Influence of the hippocampus on interneurons of the rat prefrontal cortex

Memory and the hippocampus: A synthesis from findings with rats, monkeys, and humans.

Squire, L. R. (1992) · Psychological Review · doi:10.1037/0033-295x.99.2.195 · Cited by 5,376 · see citing works

Unresponsiveness to Cannabinoids and Reduced Addictive Effects of Opiates in CB 1 Receptor Knockout Mice

Ledent, C. A., Valverde, O., Cossu, G., Petitet, F., Aubert, J.-F., Beslot, F., Böhme, G. A., Impérato, A., Pedrazzini, T., Roques, B. P., et al. (1999) · Science · doi:10.1126/science.283.5400.401 · Cited by 3,612 · see citing works

Cellular basis of working memory

Goldman-Rakic, P. S. (1995) · Neuron · doi:10.1016/0896-6273(95)90304-6 · Cited by 2,663 · see citing works

The human hippocampus and spatial and episodic memory

Burgess, N., Maguire, E. A., & O'Keefe, J. (2002) · Neuron · doi:10.1016/s0896-6273(02)00830-9 · Cited by 2,401 · see citing works

Physiologic Dysfunction of Dorsolateral Prefrontal Cortex in Schizophrenia

Weinberger, D. R. (1986) · Archives of General Psychiatry · doi:10.1001/archpsyc.1986.01800020020004 · Cited by 2,019 · see citing works

Comparative electrophysiology of pyramidal and sparsely spiny stellate neurons of the neocortex

McCormick, D. A., Connors, B. W., Lighthall, J. W., & Prince, D. A. (1985) · Journal of Neurophysiology · doi:10.1152/jn.1985.54.4.782 · Cited by 1,935 · see citing works

Cholinergic and inhibitory synapses in a pathway from motor‐axon collaterals to motoneurones

Eccles, J. C., Fatt, P., & KOKETSU, K. (1954) · The Journal of Physiology · doi:10.1113/jphysiol.1954.sp005226 · Cited by 1,198 · see citing works

Coordinated interactions between hippocampal Ripples and Cortical Spindles during Slow-Wave Sleep

Siapas, A. G., & Wilson, M. A. (1998) · Neuron · doi:10.1016/s0896-6273(00)80629-7 · Cited by 1,052 · see citing works

Organizing principles for a diversity of GABAergic interneurons and synapses in the neocortex

Gupta, A., Wang, Y., & Markram, H. (2000) · Science · doi:10.1126/science.287.5451.273 · Cited by 1,036 · see citing works

Gene expression for glutamic acid decarboxylase is reduced without loss of neurons in prefrontal cortex of schizophrenics.

Akbarian, S. (1995) · Archives of General Psychiatry · doi:10.1001/archpsyc.1995.03950160008002 · Cited by 1,002 · see citing works

Schizophrenics Show Spatial Working Memory Deficits

Park, S. (1992) · Archives of General Psychiatry · doi:10.1001/archpsyc.1992.01820120063009 · Cited by 946 · see citing works

Intracellular Features Predicted by Extracellular Recordings in the Hippocampus In Vivo

Henze, D. A., Borhegyi, Z., Csicsvari, J., Mamiya, A., Harris, K. D., & Buzsáki, G. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.84.1.390 · Cited by 942 · see citing works

Gene Expression Deficits in a Subclass of GABA Neurons in the Prefrontal Cortex of Subjects with Schizophrenia

Hashimoto, T., Volk, D. W., Eggan, S. M., Mirnics, K., Pierri, J. N., Sun, Z., Sampson, A. R., & Lewis, D. A. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-15-06315.2003 · Cited by 938 · see citing works

Chattering Cells: Superficial Pyramidal Neurons Contributing to the Generation of Synchronous Oscillations in the Visual Cortex

Gray, C. M., & McCormick, D. A. (1996) · Science · doi:10.1126/science.274.5284.109 · Cited by 906 · see citing works

Abnormally High Neuronal Density in the Schizophrenic Cortex

Selemon, L. D. (1995) · Archives of General Psychiatry · doi:10.1001/archpsyc.1995.03950220015005 · Cited by 876 · see citing works

Distribution of hippocampal CA1 and subicular efferents in the prefrontal cortex of the rat studied by means of anterograde transport of Phaseolus vulgaris ‐leucoagglutinin

Jay, T. M., & Witter, M. P. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903130404 · Cited by 841 · see citing works

