On the role of hippocampal protein synthesis in the consolidation and reconsolidation of object recognition memory

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

AChE-stained horizontal sections of the rat brain in stereotaxic coordinates

Paxinos, G., WATSON, C. R. R., & Emson, P. C. (1980) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(80)90021-7 · Cited by 4,497 · see citing works

A new one-trial test for neurobiological studies of memory in rats. 1: behavioral data

Ennaceur, A., & Delacour, J. (1988) · Behavioural Brain Research · doi:10.1016/0166-4328(88)90157-x · Cited by 3,223 · see citing works

Fear memories require protein synthesis in the amygdala for reconsolidation after retrieval

Nader, K., Schafe, G. E., & Le Doux, J. E. (2000) · Nature · doi:10.1038/35021052 · Cited by 2,706 · see citing works

Time-Dependent Processes in Memory Storage: Recent studies of learning and memory indicate that memory storage involves time-dependent processes.

McGaugh, J. L. (1966) · Science · doi:10.1126/science.153.3742.1351 · Cited by 1,468 · see citing works

Retrograde amnesia and memory consolidation: a neurobiological perspective

Squire, L. R., & Alvarez, P. (1995) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(95)80023-9 · Cited by 1,412 · see citing works

Visual Object Recognition

Logothetis, N. K., & Sheinberg, D. L. (1996) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.19.030196.003045 · Cited by 1,360 · see citing works

Memory Reconsolidation and Extinction Have Distinct Temporal and Biochemical Signatures

Suzuki, A., Josselyn, S. A., Frankland, P. W., Masushige, S., Silva, A. J., & Kida, S. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.5491-03.2004 · Cited by 1,127 · see citing works

Retrieval and reconsolidation: Toward a neurobiology of remembering

Sara, S. J. (2000) · Learning & Memory · doi:10.1101/lm.7.2.73 · Cited by 919 · see citing works

Retrograde Amnesia Produced by Electroconvulsive Shock after Reactivation of a Consolidated Memory Trace

Misanin, J. R., Miller, R. R., & Lewis, D. J. (1968) · Science · doi:10.1126/science.160.3827.554 · Cited by 872 · see citing works

Independent cellular processes for hippocampal memory consolidation and reconsolidation

Lee, J. L. C., Everitt, B. J., & Thomas, K. L. (2004) · Science · doi:10.1126/science.1095760 · Cited by 825 · see citing works

Memory traces unbound

Nader, K. (2003) · Trends in Neurosciences · doi:10.1016/s0166-2236(02)00042-5 · Cited by 763 · see citing works

Cellular and Systems Reconsolidation in the Hippocampus

Dębiec, J., LeDoux, J. E., & Nader, K. (2002) · Neuron · doi:10.1016/s0896-6273(02)01001-2 · Cited by 758 · 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

Hippocampal damage and exploratory preferences in rats: memory for objects, places, and contexts

Mumby, D. G., Gaskin, S., Glenn, M. J., Schramek, T. E., & Lehmann, H. (2002) · Learning & Memory · doi:10.1101/lm.41302 · Cited by 714 · see citing works

Spontaneous object recognition and object location memory in rats: the effects of lesions in the cingulate cortices, the medial prefrontal cortex, the cingulum bundle and the fornix

Ennaceur, A., Neave, N., & Aggleton, J. P. (1997) · Experimental Brain Research · doi:10.1007/pl00005603 · Cited by 670 · see citing works

CREB required for the stability of new and reactivated fear memories

Kida, S., Josselyn, S. A., de Ortı́z, S. P., Kogan, J. H., Chévere-Torres, I., Masushige, S., & Silva, A. J. (2002) · Nature Neuroscience · doi:10.1038/nn819 · Cited by 624 · see citing works

The labile nature of consolidation theory

Nader, K., Schafe, G. E., & LeDoux, J. E. (2000) · Nature Reviews Neuroscience · doi:10.1038/35044580 · Cited by 613 · see citing works

Mechanisms of memory stabilization: are consolidation and reconsolidation similar or distinct processes?

