Hippocampal CA1 interneurons: an in vivo intracellular labeling study

The Intrinsic Electrophysiological Properties of Mammalian Neurons: Insights into Central Nervous System Function

Llinás, R. R. (1988) · Science · doi:10.1126/science.3059497 · Cited by 2,285

The three-dimensional organization of the hippocampal formation: A review of anatomical data

Amaral, D. G., & Witter, M. P. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90424-7 · Cited by 2,180

Gamma (40-100 Hz) oscillation in the hippocampus of the behaving rat

Bragin, A., Jando, G., Nadasdy, Z., Hetke, J., Wise, K., & Buzsaki, G. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-01-00047.1995 · Cited by 1,527

Sharp wave-associated high-frequency oscillation (200 Hz) in the intact hippocampus: network and intracellular mechanisms

Ylinen, A., Bragin, A., Nadasdy, Z., Jando, G., Szabo, I., Sik, A., & Buzsaki, G. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-01-00030.1995 · Cited by 1,092

The metabotropic glutamate receptor (mGluRlα) is concentrated at perisynaptic membrane of neuronal subpopulations as detected by immunogold reaction

Baude, A., Nusser, Z., Roberts, J. D. B., Mulvihill, E., Jeffrey Mcllhinney, R. A., & Somogyi, P. (1993) · Neuron · doi:10.1016/0896-6273(93)90086-7 · Cited by 927

Neuronal Networks of the Hippocampus

Traub, R. D., & Miles, R. (1991) · doi:10.1017/cbo9780511895401 · Cited by 802

The hippocampal CA3 network: An in vivo intracellular labeling study

Li, X. ‐., Somogyi, P., Ylinen, A., & Buzsáki, G. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903390204 · Cited by 751

Parvalbumin in Most γ-Aminobutyric Acid-Containing Neurons of the Rat Cerebral Cortex

Celio, M. R. (1986) · Science · doi:10.1126/science.3945815 · Cited by 740

Calcium‐binding protein (calbindin‐D 28k ) and parvalbumin immunocytochemistry: Localization in the rat hippocampus with specific reference to the selective vulnerability of hippocampal neurons to seizure activity

Sloviter, R. S. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902800203 · Cited by 686

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

Subclass‐specific formation of perineuronal nets around parvalbumin‐expressing GABAergic neurons in Ammon's horn of the mouse hippocampus

Yamada, J., & Jinno, S. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23712 · Cited by 27

Morphology of Hippocampal Neurons

Vida, I. (2010) · Springer eBooks · doi:10.1007/978-1-4419-0996-1_2 · Cited by 30

Regulation of rhythm genesis by volume-limited, astroglia-like signals in neural networks

Savtchenko, L. P., & Rusakov, D. A. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0614 · Cited by 25

Structural Correlates of CA2 and CA3 Pyramidal Cell Activity in Freely-Moving Mice

Ding, L., Chen, H., Diamantaki, M., Coletta, S., Preston‐Ferrer, P., & Burgalossi, A. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0099-20.2020 · Cited by 29

Short‐term Effects of Kainic Acid on CA1 Hippocampal Interneurons Differentially Vulnerable to Excitotoxicity

Sanon, N. T., Carmant, L., Emond, M., Congar, P., & Lacaille, J. (2005) · Epilepsia · doi:10.1111/j.1528-1167.2005.21404.x · Cited by 24

Glutamate-Mediated Synaptic Excitation of Cortical Interneurons

Geiger, J. R. P., Roth, A., Taskin, B., & Jónás, P. (1999) · Handbook of experimental pharmacology · doi:10.1007/978-3-662-08022-1_11 · Cited by 26

Hippocampal field CA1 interneuronal nociceptive responses: modulation by medial septal region and morphine

Zheng, F., & Khanna, S. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00119-0 · Cited by 26

Calcium Dynamics in Dendrites of Hippocampal CA1 Interneurons in Awake Mice

Francavilla, R., Villette, V., Martel, O., & Topolnik, L. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00098 · Cited by 25

Synaptic kainate currents reset interneuron firing phase

Yang, E. J., Harris, A. Z., & Pettit, D. L. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.118448 · Cited by 27

Variant BDNF-Val66Met Polymorphism is Associated with Layer-Specific Alterations in GABAergic Innervation of Pyramidal Neurons, Elevated Anxiety and Reduced Vulnerability of Adolescent Male Mice to Activity-Based Anorexia

