Perisomatic Inhibition

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

Proximally targeted GABAergic synapses and gap junctions synchronize cortical interneurons

Tamás, G., Buhl, E. H., Lörincz, A., & Somogyi, P. (2000) · Nature Neuroscience · doi:10.1038/73936 · Cited by 648 · see citing works

Asynchronous GABA release generates long-lasting inhibition at a hippocampal interneuron–principal neuron synapse

Hefft, S., & Jonas, P. (2005) · Nature Neuroscience · doi:10.1038/nn1542 · Cited by 583 · see citing works

A specific ‘axo-axonal’ interneuron in the visual cortex of the rat

Somogyi, P. (1977) · Brain Research · doi:10.1016/0006-8993(77)90808-3 · Cited by 530 · see citing works

Total number and ratio of excitatory and inhibitory synapses converging onto single interneurons of different types in the CA1 area of the rat hippocampus

Gulyás, A. I., Megı́as, M., Emri, Z., & Freund, T. F. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-22-10082.1999 · Cited by 476 · see citing works

Complementary Roles of Cholecystokinin- and Parvalbumin-Expressing GABAergic Neurons in Hippocampal Network Oscillations

Klausberger, T., Marton, L. F., O'Neill, J., Huck, J. H. J., Dalezios, Y., Fuentealba, P., Suen, W. Y., Papp, E., Kaneko, T., Watanabe, M., et al. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.3269-05.2005 · Cited by 469 · see citing works

Neuronal Diversity in GABAergic Long-Range Projections from the Hippocampus

Jinno, S., Klausberger, T., Marton, L. F., Dalezios, Y., Roberts, J. D. B., Fuentealba, P., Bushong, E. A., Henze, D., Buzsáki, G., & Somogyi, P. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.1847-07.2007 · Cited by 369 · see citing works

Cell surface domain specific postsynaptic currents evoked by identified GABAergic neurones in rat hippocampus <i>in vitro</i>

Maccaferri, G., David, J., Roberts, B., Szucs, P., Cottingham, C. A., & Somogyi, P. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.t01-3-00091.x · Cited by 357 · see citing works

Cannabinoids reveal importance of spike timing coordination in hippocampal function

Robbe, D., Montgomery, S. M., Thome, A., Rueda-Orozco, P. E., McNaughton, B. L., & Buzsaki, G. (2006) · Nature Neuroscience · doi:10.1038/nn1801 · Cited by 333 · see citing works

Distinct timing in the activity of cannabinoid-sensitive and cannabinoid-insensitive basket cells

Glickfeld, L. L., & Scanziani, M. (2006) · Nature Neuroscience · doi:10.1038/nn1688 · Cited by 222 · see citing works

5-HT₃Receptors Mediate Serotonergic Fast Synaptic Excitation of Neocortical Vasoactive Intestinal Peptide/Cholecystokinin Interneurons

Férézou, I., Cauli, B., Hill, E. L., Rossier, J., Hamel, E., & Lambolez, B. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-17-07389.2002 · Cited by 215 · see citing works

Lighting the chandelier: new vistas for axo-axonic cells

Howard, A., Tamas, G., & Soltesz, I. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.04.004 · Cited by 167 · see citing works

Cholecystokinin-immunopositive basket and Schaffer collateral-associated interneurones target different domains of pyramidal cells in the CA1 area of the rat hippocampus

Cope, D. W., Maccaferri, G., Márton, L. F., Roberts, J. D. B., Cobden, P. M., & Somogyi, P. (2002) · Neuroscience · doi:10.1016/s0306-4522(01)00440-7 · Cited by 144 · see citing works

Localization of GABAB (R1) receptors in the rat hippocampus by immunocytochemistry and high resolution autoradiography, with specific reference to its localization in identified hippocampal interneuron subpopulations

Sloviter, R. (1999) · Neuropharmacology · doi:10.1016/s0028-3908(99)00132-x · Cited by 86 · see citing works

Diversity in the Neuronal Machine

Soltesz, I. (2006) · doi:10.1093/acprof:oso/9780195177015.001.1 · Cited by 68 · 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

A resource of Cre driver lines for genetic targeting of GABAergic neurons in cerebral cortex

Taniguchi, H., He, M., Wu, P., Kim, S., Paik, R., Sugino, K., Kvitsani, D., Fu, Y., Lu, J., Lin, Y., et al. (2011) · Neuron · doi:10.1016/j.neuron.2011.07.026 · Cited by 1,828 · see citing works

Hippocampal sharp wave-ripple: A cognitive biomarker for episodic memory and planning

