Dendritic Mechanisms Underlying Rapid Synaptic Activation of Fast-Spiking Hippocampal Interneurons

Ion Channels/Excitable Membranes

(2011) · Springer eBooks · doi:10.1007/springerreference_33998 · Cited by 4,066 · see citing works

Driving fast-spiking cells induces gamma rhythm and controls sensory responses

Cardin, J. A., Carlén, M., Meletis, K., Knoblich, U., Zhang, F., Deisseroth, K., Tsai, L.-H., & Moore, C. I. (2009) · Nature · doi:10.1038/nature08002 · Cited by 2,603 · see citing works

Cortical inhibitory neurons and schizophrenia

Lewis, D. A., Hashimoto, T., & Volk, D. W. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1648 · Cited by 2,297 · 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

Pattern Separation in the Dentate Gyrus and CA3 of the Hippocampus

Leutgeb, J. K., Leutgeb, S., Moser, M.-B., & Moser, E. I. (2007) · Science · doi:10.1126/science.1135801 · Cited by 1,601 · see citing works

Brain-state- and cell-type-specific firing of hippocampal interneurons in vivo

Klausberger, T., Magill, P. J., Márton, L. F., Roberts, J. D. B., Cobden, P. M., Buzsáki, G., & Somogyi, P. (2003) · Nature · doi:10.1038/nature01374 · Cited by 1,345 · see citing works

Active propagation of somatic action potentials into neocortical pyramidal cell dendrites

Stuart, G. J., & Sakmann, B. (1994) · Nature · doi:10.1038/367069a0 · Cited by 1,289 · see citing works

Enforcement of Temporal Fidelity in Pyramidal Cells by Somatic Feed-Forward Inhibition

Pouille, F., & Scanziani, M. (2001) · Science · doi:10.1126/science.1060342 · Cited by 1,097 · see citing works

Oscillatory coupling of hippocampal pyramidal cells and interneurons in the behaving rat

Csicsvari, J., Hirase, H., Czurkó, A., Mamiya, A., & Buzsáki, G. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-01-00274.1999 · Cited by 966 · see citing works

Activity-dependent action potential invasion and calcium influx into hippocampal CA1 dendrites.

Spruston, N., Schiller, Y., Stuart, G., & Sakmann, B. (1995) · Science · doi:10.1126/science.7716524 · Cited by 835 · see citing works

Spatial selectivity of unit activity in the hippocampal granular layer

Jung, M. W., & McNaughton, B. L. (1993) · Hippocampus · doi:10.1002/hipo.450030209 · Cited by 789 · see citing works

Kv3 channels: voltage-gated K+ channels designed for high-frequency repetitive firing

Rudy, B., & McBain, C. J. (2001) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01892-0 · Cited by 781 · see citing works

Disynaptic Inhibition between Neocortical Pyramidal Cells Mediated by Martinotti Cells

Silberberg, G., & Markram, H. (2007) · Neuron · doi:10.1016/j.neuron.2007.02.012 · Cited by 768 · see citing works

Diverse sources of hippocampal unitary inhibitory postsynaptic potentials and the number of synaptic release sites

Buhl, E. H., Halasy, K., & Somogyi, P. (1994) · Nature · doi:10.1038/368823a0 · Cited by 728 · see citing works

Hippocampal CA1 interneurons: an in vivo intracellular labeling study

Sik, A., Penttonen, M., Ylinen, A., & Buzsaki, G. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-10-06651.1995 · Cited by 669 · see citing works

Integrative Properties of Radial Oblique Dendrites in Hippocampal CA1 Pyramidal Neurons

Losonczy, A., & Magee, J. C. (2006) · Neuron · doi:10.1016/j.neuron.2006.03.016 · Cited by 641 · see citing works

Reliability and State Dependence of Pyramidal Cell–Interneuron Synapses in the Hippocampus

Csicsvari, J., Hirase, H., Czurko, A., & Buzsáki, G. (1998) · Neuron · doi:10.1016/s0896-6273(00)80525-5 · Cited by 606 · see citing works

Active Properties of Neuronal Dendrites

Johnston, D., Magee, J. C., Colbert, C. M., & Christie, B. R. (1996) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.19.030196.001121 · Cited by 604 · see citing works

Action potential initiation and propagation in rat neocortical pyramidal neurons

Stuart, G. J., Schiller, J., & Sakmann, B. J. (1997) · The Journal of Physiology · doi:10.1111/j.1469-7793.1997.617ba.x · Cited by 585 · see citing works

Feed‐forward dendritic inhibition in rat hippocampal pyramidal cells studied in vitro

Alger, B. E., & Nicoll, R. A. (1982) · The Journal of Physiology · doi:10.1113/jphysiol.1982.sp014255 · Cited by 528 · see citing works

