Double dissociation of function within the hippocampus: A comparison of dorsal, ventral, and complete hippocampal cytotoxic lesions

Statistical power analysis for the behavioral sciences

Cohen, J. (1990) · Computers Environment and Urban Systems · doi:10.1016/0198-9715(90)90050-4 · Cited by 65,406 · see citing works

The Rat Brain in Stereotaxic Coordinates

Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585 · see citing works

Untitled work

(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010 · see citing works

Developments of a water-maze procedure for studying spatial learning in the rat

Morris, R. (1984) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(84)90007-4 · Cited by 7,180 · see citing works

Spatial localization does not require the presence of local cues

Morris, R. G. M. (1981) · Learning and Motivation · doi:10.1016/0023-9690(81)90020-5 · Cited by 2,699 · see citing works

Modality-Specific Retrograde Amnesia of Fear

Kim, J. J., & Fanselow, M. S. (1992) · Science · doi:10.1126/science.1585183 · Cited by 2,483 · see citing works

Hippocampus, space, and memory

Olton, D. S., Becker, J. T., & Handelmann, G. E. (1979) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00062713 · Cited by 2,018 · see citing works

The Role of the Hippocampus in Feedback Regulation of the Hypothalamic-Pituitary-Adrenocortical Axis*

JACOBSON, L., & SAPOLSKY, R. (1991) · Endocrine Reviews · doi:10.1210/edrv-12-2-118 · Cited by 1,739 · see citing works

On the role of the hippocampus in learning and memory in the rat.

Jarrard, L. E. (1993) · Behavioral and Neural Biology · doi:10.1016/0163-1047(93)90664-4 · Cited by 1,125 · see citing works

The patterns of afferent innervation of the core and shell in the “Accumbens” part of the rat ventral striatum: Immunohistochemical detection of retrogradely transported fluoro‐gold

Brog, J. S., Salyapongse, A., Deutch, A. Y., & Zahm, D. S. (1993) · Journal of Comparative Neurology · doi:10.1002/cne.903380209 · Cited by 1,102 · see citing works

The hippocampus and contextual retrieval of information from memory: A theory

Hirsh, R. (1974) · Behavioral Biology · doi:10.1016/s0091-6773(74)92231-7 · Cited by 957 · see citing works

Spatial learning impairment parallels the magnitude of dorsal hippocampal lesions, but is hardly present following ventral lesions

Moser, E., Moser, M. ‐., & Andersen, P. N. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-09-03916.1993 · Cited by 916 · see citing works

Spatial learning with a minislab in the dorsal hippocampus.

Moser, M., Moser, E. I., Forrest, E., Andersen, P. N., & Morris, R. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.21.9697 · Cited by 902 · see citing works

Organization of the projections from the subiculum to the ventral striatum in the rat. A study using anterograde transport of Phaseolus vulgaris leucoagglutinin

Groenewegen, H. J., Vermeulen‐Vanderzee, E., Kortschot, A. T., & Witter, M. P. (1987) · Neuroscience · doi:10.1016/0306-4522(87)90275-2 · Cited by 867 · see citing works

The hippocampus—what does it do?

Eichenbaum, H., Otto, T., & Cohen, N. J. (1992) · Behavioral and Neural Biology · doi:10.1016/0163-1047(92)90724-i · Cited by 867 · see citing works

Comparison of spatial firing characteristics of units in dorsal and ventral hippocampus of the rat

Jung, M. W., Wiener, S. I., & McNaughton, B. L. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-12-07347.1994 · Cited by 818 · see citing works

The distribution of the projection from the hippocampal formation to the nucleus accumbens in the rat: An anterograde and retrograde-horseradish peroxidase study

Kelley, A. E., & Domesick, V. B. (1982) · Neuroscience · doi:10.1016/0306-4522(82)90198-1 · Cited by 746 · see citing works

Conservation of hippocampal memory function in rats and humans

Bunsey, M. D., & Eichenbaum, H. (1996) · Nature · doi:10.1038/379255a0 · Cited by 733 · 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

Ibotenate Lesions of Hippocampus and/or Subiculum: Dissociating Components of Allocentric Spatial Learning

Morris, R., Schenk, F., Tweedie, F., & Jarrard, L. E. (1990) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1990.tb00014.x · Cited by 661 · see citing works

Associations across time: The hippocampus as a temporary memory store

Rawlins, J. N. P. (1985) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00001291 · Cited by 561 · see citing works

A direct comparison of amphetamine-induced behaviours and regional brain dopamine release in the rat using intracerebral dialysis

Sharp, T., Zetterström, T., Ljungberg, T., & Ungerstedt, U. (1987) · Brain Research · doi:10.1016/0006-8993(87)91416-8 · Cited by 395 · see citing works

Topographical organization of the entorhinal projection to the dentate gyrus of the monkey

Witter, M., Hoesen, G. W. V., & Amaral, D. (1989) · Journal of Neuroscience · doi:10.1523/jneurosci.09-01-00216.1989 · Cited by 380 · see citing works

Configural association theory and the hippocampal formation: An appraisal and reconfiguration

Rudy, J. W., & Sutherland, R. J. (1995) · Hippocampus · doi:10.1002/hipo.450050502 · Cited by 379 · see citing works

Selective hippocampal lesions and behavior: Effects of kainic acid lesions on performance of place and cue tasks.