Chen, Y.-W., Surgent, O. J., Rana, B. S., Lee, F., & Aoki, C. J. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw210 · Cited by 25

An integrative model of the intrinsic hippocampal theta rhythm

Hummos, A., & Nair, S. S. (2017) · PLoS ONE · doi:10.1371/journal.pone.0182648 · Cited by 26

Inhibition potentiates the synchronizing action of electrical synapses

Pfeuty, B. (2007) · Frontiers in Computational Neuroscience · doi:10.3389/neuro.10.008.2007 · Cited by 24

Nerve growth factor but not neurotrophin-3 is synthesized by hippocampal GABAergic neurons that project to the medial septum

Acsády, L., Pascual, M., Rocamora, N., Soriano, E., & Freund, T. F. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00091-9 · Cited by 24

Expression of metabotropic glutamate receptor 1α in the hippocampus of rat pilocarpine model of status epilepticus

Tang, F. R., Lee, W. L., Yang, J., Sim, M. K., & Ling, E. (2001) · Epilepsy Research · doi:10.1016/s0920-1211(01)00276-5 · Cited by 25

Mild hypoxia-induced structural and functional changes of the hippocampal network

Hencz, A. J., Magony, A., Thomas, C. N., Kovacs, K., Szilagyi, G. T., Pál, J., & Attila Gabor, S. I. K. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1277375 · Cited by 27

SP–SR interneurones: A novel class of neurones of the CA2 region of the hippocampus

Mercer, A., Botcher, N. A., Eastlake, K., & Thomson, A. M. (2012) · Hippocampus · doi:10.1002/hipo.22010 · Cited by 24

Metabolic regulation of aging and age-related disease

Hamrick, M. W., & Stranahan, A. M. (2020) · Ageing Research Reviews · doi:10.1016/j.arr.2020.101175 · Cited by 27

Cellular Components of Nervous Tissue

Hof, P. R., Kidd, G. J., DeFelipe, J., de Vellis, J., Sosa, M. A. G., Elder, G. A., & Trapp, B. D. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-397179-1.00001-4 · Cited by 27

Effects of Aging on the Structure and Expression of NMDA Receptors of Somatostatin Expressing Neurons in the Mouse Hippocampus

Gramuntell, Y., Klimczak, P., Coviello, S., Pérez-Rando, M., & Nácher, J. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.782737 · Cited by 22

Brief synaptic inhibition persistently interrupts firing of fast-spiking interneurons

Chamberland, S., Nebet, E. R., Valero, M., Hanani, M., Egger, R., Larsen, S. B., Eyring, K. W., Buzsáki, G., & Tsien, R. W. (2023) · Neuron · doi:10.1016/j.neuron.2023.01.017 · Cited by 25

Temporal Dynamics of Distinct CA1 Cell Populations during Unconscious State Induced by Ketamine

Kuang, H., Lin, L., & Tsien, J. Z. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015209 · Cited by 24

Estradiol and GABAergic Transmission in the Hippocampus

Wójtowicz, T., & Mozrzymas, J. W. (2010) · Vitamins and hormones · doi:10.1016/s0083-6729(10)82015-1 · Cited by 24

Age-related deficits in the ability to encode contextual change: A place cell analysis

Oler, J. A., & Markus, E. J. (2000) · Hippocampus · doi:10.1002/1098-1063(2000)10:3 · Cited by 58

Cerebellar abnormalities in the disabled (mdab1-1) mouse

Gallagher, E., Howell, B. W., Soriano, P. M., Cooper, J. A., & Hawkes, R. B. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19981214)402:2 · Cited by 95

A Composite Sketch of Fast-Spiking Parvalbumin-Positive Neurons

Bartholomé, O., Bonardeaux, O. D. L. B., Neirinckx, V., & Rogister, B. (2020) · Cerebral Cortex Communications · doi:10.1093/texcom/tgaa026 · Cited by 23

Network recruitment to coherent oscillations in a hippocampal computer model

Stacey, W. C., Krieger, A. Μ., & Litt, B. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00643.2010 · Cited by 22

Novel strategy to selectively label excitatory and inhibitory neurons in the cerebral cortex of mice