Alberini, C. M. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2004.11.001 · Cited by 594 · see citing works

Double Dissociation between the Effects of Peri-Postrhinal Cortex and Hippocampal Lesions on Tests of Object Recognition and Spatial Memory: Heterogeneity of Function within the Temporal Lobe

Winters, B. D., Forwood, S., Cowell, R. A., Saksida, L. M., & Bussey, T. J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1346-04.2004 · Cited by 588 · see citing works

Stability of retrieved memory: Inverse correlation with trace dominance

Eisenberg, M., Kobilo, T., Berman, D. E., & Dudai, Y. (2003) · Science · doi:10.1126/science.1086881 · Cited by 518 · see citing works

Retrieval of memory in animals.

Spear, N. E. (1973) · Psychological Review · doi:10.1037/h0034326 · Cited by 505 · see citing works

Reconsolidation of memory after its reactivation

Przybyslawski, J., & Sara, S. J. (1997) · Behavioural Brain Research · doi:10.1016/s0166-4328(96)00153-2 · Cited by 493 · see citing works

Psychobiology of active and inactive memory.

Lewis, D. J. (1979) · Psychological Bulletin · doi:10.1037/0033-2909.86.5.1054 · Cited by 486 · see citing works

On the delay-dependent involvement of the hippocampus in object recognition memory

HAMMOND, R. (2004) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2004.03.005 · Cited by 476 · see citing works

Attenuation of Emotional and Nonemotional Memories after their Reactivation: Role of β Adrenergic Receptors

Przybyslawski, J., Roullet, P., & Sara, S. J. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-15-06623.1999 · Cited by 470 · see citing works

Temporally graded requirement for protein synthesis following memory reactivation

Milekic, M. H., & Alberini, C. M. (2002) · Neuron · doi:10.1016/s0896-6273(02)00976-5 · Cited by 455 · see citing works

Different molecular cascades in different sites of the brain control memory consolidation

Izquierdo, I., Bevilaqua, L. R., Rossato, J. I., Bonini, J. S., Medina, J. H., & Cammarota, M. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.07.005 · Cited by 452 · see citing works

Different Contributions of the Hippocampus and Perirhinal Cortex to Recognition Memory

Wan, H., Aggleton, J. P., & Brown, M. W. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-03-01142.1999 · Cited by 449 · see citing works

Protein Synthesis Subserves Reconsolidation or Extinction Depending on Reminder Duration

Pedreira, M. E., & Maldonado, H. (2003) · Neuron · doi:10.1016/s0896-6273(03)00352-0 · Cited by 406 · see citing works

Neural mechanisms of object recognition

Riesenhuber, M., & Poggio, T. (2002) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(02)00304-5 · Cited by 373 · see citing works

Mismatch Between What Is Expected and What Actually Occurs Triggers Memory Reconsolidation or Extinction

Pedreira, M. E., Pérez-Cuesta, L. M., & Maldonado, H. (2004) · Learning & Memory · doi:10.1101/lm.76904 · Cited by 367 · see citing works

Activation of Mitogen-Activated Protein Kinase/Extracellular Signal-Regulated Kinase in Hippocampal Circuitry Is Required for Consolidation and Reconsolidation of Recognition Memory

Kelly, A. M., Laroche, S., & Davis, S. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-12-05354.2003 · Cited by 361 · see citing works

Reconsolidation: the advantage of being refocused

Dudai, Y. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.03.010 · Cited by 357 · see citing works

Perspectives on object-recognition memory following hippocampal damage: lessons from studies in rats

Mumby, D. G. (2001) · Behavioural Brain Research · doi:10.1016/s0166-4328(01)00367-9 · Cited by 356 · see citing works

Neurotoxic lesions of the perirhinal cortex do not mimic the behavioural effects of fornix transection in the rat

Ennaceur, A., Neave, N., & Aggleton, J. P. (1996) · Behavioural Brain Research · doi:10.1016/0166-4328(96)00006-x · Cited by 351 · see citing works

A Requirement for the Immediate Early Gene zif268 in Reconsolidation of Recognition Memory after Retrieval

Bozon, B., Davis, S., & Laroche, S. (2003) · Neuron · doi:10.1016/s0896-6273(03)00674-3 · Cited by 317 · see citing works

