PKMζ maintains memories by regulating GluR2-dependent AMPA receptor trafficking

Modality-Specific Retrograde Amnesia of Fear

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

Learning induces long-term potentiation in the hippocampus

Whitlock, J. R., Heynen, A. J., Shuler, M. G., & Bear, M. F. (2006) · Science · doi:10.1126/science.1128134 · Cited by 1,913

Synaptic AMPA receptor plasticity and behavior

Kessels, H. W., & Malinow, R. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.015 · Cited by 993

Storage of spatial information by the maintenance mechanism of LTP

Pastalkova, E., Serrano, P., Pinkhasova, D., Wallace, E., Fenton, A. A., & Sacktor, T. C. (2006) · Science · doi:10.1126/science.1128657 · Cited by 848

Postsynaptic receptor trafficking underlying a form of associative learning

Rumpel, S., LeDoux, J., Zador, A., & Malinow, R. (2005) · Science · doi:10.1126/science.1103944 · Cited by 775

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

Regulation of AMPA Receptor–Mediated Synaptic Transmission by Clathrin-Dependent Receptor Internalization

Man, H., Lin, J., Ju, W. H., Ahmadian, G., Liu, L., Becker, L. E., Sheng, M., & Wang, Y. T. (2000) · Neuron · doi:10.1016/s0896-6273(00)81067-3 · Cited by 711

NSF Binding to GluR2 Regulates Synaptic Transmission

Nishimune, A., Isaac, J. T. R., Molnár, E., Noël, J., Nash, S. R., Tagaya, M., Collingridge, G. L., Nakanishi, S., & Henley, J. M. (1998) · Neuron · doi:10.1016/s0896-6273(00)80517-6 · Cited by 545

Role of the Basolateral Amygdala in the Storage of Fear Memories across the Adult Lifetime of Rats

Gale, G. D., Anagnostaras, S., Godsil, B. P., Mitchell, S., Nozawa, T., Sage, J. R., Wiltgen, B. J., & Fanselow, M. S. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.4100-03.2004 · Cited by 454

Protein kinase Mζ is necessary and sufficient for LTP maintenance

Ling, D. S. F., Benardo, L. S., Serrano, P. A., Blace, N., Kelly, M. T., Crary, J. F., & Sacktor, T. C. (2002) · Nature Neuroscience · doi:10.1038/nn829 · Cited by 419

Overexpression of protein kinase Mζ in the hippocampus mitigates Alzheimer’s disease-related cognitive deficit in rats

Amini, N., Azad, R. R., Motamedi, F., Mirzapourdelavar, H., Ghasemi, S., Aliakbari, S., & Pourbadie, H. G. (2020) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2020.11.001 · Cited by 8

The molecular diversity of plasticity mechanisms underlying memory: An evolutionary perspective

Zha, C., & Sossin, W. S. (2022) · Journal of Neurochemistry · doi:10.1111/jnc.15717 · Cited by 10

AMPA Receptor in Ventromedial Prefrontal Cortex Plays Different Roles in the Recent and Remote Retrieval of Morphine-Associated Memory

Sun, X., Wang, N., Wang, X., Sun, L., Li, Y., & Cui, C. (2019) · Neurochemical Research · doi:10.1007/s11064-019-02827-z · Cited by 8

Synaptic Correlates of Aging and Cognitive Decline

Hara, Y., & Morrison, J. H. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-418675-0.00010-9 · Cited by 8

Behavioral tagging: Plausible involvement of PKMζ, Arc and role of neurotransmitter receptor systems

Vishnoi, S., Naseem, M., Raisuddin, S., & Parvez, S. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.07.009 · Cited by 8

On the Temporary Nature of Disruption of Fear-Potentiated Startle Following PKMζ Inhibition in the Amygdale

Nader, K. (2011) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2011.00029 · Cited by 7

Fear Memory Retrieval Is Associated With a Reduction in AMPA Receptor Density at Thalamic to Amygdala Intercalated Cell Synapses

Seewald, A., Schönherr, S., Hörtnagl, H., Ehrlich, I., Schmuckermair, C., & Ferraguti, F. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.634558 · Cited by 7

Long-Term Memory Search across the Visual Brain

Fedurco, M. (2012) · Neural Plasticity · doi:10.1155/2012/392695 · Cited by 6

Sex differences in the contributions of spinal atypical PKCs and downstream targets to the maintenance of nociceptive sensitization

George, N. C., Laferrière, A., & Coderre, T. J. (2019) · Molecular Pain · doi:10.1177/1744806919840582 · Cited by 6

