Synaptic tagging: implications for late maintenance of hippocampal long-term potentiation

A synaptic model of memory: long-term potentiation in the hippocampus

Bliss, T. V. P., & Collingridge, G. L. (1993) · Nature · doi:10.1038/361031a0 · Cited by 11,566 · see citing works

Untitled work

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

Long‐lasting potentiation of synaptic transmission in the dentate area of the unanaesthetized rabbit following stimulation of the perforant path

Bliss, T. V. P., & Gardner-Medwin, A. R. (1973) · The Journal of Physiology · doi:10.1113/jphysiol.1973.sp010274 · Cited by 7,460 · see citing works

The hippocampus as a cognitive map

Passingham, R. E. (1979) · Neuroscience · doi:10.1016/0306-4522(79)90015-0 · Cited by 5,128 · see citing works

Memory consolidation, retrograde amnesia and the hippocampal complex

Nadel, L., & Moscovitch, M. (1997) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(97)80010-4 · Cited by 1,924 · see citing works

Phasic versus tonic dopamine release and the modulation of dopamine system responsivity: A hypothesis for the etiology of schizophrenia

Grace, A. A. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90196-u · Cited by 1,831 · see citing works

Metaplasticity: the plasticity of synaptic plasticity

Abraham, W. C., & Bear, M. F. (1996) · Trends in Neurosciences · doi:10.1016/s0166-2236(96)80018-x · Cited by 1,783 · see citing works

Synaptic tagging and long-term potentiation

Frey, U., & Morris, R. G. M. (1997) · Nature · doi:10.1038/385533a0 · Cited by 1,736 · see citing works

Activation of postsynaptically silent synapses during pairing-induced LTP in CA1 region of hippocampal slice

Liao, D., Hessler, N. A., & Malinow, R. (1995) · Nature · doi:10.1038/375400a0 · Cited by 1,365 · see citing works

Evidence for silent synapses: Implications for the expression of LTP

Isaac, J. T. R., Nicoll, R. A., & Malenka, R. C. (1995) · Neuron · doi:10.1016/0896-6273(95)90046-2 · Cited by 1,233 · see citing works

Effects of cAMP simulate a late stage of LTP in hippocampal CA1 neurons

Frey, U., Huang, Y.-Y., & Kandel, E. R. (1993) · Science · doi:10.1126/science.8389057 · Cited by 1,218 · see citing works

Genetic Demonstration of a Role for PKA in the Late Phase of LTP and in Hippocampus-Based Long-Term Memory

Abel, T., Nguyen, P. V., Barad, M., Deuel, T. A. S., Kandel, E. R., & Bourtchouladze, R. (1997) · Cell · doi:10.1016/s0092-8674(00)81904-2 · Cited by 1,217 · see citing works

Arc, a growth factor and activity-regulated gene, encodes a novel cytoskeleton-associated protein that is enriched in neuronal dendrites

Lyford, G. L., Yamagata, K., Kaufmann, W. E., Barnes, C. A., Sanders, L. K., Copeland, N. G., Gilbert, D. J., Jenkins, N. A., Lanahan, A. A., & Worley, P. F. (1995) · Neuron · doi:10.1016/0896-6273(95)90299-6 · Cited by 1,212 · see citing works

Cloning of the gene for a human dopamine D5 receptor with higher affinity for dopamine than D1

Sunahara, R. K., Guan, H., O’Dowd, B. F., Seeman, P. M., Laurier, L. G., Ng, G., George, S. R., Torchia, J., Tol, H. H. M. V., & Niznik, H. B. (1991) · Nature · doi:10.1038/350614a0 · Cited by 1,166 · see citing works

The Structure and Organization of Memory

Squire, L. R., Knowlton, B. J., & Musen, G. (1993) · Annual Review of Psychology · doi:10.1146/annurev.ps.44.020193.002321 · Cited by 1,121 · see citing works

The long and the short of long–term memory—a molecular framework

Goelet, P., Castellucci, V. F., Schacher, S., & Kandel, E. R. (1986) · Nature · doi:10.1038/322419a0 · Cited by 1,034 · see citing works

A Requirement for Local Protein Synthesis in Neurotrophin-Induced Hippocampal Synaptic Plasticity

Kang, H., & Schuman, E. (1996) · Science · doi:10.1126/science.273.5280.1402 · Cited by 1,010 · see citing works

Requirement of a Critical Period of Transcription for Induction of a Late Phase of LTP

Nguyen, P. V., Abel, T., & Kandel, E. R. (1994) · Science · doi:10.1126/science.8066450 · Cited by 888 · see citing works

Anisomycin, an inhibitor of protein synthesis, blocks late phases of LTP phenomena in the hippocampal CA1 region in vitro

Frey, U., Krug, M., Reymann, K. G., & Matthies, H. (1988) · Brain Research · doi:10.1016/0006-8993(88)90008-x · Cited by 806 · see citing works

Somatodendritic expression of an immediate early gene is regulated by synaptic activity.