Two Time Periods of Hippocampal mRNA Synthesis Are Required for Memory Consolidation of Fear-Motivated Learning

Igaz, L. M., Vianna, M. R. M. R., Medina, J. H., & Izquierdo, I. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-15-06781.2002 · Cited by 305 · see citing works

Effects of Visual Experience on the Representation of Objects in the Prefrontal Cortex

Rainer, G., & Miller, E. K. (2000) · Neuron · doi:10.1016/s0896-6273(00)00019-2 · Cited by 285 · see citing works

Ventromedial Prefrontal Cortex Is Obligatory for Consolidation and Reconsolidation of Object Recognition Memory

Akirav, I., & Maroun, M. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhj114 · Cited by 240 · see citing works

Interaction between Perirhinal and Medial Prefrontal Cortex Is Required for Temporal Order But Not Recognition Memory for Objects in Rats

Hannesson, D. K., Howland, J. G., & Phillips, A. G. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.5517-03.2004 · Cited by 231 · see citing works

Behavioral impairments caused by injections of the protein synthesis inhibitor anisomycin after contextual retrieval reverse with time

Lattal, K. M., & Abel, T. G. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0306546101 · Cited by 220 · see citing works

Reactivation and Reconsolidation of Long-Term Memory in the CrabChasmagnathus: Protein Synthesis Requirement and Mediation by NMDA-Type Glutamatergic Receptors

Pedreira, M. E., Pérez-Cuesta, L. M., & Maldonado, H. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-18-08305.2002 · Cited by 213 · see citing works

Reconsolidation of fresh, remote, and extinguished fear memory in medaka: old fears don't die

Eisenberg, M., & Dudai, Y. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03818.x · Cited by 204 · see citing works

Two sensitive periods for the amnesic effect of anisomycin

Grecksch, G., & Matthies, H. (1980) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(80)90145-8 · Cited by 194 · see citing works

Retrograde Amnesia for Old (Reactivated) Memory: Some Anomalous Characteristics

Mactutus, C. F., Riccio, D. C., & Ferek, J. M. (1979) · Science · doi:10.1126/science.572083 · Cited by 193 · see citing works

Retrograde and anterograde object recognition in rats with hippocampal lesions

Gaskin, S., Tremblay, A., & Mumby, D. G. (2003) · Hippocampus · doi:10.1002/hipo.10154 · Cited by 160 · see citing works

Anisomycin infused into the hippocampus fails to block “reconsolidation” but impairs extinction: The role of re-exposure durationPreprint

Power, A. E., Berlau, D. J., McGaugh, J. L., & Steward, O. (2006) · Learning & Memory · doi:10.1101/lm.91206 · Cited by 159 · see citing works

Contrasting Hippocampal and Perirhinalcortex Function using Immediate Early Gene Imaging

Aggleton, J. P., & Brown, M. W. (2005) · The Quarterly Journal of Experimental Psychology Section B · doi:10.1080/02724990444000131 · Cited by 158 · see citing works

Two Time Windows of Anisomycin-Induced Amnesia for Passive Avoidance Training in the Day-Old Chick

Freeman, F., Rose, S. P. R., & Scholey, A. B. (1995) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1995.1034 · Cited by 155 · see citing works

Characteristics of retrograde amnesia following reactivation of memory in mice

Judge, M. E., & Quartermain, D. (1982) · Physiology & Behavior · doi:10.1016/0031-9384(82)90034-8 · Cited by 145 · see citing works

Spontaneous Recovery from Extinction Depends on the Reconsolidation of the Acquisition Memory in an Appetitive Learning Paradigm in the Honeybee ( Apis mellifera )

Stollhoff, N., Menzel, R., & Eisenhardt, D. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0117-05.2005 · Cited by 126 · see citing works

Retrieval Does Not Induce Reconsolidation of Inhibitory Avoidance MemoryPreprint

Cammarota, M., Bevilaqua, L. R., Medina, J. H., & Izquierdo, I. (2004) · Learning & Memory · doi:10.1101/lm.76804 · Cited by 124 · see citing works

Retrieval induces hippocampal-dependent reconsolidation of spatial memoryPreprint