Funding for malaria genome sequencing

Hoffman, S., Bancroft, W., Michael, G., James, S., Burroughs, E. C. B., Stephenson, J., & Morgan, M. (1997) · Nature · doi:10.1038/42571 · Cited by 461 · see citing works

Amplification of EPSPs by axosomatic sodium channels in neocortical pyramidal neurons

Stuart, G. J., & Sakmann, B. (1995) · Neuron · doi:10.1016/0896-6273(95)90095-0 · Cited by 434 · see citing works

Routing of spike series by dynamic circuits in the hippocampus

Pouille, F., & Scanziani, M. (2004) · Nature · doi:10.1038/nature02615 · Cited by 434 · see citing works

Supralinear increase of recurrent inhibition during sparse activity in the somatosensory cortex

Kapfer, C., Glickfeld, L. L., Atallah, B. V., & Scanziani, M. (2007) · Nature Neuroscience · doi:10.1038/nn1909 · Cited by 427 · 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

Properties of basal dendrites of layer 5 pyramidal neurons: a direct patch-clamp recording study.

Nevian, T., Larkum, M. E., Polsky, A., & Schiller, J. (2007) · Nature Neuroscience · doi:10.1038/nn1826 · Cited by 406 · 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

Spike timing of dendrite-targeting bistratified cells during hippocampal network oscillations in vivo

Klausberger, T., Márton, L. F., Baude, A., Roberts, J. D. B., Magill, P. J., & Somogyi, P. (2004) · Nature Neuroscience · doi:10.1038/nn1159 · Cited by 393 · see citing works

Spike Transmission and Synchrony Detection in Networks of GABAergic Interneurons

Galarreta, M., & Hestrin, S. (2001) · Science · doi:10.1126/science.1061395 · Cited by 389 · see citing works

Dendritic Sodium Spikes Are Variable Triggers of Axonal Action Potentials in Hippocampal CA1 Pyramidal Neurons

Golding, N. L., & Spruston, N. (1998) · Neuron · doi:10.1016/s0896-6273(00)80635-2 · Cited by 388 · see citing works

Distal Initiation and Active Propagation of Action Potentials in Interneuron Dendrites

Martina, M., Vida, I., & Jonas, P. (2000) · Science · doi:10.1126/science.287.5451.295 · Cited by 375 · see citing works

Synaptic excitation of inhibitory cells by single CA3 hippocampal pyramidal cells of the guinea‐pig in vitro.

Miles, R. (1990) · The Journal of Physiology · doi:10.1113/jphysiol.1990.sp018200 · Cited by 315 · see citing works

Axonal initiation and active dendritic propagation of action potentials in substantia nigra neurons

Häusser, M., Stuart, G. J., Racca, C., & Sakmann, B. J. (1995) · Neuron · doi:10.1016/0896-6273(95)90152-3 · Cited by 295 · see citing works

Hippocampus of the Brain: Recurrent Inhibition in the Hippocampus with Identification of the Inhibitory Cell and its Synapses

Andersen, P. N., Eccles, J. C., & Løyning, Y. (1963) · Nature · doi:10.1038/198540a0 · Cited by 277 · see citing works

Anti-Hebbian Long-Term Potentiation in the Hippocampal Feedback Inhibitory Circuit

Lamsa, K. P., Heeroma, J. H., Somogyi, P., Rusakov, D. A., & Kullmann, D. M. (2007) · Science · doi:10.1126/science.1137450 · Cited by 261 · see citing works

EPSP Amplification and the Precision of Spike Timing in Hippocampal Neurons

Fricker, D., & Miles, R. (2000) · Neuron · doi:10.1016/s0896-6273(00)00133-1 · Cited by 254 · see citing works

Developmental expression and functional characterization of the potassium-channel subunit Kv3.1b in parvalbumin-containing interneurons of the rat hippocampus

Du, J., Zhang, L., Weiser, M., Rudy, B., & McBain, C. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-02-00506.1996 · Cited by 246 · see citing works

Voltage‐gated K+ channels in layer 5 neocortical pyramidal neurones from young rats: subtypes and gradients

Korngreen, A., & Sakmann, B. J. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.00621.x · Cited by 234 · see citing works

Facilitating pyramid to horizontal oriens‐alveus interneurone inputs: dual intracellular recordings in slices of rat hippocampus

Ali, A. B., & Thomson, A. M. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.185bu.x · Cited by 202 · see citing works

Commissural projection to the dentate gyrus of the rat: evidence for feed-forward inhibition

Buzsáki, G., & Eidelberg, E. (1981) · Brain Research · doi:10.1016/0006-8993(81)90413-3 · Cited by 179 · see citing works

PTP and LTP at a hippocampal mossy fiber-interneuron synapse

Alle, H., Jonas, P., & Geiger, J. R. P. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.251610898 · Cited by 158 · see citing works

