Lesions in the dentate hilum and CA2/CA3 regions of the rat hippocampus produce cognitive deficits that correlate with site-specific glial activation

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

Physical basis of cognitive alterations in alzheimer's disease: Synapse loss is the major correlate of cognitive impairment

Terry, R. D., Masliah, E., Salmon, D. P., Butters, N., DeTeresa, R., Hill, R., Hansen, L. A., & Katzman, R. (1991) · Annals of Neurology · doi:10.1002/ana.410300410 · Cited by 4,397 · see citing works

Statistical Principles in Experimental Design

Green, P. E., Winer, B. J., Brown, D. R., & Michels, K. M. (1992) · Journal of Marketing Research · doi:10.2307/3172747 · Cited by 4,333 · see citing works

Differential contribution of amygdala and hippocampus to cued and contextual fear conditioning.

Phillips, R. G., & LeDoux, J. E. (1992) · Behavioral Neuroscience · doi:10.1037/0735-7044.106.2.274 · Cited by 3,292 · see citing works

Differential contribution of amygdala and hippocampus to cued and contextual fear conditioning.

Phillips, R. G., & LeDoux, J. E. (1992) · Behavioral Neuroscience · doi:10.1037//0735-7044.106.2.274 · Cited by 3,262 · see citing works

Alzheimer's disease: cell-specific pathology isolates the hippocampal formation.

Hyman, B. T., Van Hoesen, G. W., Damasio, A. R., & Barnes, C. L. (1984) · Science · doi:10.1126/science.6474172 · Cited by 2,268 · 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

Human amnesia and the medial temporal region: enduring memory impairment following a bilateral lesion limited to field CA1 of the hippocampus

Zola-Morgan, S., Squire, L., & Amaral, D. (1986) · The Journal of Neuroscience · doi:10.1523/jneurosci.06-10-02950.1986 · Cited by 1,997 · 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

Configural association theory: The role of the hippocampal formation in learning, memory, and amnesia

Sutherland, R. J., & Rudy, J. W. (1989) · Psychobiology · doi:10.3758/bf03337828 · 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

Perforant pathway changes and the memory impairment of Alzheimer's disease

Hyman, B. T., Van Hoesen, G. W., Kromer, L. J., & Damasio, A. R. (1986) · Annals of Neurology · doi:10.1002/ana.410200406 · Cited by 672 · see citing works

A behavioural analysis of spatial localization following electrolytic, kainate- or colchicine-induced damage to the hippocampal formation in the rat

Sutherland, R. J., Whishaw, I. Q., & Kolb, B. (1983) · Behavioural Brain Research · doi:10.1016/0166-4328(83)90188-2 · Cited by 592 · see citing works

The Human Hippocampus

Duvernoy, H. M., Cattin, F., & Risold, P. (2013) · Springer eBooks · doi:10.1007/978-3-642-33603-4 · Cited by 567 · see citing works

Lesions of the perirhinal and parahippocampal cortices in the monkey produce long-lasting memory impairment in the visual and tactual modalities

Suzuki, W., Zola-Morgan, S. M., Squire, L., & Amaral, D. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-06-02430.1993 · Cited by 543 · see citing works

The hippocampus and space revisited

Nadel, L. (1991) · Hippocampus · doi:10.1002/hipo.450010302 · Cited by 514 · 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

Hippocampal granule cells are necessary for normal spatial learning but not for spatially-selective pyramidal cell discharge

McNaughton, B. L., Barnes, C. A., Meltzer, J., & Sutherland, R. J. (1989) · Experimental Brain Research · doi:10.1007/bf00248904 · Cited by 388 · see citing works

The hippocampal formation is necessary for rats to learn and remember configural discriminations

Rudy, J. W., & Sutherland, R. J. (1989) · Behavioural Brain Research · doi:10.1016/s0166-4328(89)80093-2 · Cited by 375 · see citing works

Complementary roles of the orbital prefrontal cortex and the perirhinal-entorhinal cortices in an odor-guided delayed-nonmatching-to-sample task.

Otto, T., & Eichenbaum, H. (1992) · Behavioral Neuroscience · doi:10.1037/0735-7044.106.5.762 · Cited by 343 · see citing works

Complementary roles of the orbital prefrontal cortex and the perirhinal-entorhinal cortices in an odor-guided delayed-nonmatching-to-sample task.

Otto, T., & Eichenbaum, H. (1992) · Behavioral Neuroscience · doi:10.1037//0735-7044.106.5.762 · Cited by 317 · see citing works

What does the hippocampus really do?

Jarrard, L. E. (1995) · Behavioural Brain Research · doi:10.1016/0166-4328(95)00034-8 · Cited by 249 · see citing works

Hippocampal cell firing correlates of delayed-match-to-sample performance in the rat.

Hampson, R. E., Heyser, C. J., & Deadwyler, S. A. (1993) · Behavioral Neuroscience · doi:10.1037/0735-7044.107.5.715 · Cited by 194 · see citing works

Preserved configural learning and spatial learning impairment in rats with hippocampal damage

Gallagher, M., & Holland, P. C. (1992) · Hippocampus · doi:10.1002/hipo.450020111 · Cited by 192 · see citing works

Hippocampal lesions do not impair negative patterning: A challenge to configural association theory.