Link, W., Konietzko, U., Kauselmann, G., Krug, M., Schwanke, B., Frey, U., & Kuhl, D. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.12.5734 · Cited by 706 · see citing works

Signaling from synapse to nucleus: postsynaptic CREB phosphorylation during multiple forms of hippocampal synaptic plasticity

Deisseroth, K., Bito, H., & Tsien, R. W. (1996) · Neuron · doi:10.1016/s0896-6273(00)80026-4 · Cited by 698 · see citing works

D1/D5 receptor agonists induce a protein synthesis-dependent late potentiation in the CA1 region of the hippocampus.

Huang, Y.-Y., & Kandel, E. R. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.7.2446 · Cited by 544 · see citing works

Anisomycin blocks the late phase of long-term potentiation in the dentate gyrus of freely moving rats

Krug, M., Lössner, B., & Ott, T. (1984) · Brain Research Bulletin · doi:10.1016/0361-9230(84)90005-4 · Cited by 509 · see citing works

NMDA application potentiates synaptic transmission in the hippocampus

Kauer, J. A., Malenka, R. C., & Nicoll, R. A. (1988) · Nature · doi:10.1038/334250a0 · Cited by 423 · see citing works

Neuronal plasticity and memory formation

Marsan, C. A., Matthies, H., & Formation, M. (1982) · Raven Press eBooks · Cited by 415 · see citing works

Hippocampal synaptic plasticity: role in spatial learning or the automatic recording of attended experience?

Morris, R., & Frey, U. (1997) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.1997.0136 · Cited by 366 · see citing works

Blockade of long-term potentiation in rat hippocampal CA1 region by inhibitors of protein synthesis

Stanton, P. K., & Sarvey, J. M. (1984) · Journal of Neuroscience · doi:10.1523/jneurosci.04-12-03080.1984 · Cited by 349 · see citing works

Dopaminergic antagonists prevent long-term maintenance of posttetanic LTP in the CA1 region of rat hippocampal slices

Frey, U., Schroeder, H., & Matthies, H. (1990) · Brain Research · doi:10.1016/0006-8993(90)91578-5 · Cited by 333 · see citing works

Depletion of norepinephrine, but not serotonin, reduces long-term potentiation in the dentate gyrus of rat hippocampal slices

Stanton, P. K., & Sarvey, J. M. (1985) · Journal of Neuroscience · doi:10.1523/jneurosci.05-08-02169.1985 · Cited by 314 · see citing works

The effect of dopaminergic D1 receptor blockade during tetanization on the expression of long-term potentiation in the rat CA1 region in vitro

Frey, U., Matthies, H., Reymann, K. G., & Matthies, H. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90732-9 · Cited by 314 · see citing works

Reduction of long‐term potentiation in the dentate gyrus of the rat following selective depletion of monoamines.

Bliss, T. V. P., Goddard, G. V., & Riives, M. L. (1983) · The Journal of Physiology · doi:10.1113/jphysiol.1983.sp014507 · Cited by 293 · see citing works

Maintenance of long-term potentiation in rat dentate gyrus requires protein synthesis but not messenger RNA synthesis immediately post-tetanization

Otani, S., Marshall, C. J., Tate, W. P., Goddard, G. V., & Abraham, W. C. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90001-8 · Cited by 274 · see citing works

Influence of actinomycin D, a RNA synthesis inhibitor, on long‐term potentiation in rat hippocampal neurons in vivo and in vitro.