Buzsáki, G. (2015) · Hippocampus · doi:10.1002/hipo.22488 · Cited by 1,759 · see citing works

Inhibitory Interneuron Deficit Links Altered Network Activity and Cognitive Dysfunction in Alzheimer Model

Verret, L., Mann, E. O., Hang, G. B., Barth, A. M. I., Cobos, I., Ho, K., Devidze, N., Masliah, E., Kreitzer, A. C., Mody, I., et al. (2012) · Cell · doi:10.1016/j.cell.2012.02.046 · Cited by 1,216 · see citing works

Network abnormalities and interneuron dysfunction in Alzheimer disease

Palop, J. J., & Mucke, L. (2016) · Nature reviews. Neuroscience · doi:10.1038/nrn.2016.141 · Cited by 1,022 · 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

A disinhibitory microcircuit for associative fear learning in the auditory cortex

Letzkus, J. J., Wolff, S. B. E., Meyer, E. M. M., Tovote, P., Courtin, J., Herry, C., & Lüthi, A. (2011) · Nature · doi:10.1038/nature10674 · Cited by 840 · see citing works

Common Mechanisms of Excitatory and Inhibitory Imbalance in Schizophrenia and Autism Spectrum Disorders

Gao, R., & Penzes, P. (2015) · Current Molecular Medicine · doi:10.2174/1566524015666150303003028 · Cited by 516 · see citing works

Prefrontal parvalbumin interneurons shape neuronal activity to drive fear expression

Courtin, J., Chaudun, F., Rozeske, R. R., Karalis, N., Gonzalez-Campo, C., Wurtz, H., Abdi, A., Baufreton, J., Bienvenu, T. C. M., & Herry, C. (2014) · Nature · doi:10.1038/nature12755 · Cited by 524 · see citing works

The Role of the Medial Prefrontal Cortex in the Conditioning and Extinction of Fear

Giustino, T. F., & Maren, S. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00298 · Cited by 519 · see citing works

A Loss of Parvalbumin-Containing Interneurons Is Associated with Diminished Oscillatory Activity in an Animal Model of Schizophrenia

Lodge, D. J., Behrens, M. M., & Grace, A. A. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5419-08.2009 · Cited by 488 · see citing works

Unique functional properties of somatostatin-expressing GABAergic neurons in mouse barrel cortex

Gentet, L. J., Kremer, Y., Taniguchi, H., Huang, Z. J., Staiger, J. F., & Petersen, C. C. H. (2012) · Nature Neuroscience · doi:10.1038/nn.3051 · Cited by 438 · see citing works

Neuronal arithmetic

Silver, R. A. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2864 · Cited by 481 · see citing works

Membrane potential dynamics of GABAergic neurons in the barrel cortex of behaving mice

Gentet, L. J., Avermann, M., Matyas, F., Staiger, J. F., & Petersen, C. C. H. (2010) · Neuron · doi:10.1016/j.neuron.2010.01.006 · Cited by 429 · see citing works

Recent advances in the neuropsychopharmacology of serotonergic hallucinogens

Halberstadt, A. L. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.07.016 · Cited by 312 · 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 &amp; Metabolism · doi:10.1038/jcbfm.2014.104 · Cited by 295 · see citing works

Autism-Associated Neuroligin-3 Mutations Commonly Disrupt Tonic Endocannabinoid Signaling

Földy, C., Malenka, R. C., & Südhof, T. C. (2013) · Neuron · doi:10.1016/j.neuron.2013.02.036 · Cited by 287 · see citing works

Nanodomain Coupling between Ca2+ Channels and Ca2+ Sensors Promotes Fast and Efficient Transmitter Release at a Cortical GABAergic Synapse

Bucurenciu, I., Kulik, A., Schwaller, B., Frotscher, M., & Jonas, P. (2008) · Neuron · doi:10.1016/j.neuron.2007.12.026 · Cited by 274 · see citing works

Classification of NPY-Expressing Neocortical Interneurons

Karagiannis, A., Gallopin, T., Dávid, C., Battaglia, D., Geoffroy, H., Rossier, J., Hillman, E. M. C., Staiger, J. F., & Cauli, B. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.0058-09.2009 · Cited by 256 · see citing works

Plasticity of Inhibition

Kullmann, D. M., Moreau, A. W., Bakiri, Y., & Nicholson, E. (2012) · Neuron · doi:10.1016/j.neuron.2012.07.030 · Cited by 234 · see citing works