Davidson, T. L., McKernan, M. G., & Jarrard, L. E. (1993) · Behavioral Neuroscience · doi:10.1037//0735-7044.107.2.227 · Cited by 164 · see citing works

Critical determinants of nonspatial working memory deficits in rats with conventional lesions of the hippocampus or fornix.

Rawlins, J. N. P., Lyford, G. L., Seferiades, A., Deacon, R. M. J., & al, E. (1993) · Behavioral Neuroscience · doi:10.1037//0735-7044.107.3.420 · Cited by 158 · see citing works

Acquisition and retention by hippocampal rats of simple, conditional, and configural tasks using tactile and olfactory cues: Implications for hippocampal function.

Whishaw, I. Q., & Tomie, J.-A. (1991) · Behavioral Neuroscience · doi:10.1037//0735-7044.105.6.787 · Cited by 155 · see citing works

Hippocampal and amygdaloid involvement in working memory for nonspatial stimuli.

Raffaele, K. C., & Olton, D. S. (1988) · Behavioral Neuroscience · doi:10.1037//0735-7044.102.3.349 · Cited by 145 · see citing works

Hippocampal lesions do not impair negative patterning: A challenge to configural association theory.

Davidson, T. L., McKernan, M. G., & Jarrard, L. E. (1993) · Behavioral Neuroscience · doi:10.1037/0735-7044.107.2.227 · Cited by 139 · see citing works

Rats with damage to the hippocampal-formation are impaired on the transverse-patterning problem but not on elemental discriminations.

Alvarado, M. C., & Rudy, J. W. (1995) · Behavioral Neuroscience · doi:10.1037//0735-7044.109.2.204 · Cited by 138 · see citing works

Rats with damage to the hippocampal-formation are impaired on the transverse-patterning problem but not on elemental discriminations.

Alvarado, M. C., & Rudy, J. W. (1995) · Behavioral Neuroscience · doi:10.1037/0735-7044.109.2.204 · Cited by 138 · see citing works

Hippocampal and amygdaloid involvement in working memory for nonspatial stimuli.

Raffaele, K. C., & Olton, D. S. (1988) · Behavioral Neuroscience · doi:10.1037/0735-7044.102.3.349 · Cited by 135 · see citing works

Hippocampal mossy cell function: A speculative view

Buckmaster, P. S., & Schwartzkroin, P. A. (1994) · Hippocampus · doi:10.1002/hipo.450040402 · Cited by 127 · see citing works

Acquisition and retention by hippocampal rats of simple, conditional, and configural tasks using tactile and olfactory cues: Implications for hippocampal function.

Whishaw, I. Q., & Tomie, J.-A. (1991) · Behavioral Neuroscience · doi:10.1037/0735-7044.105.6.787 · Cited by 124 · see citing works

Critical determinants of nonspatial working memory deficits in rats with conventional lesions of the hippocampus or fornix.

Rawlins, J. N. P., Lyford, G. L., Seferiades, A., et al. (1993) · Behavioral Neuroscience · doi:10.1037/0735-7044.107.3.420 · Cited by 123 · see citing works

Hippocampal Function and Interference

(1994) · The MIT Press eBooks · doi:10.7551/mitpress/4545.003.0005 · Cited by 115 · see citing works

Hippocampal, granule cell and CA3–4 lesions impair formation of a place learning-set in the rat and induce reflex epilepsy

Whishaw, I. Q. (1987) · Behavioural Brain Research · doi:10.1016/0166-4328(87)90036-2 · Cited by 115 · see citing works

Hippocampal connectivity and Alzheimer's dementia

Samuel, W., Masliah, E., Hill, L., Butters, N., & Terry, R. D. (1994) · Neurology · doi:10.1212/wnl.44.11.2081 · Cited by 108 · see citing works

Variations in Synaptic Plasticity and Types of Memory in Corticohippocampal Networks

Lynch, G., & Granger, R. (1992) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1992.4.3.189 · Cited by 83 · see citing works

Perirhinal cortex lesions in rats disrupt performance in a spatial DNMS task

Wiig, K. A., & Bilkey, D. K. (1994) · Neuroreport · doi:10.1097/00001756-199406270-00028 · Cited by 78 · see citing works

Separable roles of hippocampal granule cells in forgetting and pyramidal cells in remembering spatial information

Collier, T. J., Quirk, G. J., & Routtenberg, A. (1987) · Brain Research · doi:10.1016/0006-8993(87)90717-7 · Cited by 57 · see citing works

Multiple Memory Systems: What and Why, an Update

(1994) · The MIT Press eBooks · doi:10.7551/mitpress/4545.003.0003 · Cited by 51 · see citing works

Lesions of supracallosal or infracallosal hippocampal pathways in the rat: Behavioral, neurochemical, and histochemical effects