Frey, U., Frey, S., Schollmeier, F., & Krug, M. (1996) · The Journal of Physiology · doi:10.1113/jphysiol.1996.sp021179 · Cited by 273 · see citing works

cAMP Evokes Long-Term Facilitation in Aplysia Sensory Neurons That Requires New Protein Synthesis

Schacher, S., Castellucci, V. F., & Kandel, E. R. (1988) · Science · doi:10.1126/science.2454509 · Cited by 260 · see citing works

Frequency-Dependent Noradrenergic Modulation of Long-Term Potentiation in the Hippocampus

Hopkins, W. F., & Johnston, D. (1984) · Science · doi:10.1126/science.6091272 · Cited by 256 · see citing works

NMDA Receptor Activation Increases Cyclic AMP in Area CA1 of the Hippocampus via Calcium/Calmodulin Stimulation of Adenylyl Cyclase

Chetkovich, D. M., & Sweatt, J. D. (1993) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1993.tb09836.x · Cited by 212 · see citing works

Long‐lasting facilitation of excitatory postsynaptic potentials in the rat hippocampus by acetylcholine.

Markram, H., & Segal, M. (1990) · The Journal of Physiology · doi:10.1113/jphysiol.1990.sp018177 · Cited by 197 · see citing works

Protein Synthesis within Dendrites: Glycosylation of Newly Synthesized Proteins in Dendrites of Hippocampal Neurons in Culture

Torre, E. R., & Steward, O. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-19-05967.1996 · Cited by 191 · see citing works

Spatial and temporal changes in signal transduction pathways during LTP

Thomas, K. L., Laroche, S., Errington, M. L., Bliss, T. V. P., & Hunt, S. P. (1994) · Neuron · doi:10.1016/0896-6273(94)90040-x · Cited by 182 · see citing works

Protein synthesis-dependent formation of protein kinase Mzeta in long- term potentiation

Osten, P., Valsamis, L., Harris, A. Z., & Sacktor, T. C. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-08-02444.1996 · Cited by 173 · see citing works

Factors regulating the reversibility of long-term potentiation

Staubli, U., & Chun, D. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-02-00853.1996 · Cited by 169 · see citing works

A post-tetanic time window for the reinforcement of long-term potentiation by appetitive and aversive stimuli

Seidenbecher, T., Reymann, K. G., & Balschun, D. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.4.1494 · Cited by 154 · see citing works

Neuronal Activity Increases the Phosphorylation of the Transcription Factor cAMP Response Element-binding Protein (CREB) in Rat Hippocampus and Cortex

Moore, A. N., Waxham, M. N., & Dash, P. K. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.24.14214 · Cited by 144 · see citing works

Long-lasting potentiation of synaptic transmission in the dentate area of the anaesthetized rabbit following stimulation of the perforant path

Bliss, T. V. P., & Lømo, T. (1973) · The Journal of Physiology · doi:10.1113/jphysiol.1973.sp010273 · Cited by 135 · see citing works

The effect of high-frequency electrical stimulation and norepinephrine on cyclic AMP levels in normal versus norepinephrine-depleted rat hippocampal slices

Stanton, P. K., & Sarvey, J. M. (1985) · Brain Research · doi:10.1016/0006-8993(85)90981-3 · Cited by 128 · see citing works

Different Mechanisms and Multiple Stages of LTP

Matthies, H., Frey, U., Reymann, K. G., Krug, M., Jork, R., & Schröeder, H. (1990) · Advances in experimental medicine and biology · doi:10.1007/978-1-4684-5769-8_39 · Cited by 122 · see citing works

Spatial memory deficits, increased phosphorylation of the transcription factor CREB, and induction of the AP-1 complex following experimental brain injury

Dash, P. K., Moore, A., & Dixon, C. E. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-03-02030.1995 · Cited by 106 · see citing works

Protein phosphorylation in neuronal plasticity and gene expression

Schulman, H. (1995) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(95)80051-4 · Cited by 104 · see citing works

NMDA and D1 receptors regulate the phosphorylation of CREB and the induction of cfos in striatal neurons in primary culture

Das, S., Grunert, M., Williams, L., & Vincent, S. R. (1997) · Synapse · doi:10.1002/(sici)1098-2396(199703)25:3 · Cited by 103 · see citing works

Synapse Specificity and Long-Term Information Storage

Schuman, E. M. (1997) · Neuron · doi:10.1016/s0896-6273(00)81234-9 · Cited by 99 · see citing works

LTP in the lateral perforant path is β-adrenergic receptor-dependent

Bramham, C. R., Bacher-Svendsen, K., & Sarvey, J. M. (1997) · Neuroreport · doi:10.1097/00001756-199702100-00028 · Cited by 95 · see citing works

Asymptotic hippocampal long-term potentiation in rats does not preclude additional potentiation at later phases

