Gating of hippocampal activity, plasticity, and memory by entorhinal cortex long-range inhibition

A robust and high-throughput Cre reporting and characterization system for the whole mouse brain

Madisen, L., Zwingman, T. A., Sunkin, S. M., Oh, S. W., Zariwala, H. A., Gu, H., Ng, L. L., Palmiter, R. D., Hawrylycz, M. J., Jones, A. R., et al. (2010) · Nature Neuroscience · doi:10.1038/nn.2467 · Cited by 6,907 · see citing works

Ultrasensitive fluorescent proteins for imaging neuronal activity

Chen, T.-W., Wardill, T. J., Sun, Y., Pulver, S. R., Renninger, S. L., Baohan, A., Schreiter, E. R., Kerr, R. A., Orger, M. B., Jayaraman, V., et al. (2013) · Nature · doi:10.1038/nature12354 · Cited by 6,474 · see citing works

Millisecond-timescale, genetically targeted optical control of neural activity

Boyden, E. S., Zhang, F., Bamberg, E., Nagel, G., & Deisseroth, K. A. (2005) · Nature Neuroscience · doi:10.1038/nn1525 · Cited by 4,831 · see citing works

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 · see citing works

Neuronal Diversity and Temporal Dynamics: The Unity of Hippocampal Circuit Operations

Klausberger, T., & Somogyi, P. (2008) · Science · doi:10.1126/science.1149381 · Cited by 2,050 · see citing works

Memory, navigation and theta rhythm in the hippocampal-entorhinal system

Buzsáki, G., & Moser, E. I. (2013) · Nature Neuroscience · doi:10.1038/nn.3304 · Cited by 1,847 · 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

Computer Control of Microscopes Using µManager

Edelstein, A., Amodaj, N., Hoover, K., Vale, R. D., & Stuurman, N. (2010) · Current Protocols in Molecular Biology · doi:10.1002/0471142727.mb1420s92 · Cited by 1,678 · see citing works

The contextual brain: implications for fear conditioning, extinction and psychopathology

Maren, S., Phan, K. L., & Liberzon, I. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3492 · Cited by 1,547 · see citing works

Spatial representation in the entorhinal cortex

Fyhn, M., Molden, S., Witter, M. P., Moser, E. I., & Moser, M.-B. (2004) · Science · doi:10.1126/science.1099901 · Cited by 1,339 · see citing works

A new cellular mechanism for coupling inputs arriving at different cortical layers

Larkum, M. E., Zhu, J. J., & Sakmann, B. (1999) · Nature · doi:10.1038/18686 · Cited by 1,180 · see citing works

A Developmental Switch in the Response of DRG Neurons to ETS Transcription Factor Signaling

Hippenmeyer, S., Pecho‐Vrieseling, E., Sigrist, M., Portmann, T., Laengle, C., Ladle, D. R., & Arber, S. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0030159 · Cited by 1,059 · see citing works

The hippocampal CA2 region is essential for social memory

Hitti, F. L., & Siegelbaum, S. A. (2014) · Nature · doi:10.1038/nature13028 · Cited by 976 · see citing works

Impaired Recognition Memory in Rats after Damage to the Hippocampus

Clark, R. E., Zola, S. M., & Squire, L. R. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-23-08853.2000 · Cited by 740 · see citing works

Control of timing, rate and bursts of hippocampal place cells by dendritic and somatic inhibition

Royer, S., Zemelman, B. V., Losonczy, A., Kim, J., Chance, F., Magee, J. C., & Buzsáki, G. (2012) · Nature Neuroscience · doi:10.1038/nn.3077 · Cited by 728 · see citing works

Parvalbumin-expressing basket-cell network plasticity induced by experience regulates adult learning

Donato, F., Rompani, S. B., & Caroni, P. (2013) · Nature · doi:10.1038/nature12866 · Cited by 703 · see citing works

Optogenetic interrogation of neural circuits: technology for probing mammalian brain structures