Specific Functions of Synaptically Localized Potassium Channels in Synaptic Transmission at the Neocortical GABAergic Fast-Spiking Cell Synapse

Goldberg, E. M., Watanabe, S., Chang, S. Y., Joho, R. H., Huang, Z. J., Leonard, C. S., & Rudy, B. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0722-05.2005 · Cited by 108 · see citing works

Ca2+ imaging of mouse neocortical interneurone dendrites: Ia-type K+ channels control action potential backpropagation

Goldberg, J. H., Tamás, G., & Yuste, R. (2003) · The Journal of Physiology · doi:10.1111/j.1469-7793.2003.00049.x · Cited by 89 · see citing works

Back‐propagating action potentials mediate calcium signalling in dendrites of bitufted interneurons in layer 2/3 of rat somatosensory cortex

Kaiser, K. M. M., Zilberter, Y., & Sakmann, B. (2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.t01-1-00017.x · Cited by 89 · see citing works

Ca2+ imaging of mouse neocortical interneurone dendrites: Ia-type K+ channels control action potential backpropagation

Goldberg, J. H., Tamas, G., & Yuste, R. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.042580 · Cited by 89 · see citing works

Dendrites

(2007) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198566564.001.0001 · Cited by 73 · 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

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

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

GABAergic interneuron origin of schizophrenia pathophysiology

Nakazawa, K., Zsiros, V., Jiang, Z., Nakao, K., Kolata, S., Zhang, S., & Belforte, J. E. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.01.022 · Cited by 498 · see citing works

Alterations in Cortical Network Oscillations and Parvalbumin Neurons in Schizophrenia

Gonzalez-Burgos, G., Cho, R. Y., & Lewis, D. A. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.03.010 · Cited by 497 · see citing works

NMDA Receptor Hypofunction, Parvalbumin-Positive Neurons, and Cortical Gamma Oscillations in Schizophrenia

Gonzalez-Burgos, G., & Lewis, D. A. (2012) · Schizophrenia Bulletin · doi:10.1093/schbul/sbs010 · Cited by 478 · see citing works

Theta Phase Segregation of Input-Specific Gamma Patterns in Entorhinal-Hippocampal Networks

Schomburg, E. W., Fernández-Ruiz, A., Mizuseki, K., Berényi, A., Anastassiou, C. A., Koch, C., & Buzsáki, G. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.051 · Cited by 465 · see citing works

Behavior-dependent specialization of identified hippocampal interneurons

Lapray, D., Lasztóczi, B., Lagler, M., Viney, T. J., Katona, L., Valenti, O., Hartwich, K., Borhegyi, Z., Somogyi, P., & Klausberger, T. (2012) · Nature Neuroscience · doi:10.1038/nn.3176 · Cited by 262 · see citing works

Alterations of cortical GABA neurons and network oscillations in schizophrenia

Gonzalez-Burgos, G., Hashimoto, T., & Lewis, D. A. (2010) · Current Psychiatry Reports · doi:10.1007/s11920-010-0124-8 · Cited by 260 · see citing works

Frequency-invariant temporal ordering of interneuronal discharges during hippocampal oscillations in awake mice

Varga, C., Golshani, P., & Soltesz, I. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1210929109 · Cited by 253 · see citing works

GABA Neuron Alterations, Cortical Circuit Dysfunction and Cognitive Deficits in Schizophrenia

González‐Burgos, G., Fish, K. N., & Lewis, D. A. (2011) · Neural Plasticity · doi:10.1155/2011/723184 · Cited by 244 · see citing works

Synaptic Computation and Sensory Processing in Neocortical Layer 2/3

Petersen, C. C. H., & Crochet, S. (2013) · Neuron · doi:10.1016/j.neuron.2013.03.020 · Cited by 239 · see citing works

Rapid Desynchronization of an Electrically Coupled Interneuron Network with Sparse Excitatory Synaptic Input

Vervaeke, K., Lőrincz, A., Gleeson, P., Farinella, M., Nusser, Z., & Silver, R. A. (2010) · Neuron · doi:10.1016/j.neuron.2010.06.028 · Cited by 232 · see citing works

Inhibitory neurons in human cortical circuits: substrate for cognitive dysfunction in schizophrenia

Lewis, D. A. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.11.003 · Cited by 217 · see citing works

The Spiking Component of Oscillatory Extracellular Potentials in the Rat Hippocampus

Schomburg, E. W., Anastassiou, C. A., Buzsáki, G., & Koch, C. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0656-12.2012 · Cited by 205 · see citing works

Dendritic Integration in Hippocampal Dentate Granule Cells

Krueppel, R., Remy, S., & Beck, H. (2011) · Neuron · doi:10.1016/j.neuron.2011.05.043 · Cited by 199 · see citing works