Stress Impairs GABAergic Network Function in the Hippocampus by Activating Nongenomic Glucocorticoid Receptors and Affecting the Integrity of the Parvalbumin-Expressing Neuronal Network

Hu, W., Zhang, M., Czéh, B., Flügge, G., & Zhang, W. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2010.31 · Cited by 246 · see citing works

Cell-Type-Specific Circuit Connectivity of Hippocampal CA1 Revealed through Cre-Dependent Rabies Tracing

Sun, Y., Nguyen, A. Q., Nguyen, J. P., Le, L., Saur, D., Choi, J., Callaway, E. M., & Xu, X. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.02.030 · Cited by 218 · see citing works

Chronic stress increases prefrontal inhibition: a mechanism for stress-induced prefrontal dysfunction

McKlveen, J. M., Morano, R. L., Fitzgerald, M., Zoubovsky, S., Cassella, S. N., Scheimann, J. R., Ghosal, S., Mahbod, P., Packard, B. A., Myers, B., et al. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.03.2101 · Cited by 224 · see citing works

Mechanisms of Inhibition within the Telencephalon: “Where the Wild Things Are”

Fishell, G., & Rudy, B. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113717 · Cited by 233 · see citing works

Deep molecular diversity of mammalian synapses: why it matters and how to measure it

O'Rourke, N. A., Weiler, N. C., Micheva, K. D., & Smith, S. J. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3170 · Cited by 210 · see citing works

Perisomatic GABA Release and Thalamocortical Integration onto Neocortical Excitatory Cells Are Regulated by Neuromodulators

Kruglikov, I., & Rudy, B. (2008) · Neuron · doi:10.1016/j.neuron.2008.04.024 · Cited by 209 · see citing works

Target-selective GABAergic control of entorhinal cortex output

Varga, C., Lee, S. Y., & Soltesz, I. (2010) · Nature Neuroscience · doi:10.1038/nn.2570 · Cited by 219 · 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

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

The Diversity of Cortical Inhibitory Synapses

Kubota, Y., Karube, F., Nomura, M., & Kawaguchi, Y. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00027 · Cited by 180 · see citing works

Multisensory Integration of Natural Odors and Sounds in the Auditory Cortex

Cohen, L., Rothschild, G., & Mizrahi, A. (2011) · Neuron · doi:10.1016/j.neuron.2011.08.019 · Cited by 192 · 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

Synaptic Cross Talk between Perisomatic-Targeting Interneuron Classes Expressing Cholecystokinin and Parvalbumin in Hippocampus

Karson, M. A., Tang, A.-H., Milner, T. A., & Alger, B. E. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5264-08.2009 · Cited by 135 · see citing works

Hippocampal extracellular matrix alterations contribute to cognitive impairment associated with a chronic depressive-like state in rats

Riga, D., Kramvis, I., Koskinen, M. K., van Bokhoven, P., van der Harst, J. E., Heistek, T. S., Jaap Timmerman, A., van Nierop, P., van der Schors, R. C., Pieneman, A. W., et al. (2017) · Science Translational Medicine · doi:10.1126/scitranslmed.aai8753 · Cited by 128 · 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

Glutamatergic deficits and parvalbumin-containing inhibitory neurons in the prefrontal cortex in schizophrenia

Bitanihirwe, B., Lim, M., Kelley, J., Kaneko, T., & Woo, T. (2009) · BMC Psychiatry · doi:10.1186/1471-244x-9-71 · Cited by 137 · see citing works

Comparative density of CCK- and PV-GABA cells within the cortex and hippocampus

Whissell, P. D., Cajanding, J. D., Fogel, N., & Kim, J. C. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00124 · Cited by 118 · see citing works

Dual origins of functionally distinct O-LM interneurons revealed by differential 5-HT3AR expression

Chittajallu, R., Craig, M. T., McFarland, A., Yuan, X., Gerfen, S., Tricoire, L., Erkkila, B., Barron, S. C., Lopez, C. M., Liang, B. J., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3538 · Cited by 119 · see citing works

A Cortico-Hippocampal Learning Rule Shapes Inhibitory Microcircuit Activity to Enhance Hippocampal Information Flow

Basu, J., Srinivas, K. V., Cheung, S. K., Taniguchi, H., Huang, Z. J., & Siegelbaum, S. A. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.001 · Cited by 122 · see citing works

Perineuronal Nets Regulate the Inhibitory Perisomatic Input onto Parvalbumin Interneurons and γ Activity in the Prefrontal Cortex