Jarrard, L. E. (1983) · Behavioral Neuroscience · doi:10.1037//0735-7044.97.6.873 · Cited by 371 · see citing works

Neonatal lesions of the rat ventral hippocampus result in hyperlocomotion and deficits in social behaviour in adulthood

Sams-Dodd, F., Lipska, B. K., & Weinberger, D. R. (1997) · Psychopharmacology · doi:10.1007/s002130050349 · Cited by 346 · see citing works

The dependence of interresponse times upon the relative reinforcement of different interresponse times.

Anger, D. (1956) · Journal of Experimental Psychology · doi:10.1037/h0041255 · Cited by 337 · see citing works

Selective hippocampal lesions abolish the contextual specificity of latent inhibition and conditioning.

Honey, R. C., & Good, M. A. (1993) · Behavioral Neuroscience · doi:10.1037//0735-7044.107.1.23 · Cited by 336 · see citing works

Dissociating context and space within the hippocampus: Effects of complete, dorsal, and ventral excitotoxic hippocampal lesions on conditioned freezing and spatial learning.

Richmond, M. A., Yee, B. K., Pouzet, B., Veenman, L., Rawlins, J. N. P., Feldon, J., & Bannerman, D. M. (1999) · Behavioral Neuroscience · doi:10.1037/0735-7044.113.6.1189 · Cited by 332 · see citing works

On the use of ibotenic acid to lesion selectively different components of the hippocampal formation

Jarrard, L. E. (1989) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(89)90149-0 · Cited by 295 · see citing works

Convergence of hippocampal and dopaminergic input onto identified neurons in the nucleus accumbens of the rat.

Totterdell, S., & Smith, A. D. (1989) · PubMed · Cited by 266 · see citing works

Latent inhibition of conditioned dopamine release in rat nucleus accumbens

Young, A. M. J., Joseph, M. H., & Gray, J. A. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90378-s · Cited by 261 · see citing works

The cytoarchitecture, histochemistry and projections of the tuberomammillary nucleus in the rat

Köhler, C., Swanson, L. W., Haglund, L., & J-Yen, W. (1985) · Neuroscience · doi:10.1016/0306-4522(85)90049-1 · Cited by 253 · see citing works

The septo-hippocampal system and cognitive mapping

Rawlins, J. N. P., & Olton, D. S. (1982) · Behavioural Brain Research · doi:10.1016/0166-4328(82)90039-0 · Cited by 227 · see citing works

Differential Effects of Dorsal and Ventral Hippocampal Lesions

Hock, B. J., & Bunsey, M. D. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-17-07027.1998 · Cited by 220 · see citing works

Contribution of the Ventral Subiculum to Inhibitory Regulation of the Hypothalamo‐Pituitary‐Adrenocortical Axis

Herman, J. P., Cullinan, W. E., Morano, M. I., Akil, H., & Watson, S. J. (1995) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.1995.tb00784.x · Cited by 214 · see citing works

Ibotenic acid lesion of the ventral hippocampus differentially affects dopamine and its metabolites in the nucleus accumbens and prefrontal cortex in the rat

Lipska, B. K., Jaskiw, G. E., Chrapusta, S. J., Karoum, F., & Weinberger, D. R. (1992) · Brain Research · doi:10.1016/0006-8993(92)91184-g · Cited by 205 · see citing works

Topography between the entorhinal cortex and the dentate septotemporal axis in rats: I. Medial and intermediate entorhinal projecting cells

Ruth, R. E., Collier, T. J., & Routtenberg, A. (1982) · The Journal of Comparative Neurology · doi:10.1002/cne.902090107 · Cited by 186 · see citing works

Laminar origin and septotemporal distribution of entorhinal and perirhinal projections to the hippocampus in the cat

Witter, M. P., & Groenewegen, H. J. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902240305 · Cited by 178 · see citing works

Hippocampal Lesions Disrupt an Associative Mismatch Process

Honey, R. C., Watt, A. J., & Good, M. A. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-06-02226.1998 · Cited by 162 · see citing works

Similarities vs. differences in place learning and circadian activity in rats after fimbria‐fornix section or ibotenate removal of hippocampal cells

Whishaw, I. Q., & Jarrard, L. E. (1995) · Hippocampus · doi:10.1002/hipo.450050610 · Cited by 152 · see citing works

Connections of the parahippocampal cortex. I. Cortical afferents

Room, P., & Groenewegen, H. J. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902510402 · Cited by 152 · see citing works

Selective forebrain fiber tract lesions implicate ventral hippocampal structures in tonic regulation of paraventricular nucleus corticotropin-releasing hormone (CRH) and arginine vasopressin (AVP) mRNA expression

Herman, J. P., Cullinan, W. E., Young, E. A., Akil, H., & Watson, S. J. (1992) · Brain Research · doi:10.1016/0006-8993(92)91680-d · Cited by 138 · see citing works

On the preferential release of dopamine in the nucleus accumbens by amphetamine: further evidence obtained by vertically implanted concentric dialysis probes

Chiara, G. D., Tanda, G., Frau, R., & Carboni, E. (1993) · Psychopharmacology · doi:10.1007/bf02244939 · Cited by 125 · see citing works

Selective cytotoxic lesions of the hippocampal formation and DRL performance in rats.