Rossato, J. I., Bevilaqua, L. R., Medina, J. H., Izquierdo, I., & Cammarota, M. (2006) · Learning & Memory · doi:10.1101/lm.315206 · Cited by 123 · see citing works

Spontaneous recognition of object configurations in rats: effects of fornix lesions

Ennaceur, A., & Aggleton, J. P. (1994) · Experimental Brain Research · doi:10.1007/bf00227281 · Cited by 121 · see citing works

Long-term memory for instrumental responses does not undergo protein synthesis-dependent reconsolidation upon retrievalPreprint

Hernandez, P. J., & Kelley, A. E. (2004) · Learning & Memory · doi:10.1101/lm.84904 · Cited by 120 · see citing works

Dissociation in retrograde memory for object discriminations and object recognition in rats with perirhinal cortex damage

Mumby, D. G., Glenn, M. J., Nesbitt, C., & Kyriazis, D. A. (2002) · Behavioural Brain Research · doi:10.1016/s0166-4328(01)00444-2 · Cited by 120 · see citing works

Phosphorylated cAMP Response Element-Binding Protein as a Molecular Marker of Memory Processing in Rat Hippocampus: Effect of Novelty

Viola, H., Furman, M., Izquierdo, L. A., Alonso, M., Barros, D. M., de Souza, M. M., Izquierdo, I., & Medina, J. H. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-23-j0002.2000 · Cited by 119 · see citing works

Protein synthesis underlies post-retrieval memory consolidation to a restricted degree only when updated information is obtainedPreprint

Rodríguez‐Ortiz, C. J., la Cruz, V. D., Gutiérrez, R., & Bermúdez‐Rattoni, F. (2005) · Learning & Memory · doi:10.1101/lm.94505 · Cited by 117 · see citing works

Medial prefrontal cortex is involved in spatial temporal order memory but not spatial recognition memory in tests relying on spontaneous exploration in rats

Hannesson, D. K., Vacca, G., Howland, J. G., & Phillips, A. G. (2004) · Behavioural Brain Research · doi:10.1016/j.bbr.2003.12.004 · Cited by 115 · see citing works

Context memories and reactivation: constraints on the reconsolidation hypothesis.

Biedenkapp, J., & Rudy, J. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.5.956 · Cited by 115 · see citing works

Extinction Requires New RNA and Protein Synthesis and the Soma of the Cell Right Pedal Dorsal 1 inLymnaea stagnalis

Sangha, S., Scheibenstock, A., Morrow, R., & Lukowiak, K. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-30-09842.2003 · Cited by 109 · see citing works

Long‐ but not medium‐term retention of olfactory memories in honeybees is impaired by actinomycin D and anisomycin

Wüstenberg, D., Gerber, B., & Menzel, R. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00319.x · Cited by 105 · see citing works

Activation of the transcription factor NF-κB by retrieval is required for long-term memory reconsolidationPreprint

Merlo, E., Freudenthal, R., Maldonado, H., & Romano, A. G. (2005) · Learning & Memory · doi:10.1101/lm.82705 · Cited by 104 · see citing works

Acquisition, Consolidation, Reconsolidation, and Extinction of Eyelid Conditioning Responses RequireDe NovoProtein Synthesis

Inda, M. C., Delgado-Garcia, J. M., & Carrión, Á. M. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4163-04.2005 · Cited by 101 · see citing works

Paradoxical Facilitation of Object Recognition Memory after Infusion of Scopolamine into Perirhinal Cortex: Implications for Cholinergic System Function

Winters, B. D., Saksida, L. M., & Bussey, T. J. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2319-06.2006 · Cited by 97 · see citing works

Prolonged Habituation of the Gill-Withdrawal Reflex inAplysiaDepends on Protein Synthesis, Protein Phosphatase Activity, and Postsynaptic Glutamate Receptors

Ezzeddine, Y., & Glanzman, D. L. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-29-09585.2003 · Cited by 86 · see citing works

Neuronal Responses Related to Long-Term Recognition Memory Processes in Prefrontal Cortex

Xiang, J.-Z., & Brown, M. W. (2004) · Neuron · doi:10.1016/j.neuron.2004.05.013 · Cited by 86 · see citing works

Inhibition of mRNA and Protein Synthesis in the CA1 Region of the Dorsal Hippocampus Blocks Reinstallment of an Extinguished Conditioned Fear Response

Cammarota, M., Bevilaqua, L., Kerr, D., Medina, J., & Izquierdo, I. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-03-00737.2003 · Cited by 85 · see citing works

Electroconvulsive Shock Effects on a Reactivated Memory Trace: Further Examination

Dawson, R. G., & McGaugh, J. L. (1969) · Science · doi:10.1126/science.166.3904.525 · Cited by 85 · see citing works

Cue-dependent amnesia in rats.