Carceller, H., Guirado, R., Ripolles-Campos, E., Teruel-Marti, V., & Nacher, J. (2020) · The Journal of Neuroscience · doi:10.1523/jneurosci.0291-20.2020 · Cited by 112 · see citing works

Inhibitory Actions Unified by Network Integration

Seybold, B. A., Phillips, E. A. K., Schreiner, C. E., & Hasenstaub, A. R. (2015) · Neuron · doi:10.1016/j.neuron.2015.09.013 · Cited by 118 · see citing works

Cholinergic control of GABA release: emerging parallels between neocortex and hippocampus

Lawrence, J. J. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2008.03.008 · Cited by 115 · see citing works

Genetic dissection of GABAergic neural circuits in mouse neocortex

Taniguchi, H. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00008 · Cited by 106 · see citing works

M3 Muscarinic Acetylcholine Receptor Expression Confers Differential Cholinergic Modulation to Neurochemically Distinct Hippocampal Basket Cell Subtypes

Cea-del Rio, C. A., Lawrence, J. J., Tricoire, L., Erdelyi, F., Szabo, G., & McBain, C. J. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.5040-09.2010 · Cited by 99 · see citing works

Regulation of fast-spiking basket cell synapses by the chloride channel ClC-2

Földy, C., Lee, S.-H., Morgan, R. J., & Soltesz, I. (2010) · Nature Neuroscience · doi:10.1038/nn.2609 · Cited by 89 · see citing works

Gamma oscillation deficits and the onset and early progression of schizophrenia

Woo, T.-U. W., Spencer, K., & McCarley, R. W. (2010) · Harvard Review of Psychiatry · doi:10.3109/10673221003747609 · Cited by 96 · see citing works

Nerve Terminal Nicotinic Acetylcholine Receptors Initiate Quantal GABA Release from Perisomatic Interneurons by Activating Axonal T-Type (Ca_v3) Ca²⁺Channels and Ca²⁺Release from Stores

Tang, A.-H., Karson, M. A., Nagode, D. A., McIntosh, J. M., Uebele, V. N., Renger, J. J., Klugmann, M., Milner, T. A., & Alger, B. E. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.2781-11.2011 · Cited by 92 · see citing works

Cell type-specific inhibitory inputs to dendritic and somatic compartments of parvalbumin-expressing neocortical interneuron

Hioki, H., Okamoto, S., Konno, M., Kameda, H., Sohn, J., Kuramoto, E., Fujiyama, F., & Kaneko, T. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.2255-12.2013 · Cited by 83 · 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

Enriched housing enhances recovery of limb placement ability and reduces aggrecan-containing perineuronal nets in the rat somatosensory cortex after experimental stroke.

Madinier, A., Quattromani, M. J., Sjölund, C., Ruscher, K., & Wieloch, T. (2014) · PLoS ONE · doi:10.1371/journal.pone.0093121 · Cited by 82 · see citing works

Cysteine String Protein-α Prevents Activity-Dependent Degeneration in GABAergic Synapses

García-Junco-Clemente, P., Cantero, G., Gómez-Sánchez, L., Linares-Clemente, P., Martínez-López, J. A., Luján, R., & Fernández-Chacón, R. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.0924-10.2010 · Cited by 79 · see citing works

A Barrel-Related Interneuron in Layer 4 of Rat Somatosensory Cortex with a High Intrabarrel Connectivity

Koelbl, C., Helmstaedter, M., Lübke, J., & Feldmeyer, D. (2015) · Cerebral Cortex · doi:10.1093/cercor/bht263 · Cited by 68 · see citing works

Cell Type-Specific Expression of Acid-Sensing Ion Channels in Hippocampal Interneurons

Weng, J.-Y., Lin, Y.-C., & Lien, C.-C. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.0582-10.2010 · Cited by 72 · see citing works

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 · see citing works

Shank1 regulates excitatory synaptic transmission in mouse hippocampal parvalbumin‐expressing inhibitory interneurons

Mao, W., Watanabe, T., Cho, S., Frost, J. L., Truong, T., Zhao, X., & Futai, K. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.12877 · Cited by 59 · see citing works

EEG-β/γ spectral power elevation in rat: a translatable biomarker elicited by GABA_Aα2/3-positive allosteric modulators at nonsedating anxiolytic doses

Christian, E. P., Snyder, D. H., Song, W., Gurley, D. A., Smolka, J., Maier, D. L., Ding, M., Gharahdaghi, F., Liu, X. F., Chopra, M., et al. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00539.2013 · Cited by 68 · see citing works