Regional and cellular fractionation of working memory

Goldman‐Rakic, P. S. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.24.13473 · Cited by 810 · see citing works

Dual pathways connecting the dorsolateral prefrontal cortex with the hippocampal formation and parahippocampal cortex in the rhesus monkey

Goldman‐Rakic, P. S., Selemon, L. D., & Schwartz, M. L. (1984) · Neuroscience · doi:10.1016/0306-4522(84)90166-0 · Cited by 782 · see citing works

Response properties of vibrissa units in rat SI somatosensory neocortex

Simons, D. J. (1978) · Journal of Neurophysiology · doi:10.1152/jn.1978.41.3.798 · Cited by 771 · see citing works

Selective Roles for Hippocampal, Prefrontal Cortical, and Ventral Striatal Circuits in Radial-Arm Maze Tasks With or Without a Delay

Floresco, S., Seamans, J. K., & Phillips, A. G. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-05-01880.1997 · Cited by 734 · see citing works

A novel single-cell staining procedure performed in vivo under electrophysiological control: morpho-functional features of juxtacellularly labeled thalamic cells and other central neurons with biocytin or Neurobiotin

Pinault, D. (1996) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(95)00144-1 · Cited by 720 · see citing works

Postpubertal Emergence of Hyperresponsiveness to Stress and to Amphetamine after Neonatal Excitotoxic Hippocampal Damage: A Potential Animal Model of Schizophrenia

Lipska, B. K., Jaskiw, G. E., & Weinberger, D. R. (1993) · Neuropsychopharmacology · doi:10.1038/npp.1993.44 · Cited by 697 · see citing works

Cortical neuronal mechanisms in flutter-vibration studied in unanesthetized monkeys. Neuronal periodicity and frequency discrimination.

Mountcastle, V. B., Talbot, W. H., Sakata, H., & Hyvärinen, J. (1969) · Journal of Neurophysiology · doi:10.1152/jn.1969.32.3.452 · Cited by 683 · see citing works

Hippocampal Efferents Reach Widespread Areas of Cerebral Cortex and Amygdala in the Rhesus Monkey

Rosene, D. L., & Hoesen, G. W. V. (1977) · Science · doi:10.1126/science.410102 · Cited by 678 · see citing works

Integrator or coincidence detector? The role of the cortical neuron revisited

Peter König, B., Engel, A. K., & Singer, W. (1996) · Trends in Neurosciences · doi:10.1016/s0166-2236(96)80019-1 · Cited by 674 · see citing works

Correlation of physiological subgroupings of nonpyramidal cells with parvalbumin- and calbindinD28k-immunoreactive neurons in layer V of rat frontal cortex

Kawaguchi, Y., & Kubota, Y. (1993) · Journal of Neurophysiology · doi:10.1152/jn.1993.70.1.387 · Cited by 558 · see citing works

Physiological subgroups of nonpyramidal cells with specific morphological characteristics in layer II/III of rat frontal cortex

Kawaguchi, Y. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-04-02638.1995 · Cited by 533 · see citing works

A direct projection from Ammon's horn to prefrontal cortex in the rat

Swanson, L. W. (1981) · Brain Research · doi:10.1016/0006-8993(81)90192-x · Cited by 533 · 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

Reliable synaptic connections between pairs of excitatory layer 4 neurones within a single ‘barrel’ of developing rat somatosensory cortex

Feldmeyer, D., Egger, V., Lübke, J., & Sakmann, B. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.00169.x · Cited by 441 · see citing works

Parvalbumin-immunoreactive neurons are reduced in the prefrontal cortex of schizophrenics

BEASLEY, C., & REYNOLDS, G. (1997) · Schizophrenia Research · doi:10.1016/s0920-9964(96)00122-3 · Cited by 426 · see citing works

Synaptic connections and small circuits involving excitatory and inhibitory neurons in layers 2-5 of adult rat and cat neocortex: triple intracellular recordings and biocytin labelling in vitro

Thomson, A. M. (2002) · Cerebral Cortex · doi:10.1093/cercor/12.9.936 · Cited by 420 · see citing works

Dopamine gates LTP induction in lateral amygdala by suppressing feedforward inhibition

Bissière, S., Humeau, Y., & Lüthi, A. (2003) · Nature Neuroscience · doi:10.1038/nn1058 · Cited by 415 · see citing works

Destruction and Creation of Spatial Tuning by Disinhibition: GABA_ABlockade of Prefrontal Cortical Neurons Engaged by Working Memory