Lewis, D. J., Bregman, N. J., & Mahan, J. J. (1972) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0033524 · Cited by 84 · see citing works

Memory consolidation induces N-methyl-d-aspartic acid-receptor- and Ca2+/calmodulin-dependent protein kinase II-dependent modifications in α-amino-3-hydroxy-5-methylisoxazole-4-propionic acid receptor properties

Bevilaqua, L. R., Medina, J. H., Izquierdo, I., & Cammarota, M. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.08.007 · Cited by 69 · see citing works

Phosphorylation state of CREB in the rat hippocampus: A molecular switch between spatial novelty and spatial familiarity?

Moncada, D., & Viola, H. (2006) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2005.12.002 · Cited by 65 · see citing works

Reconsolidation of a context long-term memory in the terrestrial snail requires protein synthesisPreprint

Халиловна, Г. Т., Rr, T., Ismailova, A. I., Николаевна, М. Л., Samarova, E. I., Латыпович, Г. Х., & Balaban, P. M. (2005) · Learning & Memory · doi:10.1101/lm.25705 · Cited by 61 · see citing works

Post-retrieval effects of icv infusions of hemicholinium in mice are dependent on the age of the original memoryPreprint

Boccia, M. M., Blake, M. G., Acosta, G. B., & Baratti, C. M. (2006) · Learning & Memory · doi:10.1101/lm.150306 · Cited by 58 · see citing works

Inhibition of protein synthesis blocks long-term enhancement of generator potentials produced by one-trial in vivo conditioning in Hermissenda.

Crow, T., & Forrester, J. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.12.4490 · Cited by 57 · see citing works

Systems-Level Reconsolidation

Myers, K. M., & Davis, M. (2002) · Neuron · doi:10.1016/s0896-6273(02)01017-6 · Cited by 57 · see citing works

Reactivation of recent or remote memory before electroconvulsive therapy does not produce retrograde amnesia

Squire, L. R., Slater, P. C., & Chace, P. M. (1976) · Behavioral Biology · doi:10.1016/s0091-6773(76)92295-1 · Cited by 47 · see citing works

Detection of novelty, but not memory of spatial habituation, is associated with an increase in phosphorylated cAMP response element‐binding protein levels in the hippocampus

Winograd, M., & Viola, H. (2003) · Hippocampus · doi:10.1002/hipo.10153 · Cited by 46 · see citing works

Time windows for effects of protein synthesis inhibitors on Pavlovian conditioning in Hermissenda: Behavioral aspects

Epstein, H. T., Child, F. M., Kuzirian, A. M., et al. (2003) · Neurobiology of Learning and Memory · doi:10.1016/s1074-7427(02)00020-5 · Cited by 41 · see citing works

Pharmacological dissociation of memory: Anisomycin, a protein synthesis inhibitor, and leupeptin, a protease inhibitor, block different learning tasks

Staubli, U. V., Faraday, R., & LYNCH, G. S. (1985) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(85)91632-2 · Cited by 33 · see citing works

Effects of cycloheximide and puromycin on learning and retention in the cockroach, P. americana

Barraco, D. (1981) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(81)90282-3 · Cited by 28 · see citing works

Protein synthesis-dependent memory and neuronal enhancement in Hermissenda are contingent on parameters of training and retention.Preprint

Ramírez, R. R., Gandhi, C. C., Muzzio, I. A., & Matzel, L. D. (1998) · Learning & Memory · doi:10.1101/lm.4.6.462 · Cited by 24 · see citing works