Zhang, F., Gradinaru, V., Adamantidis, A. R., Durand, R., Airan, R. D., de Lecea, L., & Deisseroth, K. (2010) · Nature Protocols · doi:10.1038/nprot.2009.226 · Cited by 692 · see citing works

Major Dissociation Between Medial and Lateral Entorhinal Input to Dorsal Hippocampus

Hargreaves, E. L., Rao, G., Lee, I., & Knierim, J. J. (2005) · Science · doi:10.1126/science.1110449 · Cited by 685 · see citing works

Dendritic spikes as a mechanism for cooperative long-term potentiation

Golding, N. L., Staff, N. P., & Spruston, N. (2002) · Nature · doi:10.1038/nature00854 · Cited by 623 · see citing works

Place cells and place recognition maintained by direct entorhinal-hippocampal circuitry

Brun, V. H., Otnæss, M. K., Molden, S., Steffenach, H.-A., Witter, M. P., Moser, M.-B., & Moser, E. I. (2002) · Science · doi:10.1126/science.1071089 · Cited by 606 · see citing works

Compartmentalized dendritic plasticity and input feature storage in neurons

Losonczy, A., Makara, J. K., & Magee, J. C. (2008) · Nature · doi:10.1038/nature06725 · Cited by 598 · see citing works

Assessing rodent hippocampal involvement in the novel object recognition task. A review

Cohen, S. J., & Stackman, R. W. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.08.002 · Cited by 595 · 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

Genetic Fate Mapping Reveals That the Caudal Ganglionic Eminence Produces a Large and Diverse Population of Superficial Cortical Interneurons

Miyoshi, G., Hjerling-Leffler, J., Karayannis, T., Sousa, V. H., Butt, S. J. B., Battiste, J., Johnson, J. E., Machold, R. P., & Fishell, G. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4515-09.2010 · Cited by 559 · see citing works

Conjunctive input processing drives feature selectivity in hippocampal CA1 neurons

Bittner, K. C., Grienberger, C., Vaidya, S. P., Milstein, A. D., Macklin, J. J., Suh, J., Tonegawa, S., & Magee, J. C. (2015) · Nature Neuroscience · doi:10.1038/nn.4062 · Cited by 540 · see citing works

Dendritic Inhibition in the Hippocampus Supports Fear Learning

Lovett-Barron, M., Kaifosh, P., Kheirbek, M. A., Danielson, N., Zaremba, J. D., Reardon, T. R., Turi, G. F., Hen, R., Zemelman, B. V., & Losonczy, A. (2014) · Science · doi:10.1126/science.1247485 · Cited by 509 · see citing works

Transgenic inhibition of synaptic transmission reveals role of CA3 output in hippocampal learning

Nakashiba, T., Young, J. Z., McHugh, T. J., Buhl, D. L., & Tonegawa, S. (2008) · Science · doi:10.1126/science.1151120 · Cited by 492 · see citing works

Entorhinal cortex of the monkey: V. Projections to the dentate gyrus, hippocampus, and subicular complex

Witter, M. P., & Amaral, D. G. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903070308 · Cited by 480 · 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

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

Feed-forward inhibition in the hippocampal formation

BUZSAKI, G. (1984) · Progress in Neurobiology · doi:10.1016/0301-0082(84)90023-6 · Cited by 453 · see citing works

Coordination of entorhinal–hippocampal ensemble activity during associative learning

Igarashi, K. M., Lu, L., Colgin, L. L., Moser, M., & Moser, E. I. (2014) · Nature · doi:10.1038/nature13162 · Cited by 435 · 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

Impaired Spatial Representation in CA1 after Lesion of Direct Input from Entorhinal Cortex

Brun, V. H., Leutgeb, S., Wu, H., Schwarcz, R. M., Witter, M. P., Moser, E. I., & Moser, M. (2008) · Neuron · doi:10.1016/j.neuron.2007.11.034 · Cited by 364 · see citing works