A computational model of systems memory consolidation and reconsolidation

Helfer, P., & Shultz, T. R. (2019) · Hippocampus · doi:10.1002/hipo.23187 · Cited by 8

A role for Numb in Protein kinase M (PKM)‐mediated increase in surface AMPA receptors during facilitation in Aplysia

Farah, C. A., Dunn, T. W., Hastings, M. H., Ferguson, L., Gao, C., Gong, K., & Sossin, W. S. (2019) · Journal of Neurochemistry · doi:10.1111/jnc.14807 · Cited by 6

Increased N-Ethylmaleimide-Sensitive Factor Expression in Amygdala and Perirhinal Cortex during Habituation of Taste Neophobia

Gómez-Chacón, B., Gámiz, F., Foster, T. C., & Gallo, M. (2015) · Neural Plasticity · doi:10.1155/2016/2726745 · Cited by 6

Gone but not forgotten

Parsons, R. G. (2011) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2011.00051 · Cited by 6

Infusing zeta inhibitory peptide into the perirhinal cortex of rats abolishes long-term object recognition memory without affecting novel object location recognition

Augereau, K., Migues, P. V., & Hardt, O. M. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.1007748 · Cited by 5

Karim Nader and the unification of memory erasure: PKMζ inhibition and reconsolidation blockade

Sacktor, T. C. (2023) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2023.02.001 · Cited by 5

Up-regulation of PKMζ expression in the anterior cingulate cortex following experimental tooth movement in rats

Xin, Y., Liu, X., Cao, Y., Chen, Y., & Liu, C. (2014) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2014.04.002 · Cited by 5

Try to Remember: Interplay between Memory and Substance Use Disorder

Mohamed, R. M. P., Kumar, J., Yap, E., Mohamed, I. N., Sidi, H., Adam, R. L., & Das, S. (2018) · Current Drug Targets · doi:10.2174/1389450118666170622092824 · Cited by 5

Antinociceptive effects of lead acetate in sciatic nerve chronic constriction injury model of peripheral neuropathy in male Wistar rats

Owoyele, B. V., Bakare, A. O., Ayinla, M. T., Adeshina, K. A., Onietan, D., & Azeez, S. O. (2020) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-020-01951-w · Cited by 5

Long-Term Potentiation and Long-Term Depression

Ivanco, T. L. (2015) · Elsevier eBooks · doi:10.1016/b978-0-08-097086-8.55034-x · Cited by 5

Breaking boundaries: Dopamine’s role in prediction error, salient novelty, and memory reconsolidation

O'Neill, O. S., & Winters, B. D. (2025) · Neuroscience · doi:10.1016/j.neuroscience.2025.12.038 · Cited by 4

Molecular Mechanism of Memory Modification

Balaban, P. M. (2018) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-018-0624-2 · Cited by 4

Molecular Underpinnings of Memory Persistence and Forgetting

Dalto, J. F., Medina, J. H., & Pastor, V. E. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70089 · Cited by 4

Intracerebellar infusion of the protein kinase M zeta (PKMζ) inhibitor zeta-inhibitory peptide (ZIP) disrupts eyeblink classical conditioning.

Chihabi, K., Morielli, A. D., & Green, J. T. (2016) · Behavioral Neuroscience · doi:10.1037/bne0000140 · Cited by 4

GSK-3β activation is required for ZIP-induced disruption of learned fear

Song, S., Kim, J., Park, K., Lee, J., Park, S., Lee, S., Kim, J., Hong, I., Song, B., & Choi, S. (2020) · Scientific Reports · doi:10.1038/s41598-020-75130-5 · Cited by 5

Histone Deacetylase Inhibitor Prevents Memory Impairment by Methiothepin

Zuzina, A. B., Vinarskaya, A. K., Balaban, P. M., & Roshchin, M. V. (2021) · Advances in intelligent systems and computing · doi:10.1007/978-3-030-71637-0_71 · Cited by 4

A critical role for long-term potentiation mechanisms in the maintenance of object recognition memory in perirhinal cortex revealed by the infusion of zeta inhibitory pseudosubstrate

Outram, A. R., Brown, M. W., Warburton, E. C., & Barker, G. R. I. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.970291 · Cited by 4

Transcriptome analysis of hippocampal subfields identifies gene expression profiles associated with long-term active place avoidance memoryPreprint

Harris, R. M., Kao, H., Alarcón, J. M., Fenton, A. A., & Hofmann, H. A. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.02.05.935759 · Cited by 4

Histone deacetylase inhibitor RG2833 has therapeutic potential for Alzheimer’s disease in femalesPreprint