Sinden, J. D., Rawlins, J. N. P., Gray, J. A., & Jarrard, L. E. (1986) · Behavioral Neuroscience · doi:10.1037//0735-7044.100.3.320 · Cited by 112 · see citing works

Galanin immunoreactivity in hypothalamic histamine neurons: Further evidence for multiple chemical messengers in the tuberomammillary nucleus

Köhler, C., Ericson, H., Watanabe, T., Polak, J. M., Palay, S. L., Chan‐Palay, V., & Chan‐Palay, V. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902500105 · Cited by 110 · see citing works

Enhancement of amphetamine-induced locomotor activity and dopamine release in nucleus accumbens following excitotoxic lesions of the hippocampus

Wilkinson, L. S., Mittleman, G., Torres, E. M., Humby, T., Hall, F. S., & Robbins, T. W. (1993) · Behavioural Brain Research · doi:10.1016/0166-4328(93)90110-c · Cited by 107 · see citing works

Ca2+ dependence of the amphetamine, nomifensine, and Lu 19-005 effect on in vivo dopamine transmission

Hurd, Y. L., & Ungerstedt, U. (1989) · European Journal of Pharmacology · doi:10.1016/0014-2999(89)90067-8 · Cited by 95 · see citing works

Dorsal hippocampal lesion does not affect dopaminergic indices in the basal ganglia

Lipska, B. K., Jaskiw, G. E., Karoum, F., Phillips, I., Kleinman, J. E., & Weinberger, D. R. (1991) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(91)90342-y · Cited by 20 · see citing works

SENSITIZATION OF DA RELEASE IN THE ACCUMBENS FOLLOWING AMPHETAMINE

Warburton, E. C., Sn, M., & Mh, J. (1993) · Behavioural Pharmacology · doi:10.1097/00008877-199308000-00055 · Cited by 7 · see citing works

Are the Dorsal and Ventral Hippocampus Functionally Distinct Structures?

Fanselow, M. S., & Dong, H.-W. (2010) · Neuron · doi:10.1016/j.neuron.2009.11.031 · Cited by 3,358 · see citing works

Regional dissociations within the hippocampus-memory and anxiety

Bannerman, D. M., Rawlins, J. N. P., McHugh, S. B., Deacon, R. M. J., Yee, B. K., Bast, T., Zhang, W.-N., Pothuizen, H. H. J., & Feldon, J. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.03.004 · Cited by 1,462 · see citing works

Spatial memory, recognition memory, and the hippocampus

Broadbent, N. J., Squire, L. R., & Clark, R. E. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0406344101 · Cited by 985 · see citing works

Differential Control of Learning and Anxiety along the Dorsoventral Axis of the Dentate Gyrus

Kheirbek, M. A., Drew, L. J., Burghardt, N. S., Costantini, D. O., Tannenholz, L., Ahmari, S. E., Zeng, H., Fenton, A. A., & Hen, R. (2013) · Neuron · doi:10.1016/j.neuron.2012.12.038 · Cited by 713 · see citing works

Hippocampal synaptic plasticity, spatial memory and anxiety

Bannerman, D. M., Sprengel, R., Sanderson, D. J., McHugh, S. B., Rawlins, J. N. P., Monyer, H., & Seeburg, P. H. (2014) · Nature Reviews Neuroscience · doi:10.1038/nrn3677 · Cited by 688 · see citing works

Ventral hippocampal lesions affect anxiety but not spatial learning

Bannerman, D. M., Grubb, M., Deacon, R. M. J., Yee, B. K., Feldon, J., & Rawlins, J. N. P. (2003) · Behavioural Brain Research · doi:10.1016/s0166-4328(02)00268-1 · Cited by 530 · see citing works

Towards an immuno-precipitated neurodevelopmental animal model of schizophrenia

Meyer, U., Feldon, J., Schedlowski, M., & Yee, B. K. (2005) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.10.012 · Cited by 494 · see citing works

Amygdala and Ventral Hippocampus Contribute Differentially to Mechanisms of Fear and Anxiety.

McHugh, S. B., Deacon, R. M. J., Rawlins, J. N. P., & Bannerman, D. M. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.1.63 · Cited by 384 · see citing works

In-vivo rodent models for the experimental investigation of prenatal immune activation effects in neurodevelopmental brain disorders

Meyer, U., Feldon, J., & Fatemi, S. H. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.05.001 · Cited by 367 · see citing works

Morris water maze: a versatile and pertinent tool for assessing spatial learning and memory

Othman, M. Z., Hassan, Z., & Has, A. T. C. (2022) · EXPERIMENTAL ANIMALS · doi:10.1538/expanim.21-0120 · Cited by 375 · see citing works

Assessment of spatial memory in mice

Sharma, S., Rakoczy, S. G., & Brown‐Borg, H. M. (2010) · Life Sciences · doi:10.1016/j.lfs.2010.09.004 · Cited by 370 · see citing works

Severe Early Life Stress Hampers Spatial Learning and Neurogenesis, but Improves Hippocampal Synaptic Plasticity and Emotional Learning under High-Stress Conditions in Adulthood

Oomen, C. A., Soeters, H., Audureau, N., Vermunt, L., van Hasselt, F. N., Manders, E. M. M., Joëls, M., Lucassen, P. J., & Krugers, H. J. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0247-10.2010 · Cited by 352 · see citing works

Double dissociation of function within the hippocampus: Spatial memory and hyponeophagia.