Frey, U., Schollmeier, K., Reymann, K. G., & Seidenbecher, T. (1995) · Neuroscience · doi:10.1016/0306-4522(95)00117-2 · Cited by 93 · see citing works

Endogenous Activation of μ and δ-1 Opioid Receptors Is Required for Long-Term Potentiation Induction in the Lateral Perforant Path: Dependence on GABAergic Inhibition

Bramham, C. R., & Sarvey, J. M. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-24-08123.1996 · Cited by 89 · see citing works

Modulation by dopamine of population responses and cell membrane properties of hippocampal CA1 neurons in vitro

Gribkoff, V. K., & Ashe, J. H. (1984) · Brain Research · doi:10.1016/0006-8993(84)90768-6 · Cited by 85 · see citing works

Naloxone blocks the induction of long-term potentiation in the lateral but not in the medial perforant pathway in the anesthetized rat

Bramham, C. R., Errington, M. L., & Bliss, T. (1988) · Brain Research · doi:10.1016/0006-8993(88)91052-9 · Cited by 85 · see citing works

Modulation of long-term potentiation: Effects of adrenergic and neuroleptic drugs

Dunwiddie, T. V., Roberson, N. L., & Worth, T. S. (1982) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(82)90130-7 · Cited by 78 · see citing works

Cyclic AMP induces long-term increase in synaptic efficacy in CA1 region of rat hippocampus

Slack, J. R., & Pockett, S. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90229-m · Cited by 72 · see citing works

Chapter 16 Long-term potentiation in the hippocampal CA1 region: its induction and early temporal development

Gustafsson, B., & Wigström, H. (1990) · Progress in brain research · doi:10.1016/s0079-6123(08)61252-2 · Cited by 64 · see citing works

Discussion

Sossin, W. S. (1996) · Trends in Neurosciences · doi:10.1016/0166-2236(96)20016-5 · Cited by 63 · see citing works

Absence of long-term potentiation in the subcortically deafferented dentate gyrus

Buzsáki, G., & Gage, F. H. (1989) · Brain Research · doi:10.1016/0006-8993(89)90351-x · Cited by 62 · see citing works

Cyclic AMP and long-term potentiation in the CA1 region of rat hippocampus

Pockett, S., Slack, J. R., & Peacock, S. J. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90151-5 · Cited by 47 · see citing works

Aminergic blockade modulales long-term potentiation in the dentate gyrus of freely moving rats

Krug, M., Chepkova, A. N., Geyer, C. E., & Ott, T. (1983) · Brain Research Bulletin · doi:10.1016/0361-9230(83)90048-5 · Cited by 46 · see citing works

mRNA distribution within dendrites: Relationship to afferent innervation

Steward, O., & Wallace, C. S. (1995) · Journal of Neurobiology · doi:10.1002/neu.480260316 · Cited by 41 · see citing works

A comparison of the effects of localized brain administration of catecholamine and protein synthesis inhibitors on memory processing

Flood, J. F., Smith, G. E., & Jarvik, M. E. (1980) · Brain Research · doi:10.1016/0006-8993(80)90441-2 · Cited by 38 · see citing works

Impairment of glycoprotein fucosylation in rat hippocampus and the consequences on memory formation

Jork, R., Grecksch, G., & Matthies, H. J. G. (1986) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(86)90100-0 · Cited by 30 · see citing works

[Dopaminergic innervation of the parahippocampal and hippocampal regions in the rat].

Baulac, M., Verney, C., & Berger, B. (1986) · PubMed · Cited by 23 · see citing works

Effects of kainic acid induced seizures on immediate early gene expression in mice with a targeted mutation of the CREB gene

Blendy, J. A., Schmid, W., Kiessling, M., Schütz, G., & Gass, P. (1995) · Brain Research · doi:10.1016/0006-8993(95)00274-t · Cited by 19 · see citing works

Somatic ribosomal changes induced by long-term potentiation of the perforant path-hippocampal CA1 synapses

Wenzel, J., Desmond, N. L., & Levy, W. B. (1993) · Brain Research · doi:10.1016/0006-8993(93)91629-7 · Cited by 16 · see citing works

Dendritic spines form 'collarsʼ in hippocampal granule cells

Rusakov, D. A., Stewart, M. G., Sojka, M., et al. (1995) · Neuroreport · doi:10.1097/00001756-199507310-00023 · Cited by 11 · see citing works

Evidence that heterosynaptic depolarization underlies associativity of long‐term potentiation in rat hippocampus.