Basu, K., Gravel, C., Tomioka, R., Kaneko, T., Tamamaki, N., & Attila Gabor, S. I. K. (2008) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2008.01.016 · Cited by 21

Predicting synchronous and asynchronous network groupings of hippocampal interneurons coupled with dendritic gap junctions

Zahid, T., & Skinner, F. K. (2009) · Brain Research · doi:10.1016/j.brainres.2008.12.068 · Cited by 19

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Sekulić, V., Lawrence, J. J., & Skinner, F. K. (2014) · PLoS ONE · doi:10.1371/journal.pone.0106567 · Cited by 20

Characterizing the persistent CA3 interneuronal spiking activity in elevated extracellular potassium in the young rat hippocampus

Shin, D. S.-H., Yu, W., Fawcett, A. P., & Carlen, P. L. (2010) · Brain Research · doi:10.1016/j.brainres.2010.03.023 · Cited by 21

Nitric oxide synthase immunoreactivity in the rat hippocampus after status epilepticus induced by perforant pathway stimulation

Lumme, A., Soinila, S. O., Sadeniemi, M., Halonen, T., & Vanhatalo, S. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02487-2 · Cited by 21

Progesterone

Schumacher, M., & Robert, F. (2002) · Elsevier eBooks · doi:10.1016/b978-012532104-4/50057-3 · Cited by 21

Presynaptic cholinergic neuromodulation alters the temporal dynamics of short-term depression at parvalbumin-positive basket cell synapses from juvenile CA1 mouse hippocampus

Lawrence, J. J., Haario, H., & Stone, E. F. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00167.2014 · Cited by 19

Characterization of a novel subtype of hippocampal interneurons that express corticotropin-releasing hormone

Hooper, A., & Maguire, J. L. (2015) · Hippocampus · doi:10.1002/hipo.22487 · Cited by 20

Lateralized Decrease of Parvalbumin+ Cells in the Somatosensory Cortex of ASD Models Is Correlated with Unilateral Tactile Hypersensitivity

Deemyad, T., Puig, S., Papale, A. E., Qi, H., LaRocca, G. M., Aravind, D., LaNoce, E., & Urban, N. N. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab233 · Cited by 22

Alterations on monoamines concentration in rat hippocampus produced by lipoic acid

Santos, Í. M. D. S., de Freitas, R. L. M., Saldanha, G. B., Tomé, A. D. R., Jordán, J., & de Freitas, R. M. (2010) · Arquivos de Neuro-Psiquiatria · doi:10.1590/s0004-282x2010000300006 · Cited by 20

T‐type calcium channels contribute to NMDA receptor independent synaptic plasticity in hippocampal regular‐spiking oriens‐alveus interneurons

Nicholson, E., & Kullmann, D. M. (2017) · The Journal of Physiology · doi:10.1113/jp273695 · Cited by 19

A neural mass model of phase–amplitude coupling

Chehelcheraghi, M., Nakatani, C., Steur, E., & van Leeuwen, C. (2016) · Biological Cybernetics · doi:10.1007/s00422-016-0687-5 · Cited by 18

A quantitative analysis of the laminar distribution of synaptic boutons in field CA3 of the rat hippocampus

Matsuda, S., Kobayashi, Y., & Ishizuka, N. (2004) · Neuroscience Research · doi:10.1016/j.neures.2004.03.002 · Cited by 19

Orientation Selectivity and Its Modulation by Local and Long-Range Connections in Visual Cortex

Somers, D. C., Dragoi, V., & Sur, M. (2002) · Elsevier eBooks · doi:10.1016/b978-012552104-8/50013-4 · Cited by 18

MEA-Based Graph Deviation Network for Early Autism Syndrome Signatures in Human Forebrain Organoids

Mencattini, A., Curci, G., Riccardi, A., Casti, P., D’Orazio, M., Filippi, J., Antonelli, G., Debbi, E., Daprati, E., Zhang, W., et al. (2025) · Cyborg and Bionic Systems · doi:10.34133/cbsystems.0441 · Cited by 20

SYNAPTIC AND DENDRITIC ARCHITECTURE OF TWO TYPES OF HIPPOCAMPAL SOMATOSTATIN INTERNEURONS

Takács, V., Bardóczi, Z., Orosz, Á., Major, Á., Tar, L., Berki, P., Papp, P., Mayer, M. I., Sebők, H., Zsolt, L., et al. (2023) · PLoS Biology · doi:10.1016/j.ibneur.2023.08.600 · Cited by 20