Bannerman, D. M., Deacon, R. M. J., Offen, S., Friswell, J., Grubb, M. S., & Rawlins, J. N. P. (2002) · Behavioral Neuroscience · doi:10.1037//0735-7044.116.5.884 · Cited by 357 · see citing works

Spatial memory dissociations in mice lacking GluR1

Reisel, D., Bannerman, D. M., Schmitt, W. B., Deacon, R. M. J., Jonathan Flint, C., Borchardt, T., Seeburg, P. H., & Rawlins, J. N. P. (2002) · Nature Neuroscience · doi:10.1038/nn910 · Cited by 343 · see citing works

Dissociating context and space within the hippocampus: Effects of complete, dorsal, and ventral excitotoxic hippocampal lesions on conditioned freezing and spatial learning.

Richmond, M. A., Yee, B. K., Pouzet, B., Veenman, L., Rawlins, J. N. P., Feldon, J., & Bannerman, D. M. (1999) · Behavioral Neuroscience · doi:10.1037/0735-7044.113.6.1189 · Cited by 332 · see citing works

Hippocampal NMDA receptors and anxiety: At the interface between cognition and emotion

Barkus, C., McHugh, S. B., Sprengel, R., Seeburg, P. H., Rawlins, J. N. P., & Bannerman, D. M. (2009) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2009.10.014 · Cited by 328 · see citing works

Multiple anatomical systems embedded within the primate medial temporal lobe: Implications for hippocampal function

Aggleton, J. P. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.09.005 · Cited by 319 · see citing works

Hippocampal cytotoxic lesion effects on species-typical behaviours in mice

Deacon, R. M. J., Croucher, A. P., & Rawlins, J. N. P. (2002) · Behavioural Brain Research · doi:10.1016/s0166-4328(01)00401-6 · Cited by 307 · see citing works

Habituation in rodents: a review of behavior, neurobiology, and genetics

LEUSSIS, M., & BOLIVAR, V (2006) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2006.03.006 · Cited by 330 · see citing works

Double dissociation of function within the hippocampus: Spatial memory and hyponeophagia.

Bannerman, D. M., Deacon, R. M. J., Offen, S., Friswell, J., Grubb, M., & Rawlins, J. N. P. (2002) · Behavioral Neuroscience · doi:10.1037/0735-7044.116.5.884 · Cited by 357 · see citing works

Context representations, context functions, and the parahippocampal–hippocampal system

Rudy, J. W. (2009) · Learning & Memory · doi:10.1101/lm.1494409 · Cited by 296 · see citing works

Dissociation of function between the dorsal and the ventral hippocampus in spatial learning abilities of the rat: a within‐subject, within‐task comparison of reference and working spatial memory

Pothuizen, H. H. J., Zhang, W., Jongen‐Rêlo, A. L., Feldon, J., & Yee, B. K. (2004) · European Journal of Neuroscience · doi:10.1111/j.0953-816x.2004.03170.x · Cited by 274 · see citing works

Hippocampus and Pavlovian fear conditioning in rats: muscimol infusions into the ventral, but not dorsal, hippocampus impair the acquisition of conditional freezing to an auditory conditional stimulus.

Maren, S., & Holt, W. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.1.97 · Cited by 272 · see citing works

Hippocampal modulation of sensorimotor processes.

Bast, T., & Feldon, J. (2003) · Progress in neurobiology · doi:10.1016/s0301-0082(03)00112-6 · Cited by 267 · see citing works

Contribution of Hippocampal and Extra-Hippocampal NR2B-Containing NMDA Receptors to Performance on Spatial Learning Tasks

von Engelhardt, J., Doganci, B., Jensen, V., Hvalby, Ø., Göngrich, C., Taylor, A., Barkus, C., Sanderson, D. J., Rawlins, J. N. P., Seeburg, P. H., et al. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.039 · Cited by 250 · see citing works

Transgenic Mice Lacking NMDAR-Dependent LTD Exhibit Deficits in Behavioral Flexibility

Nicholls, R. E., Alarcón, J. M., Malleret, G., Carroll, R. C., Grody, M. B., Vronskaya, S., & Kandel, E. R. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.039 · Cited by 227 · see citing works

Striking Variations in Corticosteroid Modulation of Long-Term Potentiation along the Septotemporal Axis of the Hippocampus

Maggio, N., & Segal, M. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.0155-07.2007 · Cited by 230 · see citing works

Neurogenesis along the septo-temporal axis of the hippocampus: Are depression and the action of antidepressants region-specific?