Clark, K. A., & Collingridge, G. L. (1996) · The Journal of Physiology · doi:10.1113/jphysiol.1996.sp021157 · Cited by 10 · see citing works

About Sleep's Role in Memory

Rasch, B., & Born, J. (2013) · Physiological Reviews · doi:10.1152/physrev.00032.2012 · Cited by 2,783 · see citing works

The principal features and mechanisms of dopamine modulation in the prefrontal cortex

Seamans, J. K., & Yang, C. R. (2004) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2004.05.006 · Cited by 1,592 · see citing works

Mechanisms of CaMKII action in long-term potentiation

Lisman, J., Yasuda, R., & Raghavachari, S. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3192 · Cited by 1,134 · see citing works

Synaptic plasticity and dysconnection in schizophrenia

Stephan, K. E., Baldeweg, T., & Friston, K. J. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.10.005 · Cited by 841 · see citing works

Locus coeruleus and dopaminergic consolidation of everyday memory

Takeuchi, T., Duszkiewicz, A. J., Sonneborn, A., Spooner, P. A., Yamasaki, M., Watanabe, M., Smith, C. C., Fernández, G., Deisseroth, K., Greene, R. W., et al. (2016) · Nature · doi:10.1038/nature19325 · Cited by 827 · 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

The role of the GluR2 subunit in AMPA receptor function and synaptic plasticity

Isaac, J. T. R., Ashby, M. C., & McBain, C. J. (2007) · Neuron · doi:10.1016/j.neuron.2007.06.001 · Cited by 802 · see citing works

Visual Discrimination Task Improvement: A Multi-Step Process Occurring During Sleep

Stickgold, R., Whidbee, D., Schirmer, B., Patel, V., & Hobson, J. A. (2000) · Journal of Cognitive Neuroscience · doi:10.1162/089892900562075 · Cited by 560 · see citing works

Absolute Coding of Stimulus Novelty in the Human Substantia Nigra/VTA

Bunzeck, N., & Düzel, E. (2006) · Neuron · doi:10.1016/j.neuron.2006.06.021 · Cited by 503 · see citing works

CPEB-Mediated Cytoplasmic Polyadenylation and the Regulation of Experience-Dependent Translation of α-CaMKII mRNA at Synapses

Wu, L., Wells, D., Tay, J., Mendis, D., Abbott, M.-A., Barnitt, A., Quinlan, E., Heynen, A., Fallon, J. R., & Richter, J. D. (1998) · Neuron · doi:10.1016/s0896-6273(00)80630-3 · Cited by 488 · see citing works

Fear memory

Izquierdo, I., Furini, C. R. G., & Myskiw, J. C. (2016) · Physiological Reviews · doi:10.1152/physrev.00018.2015 · Cited by 453 · see citing works

Nonlinear dynamic causal models for fMRI

Stephan, K. E., Kasper, L., Harrison, L. M., Daunizeau, J., den Ouden, H. E. M., Breakspear, M., & Friston, K. J. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.04.262 · Cited by 416 · see citing works

Is Heterosynaptic modulation essential for stabilizing hebbian plasiticity and memory

Bailey, C. H., Giustetto, M., Huang, Y.-Y., Hawkins, R. D., & Kandel, E. R. (2000) · Nature Reviews Neuroscience · doi:10.1038/35036191 · Cited by 382 · see citing works

Induction of long-term memory by exposure to novelty requires protein synthesis: evidence for a behavioral tagging

Moncada, D., & Viola, H. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.1083-07.2007 · Cited by 370 · see citing works

A clustered plasticity model of long-term memory engrams.

Govindarajan, A., Kelleher, R. J., & Tonegawa, S. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn1937 · Cited by 355 · see citing works

The right time to learn: Mechanisms and optimization of spaced learning

Smolen, P., Zhang, Y., & Byrne, J. H. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2015.18 · Cited by 326 · see citing works

Behavioral tagging is a general mechanism of long-term memory formation

Ballarini, F., Moncada, D., Martinez, M. C., Alen, N., & Viola, H. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0907078106 · Cited by 301 · see citing works

Integration of biochemical signalling in spines

Kennedy, M. B., Beale, H. C., Carlisle, H. J., & Washburn, L. R. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1685 · Cited by 286 · see citing works