A supercritical density of Na+ channels ensures fast signaling in GABAergic interneuron axons

Hu, H., & Jonas, P. (2014) · Nature Neuroscience · doi:10.1038/nn.3678 · Cited by 179 · see citing works

Impaired Action Potential Initiation in GABAergic Interneurons Causes Hyperexcitable Networks in an Epileptic Mouse Model Carrying a Human Na_V1.1 Mutation

Hedrich, U. B. S., Liautard, C., Kirschenbaum, D., Pofahl, M., Lavigne, J., Liu, Y., Theiss, S., Slotta, J., Escayg, A., Dihné, M., et al. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.0721-14.2014 · Cited by 164 · see citing works

Contribution of sublinear and supralinear dendritic integration to neuronal computations

Tran-Van-Minh, A., Cazé, R. D., Abrahamsson, T., Cathala, L., Gutkin, B. S., & DiGregorio, D. A. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00067 · Cited by 166 · see citing works

The role of inhibitory circuits in hippocampal memory processing

Topolnik, L., & Tamboli, S. (2022) · Nature reviews. Neuroscience · doi:10.1038/s41583-022-00599-0 · Cited by 156 · see citing works

Real-time spike sorting platform for high-density extracellular probes with ground-truth validation and drift correctionPreprint

Jun, J., Mitelut, C., Lai, C., Gratiy, S. L., Anastassiou, C., & Harris, T. (2017) · bioRxiv · doi:10.1101/101030 · Cited by 164 · 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

Enhanced Intrinsic Excitability in Basket Cells Maintains Excitatory-Inhibitory Balance in Hippocampal Circuits

Campanac, E., Gasselin, C., Baude, A., Rama, S., Ankri, N., & Debanne, D. (2013) · Neuron · doi:10.1016/j.neuron.2012.12.020 · Cited by 150 · see citing works

Pathological Basis for Deficient Excitatory Drive to Cortical Parvalbumin Interneurons in Schizophrenia

Chung, D. W., Fish, K. N., & Lewis, D. A. (2016) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2016.16010025 · Cited by 148 · see citing works

Fast-spiking parvalbumin-positive interneurons in brain physiology and Alzheimer’s disease

Hijazi, S., Smit, A. B., & van Kesteren, R. E. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02168-y · Cited by 144 · see citing works

Functional fission of parvalbumin interneuron classes during fast network events

Varga, C., Oijala, M., Lish, J., Szabo, G. G., Bezaire, M., Marchionni, I., Golshani, P., & Soltesz, I. (2014) · eLife · doi:10.7554/elife.04006 · Cited by 130 · see citing works

Basket cell dichotomy in microcircuit function

Armstrong, C., & Soltész, I. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2011.223669 · Cited by 136 · see citing works

Synaptic Properties of SOM- and CCK-Expressing Cells in Dentate Gyrus Interneuron Networks

Savanthrapadian, S., Meyer, T., Elgueta, C., Booker, S. A., Vida, I., & Bartos, M. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.5433-13.2014 · Cited by 119 · see citing works

Thin Dendrites of Cerebellar Interneurons Confer Sublinear Synaptic Integration and a Gradient of Short-Term Plasticity

Abrahamsson, T., Cathala, L., Matsui, K., Shigemoto, R., & DiGregorio, D. A. (2012) · Neuron · doi:10.1016/j.neuron.2012.01.027 · Cited by 124 · see citing works

High temperatures alter physiological properties of pyramidal cells and inhibitory interneurons in hippocampus

Kim, J. A., & Connors, B. W. (2012) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2012.00027 · Cited by 135 · see citing works

Distinct nonuniform cable properties optimize rapid and efficient activation of fast-spiking GABAergic interneurons

Nörenberg, A., Hu, H., Vida, I., Bartos, M., & Jónás, P. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0910716107 · Cited by 125 · 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

Gap Junctions Compensate for Sublinear Dendritic Integration in an Inhibitory Network

Vervaeke, K., Lőrincz, A., Nusser, Z., & Silver, R. A. (2012) · Science · doi:10.1126/science.1215101 · Cited by 121 · see citing works

Morpho‐physiological criteria divide dentate gyrus interneurons into classes

Hosp, J. A., Strüber, M., Yanagawa, Y., Obata, K., Vida, I., Jonas, P., & Bartos, M. (2014) · Hippocampus · doi:10.1002/hipo.22214 · Cited by 123 · see citing works

GABAergic inhibition shapes interictal dynamics in awake epileptic mice

Muldoon, S. F., Villette, V., Tressard, T., Malvache, A., Reichinnek, S., Bartoloméi, F., & Cossart, R. (2015) · Brain · doi:10.1093/brain/awv227 · Cited by 114 · see citing works