Harnessing the power of theta: natural manipulations of cognitive performance during hippocampal theta-contingent eyeblink conditioning

Hoffmann, L. C., Cicchese, J. J., & Berry, S. D. (2015) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00050 · Cited by 20

Interneurons secrete prosaposin, a neurotrophic factor, to attenuate kainic acid-induced neurotoxicity

Nabeka, H., Saito, S., Li, X., Shimokawa, T., Khan, S., Yamamiya, K., Kawabe, S., Doihara, T., Hamada, F., Kobayashi, N., et al. (2017) · IBRO Reports · doi:10.1016/j.ibror.2017.07.001 · Cited by 18

Temporally-specific retrograde amnesia in two cases of discrete bilateral hippocampal pathology

Kapur, N., & Brooks, D. J. (1999) · Hippocampus · doi:10.1002/(sici)1098-1063(1999)9:3 · Cited by 142

Nicotinic antagonist α-bungarotoxin binding to rat hippocampal neurons containing nitric oxide synthase

Adams, C. E., & Freedman, R. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00978-5 · Cited by 18

Theta dominates cross-frequency coupling in hippocampal-medial entorhinal circuit during awake-behavior in rats

Zhou, Y., Sheremet, A., Kennedy, J. P., Qin, Y. F., DiCola, N. M., Lovett, S. D., Burke, S. N., & Maurer, A. P. (2022) · iScience · doi:10.1016/j.isci.2022.105457 · Cited by 16

Metabolic implications of axonal demyelination and its consequences for synchronized network activity: An in silico and in vitro study

Gerevich, Z., Kovács, R., Liotta, A., Hasam‐Henderson, L. A., Weh, L., Wallach, I., & Berndt, N. (2023) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x231170746 · Cited by 17

Differences in kainate receptor involvement in hippocampal mossy fibre long-term potentiation depending on slice orientation

Sherwood, J. L., Amici, M., Amici-Dargan, S., Culley, G. R., Fitzjohn, S. M., Jane, D. E., Collingridge, G. L., Lodge, D., & Bortolotto, Z. A. (2012) · Neurochemistry International · doi:10.1016/j.neuint.2012.04.021 · Cited by 17

A vitamin A-free diet results in impairment of the rat hippocampal somatostatinergic system

Hernández‐Pinto, A. M., Puebla‐Jiménez, L., & Arilla, E. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.04.034 · Cited by 17

Co-localization of calretinin and calbindin in distinct cells in the hippocampal formation of the rat

Wouterlood, F. G., Grosche, J., & Härtig, W. (2001) · Brain Research · doi:10.1016/s0006-8993(01)03220-6 · Cited by 17

AMPA receptor modulators have different impact on hippocampal pyramidal cells and interneurons

Xia, Y.-F., & Arai, A. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.06.031 · Cited by 18

Nucleus accumbens in the lizardPsammodromus algirus: chemoarchitecture and cortical afferent connections

Guirado, S., D�vila, J. C., Real, M. A., & Medina, L. M. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990301)405:1 · Cited by 33

Prenatal protein malnutrition alters the proportion but not numbers of parvalbumin-immunoreactive interneurons in the hippocampus of the adult Sprague-Dawley rat

Lister, J. P., Blatt, G. J., Kemper, T. L., Tonkiss, J., DeBassio, W. A., Galler, J. R., & Rosene, D. L. (2011) · Nutritional Neuroscience · doi:10.1179/147683011x13009738172396 · Cited by 16

Synaptic conditions for auto-associative memory storage and pattern completion in Jensen et al.’s model of hippocampal area CA3

Cheu, E. Y., Yu, J., Tan, C. H., & Tang, H. (2012) · Journal of Computational Neuroscience · doi:10.1007/s10827-012-0394-8 · Cited by 16

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McKenzie, S., & Buzsáki, G. (2016) · Research and perspectives in neurosciences · doi:10.1007/978-3-319-28802-4_1 · Cited by 16

Precocious development of parvalbumin-like immunoreactive interneurons in the hippocampal formation and entorhinal cortex of the fetal cynomolgus monkey

Berger, B., Grissac, N. D., & Alvarez, C. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990118)403:3 · Cited by 16