Jeltsch‐David, H., Cassel, J., Jackisch, R., Neufang, B., Greene, P. L., Kelche, C. R., Hertting, G., & Will, B. E. (1994) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(05)80033-0 · Cited by 38 · see citing works

The Memory Coherence Problem, Configural Associations, and the Hippocampal System

(1994) · The MIT Press eBooks · doi:10.7551/mitpress/4545.003.0006 · Cited by 36 · see citing works

Spatial learning following posterior parietal or hippocampal lesions

McDaniel, W. F., Compton, D. M., & Smith, S. R. (1994) · Neuroreport · doi:10.1097/00001756-199409080-00006 · Cited by 34 · see citing works

Perirhinal cortex lesions in rats disrupt performance in a spatial DNMS task

Wiig, K. A., & Bilkey, D. K. (1994) · Neuroreport · doi:10.1097/00001756-199406000-00029 · Cited by 13 · see citing works

Non-spatial learning following posterior parietal or hippocampal lesions

Compton, D. M., McDaniel, W. F., & Dietrich, K. L. (1994) · Neuroreport · doi:10.1097/00001756-199410270-00050 · Cited by 10 · see citing works

Strong CA2 Pyramidal Neuron Synapses Define a Powerful Disynaptic Cortico-Hippocampal Loop

Chevaleyre, V., & Siegelbaum, S. A. (2010) · Neuron · doi:10.1016/j.neuron.2010.04.013 · Cited by 324 · see citing works

Dentate gyrus-selective colchicine lesion and disruption of performance in spatial tasks: Difficulties in ?place strategy? because of a lack of flexibility in the use of environmental cues?

Xavier, G. F., Oliveira-Filho, F. J. B., & Santos, A. M. G. (1999) · Hippocampus · doi:10.1002/(sici)1098-1063(1999)9:6 · Cited by 175 · see citing works

Cognitive performance and biochemical markers in septum, hippocampus and striatum of rats after an i.c.v. injection of streptozotocin: a correlation analysis

Prickaerts, J., Fahrig, T., & Blokland, A. (1999) · Behavioural Brain Research · doi:10.1016/s0166-4328(98)00158-2 · Cited by 106 · 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

Spatial learning deficits without hippocampal neuronal loss in a model of early-onset epilepsy

Lee, C. L., Hannay, H. J., Hrachovy, R. A., Rashid, S., Antalffy, B. A., & Swann, J. W. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00327-x · Cited by 80 · see citing works

Synaptic integration by different dendritic compartments of hippocampal CA1 and CA2 pyramidal neurons

Piskorowski, R. A., & Chevaleyre, V. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0769-4 · Cited by 65 · see citing works

Delayed non-matching to position performance in aged hybrid Fischer 344 × Brown Norway rats: a longitudinal study

Blokland, A., Şık, A., & van der Staay, F. J. (2004) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2004.04.017 · Cited by 10 · see citing works

Aging potentiates Aβ-induced depletion of SNAP-25 in mouse hippocampus

Chauhan, N. B., Lichtor, T., & Siegel, G. J. (2003) · Brain Research · doi:10.1016/s0006-8993(03)03011-7 · Cited by 8 · see citing works

Gene and Protein Expression and Regulation in the Central Nervous System

Kubin, L., Gozal, D., & Czyzyk-Krzeska, M. (2002) · CRC Press eBooks · doi:10.1201/9780203910504-11 · Cited by 3 · see citing works

Gene and Protein Expression and Regulation in the Central Nervous System

Kubin, L. K., Gozal, D., & Czyzyk-Krzeska, M. (2002) · Lung biology in health and disease · doi:10.1201/9780203910504.ch5 · Cited by 2 · see citing works

Synaptic integration by different dendritic compartments of hippocampal CA1 and CA2 pyramidal neurons

Ag, S. B. (2012)

Short-Term Plasticity at the Schaffer Collateral: A New Model with Implications for Hippocampal Processing

Toland, A. (2000) · doi:10.15760/etd.756

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

Astrocytes contribute to the functional differentiation of the hippocampal longitudinal axis during reward and aversion processing in the adult male rat

Rezagholizadeh, A., Shojaei, A., Hosseinmardi, N., Mirnajafi‐Zadeh, J., Kohlmeier, K. A., & Fathollahi, Y. (2024) · Neuroscience · doi:10.1016/j.neuroscience.2024.10.011

The effects of fimbria-fornix transection, bilateral knife cut of the temporal-hippocampal pathway, and adrenalectomy-induced hippocampal dentate granule cell loss on spatial learning in the rat.

Armstrong, J. A. (1994) · doi:10.22215/etd/1994-02870

Hippocampal dentate gyrus selective lesion and performance in temporal and spatial tasks

COSTA, V. M. D. M. (1997) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)

The CA3 subregion of the hippocampus is critical for episodic memory processing by means of relational encoding in rats.

Kesner, R. P., Hunsaker, M. R., & Warthen, M. W. (2008) · Behavioral Neuroscience · doi:10.1037/a0013592 · Cited by 100 · see citing works