Rao, S. G., Williams, G. V., & Goldman-Rakic, P. S. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-01-00485.2000 · Cited by 407 · see citing works

Groupings of nonpyramidal and pyramidal cells with specific physiological and morphological characteristics in rat frontal cortex

Kawaguchi, Y. (1993) · Journal of Neurophysiology · doi:10.1152/jn.1993.69.2.416 · Cited by 390 · 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

Fast-spike Interneurons and Feedforward Inhibition in Awake Sensory Neocortex

Swadlow, H. A. (2002) · Cerebral Cortex · doi:10.1093/cercor/13.1.25 · Cited by 354 · see citing works

A role for inhibition in shaping the temporal flow of information in prefrontal cortex

Constantinidis, C., Williams, G. V., & Goldman-Rakic, P. S. (2002) · Nature Neuroscience · doi:10.1038/nn799 · Cited by 348 · see citing works

Diverse Types of Interneurons Generate Thalamus-Evoked Feedforward Inhibition in the Mouse Barrel Cortex

Porter, J. T., Johnson, C. K., & Agmon, A. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-08-02699.2001 · Cited by 344 · 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

Neuroanatomical bases of spatial memory

Becker, J. T., Walker, J. A., & Olton, D. S. (1980) · Brain Research · doi:10.1016/0006-8993(80)90922-1 · Cited by 308 · see citing works

Selectivity of the hippocampal projection to the prelimbic area of the prefrontal cortex in the rat

Jay, T. M., Glowinski, J., & Thierry, A. M. (1989) · Brain Research · doi:10.1016/0006-8993(89)91464-9 · Cited by 295 · see citing works

Up-regulation of GABAA receptor binding on neurons of the prefrontal cortex in schizophrenic subjects

Benes, F. M., Vincent, S. L., Marie, A. S., & Khan, Y. (1996) · Neuroscience · doi:10.1016/0306-4522(96)00328-4 · Cited by 274 · see citing works

GABAergic local circuit neurons and prefrontal cortical dysfunction in schizophrenia

Lewis, D. (2000) · Brain Research Reviews · doi:10.1016/s0165-0173(99)00042-9 · Cited by 257 · see citing works

Dynamic Properties of Corticothalamic Neurons and Local Cortical Interneurons Generating Fast Rhythmic (30–40 Hz) Spike Bursts

Steriade, M., Timofeev, I., Dürmüller, N., & Grenier, F. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.79.1.483 · 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

Anatomical and electrophysiological evidence for a direct projection from ammon's horn to the medial prefrontal cortex in the rat

Ferino, F., Thierry, A. M., & Glowinski, J. (1987) · Experimental Brain Research · doi:10.1007/bf00236315 · Cited by 246 · see citing works

Differentially Interconnected Networks of GABAergic Interneurons in the Visual Cortex of the Cat

Tamás, G., Somogyi, P., & Buhl, E. H. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-11-04255.1998 · Cited by 242 · see citing works

Excitatory amino acid pathway from the hippocampus to the prefrontal cortex. Contribution of AMPA receptors in hippocampo-prefrontal cortex transmission

Jay, T. M., Thierry, A., Wiklund, L., & Glowinski, J. (1992) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1992.tb00154.x · Cited by 187 · see citing works

The effects of fornix and medial prefrontal lesions on delayed non-matching-to-sample by rats

Shaw, C., & Aggleton, J. P. (1993) · Behavioural Brain Research · doi:10.1016/0166-4328(93)90051-q · Cited by 181 · see citing works

GABAA Receptor Subunit Gene Expression in Human Prefrontal Cortex: Comparison of Schizophrenics and Controls

Akbarian, S., Huntsman, M. M., Kim, J. J., Tafazzoli, A., Potkin, S. G., Bunney, W. E., & Jones, E. G. (1995) · Cerebral Cortex · doi:10.1093/cercor/5.6.550 · Cited by 181 · see citing works

Functional role of rat prelimbic-infralimbic cortices in spatial memory: evidence for their involvement in attention and behavioural flexibility

Delatour, B., & Gisquet-Verrier, P. (2000) · Behavioural Brain Research · doi:10.1016/s0166-4328(99)00168-0 · Cited by 170 · see citing works

Stress-induced activation of nitric oxide-producing neurons in the rat brain

Krukoff, T. L., & Khalili, P. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970127)377:4 · Cited by 167 · see citing works

Electrophysiological Properties of Pyramidal Neurons in the Rat Prefrontal Cortex: An In Vivo Intracellular Recording Study