Ndukwe, K., Serrano, P. A., Rockwell, P., Xie, L., & Figueiredo‐Pereira, M. E. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.26.573348 · Cited by 4

Glutamate receptors as regulators of synaptic plasticity in neuropsychiatric disorders: pathological insight and translational perspectives

Srivastava, J., Yadav, J., & Dubey, N. (2026) · Cognitive Neurodynamics · doi:10.1007/s11571-026-10446-y · Cited by 3

Long-term memory persistence

Izquierdo, I., Cammarota, M., & Medina, J. H. (2010) · Future Neurology · doi:10.2217/fnl.10.60 · Cited by 3

Intra-periaqueductal gray infusion of zeta inhibitory peptide attenuates pain-conditioned place avoidance in rats

Sun, J., Lu, B., Yao, J., Lei, W., Huang, Y., Zhang, H., & Xiao, C. (2014) · Brain Research · doi:10.1016/j.brainres.2014.07.027 · Cited by 3

Synaptic Tagging and Capture: Functional Implications and Molecular Mechanisms

Prodan, A., & Morris, R. (2024) · Springer eBooks · doi:10.1007/978-3-031-54864-2_1 · Cited by 3

AMPA receptor trafficking in recent vs. remote memory

Ghazal, P. (2016) · Brain Research · doi:10.1016/j.brainres.2016.09.010 · Cited by 3

Roles of Protein Kinase C and Protein Kinase M in Aplysia Learning

Hastings, M. H., Farah, C. A., & Sossin, W. S. (2013) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-415823-8.00018-6 · Cited by 3

PKMζ Maintains Remote Contextual Fear Memory by Inhibiting GluA2-Dependent AMPA Receptor Endocytosis in the Prelimbic Cortex

Marcondes, L. A., Myskiw, J. D. C., Nachtigall, E. G., Narvaes, R. F., Izquierdo, I., & Furini, C. R. G. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.12.028 · Cited by 3

Fear learning-induced changes in AMPAR and NMDAR expression in the fear circuitPreprint

Shultz, B., Farkash, A., Collins, B., Mohammadmirzaei, N., & Knox, D. (2022) · Learning & Memory · doi:10.1101/lm.053525.121 · Cited by 3

Fear Axis Disorders

Masson, S., Bleuer‐Elsner, S., Muller, G., Médam, T., Chevallier, J., & Gaultier, E. (2024) · Springer eBooks · doi:10.1007/978-3-031-53012-8_8 · Cited by 2

Amygdala stimulation transforms short-term memory into remote memory by persistent activation of atypical PKC in the anterior cingulate cortex

Almaguer‐Melian, W., Mercerón‐Martínez, D., Alacán‐Ricardo, L., Pina, A. B., Hsieh, C., Bergado, J. A., & Sacktor, T. C. (2024) · Neuroscience · doi:10.1016/j.neuroscience.2025.01.065 · Cited by 2

Persistently Increased Expression of PKMzeta and Unbiased Gene Expression Profiles Identify Hippocampal Molecular Traces of a Long‐Term Active Place Avoidance Memory and “Shadow” Proteins

Han, J., Grau-Perales, A. B., Harris, R. M., Lesburguères, E., Kao, H., Pal, A., Alarcón, J. M., Sacktor, T. C., Martiniani, S., Hofmann, H. A., et al. (2026) · Advanced Science · doi:10.1002/advs.202521254 · Cited by 4

PKMζ Is Not Required for Development of Postsurgical Pain

Liu, S., Li, C., Yan, G., Xing, Y., & Tao, F. (2017) · Molecular Neurobiology · doi:10.1007/s12035-017-0499-1 · Cited by 2

Influence of moxibustion on NR2B and PKMζ after neural stem cell transplantation in the rats with vascular dementia

Sun, R., Yang, J., Wang, P., Fan, Y., Cui, J., Zhang, W., Wang, S., & (季荣), R. J. (2021) · 世界针灸杂志：英文版 · doi:10.1016/j.wjam.2021.05.007 · Cited by 2

Can RNA Affect Memory Modulation? Implications for PTSD Understanding and Treatment

Cohen, T., & Shomron, N. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241612908 · Cited by 2

GDNF facilitates cognitive function recovery following neonatal surgical-induced learning and memory impairment via activation of the RET pathway and modulation of downstream effectors PKMζ and Kalirin in rats

Chen, Y., Zheng, Y.-X., Li, Y., Jia, Z. Y., & Yuan, Y. (2024) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2024.111078 · Cited by 2

Neuroplasticity in the Pain, Emotion, and Cognition Nexus

Pickering, G. P. (2015) · Springer eBooks · doi:10.1007/978-3-319-12033-1_5 · Cited by 3