Memory formation for an appetitive visual discrimination task in young chicks

Gibbs, M. E., & Ng, K. (1978) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(78)90315-5 · Cited by 21 · see citing works

Cue-dependent amnesia: Permanence and Memory Return☆

Bregman, N. J., Nicholas, T. W., & Lewis, D. A. (1976) · Physiology & Behavior · doi:10.1016/0031-9384(76)90075-5 · Cited by 11 · see citing works

Reconsolidation: maintaining memory relevance

Lee, J. L. C. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2009.05.002 · Cited by 516 · 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

Plastic modifications induced by object recognition memory processing

Clarke, J. R., Cammarota, M., Gruart, A., Izquierdo, I., & Delgado-García, J. M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0915059107 · Cited by 273 · see citing works

The consolidation of object and context recognition memory involve different regions of the temporal lobe

Balderas, I., Rodriguez-Ortiz, C. J., Salgado-Tonda, P., Chavez-Hurtado, J., McGaugh, J. L., & Bermudez-Rattoni, F. (2008) · Learning & Memory · doi:10.1101/lm.1028008 · Cited by 213 · see citing works

HDAC inhibition modulates hippocampus-dependent long-term memory for object location in a CBP-dependent manner

Haettig, J., Stefanko, D. P., Multani, M. L., Figueroa, D. X., McQuown, S. C., & Wood, M. A. (2011) · Learning & Memory · doi:10.1101/lm.1986911 · Cited by 211 · see citing works

The hippocampus is crucial for forming non-hippocampal long-term memory during sleep

Sawangjit, A., Oyanedel, C. N., Niethard, N., Salazar, C., Born, J., & Inostroza, M. (2018) · Nature · doi:10.1038/s41586-018-0716-8 · Cited by 208 · see citing works

The role of metaplasticity mechanisms in regulating memory destabilization and reconsolidation

Finnie, P. S. B., & Nader, K. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.03.008 · Cited by 189 · see citing works

Caloric restriction increases learning consolidation and facilitates synaptic plasticity through mechanisms dependent on NR2B subunits of the NMDA receptor

Fontán-Lozano, Á., Sáez-Cassanelli, J. L., Inda, M. C., de los Santos-Arteaga, M., Sierra-Domínguez, S. A., López-Lluch, G., Delgado-García, J. M., & Carrión, Á. M. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.2757-07.2007 · Cited by 195 · see citing works

Distinct contributions of the hippocampus and medial prefrontal cortex to the “what–where–when” components of episodic-like memory in mice

DeVito, L. M., & Eichenbaum, H. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.09.014 · Cited by 164 · 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

Adolescent exposure to nicotine and/or the cannabinoid agonist CP 55,940 induces gender-dependent long-lasting memory impairments and changes in brain nicotinic and CB ₁ cannabinoid receptors

Mateos, B., Borcel, E., Loriga, R., Luesu, W., Bini, V, Llorente, R., Castelli, M., & Viveros, M.-P. (2011) · Journal of Psychopharmacology · doi:10.1177/0269881110370503 · Cited by 108 · see citing works

Posttraining activation of CB1 cannabinoid receptors in the CA1 region of the dorsal hippocampus impairs object recognition long-term memory

Clarke, J. R., Rossato, J. I., Monteiro, S., Bevilaqua, L. R. M., Izquierdo, I., & Cammarota, M. (2008) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2008.04.009 · Cited by 97 · see citing works

Brain networks activated to form object recognition memory

Tanimizu, T., Kono, K., & Kida, S. (2018) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2017.05.017 · Cited by 81 · see citing works

Nuclear Factor κB-Dependent Histone Acetylation is Specifically Involved in Persistent Forms of Memory

Federman, N., de la Fuente, V., Zalcman, G., Corbi, N., Onori, A., Passananti, C., & Romano, A. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.4181-12.2013 · Cited by 73 · see citing works

β‐Adrenergic receptors link NO/sGC/PKG signaling to BDNF expression during the consolidation of object recognition long‐term memory

Furini, C. R., Rossato, J. I., Bitencourt, L. L., Medina, J. H., Izquierdo, I., & Cammarota, M. (2010) · Hippocampus · doi:10.1002/hipo.20656 · Cited by 72 · see citing works