Dégenètais, E. (2002) · Cerebral Cortex · doi:10.1093/cercor/12.1.1 · Cited by 152 · see citing works

GABAergic neuronal subtypes in the human frontal cortex — development and deficits in schizophrenia

Reynolds, G. P., & Beasley, C. L. (2001) · Journal of Chemical Neuroanatomy · doi:10.1016/s0891-0618(01)00113-2 · Cited by 138 · see citing works

Hippocampal inputs to identified neurons in an in vitro slice preparation of the rat nucleus accumbens: evidence for feed-forward inhibition

Pennartz, C. M. A., & Kitai, S. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-09-02838.1991 · Cited by 137 · see citing works

Comparisons of behavioral effects of hippocampal and prefrontal cortex lesions in the rat.

Nonneman, A. J., Voigt, J., & Kolb, B. E. (1974) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0036864 · Cited by 136 · see citing works

Subunit Composition, Kinetic, and Permeation Properties of AMPA Receptors in Single Neocortical Nonpyramidal Cells

Angulo, M. C., Lambolez, B., Audinat, É., Hestrin, S., & Rossier, J. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-17-06685.1997 · Cited by 136 · see citing works

Synaptic Influence of Hippocampus on Pyramidal Cells of the Rat Prefrontal Cortex: An In Vivo Intracellular Recording Study

Dégenètais, E. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.7.782 · Cited by 127 · see citing works

Activity of different classes of neurons of the motor cortex during locomotion

Beloozerova, I. N., Sirota, M. G., & Swadlow, H. A. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-03-01087.2003 · Cited by 126 · see citing works

Morphological evidence that CA1 hippocampal afferents monosynaptically innervate PV-containing neurons and NADPH-diaphorase reactive cells in the medial prefrontal cortex (Areas 25/32) of the rat

Gabbott, P., Headlam, A., & Busby, S. (2002) · Brain Research · doi:10.1016/s0006-8993(02)02487-3 · Cited by 101 · see citing works

Learning-related changes in response patterns of prefrontal neurons during instrumental conditioning.

Mulder, A. B., Nordquist, R. E., Örgüt, O., & Pennartz, C. M. A. (2003) · Behavioural Brain Research · doi:10.1016/j.bbr.2003.09.016 · Cited by 84 · see citing works

The Influence of Single VB Thalamocortical Impulses on Barrel Columns of Rabbit Somatosensory Cortex

Swadlow, H. A., & Gusev, A. G. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.83.5.2802 · Cited by 84 · see citing works

Role of the prefrontal cortex of the rat in learning and decision making: effects of transient inactivation

de Bruin, J. P. C., Feenstra, M. G. P., Broersen, L. M., van Leeuwen, M., Arens, C., de Vries, S. I., & Joosten, R. N. J. M. A. (2000) · Progress in brain research · doi:10.1016/s0079-6123(00)26010-x · Cited by 72 · see citing works

Interhemispheric and subcortical collaterals of medial prefrontal cortical neurons in the rat

Ferino, F., Thierry, A. M., Saffroy, M., & Glowinski, J. (1987) · Brain Research · doi:10.1016/0006-8993(87)90450-1 · Cited by 72 · see citing works

Unit activity of the medial wall of the frontal cortex during delayed performance in rats

Batuev, A. S. (1990) · Behavioural Brain Research · doi:10.1016/0166-4328(90)90145-5 · Cited by 67 · see citing works

Effects of lesions of prefrontal cortex and dorsomedial thalamus on delayed go/no-go alternation in rats

Sakurai, Y., & Sugimoto, S. (1985) · Behavioural Brain Research · doi:10.1016/0166-4328(85)90045-2 · Cited by 56 · see citing works

Behavioral effects of large and small lesions of the rat medial frontal cortex

Silva, M. G., Boyle, M. A., Finger, S., Numan, B., Bouzrara, A., & Almli, C. R. (1986) · Experimental Brain Research · doi:10.1007/bf00243840 · Cited by 34 · see citing works

Large and small medial frontal cortex lesions and spatial performance of the rat

Wolf, C., Waksman, D., Finger, S., & Almli, C. R. (1987) · Brain Research Bulletin · doi:10.1016/0361-9230(87)90025-6 · Cited by 32 · see citing works

Chandelier cells: shedding light on altered cortical circuitry in schizophrenia

Lewis, D. A. (1998) · Molecular Psychiatry · doi:10.1038/sj.mp.4000469 · Cited by 17 · see citing works