Tanti, A., & Belzung, C. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.08.017 · Cited by 220 · see citing works

Disconnection of the hippocampal–prefrontal cortical circuits impairs spatial working memory performance in rats

Wang, G.-W., & Cai, J. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.09.002 · Cited by 205 · see citing works

The case for episodic memory in animals

Dere, E., KARTTEKE, E., Huston, J. P., & DESOUZASILVA, M. (2006) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2006.09.005 · Cited by 202 · see citing works

Hippocampal lesions, species-typical behaviours and anxiety in mice

Deacon, R. M. J., & Rawlins, J. N. P. (2004) · Behavioural Brain Research · doi:10.1016/j.bbr.2004.05.027 · Cited by 193 · see citing works

Spatial Cognition and the Hippocampus: The Anterior–Posterior Axis

Nadel, L., Hoscheidt, S. M., & Ryan, L. (2012) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00313 · Cited by 191 · see citing works

Effects of cytotoxic hippocampal lesions in mice on a cognitive test battery

Deacon, R. M. J., Bannerman, D. M., Kirby, B. P., Croucher, A. P., & Rawlins, J. N. P. (2002) · Behavioural Brain Research · doi:10.1016/s0166-4328(01)00451-x · Cited by 189 · see citing works

An aluminum-based rat model for Alzheimer’s disease exhibits oxidative damage, inhibition of PP2A activity, hyperphosphorylated tau, and granulovacuolar degeneration

Walton, J. R. (2007) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2007.06.001 · Cited by 183 · see citing works

Double dissociation of the effects of selective nucleus accumbens core and shell lesions on impulsive‐choice behaviour and salience learning in rats

Pothuizen, H. H. J., Jongen‐Rêlo, A. L., Feldon, J., & Yee, B. K. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04388.x · Cited by 183 · see citing works

Lesions of the ventral hippocampus, but not the dorsal hippocampus, impair conditioned fear expression and inhibitory avoidance on the elevated T-maze

Trivedi, M. (2004) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2004.02.005 · Cited by 179 · see citing works

Spatial long-term memory is related to mossy fiber synaptogenesis

Ramı́rez-Amaya, V., Balderas, I., Sandoval, J., Escobar, M. L., & Bermúdez-Rattoni, F. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-18-07340.2001 · Cited by 177 · see citing works

A comparison of 129S2/SvHsd and C57BL/6JOlaHsd mice on a test battery assessing sensorimotor, affective and cognitive behaviours: implications for the study of genetically modified mice

Contet, C. (2001) · Behavioural Brain Research · doi:10.1016/s0166-4328(01)00231-5 · Cited by 176 · see citing works

Individual Differences and Social Influences on the Neurobehavioral Pharmacology of Abused Drugs

Bardo, M. T., Neisewander, J. L., & Kelly, T. H. (2013) · Pharmacological Reviews · doi:10.1124/pr.111.005124 · Cited by 167 · see citing works

Watermaze Learning Enhances Excitability of CA1 Pyramidal Neurons

Oh, M. M., Kuo, A. G., Wu, W., Sametsky, E. A., & Disterhoft, J. F. (2003) · Journal of Neurophysiology · doi:10.1152/jn.01177.2002 · Cited by 165 · see citing works

Neural basis of psychosis-related behaviour in the infection model of schizophrenia

Meyer, U., & Feldon, J. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.12.022 · Cited by 158 · see citing works

Perspectives for the development of animal models of bipolar disorder

Machado-Vieira, R., Kapczinski, F., & Soares, J. C. (2004) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2003.10.015 · Cited by 158 · see citing works

From ear to uncertainty: vestibular contributions to cognitive function

Smith, P. F., & Zheng, Y. (2013) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2013.00084 · Cited by 154 · see citing works

Malaise in the water maze: Untangling the effects of LPS and IL-1β on learning and memory

Cunningham, C. M., & Sanderson, D. J. (2008) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2008.05.007 · Cited by 151 · see citing works

Retrograde amnesia: neither partial nor complete hippocampal lesions in rats result in preferential sparing of remote spatial memory, even after reminding

Martin, S. J., de Hoz, L., & Morris, R. (2004) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2004.07.007 · Cited by 151 · see citing works

Early behavioural changes in scrapie‐affected mice and the influence of dapsone

Guenther, K. M., Deacon, R. M. J., Perry, V. H., & Rawlins, J. N. P. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01645.x · Cited by 150 · see citing works

The Ventral Hippocampus Supports a Memory Representation of Context and Contextual Fear Conditioning: Implications for a Unitary Function of the Hippocampus.

Rudy, J. W., & Matus-Amat, P. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.1.154 · Cited by 147 · see citing works

Double dissociation between hippocampal and prefrontal lesions on an operant delayed matching task and a water maze reference memory task

Sloan, H. L., Good, M. A., & Dunnett, S. B. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.03.030 · Cited by 149 · see citing works

Dissecting spatial knowledge from spatial choice by hippocampal NMDA receptor deletion

Bannerman, D. M., Bus, T., Taylor, A. M., Sanderson, D. J., Schwarz, I., Jensen, V., Hvalby, Ø., Rawlins, J. N. P., Seeburg, P. H., & Sprengel, R. (2012) · Nature Neuroscience · doi:10.1038/nn.3166 · Cited by 142 · see citing works

Anxiolytic effects of cytotoxic hippocampal lesions in rats.