Entorhinal Cortex Layer III Input to the Hippocampus Is Crucial for Temporal Association Memory

Suh, J., Rivest, A. J., Nakashiba, T., Tominaga, T., & Tonegawa, S. (2011) · Science · doi:10.1126/science.1210125 · Cited by 352 · see citing works

Long-range-projecting GABAergic neurons modulate inhibition in hippocampus and entorhinal cortex

Melzer, S., Michael, M., Caputi, A., Eliava, M., Fuchs, E. C., Whittington, M. A., & Monyer, H. (2012) · Science · doi:10.1126/science.1217139 · Cited by 333 · see citing works

Island Cells Control Temporal Association Memory

北村, 貴., Pignatelli, M., Suh, J., Kohara, K., Yoshiki, A., Abe, K., & Tonegawa, S. (2014) · Science · doi:10.1126/science.1244634 · Cited by 327 · see citing works

The rodent hippocampus is essential for nonspatial object memory

Cohen, S. J., Munchow, A. H., Rios, L. M., Zhang, G., Ásgeirsdóttir, H. N., & Stackman, R. W. (2013) · Current Biology · doi:10.1016/j.cub.2013.07.002 · Cited by 325 · see citing works

Pathway Interactions and Synaptic Plasticity in the Dendritic Tuft Regions of CA1 Pyramidal Neurons

Takahashi, H., & Magee, J. C. (2009) · Neuron · doi:10.1016/j.neuron.2009.03.007 · Cited by 312 · see citing works

Conditional dendritic spike propagation following distal synaptic activation of hippocampal CA1 pyramidal neurons

Jarsky, T., Roxin, A., Kath, W. L., & Spruston, N. (2005) · Nature Neuroscience · doi:10.1038/nn1599 · Cited by 301 · see citing works

Chemical and Genetic Engineering of Selective Ion Channel–Ligand Interactions

Magnus, C. J., Lee, P. H., Atasoy, D., Su, H. H., Looger, L. L., & Sternson, S. M. (2011) · Science · doi:10.1126/science.1206606 · Cited by 296 · see citing works

A Blueprint for the Spatiotemporal Origins of Mouse Hippocampal Interneuron Diversity

Tricoire, L., Pelkey, K. A., Erkkila, B. E., Jeffries, B. W., Yuan, X., & McBain, C. J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0323-11.2011 · Cited by 292 · see citing works

Feedforward excitation of the hippocampus by afferents from the entorhinal cortex: redefinition of the role of the trisynaptic pathway.

Yeckel, M. F., & Berger, T. W. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.15.5832 · Cited by 286 · see citing works

Parvalbumin-positive CA1 interneurons are required for spatial working but not for reference memory

Murray, A., Sauer, J., Riedel, G., McClure, C., Ansel-Bollepalli, L., Cheyne, L., Bartos, M., Wisden, W., & Wulff, P. (2011) · Nature Neuroscience · doi:10.1038/nn.2751 · Cited by 276 · see citing works

Physiological and morphological diversity of immunocytochemically defined parvalbumin‐ and cholecystokinin‐positive interneurones in CA1 of the adult rat hippocampus

Pawelzik, H., Hughes, D. I., & Thomson, A. M. (2002) · Journal of Comparative Neurology · doi:10.1002/cne.10118 · Cited by 262 · see citing works

Sensory-evoked LTP driven by dendritic plateau potentials in vivo

Gambino, F., Pagès, S., Kehayas, V., Baptista, D., Tatti, R., Carleton, A., & Holtmaat, A. (2014) · Nature · doi:10.1038/nature13664 · Cited by 253 · 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

Calcium transient prevalence across the dendritic arbour predicts place field properties

Sheffield, M. E. J., & Dombeck, D. A. (2014) · Nature · doi:10.1038/nature13871 · Cited by 250 · see citing works

SIMA: Python software for analysis of dynamic fluorescence imaging data

Kaifosh, P., Zaremba, J. D., Danielson, N., & Losonczy, A. (2014) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2014.00080 · Cited by 225 · see citing works

