plasticity at Hippocampal Mossy Fiber Synapses Is Induced by Natural Activity Patterns and Associated with Vesicle Pool Engram Formation

Vandael, D., Borges-Merjane, C., Zhang, X., & Jonas, P. (2020) · Neuron · doi:10.1016/j.neuron.2020.05.013 · Cited by 114 · see citing works

Facilitation of currents through rat Ca²⁺‐permeable AMPA receptor channels by activity‐dependent relief from polyamine block

Rozov, A., Zilberter, Y., Wollmuth, L. P., & Burnashev, N. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.361bh.x · Cited by 114 · see citing works

Target-Specific Properties of Thalamocortical Synapses onto Layer 4 of Mouse Primary Visual Cortex

Kloc, M., & Maffei, A. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.2595-14.2014 · Cited by 99 · see citing works

AMPA receptor channels with long-lasting desensitization in bipolar interneurons contribute to synaptic depression in a novel feedback circuit in layer 2/3 of rat neocortex

Rozov, A., Jerecic, J., Sakmann, B., & Burnashev, N. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-20-08062.2001 · Cited by 103 · see citing works

Role of Ionotropic Glutamate Receptors in Long-Term Potentiation in Rat Hippocampal CA1 Oriens-Lacunosum Moleculare Interneurons

Oren, I., Nissen, W., Kullmann, D. M., Somogyi, P., & Lamsa, K. P. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.3251-08.2009 · Cited by 93 · see citing works

Diverse roles for ionotropic glutamate receptors on inhibitory interneurons in developing and adult brain

Akgül, G., & McBain, C. J. (2016) · The Journal of Physiology · doi:10.1113/jp271764 · Cited by 87 · see citing works

Associative Plasticity at Excitatory Synapses Facilitates Recruitment of Fast-Spiking Interneurons in the Dentate Gyrus

Sambandan, S., Sauer, J.-F., Vida, I., & Bartos, M. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.2012-10.2010 · Cited by 82 · see citing works

Dopamine D₄Receptors Regulate AMPA Receptor Trafficking and Glutamatergic Transmission in GABAergic Interneurons of Prefrontal Cortex

Yuen, E. Y., & Yan, Z. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5050-08.2009 · Cited by 81 · see citing works

Differential Regulation of Metabotropic Glutamate Receptor- and AMPA Receptor-Mediated Dendritic Ca²⁺Signals by Presynaptic and Postsynaptic Activity in Hippocampal Interneurons

Topolnik, L., Congar, P., & Lacaille, J.-C. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.4388-04.2005 · Cited by 73 · see citing works

Glutamate and nicotinic receptor interactions in working memory: importance for the cognitive impairment of schizophrenia

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