Dopamine and Memory: Modulation of the Persistence of Memory for Novel Hippocampal NMDA Receptor-Dependent Paired Associates

Bethus, I., Tse, D., & Morris, R. G. M. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.2721-09.2010 · Cited by 270 · see citing works

NOvelty-related Motivation of Anticipation and exploration by Dopamine (NOMAD): Implications for healthy aging

Düzel, E., Bunzeck, N., Guitart-Masip, M., & Düzel, S. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.08.006 · Cited by 249 · see citing works

Relevance of synaptic tagging and capture to the persistence of long-term potentiation and everyday spatial memory

Wang, S.-H., Redondo, R. L., & Morris, R. G. M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1008638107 · Cited by 251 · see citing works

Functional imaging of the human dopaminergic midbrain

Düzel, E., Bunzeck, N., Guitart-Masip, M., Wittmann, B., Schott, B. H., & Tobler, P. N. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2009.02.005 · Cited by 216 · see citing works

The temporal paradox of Hebbian learning and homeostatic plasticity

Zenke, F., Gerstner, W., & Ganguli, S. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.03.015 · Cited by 201 · see citing works

Localization and translation of mRNA in dentrites and axons

Job, C., & Eberwine, J. (2001) · Nature Reviews Neuroscience · doi:10.1038/35104069 · Cited by 202 · see citing works

Synaptic evidence for the efficacy of spaced learning

Kramár, E. A., Babayan, A. H., Gavin, C. F., Cox, C. D., Jafari, M., Gall, C. M., Rumbaugh, G., & Lynch, G. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1120700109 · Cited by 192 · see citing works

Dopamine regulates aversive contextual learning and associated in vivo synaptic plasticity in the Hippocampus

Broussard, J. I., Yang, K., Levine, A. T., Tsetsenis, T., Jenson, D., Cao, F., Garcia, I., Arenkiel, B. R., Zhou, F.-M., De Biasi, M., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.01.070 · Cited by 180 · see citing works

Identification of transmitter systems and learning tag molecules involved in behavioral tagging during memory formation

Moncada, D., Ballarini, F., Martinez, M. C., Frey, J. U., & Viola, H. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1104495108 · Cited by 171 · see citing works

A Mechanism for Ca ²⁺ /Calmodulin-Dependent Protein Kinase II Clustering at Synaptic and Nonsynaptic Sites Based on Self-Association

Hudmon, A., LeBel, E., Roy, H., Sik, A., Schulman, H., Waxham, M. N., & De Koninck, P. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.4698-04.2005 · Cited by 159 · see citing works

The Role of Extracellular Regulated Kinases I/II in Late-Phase Long-Term Potentiation

Rosenblum, K., Futter, M., Voss, K., Erent, M., Skehel, P. A., French, P., Obosi, L., Jones, M. W., & Bliss, T. V. P. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-13-05432.2002 · Cited by 155 · see citing works

An Associational Model of Birdsong Sensorimotor Learning I. Efference Copy and the Learning of Song Syllables

Troyer, T. W., & Doupe, A. J. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.84.3.1204 · Cited by 145 · see citing works

Chapter 7 ‘Synaptic tagging’ and ‘cross-tagging’ and related associative reinforcement processes of functional plasticity as the cellular basis for memory formation

Frey, S., & Frey, J. U. (2008) · Progress in brain research · doi:10.1016/s0079-6123(07)00007-6 · Cited by 139 · see citing works

Translational Control in the Brain in Health and Disease

Sossin, W. S., & Costa-Mattioli, M. (2019) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a032912 · Cited by 138 · see citing works

Memory consolidation as an adaptive process

Cowan, E. T., Schapiro, A. C., Dunsmoor, J. E., & Murty, V. P. (2021) · Psychonomic Bulletin & Review · doi:10.3758/s13423-021-01978-x · Cited by 133 · see citing works

The learning of fear extinction

Furini, C., Myskiw, J., & Izquierdo, I. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.10.016 · Cited by 124 · see citing works

Epigenetic memory: The Lamarckian brain

Fischer, A. (2014) · The EMBO Journal · doi:10.1002/embj.201387637 · Cited by 107 · see citing works

Locus Coeruleus and Dopamine-Dependent Memory Consolidation

Yamasaki, M., & Takeuchi, T. (2017) · Neural Plasticity · doi:10.1155/2017/8602690 · Cited by 91 · see citing works