Action Potential Initiation in Neocortical Inhibitory Interneurons

Li, T., Tian, C., Scalmani, P., Frassoni, C., Mantegazza, M., Wang, Y., Yang, M., Wu, S., & Shu, Y. (2014) · PLoS Biology · doi:10.1371/journal.pbio.1001944 · Cited by 115 · see citing works

Global and Multiplexed Dendritic Computations under In Vivo-like Conditions

Ujfalussy, B. B., Makara, J. K., Lengyel, M., & Branco, T. (2018) · Neuron · doi:10.1016/j.neuron.2018.08.032 · Cited by 114 · see citing works

Frequency-Tuned Distribution of Inhibition in the Dentate Gyrus

Ewell, L. A., & Jones, M. V. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1854-10.2010 · Cited by 107 · see citing works

Dendritic Spikes Induce Ripples in Parvalbumin Interneurons during Hippocampal Sharp Waves

Chiovini, B., Turi, G. F., Katona, G., Kaszás, A., Pálfi, D., Maák, P. A., Szalay, G., Szabó, M. F., Szabó, G., Szadai, Z., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.04.004 · Cited by 99 · see citing works

Challenging the point neuron dogma: FS basket cells as 2-stage nonlinear integrators

Tzilivaki, A., Kastellakis, G., & Poirazi, P. (2019) · Nature Communications · doi:10.1038/s41467-019-11537-7 · Cited by 112 · see citing works

Distinct Dendritic Arborization andIn VivoFiring Patterns of Parvalbumin-Expressing Basket Cells in the Hippocampal Area CA3

Tukker, J. J., Lasztóczi, B., Katona, L., Roberts, J. D. B., Pissadaki, E. K., Dalezios, Y., Márton, L. F., Zhang, L., Klausberger, T., & Somogyi, P. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5052-12.2013 · Cited by 90 · see citing works

Distinct synaptic properties of perisomatic inhibitory cell types and their different modulation by cholinergic receptor activation in the CA3 region of the mouse hippocampus

Szabo, G. G., Holderith, N. B., Gulyás, A. I., Freund, T. F., & Hájos, N. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07292.x · Cited by 90 · see citing works

Firing Frequency Maxima of Fast-Spiking Neurons in Human, Monkey, and Mouse Neocortex

Wang, B., Wei, K., Guang, J., Chen, G., Yin, L., Deng, S., He, Q., Liu, Y., He, T., Zheng, R., et al. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00239 · Cited by 89 · see citing works

Perisomatic inhibition and cortical circuit dysfunction in schizophrenia

Lewis, D. A., Fish, K. N., Arion, D., & Gonzalez-Burgos, G. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.05.013 · Cited by 87 · see citing works

Active dendrites support efficient initiation of dendritic spikes in hippocampal CA3 pyramidal neurons

Kim, S., Guzman, S. J., Hu, H., & Jónás, P. (2012) · Nature Neuroscience · doi:10.1038/nn.3060 · Cited by 85 · see citing works

The Guide to Dendritic Spikes of the Mammalian Cortex In Vitro and In Vivo

Larkum, M. E., Wu, J., Duverdin, S., & Gidon, A. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.02.009 · Cited by 81 · see citing works

Multiple clusters of release sites formed by individual thalamic afferents onto cortical interneurons ensure reliable transmission

Bagnall, M. W., Hull, C., Bushong, E. A., Ellisman, M. H., & Scanziani, M. (2011) · Neuron · doi:10.1016/j.neuron.2011.05.032 · Cited by 80 · see citing works

Dendritic NMDA receptors in parvalbumin neurons enable strong and stable neuronal assemblies

Cornford, J. H., Mercier, M. S., Leite, M., Magloire, V., Häusser, M., & Kullmann, D. M. (2019) · eLife · doi:10.7554/elife.49872 · Cited by 82 · see citing works

The role of glutamatergic inputs onto parvalbumin-positive interneurons: relevance for schizophrenia

Rotaru, D. C., Lewis, D. A., & González‐Burgos, G. (2012) · Reviews in the Neurosciences · doi:10.1515/revneuro-2011-0059 · Cited by 80 · see citing works

Roller Coaster Scanning reveals spontaneous triggering of dendritic spikes in CA1 interneurons

Katona, G., Kaszás, A., Turi, G. F., Hájos, N., Tamás, G., Vizi, E. S., & Rózsa, B. J. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1009270108 · Cited by 77 · see citing works

Dendritic ion channelopathy in acquired epilepsy

Poolos, N. P., & Johnston, D. (2012) · Epilepsia · doi:10.1111/epi.12033 · Cited by 75 · see citing works

Dendritic Calcium Nonlinearities Switch the Direction of Synaptic Plasticity in Fast-Spiking Interneurons

Camiré, O., & Topolnik, L. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2253-13.2014 · Cited by 74 · see citing works