Deacon, R. M. J., Bannerman, D. M., & Rawlins, J. N. P. (2002) · Behavioral Neuroscience · doi:10.1037//0735-7044.116.3.494 · Cited by 142 · see citing works

Dissociable contributions of the ventral hippocampus and orbitofrontal cortex to decision‐making with a delayed or uncertain outcome

Abela, A. R., & Chudasama, Y. (2012) · European Journal of Neuroscience · doi:10.1111/ejn.12071 · Cited by 142 · see citing works

Longitudinal axis of the hippocampus: Both septal and temporal poles of the hippocampus support water maze spatial learning depending on the training protocol

de Hoz, L., Knox, J., & Morris, R. (2003) · Hippocampus · doi:10.1002/hipo.10079 · Cited by 135 · see citing works

Restoration of spatial working memory by genetic rescue of GluR-A–deficient mice

Schmitt, W. B., Sprengel, R., Mack, V., Draft, R. W., SEEBURG, P. H., Deacon, R. M. J., Rawlins, J. N. P., & Bannerman, D. M. (2005) · Nature Neuroscience · doi:10.1038/nn1412 · Cited by 131 · see citing works

Phospholipase C-β1 knockout mice exhibit endophenotypes modeling schizophrenia which are rescued by environmental enrichment and clozapine administration

Mcomish, C., Burrows, E., Howard, M., Scarr, E., Kim, D., Shin, H.-S., Dean, B., van den Buuse, M., & Hannan, A. (2008) · Molecular Psychiatry · doi:10.1038/sj.mp.4002046 · Cited by 136 · see citing works

Dissociating the roles of dorsal and ventral CA1 for the temporal processing of spatial locations, visual objects, and odors.

Hunsaker, M. R., Fieldsted, P. M., Rosenberg, J. S., & Kesner, R. P. (2008) · Behavioral Neuroscience · doi:10.1037/0735-7044.122.3.643 · Cited by 127 · see citing works

Spatial Memory Deficits Induced by Perinatal Treatment of Rats with PCP and Reversal Effect of D-Serine

Andersen, J. D., & Pouzet, B. (2004) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300394 · Cited by 126 · see citing works

Late prenatal immune activation causes hippocampal deficits in the absence of persistent inflammation across aging

Giovanoli, S., Notter, T., Richetto, J., Labouesse, M. A., Vuillermot, S., Riva, M. A., & Meyer, U. (2015) · Journal of Neuroinflammation · doi:10.1186/s12974-015-0437-y · Cited by 124 · see citing works

Both dorsal and ventral hippocampus contribute to spatial learning in Long–Evans rats

Ferbinteanu, J., Ray, C. A., & McDonald, R. J. (2003) · Neuroscience Letters · doi:10.1016/s0304-3940(03)00473-7 · Cited by 124 · see citing works

Chapter 9 The role of the GluR-A (GluR1) AMPA receptor subunit in learning and memory

Sanderson, D. J., Good, M. A., Seeburg, P. H., Sprengel, R., Rawlins, J. N. P., & Bannerman, D. M. (2008) · Progress in brain research · doi:10.1016/s0079-6123(07)00009-x · Cited by 123 · see citing works

How do animals actually solve the T maze?

Dudchenko, P. A. (2001) · Behavioral Neuroscience · doi:10.1037/0735-7044.115.4.850 · Cited by 123 · see citing works

Differential contributions of dorsal vs. ventral hippocampus to auditory trace fear conditioning

Yoon, T., & Otto, T. (2007) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2006.12.006 · Cited by 122 · see citing works

Adult hippocampal neurogenesis shapes adaptation and improves stress response: a mechanistic and integrative perspective

Surget, A., & Belzung, C. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01136-8 · Cited by 122 · see citing works

Perineuronal nets, inhibitory interneurons and anxiety-related ventral hippocampal neuronal oscillations are altered by early life adversity

Murthy, S., Kane, G. A., Katchur, N. J., Lara Mejia, P. S., Obiofuma, G., Buschman, T. J., McEwen, B. S., & Gould, E. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.02.021 · Cited by 118 · see citing works

Glucocorticoid and mineralocorticoid receptor expression in the human hippocampus in major depressive disorder

Medina, A., Seasholtz, A. F., Sharma, V., Burke, S., Bunney, W. E., Myers, R., Schatzberg, A. F., Akil, H., & Watson, S. J. (2012) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2012.11.002 · Cited by 120 · see citing works

Impulsive choice in hippocampal but not orbitofrontal cortex‐lesioned rats on a nonspatial decision‐making maze task

Mariano, T. Y., Bannerman, D. M., McHugh, S. B., Preston, T. J., Rudebeck, P. H., Rudebeck, S. R., Rawlins, J. N. P., Walton, M. E., Rushworth, M. F. S., Baxter, M. G., et al. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06837.x · Cited by 107 · see citing works

Flavonoids as modulators of memory and learning: molecular interactions resulting in behavioural effects

Rendeiro, C., Guerreiro, J. D. T., Williams, C. M., & Spencer, J. P. E. (2012) · Proceedings of The Nutrition Society · doi:10.1017/s0029665112000146 · Cited by 112 · see citing works

Dorsal, but not ventral, hippocampal lesions disrupt cocaine place conditioning

Meyers, R. A., Zavala, A. R., & Neisewander, J. L. (2003) · Neuroreport · doi:10.1097/00001756-200311140-00023 · Cited by 109 · see citing works

Age Sensitivity of Behavioral Tests and Brain Substrates of Normal Aging in Mice

Kennard, J. A., & Woodruff-Pak, D. (2011) · Front. Ag. Neurosci. · doi:10.3389/fnagi.2011.00009 · Cited by 116 · see citing works

A neural model of cortico-cerebellar interactions during attentive imitation and predictive learning of sequential handwriting movements

Grossberg, S., & Paine, R. W. (2000) · Neural Networks · doi:10.1016/s0893-6080(00)00065-4 · Cited by 106 · see citing works

Why do lesions in the rodent anterior thalamic nuclei cause such severe spatial deficits?

