MAP Kinase Translocates into the Nucleus of the Presynaptic Cell and Is Required for Long-Term Facilitation in Aplysia

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

Specificity of receptor tyrosine kinase signaling: Transient versus sustained extracellular signal-regulated kinase activation

Marshall, C. J. (1995) · Cell · doi:10.1016/0092-8674(95)90401-8 · Cited by 3,906

PD 098059 Is a Specific Inhibitor of the Activation of Mitogen-activated Protein Kinase Kinase in Vitro and in Vivo

Alessi, D. R., Cuenda, A., Cohen, P., Dudley, D. T., & Saltiel, A. R. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.46.27489 · Cited by 3,374

A synthetic inhibitor of the mitogen-activated protein kinase cascade.

Dudley, D. T., Pang, L., Decker, S. J., Bridges, A. J., & Saltiel, A. R. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.17.7686 · Cited by 2,679

Synaptic tagging and long-term potentiation

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

Protein synthesis and memory: A review.

Davis, H. P., & Squire, L. R. (1984) · Psychological Bulletin · doi:10.1037/0033-2909.96.3.518 · Cited by 1,505

Coupling of the RAS-MAPK Pathway to Gene Activation by RSK2, a Growth Factor-Regulated CREB Kinase

Xing, J. W., Ginty, D. D., & Greenberg, M. E. (1996) · Science · doi:10.1126/science.273.5277.959 · Cited by 1,246

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

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

cAMP Activates MAP Kinase and Elk-1 through a B-Raf- and Rap1-Dependent Pathway

Vossler, M. R., Yao, H. W., York, R. D., Pan, M., Rim, C. S., & Stork, P. A. (1997) · Cell · doi:10.1016/s0092-8674(00)80184-1 · Cited by 1,044

Persistent Long-Term Facilitation at an Identified Synapse Becomes Labile with Activation of Short-Term Heterosynaptic Plasticity

Hu, J., & Schacher, S. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0098-14.2014 · Cited by 13

The Contribution of Spatial and Temporal Molecular Networks in the Induction of Long-term Memory and Its Underlying Synaptic Plasticity

Mirisis, A. A., Alexandrescu, A., Carew, T. J., & Kopec, A. M. (2016) · AIMS neuroscience · doi:10.3934/neuroscience.2016.3.356 · Cited by 12

Antioxidant‐Mediated Reversal of Oxidative Damage in Mouse Modeling of Complex I Inhibition

Parameshwaran, K., Irwin, M. H., Steliou, K., Suppiramaniam, V. D., & Pinkert, C. A. (2015) · Drug Development Research · doi:10.1002/ddr.21242 · Cited by 12

Critical role of the circadian clock in memory formation: lessons from Aplysia

Lyons, L. C. (2011) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2011.00052 · Cited by 12

Changes in Metabolism and Proteostasis Drive Aging Phenotype in Aplysia californica Sensory Neurons

Kron, N. S., Schmale, M. C., & Fieber, L. A. (2020) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2020.573764 · Cited by 13

Timing-Dependent Protection of Swimming Exercise against d-Galactose-Induced Aging-Like Impairments in Spatial Learning/Memory in Rats

Li, X., Wang, L., Zhang, S., Hu, X., Yang, H.-J., & Xi, L. (2019) · Brain Sciences · doi:10.3390/brainsci9090236 · Cited by 12

Learning abilities

Lafontaine, M. P., Knoth, I. S., & Lippé, S. (2020) · Handbook of clinical neurology · doi:10.1016/b978-0-444-64150-2.00021-6 · Cited by 12

Targeting the PDZ domains of molecular scaffolds of transmembrane ion channels

Piserchio, A., Spaller, M. R., & Mierke, D. F. (2006) · The AAPS Journal · doi:10.1007/bf02854911 · Cited by 12

Glycosides, Depression and Suicidal Behaviour: The Role of Glycoside-Linked Proteins

Serafini, G., Pompili, M., Innamorati, M., Giordano, G., Tatarelli, R., Lester, D., Girardi, P., & Dwivedi, Y. K. (2011) · Molecules · doi:10.3390/molecules16032688 · Cited by 9

Multifunctional Role of Protein Kinase C in Regulating the Formation and Maturation of Specific Synapses