Distinct KvChannel Subtypes Contribute to Differences in Spike Signaling Properties in the Axon Initial Segment and Presynaptic Boutons of Cerebellar Interneurons

Rowan, M. J., Tranquil, E., & Christie, J. M. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4208-13.2014 · Cited by 74 · see citing works

Normal and epilepsy-associated pathologic function of the dentate gyrus

Dengler, C. G., & Coulter, D. A. (2016) · Progress in brain research · doi:10.1016/bs.pbr.2016.04.005 · Cited by 70 · see citing works

Persistent Discharges in Dentate Gyrus Perisoma-Inhibiting Interneurons Require Hyperpolarization-Activated Cyclic Nucleotide-Gated Channel Activation

Elgueta, C., Köhler, J., & Bartos, M. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.3671-14.2015 · Cited by 57 · see citing works

Complementary Tuning of Na+ and K+ Channel Gating Underlies Fast and Energy-Efficient Action Potentials in GABAergic Interneuron Axons

Hu, H., Roth, F. C., Vandael, D. H. F., & Jónás, P. (2018) · Neuron · doi:10.1016/j.neuron.2018.02.024 · Cited by 62 · see citing works

Dynamic functions of GABA signaling during granule cell maturation

Dieni, C. V., Chancey, J. H., & Overstreet‐Wadiche, L. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00113 · Cited by 61 · see citing works

Lower gene expression for KCNS3 potassium channel subunit in parvalbumin-containing neurons in the prefrontal cortex in schizophrenia

Georgiev, D., Arion, D., Enwright, J. F., Kikuchi, M., Minabe, Y., Corradi, J. P., Lewis, D. A., & Hashimoto, T. (2014) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2013.13040468 · Cited by 61 · see citing works

An axon-specific expression of HCN channels catalyzes fast action potential signaling in GABAergic interneurons

Roth, F. C., & Hu, H. (2020) · Nature Communications · doi:10.1038/s41467-020-15791-y · Cited by 61 · see citing works

Flexible Nanopipettes for Minimally Invasive Intracellular Electrophysiology In Vivo

Jayant, K., Wenzel, M., Bando, Y., Hamm, J. P., Mandriota, N., Rabinowitz, J. H., Plante, I. J., Owen, J. S., Şahin, Ö., Shepard, K. L., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2018.12.019 · Cited by 57 · see citing works

Toward a full-scale computational model of the rat dentate gyrus

Schneider, C. J., Bezaire, M. J., & Soltész, I. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00083 · Cited by 60 · see citing works

Membrane Properties and the Balance between Excitation and Inhibition Control Gamma-Frequency Oscillations Arising from Feedback Inhibition

Economo, M. N., & White, J. A. (2012) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002354 · Cited by 58 · see citing works

Functional Properties of Dendritic Gap Junctions in Cerebellar Golgi Cells

Szoboszlay, M., Lőrincz, A., Lanore, F., Vervaeke, K., Silver, R. A., & Nusser, Z. (2016) · Neuron · doi:10.1016/j.neuron.2016.03.029 · Cited by 60 · see citing works

Differential Dendritic Integration of Synaptic Potentials and Calcium in Cerebellar Interneurons

Tran-Van-Minh, A., Abrahamsson, T., Cathala, L., & DiGregorio, D. A. (2016) · Neuron · doi:10.1016/j.neuron.2016.07.029 · Cited by 61 · see citing works

Developmental pruning of excitatory synaptic inputs to parvalbumin interneurons in monkey prefrontal cortex

Chung, D. W., Wills, Z. P., Fish, K. N., & Lewis, D. A. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1610077114 · Cited by 59 · see citing works

Conditional Spike Transmission Mediated by Electrical Coupling Ensures Millisecond Precision-Correlated Activity among Interneurons In Vivo

van Welie, I., Roth, A., Ho, S. S. N., Komai, S., & Häusser, M. (2016) · Neuron · doi:10.1016/j.neuron.2016.04.013 · Cited by 55 · see citing works

Principles of dendritic integration

Spruston, N., Stuart, G. J., & Häusser, M. (2016) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198745273.003.0012 · Cited by 57 · see citing works

Cortical Interneuron Subtypes Vary in Their Axonal Action Potential Properties

Casale, A. E., Foust, A. J., Bal, T., & McCormick, D. A. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1467-13.2015 · Cited by 53 · see citing works

Enhanced hippocampal neuronal excitability and LTP persistence associated with reduced behavioral flexibility in the maternal immune activation model of schizophrenia

Savanthrapadian, S., Wolff, A. R., Logan, B. J., Eckert, M. J., Bilkey, D. K., & Abraham, W. C. (2013) · Hippocampus · doi:10.1002/hipo.22193 · Cited by 51 · see citing works

Parvalbumin‐producing cortical interneurons receive inhibitory inputs on proximal portions and cortical excitatory inputs on distal dendrites