Variable Kainate Receptor Distributions of Oriens Interneurons

Yang, E. J., Harris, A. Z., & Pettit, D. L. (2006) · Journal of Neurophysiology · doi:10.1152/jn.01332.2005 · Cited by 15

Progressive Alterations in Synaptic Transmission and Plasticity of Area CA1 Precede the Cognitive Impairment Associated with Neonatal Administration of MK-801

Hernández‐Frausto, M., López‐Rubalcava, C., & Galván, E. J. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.01.036 · Cited by 15

Proportional loss of parvalbumin‐immunoreactive synaptic boutons and granule cells from the hippocampus of sea lions with temporal lobe epilepsy

Cameron, S., Lopez, A., Glabman, R. A., Abrams, E., Johnson, S., Field, C. L., Gulland, F. M. D., & Buckmaster, P. S. (2019) · The Journal of Comparative Neurology · doi:10.1002/cne.24680 · Cited by 15

Multiplexing of Information about Self and Others in Hippocampal Ensembles

Bos, J. J., Vinck, M. A., Marchesi, P., Keestra, A., Mourik-Donga, L. A. V., Jackson, J. C., Verschure, P. F. M. J., & Pennartz, C. M. A. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.11.057 · Cited by 14

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Dubanet, O., Silva, A. F. G. D., Frick, A., Hirase, H., Beyeler, A., & Leinekugel, X. (2020) · Cell Reports · doi:10.1016/j.celrep.2021.109381 · Cited by 15

Effects of neonatal stress on gamma oscillations in hippocampus

Dricks, S. (2016) · Scientific Reports · doi:10.1038/srep29007 · Cited by 15

High-frequency oscillations and sequence generation in two-population models of hippocampal region CA1

Braun, W., & Memmesheimer, R.-M. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009891 · Cited by 14

Phase response theory explains cluster formation in sparsely but strongly connected inhibitory neural networks and effects of jitter due to sparse connectivity

Tikidji-Hamburyan, R. A., Leonik, C., & Canavier, C. C. (2019) · Journal of Neurophysiology · doi:10.1152/jn.00728.2018 · Cited by 14

Synergy of Glutamatergic and Cholinergic Modulation Induces Plateau Potentials in Hippocampal OLM Interneurons

Hagger‐Vaughan, N., & Storm, J. F. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00508 · Cited by 14

Discrete Synaptic Events Induce Global Oscillations in Balanced Neural Networks

Goldobin, D. S., di Volo, M., & Torcini, A. (2024) · Physical Review Letters · doi:10.1103/physrevlett.133.238401 · Cited by 14

Directional spike propagation in a recurrent network: Dynamical firewall as anisotropic recurrent inhibition

Samura, T., & Hayashi, H. (2012) · Neural Networks · doi:10.1016/j.neunet.2012.05.010 · Cited by 13

Synaptic organisation and behaviour-dependent activity of mGluR8a-innervated GABAergic trilaminar cells projecting from the hippocampus to the subiculum

Katona, L., Hartwich, K., Tomioka, R., Somogyi, J., Roberts, J. D. B., Wagner, K., Joshi, A., Klausberger, T., Rockland, K. S., & Somogyi, P. (2020) · Brain Structure and Function · doi:10.1007/s00429-020-02029-2 · Cited by 14

Temporally Targeted Interactions With Pathologic Oscillations as Therapeutical Targets in Epilepsy and Beyond

Földi, T., Lörincz, M. L., & Berényi, A. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.784085 · Cited by 14

Mechanism-Based and Input-Output Modeling of the Key Neuronal Connections and Signal Transformations in the CA3-CA1 Regions of the Hippocampus

Geng, K., Shin, D. C., Song, D. B., Hampson, R. E., Deadwyler, S. A., Berger, T. W., & Marmarelis, V. Z. (2017) · Neural Computation · doi:10.1162/neco_a_01031 · Cited by 13

Hippocampal Slice Cultures

F�rster, E., Bartos, M., & Zhao, S. (2005) · KARGER eBooks · doi:10.1159/000083427 · Cited by 12

Methods for single-cell recording and labeling in vivo

Cid, E., & de la Prida, L. M. (2019) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2019.108354 · Cited by 13

Interneuronal network model of theta-nested fast oscillations predicts differential effects of heterogeneity, gap junctions and short term depression for hyperpolarizing versus shunting inhibition