Hu, J., Chen, Y., & Schacher, S. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3305-07.2007 · Cited by 12

A new genetic model of activity-induced Ras signaling dependent pre-synaptic plasticity in Drosophila

Freeman, A. A. H., Bowers, M. E., Vrailas‐Mortimer, A. D., Timmerman, C., Roux, S., Ramaswami, M., & Sanyal, S. (2010) · Brain Research · doi:10.1016/j.brainres.2010.02.061 · Cited by 11

Diversity matters: combinatorial information coding by GABAA receptor subunits during spatial learning and its allosteric modulation

Szodorai, E., Bampali, K., Romanov, R. A., Kasper, S. F., Hökfelt, T. G. M., Ernst, M. C., Lübec, G., & Harkany, T. (2018) · Cellular Signalling · doi:10.1016/j.cellsig.2018.07.003 · Cited by 11

Local synaptic integration of mitogen-activated protein kinase and protein kinase A signaling mediates intermediate-term synaptic facilitation in Aplysia

Ye, X., Marina, A., & Carew, T. J. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1209956109 · Cited by 11

Essential Role of Somatic and Synaptic Protein Synthesis and Axonal Transport in Long-Term Synapse-Specific Facilitation at Distal Sensorimotor Connections inAplysia

Guan, X., & Clark, G. A. (2006) · Biological Bulletin · doi:10.2307/4134561 · Cited by 11

Sensitization and Habituation: Invertebrate

Fioravante, D., Antzoulatos, E. G., & Byrne, J. H. (2008) · Elsevier eBooks · doi:10.1016/b978-012370509-9.00005-x · Cited by 11

Nonredundant roles for hippocampal and entorhinal cortical plasticity in spatial memory storage

Hebert, A. E., & Dash, P. K. (2004) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2004.06.016 · Cited by 11

Aplysia Neurons as a Model of Alzheimer’s Disease: Shared Genes and Differential Expression

Kron, N. S., & Fieber, L. A. (2021) · Journal of Molecular Neuroscience · doi:10.1007/s12031-021-01918-3 · Cited by 10

Bilateral phosphorylation of ERK in the lateral and centrolateral amygdala during unilateral storage of fear memories

Tarpley, J. W., Shlifer, I. G., Birnbaum, M. S., Halladay, L. R., & Blair, H. T. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.08.071 · Cited by 14

Differential signaling cascade of MAP kinase and S6 kinase depends on 3′,5′-monophosphate concentration in Schwann cells: correlation to cellular differentiation and proliferation

Mutoh, T., Li, M., Yamamoto, M., Mitsuma, T., & Sobue, G. (1998) · Brain Research · doi:10.1016/s0006-8993(98)00933-0 · Cited by 10

Contribution of T cells to the development of autoimmune diabetes in the NOD mouse model

Toyoda, H., & Formby, B. (1998) · BioEssays · doi:10.1002/(sici)1521-1878(199809)20:9 · Cited by 34

Long-Term Potentiation and Memory

(2012) · Springer eBooks · doi:10.1007/springerreference_169302 · Cited by 10

Autocrine signaling by an Aplysia neurotrophin forms a presynaptic positive feedback loop

Jin, I., Udo, H., Nicholls, R. E., Kassabov, S., Zhu, H., Kandel, E. R., & Hawkins, R. D. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1810649115 · Cited by 9

Certain ortho-hydroxylated brominated ethers are promiscuous kinase inhibitors that impair neuronal signaling and neurodevelopmental processes

Poston, R. G., Murphy, L., Rejepova, A., Ghaninejad-Esfahani, M., Segales, J. S., Mulligan, K. A., & Saha, R. N. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.011138 · Cited by 9

Monocular deprivation enhances the nuclear signalling of extracellular signal‐regulated kinase in the developing visual cortex

Takamura, H., Ichisaka, S., Hayashi, C., Maki, H., & Hata, Y. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05908.x · Cited by 9

Anterograde and retrograde signaling by an Aplysia neurotrophin forms a transsynaptic functional unit

Jin, I., Udo, H., Kassabov, S. R., Kosmidis, S., Zhu, H., Kandel, E. R., & Hawkins, R. D. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1810650115 · Cited by 8