Tasks for inhibitory interneurons in intact brain circuits

Roux, L., & Buzsáki, G. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.09.011 · Cited by 218 · see citing works

4‐ to 6‐week‐old adult‐born hippocampal neurons influence novelty‐evoked exploration and contextual fear conditioning

Denny, C. A., Burghardt, N. S., Schachter, D., Hen, R., & Drew, M. R. (2011) · Hippocampus · doi:10.1002/hipo.20964 · Cited by 199 · see citing works

A role for synaptic inputs at distal dendrites: instructive signals for hippocampal long-term plasticity

Dudman, J. T., Tsay, D., & Siegelbaum, S. A. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.020 · Cited by 192 · see citing works

Unitary IPSPs evoked by interneurons at the stratum radiatum‐stratum lacunosum‐moleculare border in the CA1 area of the rat hippocampus <i>in vitro</i>

Vida, I., Halasy, K., Szinyei, C., Somogyi, P., & Buhl, E. H. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.755bv.x · Cited by 190 · see citing works

Septo-hippocampal GABAergic signaling across multiple modalities in awake mice

Kaifosh, P., Lovett-Barron, M., Turi, G. F., Reardon, T. R., & Losonczy, A. (2013) · Nature Neuroscience · doi:10.1038/nn.3482 · Cited by 155 · see citing works

Asynchronous Transmitter Release from Cholecystokinin-Containing Inhibitory Interneurons Is Widespread and Target-Cell Independent

Daw, M. I., Tricoire, L., Erdelyi, F., Szabo, G., & McBain, C. J. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5760-08.2009 · Cited by 151 · 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

The role of the hippocampus in object recognition in rats: examination of the influence of task parameters and lesion size

Ainge, J. A., Heron-Maxwell, C., Theofilas, P., Wright, P., de Hoz, L., & Wood, E. R. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2005.09.005 · Cited by 140 · see citing works

A multifunctional reporter mouse line for Cre‐ and FLP‐dependent lineage analysis

Yamamoto, M., Shook, N. A., Kanisicak, O., Yamamoto, S., Wosczyna, M. N., Camp, J. R., & Goldhamer, D. J. (2009) · genesis · doi:10.1002/dvg.20474 · Cited by 136 · 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

Distinct Endocannabinoid Control of GABA Release at Perisomatic and Dendritic Synapses in the Hippocampus

Lee, S.-H., Foldy, C., & Soltesz, I. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.6238-09.2010 · Cited by 114 · see citing works

Cannabinoid CB1 receptor deficiency increases contextual fear memory under highly aversive conditions and long-term potentiation in vivo

Jacob, W., Marsch, R., Marsicano, G., Lutz, B., & Wotjak, C. T. (2012) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2012.04.008 · Cited by 78 · see citing works

Presynaptic Inhibition of GABA_A Receptor-Mediated Unitary IPSPs by Cannabinoid Receptors at Synapses Between CCK-Positive Interneurons in Rat Hippocampus

Ali, A. B. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00156.2007 · Cited by 62 · see citing works

Reelin Signaling Specifies the Molecular Identity of the Pyramidal Neuron Distal Dendritic Compartment

Kupferman, J. V., Basu, J., Russo, M. J., Guevarra, J., Cheung, S. K., & Siegelbaum, S. A. (2014) · Cell · doi:10.1016/j.cell.2014.07.035 · Cited by 62 · 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

CA1 Pyramidal Cell Theta-Burst Firing Triggers Endocannabinoid-Mediated Long-Term Depression at Both Somatic and Dendritic Inhibitory Synapses

Younts, T. J., Chevaleyre, V., & Castillo, P. E. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0817-13.2013 · Cited by 51 · see citing works

Requirement for CB1 but not GABAB receptors in the cholecystokinin mediated inhibition of GABA release from cholecystokinin expressing basket cells

Lee, S.-H., & Soltész, I. (2010) · The Journal of Physiology · doi:10.1113/jphysiol.2010.198499 · Cited by 49 · see citing works

Cortico-hippocampal communication by way of parallel parahippocampal-subicular pathways.