Aggleton, J. P., & Nelson, A. J. D. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.08.013 · Cited by 105 · see citing works

The role of habituation in hippocampus‐dependent spatial working memory tasks: Evidence from GluA1 AMPA receptor subunit knockout mice

Sanderson, D. J., & Bannerman, D. M. (2010) · Hippocampus · doi:10.1002/hipo.20896 · Cited by 103 · see citing works

Ventral Hippocampal CA1 and CA3 Differentially Mediate Learned Approach-Avoidance Conflict Processing

Schumacher, A., Villaruel, F. R., Ussling, A., Riaz, S., Lee, A. C. H., & Ito, R. (2018) · Current Biology · doi:10.1016/j.cub.2018.03.012 · Cited by 101 · see citing works

Unique regulation of long term potentiation in the rat ventral hippocampus

Maggio, N., & Segal, M. (2007) · Hippocampus · doi:10.1002/hipo.20237 · Cited by 100 · see citing works

Sex differences in contextual fear conditioning are associated with differential ventral hippocampal extracellular signal-regulated kinase activation

Gresack, J. E., Schafe, G. E., Orr, P. T., & Frick, K. M. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.01.009 · Cited by 99 · see citing works

Medial Septal Lesions Mimic Effects of Both Selective Dorsal and Ventral Hippocampal Lesions.

Bannerman, D. M., Matthews, P. M., Deacon, R. M. J., & Rawlins, J. N. P. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.5.1033 · Cited by 98 · see citing works

Hippocampal tauopathy in tau transgenic mice coincides with impaired hippocampus-dependent learning and memory, and attenuated late-phase long-term depression of synaptic transmission

der Jeugd, A. V., Ahmed, T., Burnouf, S., Bélarbi, K., Hamdame, M., Grosjean, M., Humez, S., Balschun, D., Blum, D. L., Buée, L., et al. (2010) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2010.12.005 · Cited by 98 · see citing works

Which Memory Task for My Mouse? A Systematic Review of Spatial Memory Performance in the Tg2576 Alzheimer's Mouse Model

Stewart, S., Cacucci, F., & Lever, C. (2011) · Journal of Alzheimer s Disease · doi:10.3233/jad-2011-101827 · Cited by 94 · see citing works

Hippocampal Lesions Impair Rapid Learning of a Continuous Spatial Alternation Task

Kim, S. M., & Frank, L. M. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005494 · Cited by 95 · see citing works

Fmr1 knockout mice show reduced anxiety and alterations in neurogenesis that are specific to the ventral dentate gyrus

Eadie, B. D., Zhang, W. N., Boehme, F., Gil‐Mohapel, J., Kainer, L., Simpson, J. M., & Christie, B. R. (2009) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.08.001 · Cited by 94 · see citing works

Inhibitory Control Deficits in Rats with Ventral Hippocampal Lesions

Abela, A. R., Dougherty, S. D., Fagen, E. D., Hill, C. J. R., & Chudasama, Y. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs121 · Cited by 94 · see citing works

Effects of ventral and dorsal CA1 subregional lesions on trace fear conditioning

Rogers, J. L., Hunsaker, M. R., & Kesner, R. P. (2006) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2006.01.002 · Cited by 95 · see citing works

Dorsal versus ventral hippocampal contributions to trace and contextual conditioning: Differential effects of regionally selective nmda receptor antagonism on acquisition and expression

Czerniawski, J. L., Ree, F., Chia, C., & Otto, T. (2011) · Hippocampus · doi:10.1002/hipo.20992 · Cited by 91 · see citing works

A stereological comparison of GAD67 and reelin expression in the hippocampal stratum oriens of offspring from two mouse models of maternal inflammation during pregnancy

Harvey, L., & Boksa, P. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.11.022 · Cited by 92 · see citing works

Topography of Arc/Arg3.1 mRNA Expression in the Dorsal and Ventral Hippocampus Induced by Recent and Remote Spatial Memory Recall: Dissociation of CA3 and CA1 Activation

Gusev, P. A., Cui, C., Alkon, D. L., & Gubin, A. N. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0832-05.2005 · Cited by 90 · see citing works

The Importance of Having Arc: Expression of the Immediate-Early Gene Arc Is Required for Hippocampus-Dependent Fear Conditioning and Blocked by NMDA Receptor Antagonism

Czerniawski, J. L., Ree, F., Chia, C., Ramamoorthi, K., Kumata, Y., & Otto, T. A. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2211-11.2011 · Cited by 91 · see citing works

Dorsal and ventral hippocampal adult-born neurons contribute to context fear memory

Huckleberry, K. A., Shue, F., Copeland, T., Chitwood, R. A., Yin, W., & Drew, M. R. (2018) · Neuropsychopharmacology · doi:10.1038/s41386-018-0109-6 · Cited by 91 · see citing works

Spatial memory tasks in rodents: what do they model?