Epigenetics and the Formation of Long-Term Memory

Grinkevich, L. N. (2014) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-014-9897-2 · Cited by 8

The PDZ-GEF Gef26 regulates synapse development and function via FasII and Rap1 at the Drosophila neuromuscular junction

Ou, M., Wang, S., Sun, M., An, J., Lv, H., Zeng, K. X., Hou, X. S., & Xie, W. (2018) · Experimental Cell Research · doi:10.1016/j.yexcr.2018.12.008 · Cited by 8

Possible molecular-cellular mechanisms of the regulation of gene expression during learning

Grinkevich, L. N., & Vasil’ev, G. V. (2000) · Neuroscience and Behavioral Physiology · doi:10.1007/bf02471781 · Cited by 8

Differentiation and De-Differentiation—Neuronal Cell-Cycle Regulation During Development and Age-Related Neurodegenerative Disorders

Arendt, T. (2008) · Springer eBooks · doi:10.1007/978-0-387-32671-9_8 · Cited by 8

Neural Analysis of Learning in Simple Systems

Krasne, F. (2002) · Wiley eBooks · doi:10.1002/0471214426.pas0304 · Cited by 8

Differential patterns of extracellular signal-regulated kinase-1 and -2 phosphorylation in rat limbic brain regions after short-term and long-term inhibitory avoidance learning

Chai, S.-C., Holahan, M. R., Shyu, B., & Wang, C. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.10.009 · Cited by 7

Analysis of 5-HT–Induced Short-Term Facilitation atAplysiaSensorimotor Synapse During Bursts: Increased Synaptic Gain That Does Not Require ERK Activation

Phares, G. A., & Byrne, J. H. (2005) · Journal of Neurophysiology · doi:10.1152/jn.01261.2004 · Cited by 7

A Comparative Analysis of the Molecular Mechanisms Contributing to Implicit and Explicit Memory Storage in Aplysia and in the Hippocampus ☆

Hawkins, R. D., Mayford, M. R., & Kandel, E. R. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21095-x · Cited by 6

Identification of Short-Term and Long-Term Functional Synaptic Plasticity From Spiking Activities

Song, D. B., Robinson, B. S., & Berger, T. W. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-812976-0.00017-8 · Cited by 6

Characterization and reversal of Doxorubicin-mediated biphasic activation of ERK and persistent excitability in sensory neurons of Aplysia californica

Harini, L., Coughlin, B. L., Darr, A. S., & Byrne, J. H. (2017) · Scientific Reports · doi:10.1038/s41598-017-04634-4 · Cited by 6

Cell Adhesion Molecules of the NCAM Family and Their Roles at Synapses

Owczarek, S., Kristiansen, L. V., Hortsch, M., & Walmod, P. S. (2009) · Springer eBooks · doi:10.1007/978-0-387-92708-4_13 · Cited by 7

Nerve injury-associated kinase: a sterile 20-like protein kinase up-regulated in dorsal root ganglia in a rat model of neuropathic pain

Rausch, O., Newton, R. A., Bingham, S., MacDonald, R. E., Case, C. P., Sanger, G. J., Lawson, S. N., & Reith, A. D. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00392-4 · Cited by 6

A first partial Aplysia californica proteome

Sun, Y., Monje, F. J., Pollak, D. D., & Lübec, G. (2010) · Amino Acids · doi:10.1007/s00726-010-0795-9 · Cited by 6

Characterization of memories and ignorant (S6KII) mutants in operant conditioning in the heat-box

Putz, G. (2002) · Online Publication Service of Würzburg University (Würzburg University) · Cited by 6

From nociception in aneural animals to human suffering: toward a comparative biology of pain

Walters, E. T. (2025) · Journal of Experimental Biology · doi:10.1242/jeb.251210 · Cited by 8

Presynapses go nuclear!

Kravchick, D. O., & Jordan, B. A. (2015) · The EMBO Journal · doi:10.15252/embj.201591331 · Cited by 5

The Role of CREB in Neuronal Plasticity, Learning and Memory, and in Neuropsychiatric Disorders

(2012) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/978160805257811201010022 · Cited by 5

Aversive conditioning in the tardigrade, Dactylobiotus dispar.