Lavenex (2000) · Pure Amsterdam UMC · doi:10.1002/1098-1063(2000)10:4 · Cited by 1 · 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

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

Layer-specific modulation of neocortical dendritic inhibition during active wakefulness

Muñoz, W., Tremblay, R., Levenstein, D., & Rudy, B. (2017) · Science · doi:10.1126/science.aag2599 · Cited by 305 · see citing works

Interneuronal mechanisms of hippocampal theta oscillations in a full-scale model of the rodent CA1 circuit

Bezaire, M. J., Raikov, I., Burk, K., Vyas, D., & Soltesz, I. (2016) · eLife · doi:10.7554/elife.18566 · Cited by 198 · see citing works

The medial prefrontal cortex - hippocampus circuit that integrates information of object, place and time to construct episodic memory in rodents: Behavioral, anatomical and neurochemical properties

Chao, O. Y., de Souza Silva, M. A., Yang, Y.-M., & Huston, J. P. (2020) · Neuroscience &amp; Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.04.007 · Cited by 158 · see citing works

Input-Timing-Dependent Plasticity in the Hippocampal CA2 Region and Its Potential Role in Social Memory

Leroy, F., Brann, D. H., Meira, T., & Siegelbaum, S. A. (2017) · Neuron · doi:10.1016/j.neuron.2017.07.036 · Cited by 91 · see citing works

Prefrontal feature representations drive memory recall

Yadav, N., Noble, C., Niemeyer, J. E., Terceros, A., Victor, J., Liston, C., & Rajasethupathy, P. (2022) · Nature · doi:10.1038/s41586-022-04936-2 · Cited by 61 · see citing works

Mental navigation and the neural mechanisms of insight

Aru, J., Drüke, M., Pikamäe, J., & Larkum, M. E. (2023) · Trends in Neurosciences · doi:10.1016/j.tins.2022.11.002 · Cited by 38 · see citing works

Serotonergic neuromodulation of synaptic plasticity

Higa, G. S. V., Viana, F. J. C., Francis-Oliveira, J., Cruvinel, E., Franchin, T. S., Marcourakis, T., Ulrich, H., & De Pasquale, R. (2024) · Neuropharmacology · doi:10.1016/j.neuropharm.2024.110036 · Cited by 29 · see citing works

381. Sensory gating: new vistas

Boutros, N. N., Yee-Bradbury, C., Ruhrmann, S., Jin, Y., & Jansen, B. (2000) · Biological Psychiatry · doi:10.1016/s0006-3223(00)00645-4

P03-21 - Sensory Gating of Auditory Evoked Potentials in Schizophrenia: Effects of Gating-Out and Gating-In Paradigms in Relation to Psychopathology

Vedeniapin, A. B., Gjini, K., & Boutros, N. N. (2010) · European Psychiatry · doi:10.1016/s0924-9338(10)71131-7

64. Correlations between four components of sensory gating

Boutros, N. N., Campbell, D., & Torello, M. W. (2000) · Biological Psychiatry · doi:10.1016/s0006-3223(00)00326-7

Sensory gating of auditory evoked potentials in rats: effects of repetitive stimulation and the interstimulus interval

de Bruin, N. M. W. J., Ellenbroek, B. A., van Schaijk, W. J., Cools, A. R., Coenen, A. M. L., & van Luijtelaar, E. L. J. M. (2001) · Biological Psychology · doi:10.1016/s0301-0511(00)00084-3 · Cited by 46 · see citing works

Consistency of abnormal sensory gating in first‐admission and chronic schizophrenia across quantification methods

Schubring, D., Popov, T. G., Miller, G. A., & Rockstroh, B. S. (2017) · Psychophysiology · doi:10.1111/psyp.13006 · Cited by 15 · see citing works