Via, G., Baravalle, R., Fernandez, F. R., White, J. A., & Canavier, C. C. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1010094 · Cited by 14

On the role of the entorhinal cortex in the effective connectivity of the hippocampal formation

López‐Madrona, V. J., Matias, F. S., Pereda, E., Canals, S., & Mirasso, C. R. (2017) · Chaos An Interdisciplinary Journal of Nonlinear Science · doi:10.1063/1.4979001 · Cited by 12

Intracellular recording and labeling of neurons in midline structures of the rat brain in vivo using sharp electrodes

Konopacki, J., Bland, B. H., & Dyck, R. H. (2003) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(03)00126-2 · Cited by 12

Uncovering the organization of neural circuits with Generalized Phase Locking Analysis

Safavi, S., Panagiotaropoulos, T. I., Kapoor, V., Ramírez-Villegas, J. F., Logothetis, N. K., & Besserve, M. (2023) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1010983 · Cited by 18

Developmental Age Differentially Mediates the Calcium-Binding Protein Parvalbumin in the Rat: Evidence for a Selective Decrease in Hippocampal Parvalbumin Cell Counts

Honeycutt, J. A., Keary, K. M., Kania, V. M., & Chrobak, J. J. (2016) · Developmental Neuroscience · doi:10.1159/000444447 · Cited by 11

Group I metabotropic glutamate receptors generate two types of intrinsic membrane oscillations in hippocampal oriens/alveus interneurons

Govindaiah, G., Kang, Y., Lewis, H. E. S., Chung, L., Clement, E. M., Greenfield, L. J., García‐Rill, E., & Lee, S.-H. (2018) · Neuropharmacology · doi:10.1016/j.neuropharm.2018.06.035 · Cited by 11

Coupled Oscillators Model of Hyperexcitable Neuroglial Networks

Farah, F. H., Grigorovsky, V., & Bardakjian, B. L. (2018) · International Journal of Neural Systems · doi:10.1142/s0129065718500417 · Cited by 11

Structural and Functional Properties of Hippocampal Neurons

Spruston, N., Piskorowski, R. A., Chevaleyre, V., Eyre, M. D., McBain, C. J., & Bartos, M. (2025) · Oxford University Press eBooks · doi:10.1093/med/9780190065324.003.0005 · Cited by 11

Morphology of CA3 non-pyramidal cells in the developing rat hippocampus

Gaïarsa, J., Khalilov, I., GOZLAN, H., & Ben‐Ari, Y. (2001) · Developmental Brain Research · doi:10.1016/s0165-3806(01)00130-4 · Cited by 12

Neurocalcin-immunoreactive cells in the rat hippocampus are GABAergic interneurons

Martinez-Guijarro, F. J., Briñón, J. G., Blasco-Ib��ez, J. M., Okazaki, K., Hidaka, H., & Alonso, J. R. (1998) · Hippocampus · doi:10.1002/(sici)1098-1063(1998)8:1 · Cited by 11

Differential induction of long term synaptic plasticity in inhibitory synapses of the hippocampus

Mendoza, E., Galarraga, E., Tapia, D., Laville, A., Hernández, E., & Bargas, J. (2006) · Synapse · doi:10.1002/syn.20331 · Cited by 11

Dynamics and diversity in interneurons: a model exploration with slowly inactivating potassium currents

Saraga, F., & Skinner, F. K. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00168-9 · Cited by 10

Inhibitory interneurons in hippocampus

Jones, S., & Yakel, J. L. (1999) · Cell Biochemistry and Biophysics · doi:10.1007/bf02738173 · Cited by 10

Synchronization through nonreciprocal connections in a hybrid hippocampus microcircuit

Hilscher, M. M., Leão, K. E., & Leão, R. N. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00120 · Cited by 11

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Hoshi, M. M. (2020) · British Journal of Pharmacology · doi:10.1111/bph.15174 · Cited by 10

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Cona, F., Zavaglia, M., & Ursino, M. (2012) · International Journal of Neural Systems · doi:10.1142/s0129065712500037 · Cited by 9

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Colavita, M., Terral, G., Lemercier, C. E., Drago, F., Marsicano, G., & Massa, F. (2016) · Scientific Reports · doi:10.1038/srep28454 · Cited by 9

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