Untitled work

(1996) · doi:10.1002/(sici)1096-9861(19960520)369:1

NMDA Receptor Hypofunction Produces Opposite Effects on Prefrontal Cortex Interneurons and Pyramidal Neurons

Homayoun, H., & Moghaddam, B. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.2213-07.2007 · Cited by 1,231 · see citing works

Prefrontal phase locking to hippocampal theta oscillations

Siapas, A. G., Lubenov, E. V., & Wilson, M. A. (2005) · Neuron · doi:10.1016/j.neuron.2005.02.028 · Cited by 1,014 · see citing works

Entrainment of Neocortical Neurons and Gamma Oscillations by the Hippocampal Theta Rhythm

Sirota, A., Montgomery, S., Fujisawa, S., Isomura, Y., Zugaro, M., & Buzsáki, G. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.014 · Cited by 1,015 · see citing works

Coherent theta oscillations and reorganization of spike timing in the hippocampal- prefrontal network upon learning

Benchenane, K., Peyrache, A., Khamassi, M., Tierney, P. L., Gioanni, Y., Battaglia, F. P., & Wiener, S. I. (2010) · Neuron · doi:10.1016/j.neuron.2010.05.013 · Cited by 872 · see citing works

Synchronized activity between the ventral hippocampus and the medial prefrontal cortex during anxiety

Adhikari, A., Topiwala, M. A., & Gordon, J. A. (2010) · Neuron · doi:10.1016/j.neuron.2009.12.002 · Cited by 729 · see citing works

The prefrontal cortex as a key target of the maladaptive response to stress

Cerqueira, J. J., Mailliet, F., Almeida, O. F. X., Jay, T. M., & Sousa, N. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.4372-06.2007 · Cited by 599 · 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

Stress-induced prefrontal reorganization and executive dysfunction in rodents

Holmes, A., & Wellman, C. L. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.11.005 · Cited by 469 · see citing works

Oscillations in the prefrontal cortex: a gateway to memory and attention

Benchenane, K., Tiesinga, P. H., & Battaglia, F. P. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.01.004 · Cited by 366 · see citing works

Short- and Long-Term Consequences of Nicotine Exposure during Adolescence for Prefrontal Cortex Neuronal Network Function

Goriounova, N. A., & Mansvelder, H. D. (2012) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a012120 · Cited by 307 · see citing works

Prefrontal-Hippocampal Interactions in Memory and Emotion

Jin, J., & Maren, S. (2015) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00170 · Cited by 313 · see citing works

State-dependent spike-timing relationships between hippocampal and prefrontal circuits during sleep

Wierzynski, C. M., Lubenov, E. V., Gu, M., & Siapas, A. G. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.011 · Cited by 289 · see citing works

Inactivation of the ventromedial prefrontal cortex reduces expression of conditioned fear and impairs subsequent recall of extinction

Sierra‐Mercado, D., Corcoran, K. A., Lebrón‐Milad, K., & Quirk, G. J. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05014.x · Cited by 255 · see citing works

Theta oscillations mediate interaction between prefrontal cortex and medial temporal lobe in human memory

Anderson, K. L., Rajagovindan, R., Ghacibeh, G. A., Meador, K. J., & Ding, M. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhp223 · Cited by 222 · see citing works

Hippocampus-driven feed-forward inhibition of the prefrontal cortex mediates relapse of extinguished fear

Marek, R., Jin, J., Goode, T. D., Giustino, T. F., Wang, Q., Acca, G. M., Holehonnur, R., Ploski, J. E., Fitzgerald, P. J., Lynagh, T., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0073-9 · Cited by 226 · see citing works

Dopaminergic Regulation of Inhibitory and Excitatory Transmission in the Basolateral Amygdala–Prefrontal Cortical Pathway

Floresco, S. B., & Tse, M. T. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5474-06.2007 · Cited by 204 · see citing works

Coupled oscillations mediate directed interactions between prefrontal cortex and hippocampus of the neonatal rat

Brockmann, M. D., Pöschel, B., Cichon, N., & Hanganu-Opatz, I. L. (2011) · Neuron · doi:10.1016/j.neuron.2011.05.041 · Cited by 186 · see citing works

Prefrontal cortex and drug abuse vulnerability: Translation to prevention and treatment interventions