Morellini, F. (2013) · Cell and Tissue Research · doi:10.1007/s00441-013-1668-9 · Cited by 90 · see citing works

Dissociating space and trace in dorsal and ventral hippocampus

Czerniawski, J. L., Yoon, T., & Otto, T. (2008) · Hippocampus · doi:10.1002/hipo.20469 · Cited by 90 · see citing works

Hippocampal and extrahippocampal systems compete for control of contextual fear: Role of ventral subiculum and amygdalaPreprint

Biedenkapp, J. C., & Rudy, J. W. (2008) · Learning & Memory · doi:10.1101/lm.1099109 · Cited by 89 · see citing works

Dentate gyrus and spatial behaviour

Xavier, G. F., & Costa, V. C. I. (2009) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2009.03.036 · Cited by 83 · see citing works

Molecular heterogeneity along the dorsal–ventral axis of the murine hippocampal CA1 field: a microarray analysis of gene expression

Leonardo, E. D., Richardson-Jones, J. W., Sibille, E. L., Kottman, A., & Hen, R. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.08.082 · Cited by 84 · see citing works

Regulation of corticosteroid receptors in the rat brain: the role of serotonin and stress

Robertson, D. A. F., Beattie, J., Reid, I., & Balfour, D. J. K. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.03990.x · Cited by 84 · see citing works

Age-dependent phenotypic characteristics of a triple transgenic mouse model of Alzheimer disease.

Pietropaolo, S., Feldon, J., & Yee, B. K. (2008) · Behavioral Neuroscience · doi:10.1037/a0012520 · Cited by 84 · see citing works

The role of the entorhinal cortex in two forms of spatial learning and memory

Bannerman, D. M., Yee, B. K., Lemaire, M., Wilbrecht, L., Jarrard, L. E., Iversen, S. D., Rawlins, J. N. P., & Good, M. A. (2001) · Experimental Brain Research · doi:10.1007/s002210100868 · Cited by 83 · see citing works

Interleukin-1β with learning and memory

Huang, Z., & Sheng, G. (2010) · Neuroscience Bulletin · doi:10.1007/s12264-010-6023-5 · Cited by 86 · see citing works

The Longitudinal Axis of the Hippocampal Formation: Its Anatomy, Circuitry, and Role in Cognitive Function

Small, S. A. (2002) · Reviews in the Neurosciences · doi:10.1515/revneuro.2002.13.2.183 · Cited by 82 · see citing works

Brain tissue oxygen amperometry in behaving rats demonstrates functional dissociation of dorsal and ventral hippocampus during spatial processing and anxiety

McHugh, S. B., Fillenz, M., Lowry, J. P., Rawlins, J. N. P., & Bannerman, D. M. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07497.x · Cited by 80 · see citing works

Hippocampal activation during retrieval of spatial context from episodic and semantic memory

Hoscheidt, S. M., Nadel, L., Payne, J. D., & Ryan, L. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.04.010 · Cited by 81 · see citing works

The role of the ventral dentate gyrus in anxiety-based behaviors

Weeden, C. S. S., Roberts, J. M., Kamm, A. M., & Kesner, R. P. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.12.002 · Cited by 80 · see citing works

How Many Ways Can Mouse Behavioral Experiments Go Wrong? Confounding Variables in Mouse Models of Neurodegenerative Diseases and How to Control Them

Schellinck, H. M., Cyr, D. P., & Brown, R. E. (2010) · Advances in the study of behavior · doi:10.1016/s0065-3454(10)41007-4 · Cited by 77 · see citing works

Double dissociation of function within the hippocampus: Spatial memory and hyponeophagia.

Bannerman, D. M., Deacon, R. M. J., Offen, S., Friswell, J., Grubb, M. S., & Rawlins, J. N. P. (2002) · Behavioral Neuroscience · doi:10.1037//0735-7044.116.5.884 · Cited by 357 · see citing works

Dissociation of function between the dorsal and the ventral hippocampus in spatial learning abilities of the rat: a within‐subject, within‐task comparison of reference and working spatial memory

Pothuizen, H. H. J., Zhang, W., Jongen‐Rêlo, A. L., Feldon, J., & Yee, B. K. (2004) · European Journal of Neuroscience · doi:10.1111/j.0953-816x.2004.03170.x · Cited by 274 · see citing works

Dorsal and ventral hippocampus: Same or different?

Ferbinteanu, J., & McDonald, R. J. (2000) · Psychobiology · doi:10.3758/bf03331990 · Cited by 42 · see citing works

Dissociation of Motor Hyperactivity and Spatial Memory Deficits by Selective Hippocampal Lesions in the Neonatal Rat

van Praag, H., Dreyfus, C. F., & Black, I. B. (1994) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1994.6.4.321 · Cited by 21 · see citing works

Dorsal and ventral hippocampal lesions and behavior

Nadel, L. (1968) · Physiology & Behavior · doi:10.1016/0031-9384(68)90174-1 · Cited by 249 · see citing works