Cortical zeta-inhibitory peptide injection reduces local sleep need

Carroll, C. M., Hsiang, H. W., Snyder, S., Forsberg, J., & Dash, M. B. (2019) · SLEEP · doi:10.1093/sleep/zsz028 · Cited by 2

Persistent Increases of PKMM in Sensorimotor Cortex Maintain Procedural long-Term Memory StoragePreprint

Gao, P. P., Goodman, J. H., Sacktor, T. C., & Francis, J. T. (2018) · SSRN Electronic Journal · doi:10.2139/ssrn.3188398 · Cited by 2

Females outperform males in spatial learning despite increased amyloid plaques and microgliosis in a TgF344-AD rat model of Alzheimer’s diseasePreprint

Chaudry, O., Ndukwe, K., Xie, L., Serrano, P. A., Figueiredo‐Pereira, M. E., & Rockwell, P. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.03.27.485975 · Cited by 2

Collapsin response mediator protein 2 modulates synaptic function by stabilizing the surface expression of phosphorylated AMPA receptor GluA2 subunits

Wu, J., Ren, B., Yin, Y., Cheng, L., Li, J., Chen, K., Guo, G., & Zhang, J. (2025) · Brain Research · doi:10.1016/j.brainres.2025.149798 · Cited by 1

Enrichment-induced forgetting is associated with white matter microstructure in mice

Gazdzinski, L. M., Mak, J., Lin, X. (., Lerch, J. P., Sled, J. G., Nieman, B. J., & Wheeler, A. L. (2025) · Behavioural Brain Research · doi:10.1016/j.bbr.2025.115878 · Cited by 1

HDAC Inhibition Reshapes Splicing of Synaptic Plasticity-Related Genes and Neural Network Dynamics

Beletskiy, A., Leontovich, Y. A., Aseyev, N., Balaban, P. M., & Borodinova, A. A. (2026) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-026-01693-y · Cited by 1

Effects of methamphetamine on sexual behavior

Frohmader, K. S. (2011) · Scholarship@Western (Western University) · Cited by 1

Involvement of Protein Kinase Mζ in the Maintenance of Long-Term Memory for Taste Aversion Learning in Young Chicks

Тиунова, А. А., Bezryadnov, D. V., & Анохин, К. В. (2015) · Bulletin of Experimental Biology and Medicine · doi:10.1007/s10517-015-2813-0 · Cited by 1

Multiple Stages of Memory Formation and Persistence

Medina, J. H., & Cammarota, M. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21099-7 · Cited by 1

21st century excitatory amino acid research: A Q & A with Jeff Watkins and Dick Evans

Watkins, J. C., Evans, R. H., Bayés, À., Booker, S. A., Gibb, A. J., Mabb, A. M., Mayer, M. L., Mellor, J. R., Molnár, E., Niu, L., et al. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108743 · Cited by 2

Involvement of PKMζ in Stress Response and Depression

Liu, J. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.907767 · Cited by 1

Protein Kinase Mζ-Dependent Maintenance of GluA2 at the Synapse: A Possible Target for Preventing or Treating Age-Related Memory Decline?

Aicardi, G. (2013) · Rejuvenation Research · doi:10.1089/rej.2013.1448 · Cited by 1

An integrative model of AMPA receptor trafficking reveals the central contribution of local translation in subtype-specific kineticsPreprint

Wagle, S., Kracht, M. K., Bührke, A., Acker‐Palmer, A., Kraynyukova, N., Hafner, A., Schuman, E. M., & Tchumatchenko, T. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.08.637220 · Cited by 1

Abolition of the Morphological Correlate of Long-Term Facilitation in Aplysia

Sun, P. Y. (2013) · eScholarship (California Digital Library)

Protein Kinases in Spinal Plasticity: A Role for Metabotropic Glutamate Receptors

Russell, J. A., & Adam, R. (2012) · InTech eBooks · doi:10.5772/37788

Mecanismos neurobiológicos involucrados en la persistencia de la memoria de largo término: rol de C-fos en hipocampo y corteza retrosplenial

Katche, C. (2011) · Repositorio Digital Institucional de la Universidad de Buenos Aires (Universidad de Buenos Aires)

Stress, emotional learning and AMPA receptors: from behavior to molecule

Mengyuan, Z. (2011) · UvA-DARE (University of Amsterdam)

Sistemas neurales implicados en aprendizaje aversivo gustativo complejo: comparación con otros tipos de memoria y efecto de la edad

Gámiz, F. (2012) · Institutional Repository of the University of Granada (University of Granada)