Asynchronous release of GABA via tonic cannabinoid receptor activation at identified interneuron synapses in rat CA1

Ali, A. B., & Todorova, M. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07165.x · Cited by 66 · see citing works

Deletion of selenoprotein P results in impaired function of parvalbumin interneurons and alterations in fear learning and sensorimotor gating

Pitts, M. W., Raman, A. V., Hashimoto, A. C., Todorovic, C., Nichols, R. A., & Berry, M. J. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.02.017 · Cited by 67 · see citing works

Properties and dynamics of inhibitory synaptic communication within the CA3 microcircuits of pyramidal cells and interneurons expressing parvalbumin or cholecystokinin

Kohus, Z., Káli, S., Rovira‐Esteban, L., Schlingloff, D., Papp, O., Freund, T. F., Hájos, N., & Gulyás, A. I. (2016) · The Journal of Physiology · doi:10.1113/jp272231 · Cited by 66 · see citing works

Differential GABA_B-Receptor-Mediated Effects in Perisomatic- and Dendrite-Targeting Parvalbumin Interneurons

Booker, S. A., Gross, A., Althof, D., Shigemoto, R., Bettler, B., Frotscher, M., Hearing, M., Wickman, K., Watanabe, M., Kulik, Á., et al. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.1186-12.2013 · Cited by 58 · see citing works

Cholinergic modulation amplifies the intrinsic oscillatory properties of CA1 hippocampal cholecystokinin‐positive interneurons

Cea‐del Rio, C. A., Lawrence, J. J., Erdelyi, F., Szabo, G., & McBain, C. J. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2010.199422 · Cited by 53 · see citing works

Direct Alteration of a Specific Inhibitory Circuit of the Hippocampus by Antidepressants

Méndez, P., Pazienti, A., Szabó, G., & Bacci, A. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.1720-12.2012 · Cited by 53 · see citing works

Altered gamma oscillations during pregnancy through loss of δ subunit-containing GABAA receptors on parvalbumin interneurons

Ferando, I., & Mody, I. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00144 · Cited by 52 · see citing works

Cell-type specific inactivation of hippocampal CA1 disrupts location-dependent object recognition in the mouse

Haettig, J., Sun, Y., Wood, M. A., & Xu, X. (2013) · Learning &amp; Memory · doi:10.1101/lm.027847.112 · Cited by 41 · see citing works

GABA Transporter GAT1: A Crucial Determinant of GABAB Receptor Activation in Cortical Circuits?

Gonzalez-Burgos, G. (2010) · Advances in Pharmacology · doi:10.1016/s1054-3589(10)58008-6 · Cited by 38 · see citing works

Presynaptic Kainate Receptor Activation Preserves Asynchronous GABA Release Despite the Reduction in Synchronous Release from Hippocampal Cholecystokinin Interneurons

Daw, M. I., Pelkey, K. A., Chittajallu, R., & McBain, C. J. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.6334-09.2010 · Cited by 43 · see citing works

5-HT3a Receptors Modulate Hippocampal Gamma Oscillations by Regulating Synchrony of Parvalbumin-Positive Interneurons

Huang, Y., Yoon, K., Ko, H., Jiao, S., Ito, W., Wu, J.-Y., Yung, W.-H., Lu, B., & Morozov, A. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu209 · Cited by 27 · see citing works

KCTD12 Auxiliary Proteins Modulate Kinetics of GABA_BReceptor-Mediated Inhibition in Cholecystokinin-Containing Interneurons

Booker, S. A., Althof, D., Gross, A., Loreth, D., Müller, J., Unger, A., Fakler, B., Varro, A., Watanabe, M., Gassmann, M., et al. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw090 · Cited by 25 · see citing works

Progressive excitability changes in the medial entorhinal cortex in the 3xTg mouse model of Alzheimer’s disease pathology

Chen, L., Christenson Wick, Z., Vetere, L. M., Vaughan, N., Jurkowski, A., Galas, A., Diego, K. S., Philipsberg, P. A., Soler, I., Feng, Y., et al. (2023) · The Journal of Neuroscience · doi:10.1523/jneurosci.1204-23.2023 · Cited by 21 · see citing works

Response to Comment on “Principles of connectivity among morphologically defined cell types in adult neocortex”

Jiang, X., Shen, S., Sinz, F., Reimer, J., Cadwell, C. R., Berens, P., Ecker, A. S., Patel, S., Denfield, G. H., Froudarakis, E., et al. (2016) · Science · doi:10.1126/science.aaf6102 · Cited by 13 · see citing works