A mismatch-based model for memory reconsolidation and extinction in attractor networks

Osan, R., Tort, A. B. L., & Amaral, O. B. (2011) · PLoS ONE · doi:10.1371/journal.pone.0023113 · Cited by 63 · see citing works

Spatiotemporally resolved protein synthesis as a molecular framework for memory consolidation

Shrestha, P., & Klann, E. (2022) · Trends in Neurosciences · doi:10.1016/j.tins.2022.01.004 · Cited by 54 · see citing works

GluN1 and GluN2A NMDA receptor subunits increase in the hippocampus during memory consolidation in the Rat

Cercato, M. C., Vázquez, C. A., Kornisiuk, E., Aguirre, A. I., Colettis, N., Snitcofsky, M., Jerusalinsky, D. A., & Baez, M. V. (2017) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2016.00242 · Cited by 55 · see citing works

Nicotinic receptor activation in perirhinal cortex and hippocampus enhances object memory in rats

Melichercik, A. M., Elliott, K. S., Bianchi, C., Ernst, S. M., & Winters, B. D. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.01.008 · Cited by 54 · see citing works

State-dependent effect of dopamine D1/D5 receptors inactivation on memory destabilization and reconsolidation

Rossato, J. I., Köhler, C. A., Radiske, A., Lima, R. H., Bevilaqua, L. R. M., & Cammarota, M. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.09.009 · Cited by 48 · see citing works

Infusion of protein synthesis inhibitors in the entorhinal cortex blocks consolidation but not reconsolidation of object recognition memory

Lima, R. H., Rossato, J. I., Furini, C. R., Bevilaqua, L. R., Izquierdo, I., & Cammarota, M. (2009) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2008.12.009 · Cited by 49 · see citing works

Evidence of VTA and LC control of protein synthesis required for the behavioral tagging process

Moncada, D. (2017) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.06.003 · Cited by 50 · see citing works

Dopamine D1 receptor activity modulates object recognition memory consolidation in the perirhinal cortex but not in the hippocampus

Balderas, I., Moreno‐Castilla, P., & Bermudez‐Rattoni, F. (2013) · Hippocampus · doi:10.1002/hipo.22143 · Cited by 46 · see citing works

Distinct roles of the hippocampus and perirhinal cortex in GABAA receptor blockade-induced enhancement of object recognition memory

Kim, J. M., Kim, D. H., Lee, Y., Park, S. J., & Ryu, J. H. (2014) · Brain Research · doi:10.1016/j.brainres.2014.01.024 · Cited by 35 · see citing works

Hippocampal NMDA receptors are involved in rats’ spontaneous object recognition only under high memory load condition

Sugita, M., Yamada, K., Iguchi, N., & Ichitani, Y. (2015) · Brain Research · doi:10.1016/j.brainres.2015.08.001 · Cited by 14 · see citing works

Reactivation with a simple exposure to the experimental environment is sufficient to induce reconsolidation requiring protein synthesis in the hippocampal CA3 region in mice

Artinian, J., Jaeger, X. D., Fellini, L., Blanquat, P. D. S., & Roullet, P. (2007) · Hippocampus · doi:10.1002/hipo.20256 · Cited by 41 · see citing works

Cellular and Systems Reconsolidation in the Hippocampus

Dębiec, J., LeDoux, J. E., & Nader, K. (2002) · Neuron · doi:10.1016/s0896-6273(02)01001-2 · Cited by 758 · see citing works

Inhibition of prefrontal protein synthesis following recall does not disrupt memory for trace fear conditioning

Blum, S., Runyan, J. D., & Dash, P. K. (2006) · BMC Neuroscience · doi:10.1186/1471-2202-7-67 · Cited by 39 · see citing works

State-dependent effect of dopamine D1/D5 receptors inactivation on memory destabilization and reconsolidation

Rossato, J. I., Köhler, C. A., Radiske, A., Lima, R. H., Bevilaqua, L. R. M., & Cammarota, M. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.09.009 · Cited by 48 · see citing works

Faculty Opinions recommendation of Cellular and systems reconsolidation in the hippocampus.

Giese, K.-P. (2002) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1002838.152907