Zhou, S., DeFranco, J. P., Blaha, N. T., Dwivedy, P., Culver, A., Nallamala, H., Chelluri, S., & Dumas, T. C. (2019) · Journal of Experimental Psychology Animal Learning and Cognition · doi:10.1037/xan0000218 · Cited by 5

Dynamics and Mechanisms of ERK Activation after Different Protocols that Induce Long-Term Synaptic Facilitation in Aplysia

Zhang, Y., Liu, R., Smolen, P. D., Cleary, L. J., & Byrne, J. H. (2022) · Oxford Open Neuroscience · doi:10.1093/oons/kvac014 · Cited by 6

Bifurcation analysis of a delay differential equation model associated with the induction of long-term memory

Hao, L., Yang, Z., & Lei, J. (2015) · Chaos Solitons & Fractals · doi:10.1016/j.chaos.2015.09.013 · Cited by 5

Enhancing resilience to stress: the role of signaling cascades

Yuan, P., Zhou, R., Farzad, N., Gould, T. D., Gray, N. A., Du, J., & Manji, H. K. (2005) · Techniques in the behavioral and neural sciences · doi:10.1016/s0921-0709(05)80040-9 · Cited by 5

Glutamatergic Synapses: Molecular Organization

Sheng, M., & Lin, J. (2001) · Wiley eBooks · doi:10.1038/npg.els.0000235 · Cited by 5

Fast retrograde effects on neuronal death and dendritic organization in development: the role of calcium influx

Posada, A., & Clarke, P. G. H. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00442-4 · Cited by 5

Enhancing Associative Learning in Rats With a Computationally Designed Training Protocol

Zhang, X. O., Zhang, Y., Cho, C. E., Engelke, D. S., Smolen, P. D., Byrne, J. H., & Monte, F. H. D. (2023) · Biological Psychiatry Global Open Science · doi:10.1016/j.bpsgos.2023.07.006 · Cited by 4

The VR1-Positive Primary Afferent-Mediated Expression of pERK in the Lumbosacral Neurons in Response to Mechanical and Chemical Stimulation of the Urinary Bladder in Rats

Yoo, C. J., & Hwang, S. J. (2007) · Journal of Korean Neurosurgical Society · doi:10.3340/jkns.2007.42.6.462 · Cited by 4

Location, location, location: The many addresses of memory formation

Yin, J. C. P. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.18.9985 · Cited by 4

Differential responses of phosphorylated mitogen-activated protein kinase and phosphorylated cyclic-AMP response element-binding protein immunoreactivity in the rat brain to sub-convulsive pentylenetetrazol

Reijmers, L. G. J. E., Hernándo, F., van Ree, J. M., Spruijt, B. M., & Burbach, J. P. H. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00394-8 · Cited by 4

Evolutionary Aspects of Nociception and Pain

Walters, E. T. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.24237-5 · Cited by 4

Postsynaptic effects of Aplysia cysteine-rich neurotrophic factor in the induction of activity-dependent long-term facilitation in Aplysia californicaPreprint

Alexandrescu, A., & Carew, T. J. (2020) · Learning & Memory · doi:10.1101/lm.051011.119 · Cited by 3

Synaptic Mechanisms of Induction and Maintenance of Long-Term Sensitization Memory in Aplysia

Glanzman, D. L. (2013) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-415823-8.00017-4 · Cited by 3

Synaptic generation of an intracellular retrograde signal requires activation of the tyrosine kinase and mitogen-activated protein kinase signaling cascades in Aplysia

Stough, S., Kopec, A. M., & Carew, T. J. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.07.017 · Cited by 3

Structural functional characteristic of neuronal serotonin receptors and molecular mechanisms of their coupling with G-proteins

Shpakov, A. O. (2009) · Neurochemical Journal · doi:10.1134/s1819712409010012 · Cited by 3

Mechanisms of protein kinase C-induced sustained activation of extracellular signal-regulated kinase in the hippocampus

Kamboj, K., Jana, S., & Sharma, S. K. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.10.046 · Cited by 5

Molecular cloning, characterization, and expression of two 5-HTRs from the pearl oyster Pinctada fucata martensii

Zhu, S., He, Y., Xu, Q., Zhang, J., Yang, C., Hao, R., Li, J., & Deng, Y. (2022) · Frontiers in Marine Science · doi:10.3389/fmars.2022.1011420 · Cited by 3