Kameda, H., Hioki, H., Tanaka, Y. H., Tanaka, T., Sohn, J., Sonomura, T., Furuta, T., Fujiyama, F., & Kaneko, T. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08027.x · Cited by 51 · see citing works

Role of microcircuit structure and input integration in hippocampal interneuron recruitment and plasticity

Bartos, M., Alle, H., & Vida, I. (2010) · Neuropharmacology · doi:10.1016/j.neuropharm.2010.12.017 · Cited by 50 · see citing works

A Subtype of Inhibitory Interneuron with Intrinsic Persistent Activity in Human and Monkey Neocortex

Wang, B., Yin, L., Zou, X., Ye, M., Liu, Y., He, T., Deng, S., Jiang, Y., Zheng, R., Wang, Y., et al. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.02.018 · Cited by 40 · see citing works

Impaired GABAergic neurotransmission in schizophrenia underlies impairments in cortical gamma band oscillations

McNally, J. M., McCarley, R. W., & Brown, R. E. (2013) · Current Psychiatry Reports · doi:10.1007/s11920-012-0346-z · Cited by 47 · see citing works

Role of active dendritic conductances in subthreshold input integration

Remme, M. W. H., & Rinzel, J. (2010) · Journal of Computational Neuroscience · doi:10.1007/s10827-010-0295-7 · Cited by 47 · see citing works

Rapid Dynamic Changes of Dendritic Inhibition in the Dentate Gyrus by Presynaptic Activity Patterns

Liu, Y., Cheng, J., & Lien, C. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2566-13.2014 · Cited by 45 · see citing works

NMDA receptor-dependent function and plasticity in inhibitory circuits

Moreau, A. W., & Kullmann, D. M. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.03.004 · Cited by 44 · see citing works

The ins and outs of inhibitory synaptic plasticity: Neuron types, molecular mechanisms and functional roles

Capogna, M., Castillo, P. E., & Maffei, A. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14907 · Cited by 41 · see citing works

Parvalbumin interneuron dendrites enhance gamma oscillations

Kriener, B., Hu, H., & Vervaeke, K. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110948 · Cited by 41 · see citing works

Fast activation of feedforward inhibitory neurons from thalamic input and its relevance to the regulation of spike sequences in the barrel cortex

Kimura, F., Itami, C., Ikezoe, K., Tamura, H., Fujita, I., Yanagawa, Y., Obata, K., & Ohshima, M. (2010) · The Journal of Physiology · doi:10.1113/jphysiol.2010.188177 · Cited by 40 · see citing works

Active Action Potential Propagation But Not Initiation in Thalamic Interneuron Dendrites

Casale, A. E., & McCormick, D. A. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4417-11.2011 · Cited by 38 · see citing works

Dendritic inhibition differentially regulates excitability of dentate gyrus parvalbumin-expressing interneurons and granule cells

Elgueta, C., & Bartos, M. (2019) · Nature Communications · doi:10.1038/s41467-019-13533-3 · Cited by 38 · see citing works

Synchronization of Firing in Cortical Fast-Spiking Interneurons at Gamma Frequencies: A Phase-Resetting Analysis

Gouwens, N. W., Zeberg, H., Tsumoto, K., Tateno, T., Aihara, K., & Robinson, H. P. C. (2010) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000951 · Cited by 36 · see citing works

Multiscale and multimodal reconstruction of cortical structure and functionPreprint

Turner, N. L., Macrina, T., Bae, J. A., Yang, R., Wilson, A. M., Schneider-Mizell, C. M., Lee, K., Lu, R., Wu, J., Bodor, Á. L., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.10.14.338681 · Cited by 37 · see citing works

Computational modeling of GABAA receptor-mediated paired-pulse inhibition in the dentate gyrus

Jedlička, P., Deller, T., & Schwarzacher, S. W. (2010) · Journal of Computational Neuroscience · doi:10.1007/s10827-010-0214-y · Cited by 37 · see citing works

Transcranial alternating current stimulation (tACS) at gamma frequency: an up-and-coming tool to modify the progression of Alzheimer’s Disease

Paolis, M. L. D., Paoletti, I., Zaccone, C., Capone, F., D’Amelio, M., & Krashia, P. (2024) · Translational Neurodegeneration · doi:10.1186/s40035-024-00423-y · Cited by 39 · see citing works

Inhibitory Networks of Fast-Spiking Interneurons Generate Slow Population Activities due to Excitatory Fluctuations and Network Multistability

Ho, E. C. Y., Strüber, M., Bartos, M., Zhang, L., & Skinner, F. K. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5446-11.2012 · Cited by 32 · see citing works

Spatial Clustering of Inhibition in Mouse Primary Visual Cortex

D’Souza, R. D., Bista, P., Meier, A. M., Ji, W., & Burkhalter, A. (2019) · Neuron · doi:10.1016/j.neuron.2019.09.020 · Cited by 34 · see citing works