Perry, J. L., Joseph, J. E., Jiang, Y., Zimmerman, R. S., Kelly, T. H., Darna, M., Huettl, P., Dwoskin, L. P., & Bardo, M. T. (2011) · Brain Research Reviews · doi:10.1016/j.brainresrev.2010.09.001 · Cited by 180 · 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 & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.04.007 · Cited by 158 · see citing works

5-HT1A receptor agonists enhance pyramidal cell firing in prefrontal cortex through a preferential action on GABA interneurons

Llado-Pelfort, L., Santana, N., Ghisi, V., Artigas, F., & Celada, P. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr220 · Cited by 156 · see citing works

Context-dependent prefrontal cortex regulation of cocaine self-administration and reinstatement behaviors in rats

Di Pietro, N. C., Black, Y. D., & Kantak, K. M. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05193.x · Cited by 107 · see citing works

The Blockade of the Transient Receptor Potential Vanilloid Type 1 and Fatty Acid Amide Hydrolase Decreases Symptoms and Central Sequelae in the Medial Prefrontal Cortex of Neuropathic Rats

de Novellis, V., Vita, D., Gatta, L., Luongo, L., Bellini, G., De Chiaro, M., Marabese, I., Siniscalco, D., Boccella, S., Piscitelli, F., et al. (2011) · Molecular Pain · doi:10.1186/1744-8069-7-7 · Cited by 90 · see citing works

Ontogeny of altered dendritic morphology in the rat prefrontal cortex, hippocampus, and nucleus accumbens following Cesarean delivery and birth anoxia

Juárez, I., Gratton, A., & Flores, G. (2008) · Journal of Comparative Neurology · doi:10.1002/cne.21651 · Cited by 89 · see citing works

Divisions of identified parvalbumin-expressing basket cells during working memory-guided decision making

Lagler, M., Ozdemir, A. T., Lagoun, S., Malagon-Vina, H., Borhegyi, Z., Hauer, R., Jelem, A., & Klausberger, T. (2016) · Neuron · doi:10.1016/j.neuron.2016.08.010 · Cited by 67 · see citing works

Nicotine exposure during adolescence alters the rules for prefrontal cortical synaptic plasticity during adulthood

Goriounova, N. A., & Mansvelder, H. D. (2012) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2012.00003 · Cited by 65 · see citing works

Chronic stress disrupts neural coherence between cortico-limbic structures

Oliveira, J. F., Dias, N. S., Correia, M., Gama-Pereira, F., Sardinha, V. M., Lima, A., Oliveira, A. F., Jacinto, L. R., Ferreira, D. S., Silva, A. M., et al. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00010 · Cited by 55 · see citing works

Altered short-term plasticity in the prefrontal cortex after early life seizures

Hernan, A. E., Holmes, G. L., Isaev, D., Scott, R. C., & Isaeva, E. (2013) · Neurobiology of Disease · doi:10.1016/j.nbd.2012.10.007 · Cited by 49 · see citing works

Pathways for Contextual Memory: The Primate Hippocampal Pathway to Anterior Cingulate Cortex

Wang, J., John, Y., & Barbas, H. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhaa333 · Cited by 39 · see citing works

Amygdala Inputs to the Prefrontal Cortex Elicit Heterosynaptic Suppression of Hippocampal Inputs

Tejeda, H. A., & O'Donnell, P. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.0837-14.2014 · Cited by 11 · see citing works

Effects of Inhibitory Signal on Criticality in Excitatory-Inhibitory Networks*

Wang, F., & Wang, S.-J. (2019) · Communications in Theoretical Physics · doi:10.1088/0253-6102/71/6/746 · Cited by 3 · see citing works

[Interaction of excitatory and inhibitory processes in the proposed inhibitory interneurons of the hippocampus].

Artemenko, D. P. (1980) · PubMed · Cited by 3 · see citing works

Difference in axon diameter and myelin thickness between excitatory and inhibitory callosally projecting axons in mice

Basu, K., Appukuttan, S., Manchanda, R., & Attila Gabor, S. I. K. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac329 · Cited by 28 · see citing works

What is the Source of the EEG?

Kirschstein, T., & Köhling, R. (2009) · Clinical EEG and Neuroscience · doi:10.1177/155005940904000305 · Cited by 206 · see citing works

Excitatory and Inhibitory Responses of the Ongoing Sympathetic Discharge in Single Renal Neurons to Liminal Stimulation of Aortic C-Fibres in the Rabbit

Lupa, K., Wójcik, G., Kruk, A., et al. (1999) · Archives of Physiology and Biochemistry · doi:10.1076/apab.107.2.113.4338