Paradoxical LTP maintenance with inhibition of protein synthesis and the proteasome suggests a novel protein synthesis requirement for early LTP reversal

Smolen, P. D., Baxter, D. A., & Byrne, J. H. (2018) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2018.08.026 · Cited by 2

Chapter XI Elk-1: an important regulator of immediate early gene expression in the brain

Vanhoutte, P., & Caboche, J. (2002) · Handbook of chemical neuroanatomy · doi:10.1016/s0924-8196(02)80022-7 · Cited by 2

Comparative Analysis of the Activation of the Elk-1 Transcription Factor in the Central Nervous System of Animals with Different Learning Capacities

Grinkevich, L. N., Lisachev, P. D., Gudzik, K. A., Grinkevich, V. V., & Kharchenko, O. A. (2004) · Doklady Biological Sciences · doi:10.1023/b:dobs.0000039688.51578.78 · Cited by 3

Comparative analysis of the activation of MAP/ERK kinases in the CNS of animals with different learning abilities

Grinkevich, L. N., Lisachev, P. D., Baranova, K. A., & Kharchenko, O. A. (2007) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-007-0072-x · Cited by 3

Synaptic and Cellular Basis of Learning

Bailey, C. H., & Kandel, E. R. (2009) · Wiley eBooks · doi:10.1002/9780470478509.neubb001028 · Cited by 3

The Cell Biology of Learning and Memory in Aplysia

Glanzman, D. L. (2008) · Advances in psychology · doi:10.1016/s0166-4115(08)10021-8 · Cited by 2

Nicorandil, an Adenosine Triphosphate-Sensitive Potassium Channel Opener, Inhibits Muscarinic Acetylcholine Receptor-Mediated Activation of Extracellular Signal-Regulated Kinases in PC12 Cells

Niinomi, K., Banno, Y., Iida, H., & Dohi, S. (2008) · Anesthesia & Analgesia · doi:10.1213/ane.0b013e31818880a8 · Cited by 2

Innovative rehabilitation for orofacial praxis

Fellus, P. (2021) · International Dental Journal · doi:10.1016/j.identj.2021.08.014 · Cited by 2

The role of cAMP-dependent protein kinase A in the formation of long-term memory in Bactrocera dorsalis

Yu, J., Hui, Y., He, J., Yu, Y., Wang, Z., Ling, S., Wang, W., Zeng, X., & Liu, J. (2023) · Journal of Integrative Agriculture · doi:10.1016/j.jia.2023.07.016 · Cited by 2

Neurobiology of addiction: Neuroanatomical, neurochemical, molecular and genetic aspects of morphine and cocaine addiction. Part II

Antón, B., Calva, J. J., Valdez, A. D. P., Acevedo, R., Morales, A., Medécigo, M., & Leff, P. (2000) · Redalyc (Universidad Autónoma del Estado de México) · Cited by 2

Brain MAPK s Levels are Differentially Associated with Seizures Threshold and Severity Progression in Pentylenetetrazole‐Kindled Mice

Ben, J., Gonçalves, F. M., de Oliveira, P. A., Peres, T. V., Hohl, A., Leal, R. B., Cavalheiro, É. A., Prediger, R. D., & Walz, R. (2013) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.12147 · Cited by 2

Biology of Learning and Memory Genes

Stanl y Pradeep, F., Pradeep, B. V., & Palaniswamy, M. (2011) · Journal of Neurology & Neurophysiology · doi:10.4172/2155-9562.1000118 · Cited by 2

Effects of Axotomy on Cultured Sensory Neurons ofAplysia: Long-Term Injury-Induced Changes in Excitability and Morphology Are Mediated by Different Signaling Pathways

Bedi, S. S., Cai, D., & Glanzman, D. L. (2008) · Journal of Neurophysiology · doi:10.1152/jn.90539.2008 · Cited by 2

Cellular and Molecular Mechanisms of Memory in Mollusks

Byrne, J. H., Hochner, B., & Kemenes, G. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21097-3 · Cited by 3

Relationship of ERK1/2 phosphorylation to D1 dopamine receptor activation, behavioral sensitization, and structural plasticity in the neonate 6-hydroxydopamine-lesioned rat