Selective Expression of KCNS3 Potassium Channel α-Subunit in Parvalbumin-Containing GABA Neurons in the Human Prefrontal Cortex

Георгиев, Д., González‐Burgos, G., Kikuchi, M., Minabe, Y., Lewis, D. A., & Hashimoto, T. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043904 · Cited by 32 · see citing works

Biophysical Kv3 channel alterations dampen excitability of cortical PV interneurons and contribute to network hyperexcitability in early Alzheimer’s

Oláh, V. J., Goettemoeller, A. M., Rayaprolu, S., Dammer, E. B., Seyfried, N. T., Rangaraju, S., Dimidschstein, J., & Rowan, M. J. (2022) · eLife · doi:10.7554/elife.75316 · Cited by 32 · see citing works

Community-based reconstruction and simulation of a full-scale model of the rat hippocampus CA1 region

Romani, A., Antonietti, A., Bella, D., Budd, J., Giacalone, E., Kurban, K., Sáray, S., Abdellah, M., Arnaudon, A., Boci, E., et al. (2024) · PLOS Biology · doi:10.1371/journal.pbio.3002861 · Cited by 39 · see citing works

Errors in the measurement of voltage-activated ion channels in cell-attached patch-clamp recordings

Williams, S. R., & Wozny, C. (2011) · Nature Communications · doi:10.1038/ncomms1225 · Cited by 32 · see citing works

Synaptic Integration in Cortical Inhibitory Neuron Dendrites

Hu, H., & Vervaeke, K. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.06.065 · Cited by 30 · see citing works

Cell type‐specific and activity‐dependent dynamics of action potential‐evoked Ca2+ signals in dendrites of hippocampal inhibitory interneurons

Evstratova, A., Chamberland, S., & Topolnik, L. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2010.204255 · Cited by 31 · see citing works

Functional Distinctions between Spine and Dendritic Synapses Made onto Parvalbumin-Positive Interneurons in Mouse Cortex

Sancho, L., & Bloodgood, B. L. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.07.070 · Cited by 30 · see citing works

M1-like muscarinic acetylcholine receptors regulate fast-spiking interneuron excitability in rat dentate gyrus

Chiang, P., Yeh, W. C., Lee, C. T., Weng, J.-Y., Huang, Y. Y., & Lien, C. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.04.051 · Cited by 30 · see citing works

Physiological features of parvalbumin-expressing GABAergic interneurons contributing to high-frequency oscillations in the cerebral cortex

Milicevic, K. D., Barbeau, B. L., Lovic, D. D., Patel, A. A., Ivanova, V. O., & Antic, S. D. (2023) · Current Research in Neurobiology · doi:10.1016/j.crneur.2023.100121 · Cited by 30 · see citing works

Gap Junctions Interconnect Different Subtypes of Parvalbumin-Positive Interneurons in Barrels and Septa with Connectivity Unique to Each Subtype

Shigematsu, N., Nishi, A., & Fukuda, T. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy038 · Cited by 29 · see citing works

Challenging the point neuron dogma: FS basket cells as 2-stage nonlinear integratorsPreprint

Tzilivaki, A., Kastellakis, G., & Poirazi, P. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/251314 · Cited by 30 · see citing works

The computational power of the human brain

Gebicke‐Haerter, P. J. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1220030 · Cited by 30 · see citing works

Different input and output properties characterize parvalbumin‐positive basket and Axo‐axonic cells in the hippocampal CA3 subfield

Papp, O. I., Karlócai, M. R., Tóth, I. E., Freund, T. F., & Hájos, N. (2013) · Hippocampus · doi:10.1002/hipo.22147 · Cited by 27 · see citing works

Spatial integration of dendrites in fast-spiking basket cells

Liu, M., & Sun, X. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1132980 · Cited by 2 · see citing works

Distinct nonuniform cable properties optimize rapid and efficient activation of fast-spiking GABAergic interneurons

Nörenberg, A., Hu, H., Vida, I., Bartos, M., & Jónás, P. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0910716107 · Cited by 125 · see citing works

Dendritic Spikes Are Enhanced by Cooperative Network Activity in the Intact Hippocampus

Kamondi, A., Acsády, L., & Buzsáki, G. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-10-03919.1998 · Cited by 252 · see citing works

Distal Initiation and Active Propagation of Action Potentials in Interneuron Dendrites

Martina, M., Vida, I., & Jonas, P. (2000) · Science · doi:10.1126/science.287.5451.295 · Cited by 375 · see citing works

Efficient Ca2+ buffering in fast‐spiking basket cells of rat hippocampus

Aponte, Y., Bischofberger, J., & Jónás, P. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2007.147298 · Cited by 80 · see citing works