Selective rapid eye movement sleep deprivation impairs the maintenance of long‐term potentiation in the rat hippocampus

Ishikawa, A., Kanayama, Y., Matsumura, H., Tsuchimochi, H., Ishida, Y., & Nakamura, S. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04874.x · Cited by 100 · see citing works

Differences between synaptic plasticity thresholds result in new timing rules for maximizing long-term potentiation

Lynch, G., Kramár, E. A., Babayan, A. H., Rumbaugh, G., & Gall, C. M. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.07.006 · Cited by 97 · see citing works

Cognitive neuroscience perspective on memory: overview and summary

Sridhar, S., Khamaj, A., & Asthana, M. K. (2023) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2023.1217093 · Cited by 80 · see citing works

Amygdala modulation of memory-related processes in the hippocampus: potential relevance to PTSD

Tsoory, M. M., Vouimba, R. M., Akirav, I., Kavushansky, A., Avital, A., & Richter-Levin, G. (2007) · Progress in Brain Research · doi:10.1016/s0079-6123(07)67003-4 · Cited by 78 · see citing works

The sleep benefit in episodic memory: An integrative review and a meta-analysis.

Berres, S., & Erdfelder, E. (2021) · Psychological Bulletin · doi:10.1037/bul0000350 · Cited by 74 · see citing works

Role of amygdala oscillations in the consolidation of emotional memories

Pelletier, J. G., & Paré, D. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2003.08.019 · Cited by 71 · see citing works

D1 and D5 dopamine receptors participate on the consolidation of two different memories

Furini, C. R. G., Myskiw, J. C., Schmidt, B. E., Marcondes, L. A., & Izquierdo, I. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.06.027 · Cited by 60 · see citing works

Sensorimotor Modulation of Mood and Depression: In Search of an Optimal Mode of Stimulation

Canbeyli, R. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00428 · Cited by 42 · see citing works

Memory corticalization triggered by REM sleep: mechanisms of cellular and systems consolidation

Almeida-Filho, D. G., Queiroz, C. M., & Ribeiro, S. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-018-2886-9 · Cited by 38 · see citing works

Memory reconsolidation allows the consolidation of a concomitant weak learning through a synaptic tagging and capture mechanism

Cassini, L. F., Sierra, R. O., Haubrich, J., Crestani, A. P., Santana, F., de Oliveira Alvares, L., & Quillfeldt, J. A. (2013) · Hippocampus · doi:10.1002/hipo.22149 · Cited by 36 · see citing works

On the role of epigenetic modifications of HPA axis in posttraumatic stress disorder and resilience

Khan, Z., Messiri, N. E., Iqbal, E., Hassan, H., Tanweer, M. S., Sadia, S. R., Taj, M., Zaidi, U., Yusuf, K., Syed, N. I., et al. (2025) · Journal of Neurophysiology · doi:10.1152/jn.00345.2024 · Cited by 32 · see citing works

Critical Involvement of Postsynaptic Protein Kinase Activation in Long-Term Potentiation at Hippocampal Mossy Fiber Synapses on CA3 Interneurons

Galván, E. J., Cosgrove, K. E., Mauna, J. C., Card, J. P., Thiels, E., Meriney, S. D., & Barrionuevo, G. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.5269-09.2010 · Cited by 28 · see citing works

Cellular and Molecular Bases of Memory: Synaptic and Neuronal Plasticity

Wang, J., Ko, G. Y. ‐., & Kelly, P. T. (1997) · Journal of Clinical Neurophysiology · doi:10.1097/00004691-199707000-00002 · Cited by 74 · see citing works

Synaptic Plasticity and AMPA Receptor Trafficking

Malenka, R. C. (2003) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1300.001 · Cited by 324 · see citing works

Inverse synaptic tagging: An inactive synapse-specific mechanism to capture activity-induced Arc/arg3.1 and to locally regulate spatial distribution of synaptic weights

Okuno, H., Minatohara, K., & Bito, H. (2017) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2017.09.025 · Cited by 43 · see citing works

Chronic Inactivation of a Neural Circuit Enhances LTP by Inducing Silent Synapse Formation

Arendt, K. L., Sarti, F., & Chen, L. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3880-12.2013 · Cited by 77 · see citing works

Synapse Number and Synaptic Efficacy Are Regulated by Presynaptic cAMP and Protein Kinase A

Munno, D. W., Prince, D. J., & Syed, N. I. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-10-04146.2003 · Cited by 29 · see citing works