Papadeas, S. T. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/xraa-7j71 · Cited by 2

Expression of pERK in the Neurons and Microglia in the Spinal Cord of the Rat with Neuropathic Pain

Kim, K. J., Lee, S., Hwang, S. J., & Oh, S. J. (2005) · Journal of Korean Neurotraumatology Society · doi:10.13004/jknts.2005.1.1.19 · Cited by 2

Genetic Mechanisms of Memory Disorders (Excluding Alzheimer's Disease)

Kaas, G. A., Hawkins, K. E., & Sweatt, J. D. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21125-5 · Cited by 3

MAP kinases and their roles in pancreatic β-cells

Khoo, S., Gibson, T. B., Arnette, D., Lawrence, M. C., January, B., McGlynn, K., Vanderbilt, C. A., Griffen, S. C., German, M. S., & Cobb, M. H. (2004) · Cell Biochemistry and Biophysics · doi:10.1007/bf02739023 · Cited by 2

Spatial and single-cell transcriptomics reveal neuron-astrocyte interplay in long-term memoryPreprint

Sun, W., Liu, Z., Jiang, X., Chen, M. B., Dong, H., Liu, J. Z., Südhof, T. C., & Quake, S. R. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.03.20.533566 · Cited by 2

The serotonin receptor 5-HTR modulates larval settlement and metamorphosis in Manila clam Ruditapes philippinarum

Yang, H., Zhang, L., Wu, B., Liu, Z., Zhou, L., Ma, P., Li, Z., & Sun, X. (2026) · Aquaculture Reports · doi:10.1016/j.aqrep.2026.103445 · Cited by 1

Hippocampal ERK2 dimerization regulates inhibitory avoidance memory reconsolidation and synaptic plasticity

Ramos, S. O., Medina, C., Krawczyk, M. D. C., Millan, J., Acutain, M. F., Romano, A. G., Báez, M. V., Urbano, F. J., Boccia, M. M., & Feld, M. (2026) · iScience · doi:10.1016/j.isci.2026.116649 · Cited by 1

Cell Cycle Activation in Neurons

Arendt, T. (2005) · Springer eBooks · doi:10.1007/0-387-29390-6_1 · Cited by 1

Presynaptic Mechanisms of Plasticity and Memory in Aplysia and Other Learning-Related Experimental Systems

Hawkins, R. D., Bailey, C. H., & Kandel, E. R. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21111-5 · Cited by 1

Identification of Neural Plasticity From Spikes

Song, D. B., Robinson, B. S., Chan, R. H. M., & Berger, T. W. (2018) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-812028-6.00007-0 · Cited by 1

Specificity of synapse formation in Aplysia: paracrine and autocrine signaling regulates bidirectional molecular interactions between sensory and non-target motor neurons

Alexandrescu, A., & Carew, T. J. (2020) · Scientific Reports · doi:10.1038/s41598-020-62099-4 · Cited by 1

DNA methylation inhibition participates in the anterograde amnesia key mechanism through the suppression of the transcription of genes involved in memory formation in grape snails

Solntseva, S. V., Nikitin, V. P., Kozyrev, S. A., & Nikitin, P. V. (2022) · Behavioural Brain Research · doi:10.1016/j.bbr.2022.114118 · Cited by 1

Neurobiologia do condicionamento pavloviano e condicionamento operante – Revisão narrativa

Silva, W. D. S. (2024) · Research Society and Development · doi:10.33448/rsd-v13i11.47523 · Cited by 3

Heterosynaptic plasticity: one name for several phenomena

Смирнов, И. В., & Malyshev, A. Y. (2024) · Журнал высшей нервной деятельности им И П Павлова · doi:10.31857/s0044467724060019 · Cited by 1

Signal Transduction Pathways in Well-Defined Models of Learning and Memory

Müller, U. (2000) · doi:10.1007/978-1-59259-019-3_3 · Cited by 1

BIOCHEMISTRY OF SHORT-TERM AND LONG-TERM MEMORY

Stepanov, G. F., Yasinenko, N. Y., Vasylieva, A. G., & Davydenko, V. L. (2021) · Odes’kij medičnij žurnal (The Odessa Medical Journal) · doi:10.54229/2226-2008-2021-5-10 · Cited by 1

In conversation with Kelsey Martin

Wiseman, S. L. (2023) · Nature Neuroscience · doi:10.1038/s41593-023-01533-y · Cited by 1

Transcription Factors CREB and NF-KB: Involvement in Synaptic Plasticity and Memory Formation

Albensi, B. C., Barger, S. W., Carrión, Á. M., Fontán‐Lozano, Á., Grilli, M., Josselyn, S. A., Mao, X. R., Meneghini, V., Murphy, K. J., Odero, G. L., et al. (2018) · Cited by 1

Psychotropic drug tenoten activates mitogen-activated MAP/ERK kinase regulatory cascade controlling the neuroprotective effects

Epstein, O. I., Vorobieva, O. V., Grinkevich, L. N., Kharchenko, O. A., & Shtark, M. B. (2007) · Bulletin of Experimental Biology and Medicine · doi:10.1007/s10517-007-0322-5 · Cited by 1

Synaptic Growth and Transcriptional Regulation in Drosophila

Barber, C. F., & Littleton, J. T. (2007) · Springer eBooks · doi:10.1007/978-0-387-73609-9_13 · Cited by 1

Synapse Formation between Identified Molluscan Neurons: A Model System Approach

Wiersma-Meems, R., & Syed, N. I. (2006) · Springer eBooks · doi:10.1007/978-0-387-32562-0_3 · Cited by 1

Postsynaptic Mechanisms of Trophic Factor-Induced Excitatory Synapse Formation in Lymnaea stagnalis

Flynn, N. (2015) · Libraries and Cultural Resources (University of Calgary) · doi:10.11575/prism/27390 · Cited by 1

Circular RNAs may embed pieces of real-world sensory information into an episodic memoryPreprint

Asok, A. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.06.511043 · Cited by 1

Hippocampal ERK2 dimerization is critical for memory reconsolidation and synaptic plasticityPreprint

Ramos, S. O., Medina, C., Krawczyk, M. D. C., Millan, J., Acutain, M. F., Romano, A. G., Baez, M. V., Urbano, F. J., Boccia, M. M., & Feld, M. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.06.611755 · Cited by 1

Neural mechanisms of memory reconsolidation

Exton-McGuinness, M. T. J. (2014) · University of Birmingham Institutional Research Archive (University of Birmingham) · Cited by 1

The dynamics, interactions and phenotypes associated with the three members of the 14-3-3 family in Drosophila melanogaster

Acevedo, S. F. (2005) · OakTrust (Texas A&M University Libraries) · Cited by 1

Signaling Between Synapse and Nucleus During Synaptic Plasticity

Lai, K., Wang, D., & Martin, K. C. (2009) · Research and perspectives in Alzheimer's disease · doi:10.1007/978-3-540-87941-1_6

Repeated pulses of serotonin required for long-term facilitation activate mitogen-activated protein kinase in sensory neurons of Aplysia

Michael, D., Martin, K. C., Seger, R., Ning, M., Baston, R., & Kandel, E. R. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.4.1864 · Cited by 139

Local synaptic integration of mitogen-activated protein kinase and protein kinase A signaling mediates intermediate-term synaptic facilitation in Aplysia

Ye, X., Marina, A., & Carew, T. J. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1209956109 · Cited by 11

Mutation in the Phosphorylation Sites of MAP Kinase Blocks Learning-Related Internalization of apCAM in Aplysia Sensory Neurons

Bailey, C. H., Kaang, B., Chen, M., Martin, K. C., Lim, C., Casadio, A., & Kandel, E. R. (1997) · Neuron · doi:10.1016/s0896-6273(00)80331-1 · Cited by 180

Serotonin Regulates the Secretion and Autocrine Action of a Neuropeptide to Activate MAPK Required for Long-Term Facilitation in Aplysia

Hu, J., Glickman, L., Wu, F., & Schacher, S. (2004) · Neuron · doi:10.1016/j.neuron.2004.07.011 · Cited by 72

Differential Role of Mitogen-Activated Protein Kinase in Three Distinct Phases of Memory for Sensitization in Aplysia

Sharma, S. K., Sherff, C. M., Shobe, J., Bagnall, M. W., Sutton, M. A., & Carew, T. J. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-09-03899.2003 · Cited by 125