WntSignalinginAmygdala-DependentLearning andMemory

Maguschak, K. A. (2011)

Nociceptors via Protein Kinase C Sensory Nerve Terminal Mitochondrial Dysfunction Induces Hyperexcitability in Airway

Kays, J. S., Hodgdon, K. E., Sacktor, T. C., Nicol, G. D., Strey, K. A., Nichols, N. L., Baertsch, N. A., Broytman, O., Tracy, L. M., Hadley, S. H., et al. (2015)

An Alternative Mechanism for Long-Term Memory Formation

Radwańska, K., & Giese, K.-P. (2015) · Springer eBooks · doi:10.1007/978-3-319-24364-1_5

The organization of proteins involved in synaptic plasticity

Jacob, A. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/6mpm-0w63

Plasticity and Memory in Cerebral Cortex

Finnie, P. S. B., Bear, M. F., & Cooke, S. F. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21079-1

Role of the Anterior Cingulate Cortex in Fear Learning and Sensation Related Behaviors

Descalzi, G. (2014) · TSpace (University of Toronto)

The Role of Acetylcholine Nicotinic Receptors, Protein Kinase B and Protein Kinase M on the Protective Effect of Rosmarinic Acid in Beta Amyloid (25-35) Induced Rat Model of Alzheimer’s Disease

Baluchnejadmojarad, T., Roghani, M., & Kazemloo, P. (2017) · Journal of Advances in Medical and Biomedical Research

A post-synaptic forgetting mechanism controlled by synaptotagmin 3

Awasthi, A. (2018) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-6858

Reversing Cocaine-Induced Plasticity with Zeta Inhibitory Peptide

Deutschmann, A. U., Lenz, J. D., McGrath, A. G., & Briand, L. A. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.1367-19.2019

Neurogenesis-mediated Forgetting in Morris Water Maze

Duan, C. (2020) · TSpace (University of Toronto)

GluR2Q and GluR2R AMPA Subunits are not Targets of lypd2 Interaction

Lauriello, A., McVeigh, Q., & Sung, R. (2022) · PLoS ONE · doi:10.1371/journal.pone.0278278

Amygdala stimulation transforms short-term memory into remote memory by persistent activation of atypical PKC in the anterior cingulate cortexPreprint

Almaguer‐Melian, W., Mercerón‐Martínez, D., Alacán‐Ricardo, L., Pina, A. B., Hsieh, C., Bergado, J. A., & Sacktor, T. C. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.17.613040

Unraveling engrams: Tracing memories through time

Lee, J. J., Zaheer, M., Zbaranska, S., & Josselyn, S. A. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15754-7.00040-7

Environmental Enrichment During Adolescence Improves Spatial Learning and Modulates Glua2 Containing Spines in the HippocampusPreprint

Alliger, A. A., Luine, V. N., Carvajal, B. V., Omelchenko, A., Sanchez, S., Avila, J. A., & Serrano, P. A. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.4977829

Role of the Hippocampus in Adaptive Forgetting: A Question of Synaptic Depression?

Malleret, G. (2025) · IntechOpen eBooks · doi:10.5772/intechopen.1008782

Disorders Related to Dysregulation of the Fear Axis

Bleuer‐Elsner, S., Masson, S., Lacoste, M., & Muller, G. (2026) · Springer eBooks · doi:10.1007/978-3-032-06260-4_8

PKMζ in the prefrontal cortex alters cocaine cue-induced reinstatement in a sex-specific manner

Kniffin, A. R., English, E. A., Peiris, M. R., & Briand, L. A. (2026) · Psychopharmacology · doi:10.1007/s00213-026-07024-9

Investigating the role of hippocampo-thalamic-cortical communication during memory consolidation and fear expression

Andrews, C. (2023) · theses.fr (ABES) · doi:10.70675/f6440870zaf96z4fffz911cz1de8d0a8ad0e

Generating models for isoform-specific PKM-KIBRA interactions with BIFC, stabilization and AlphaFold 3

Amoah, E., Dunn, T. W., Ferguson, L., Diaz, K. B., O’Donnell, C., Kremerskoten, J., & Sossin, W. S. (2026) · Molecular Brain · doi:10.1186/s13041-026-01321-2

Myosin IIB Maintains Long‐Term Memory

Silva, M. O., Leite, L. M., Lunardi, P. S., Popik, B., Porto, R. R., Medeiros, M. D. S., & Alvares, L. D. O. (2026) · Hippocampus · doi:10.1002/hipo.70112

PKMζ Maintains Late Long-Term Potentiation by N -Ethylmaleimide-Sensitive Factor/GluR2-Dependent Trafficking of Postsynaptic AMPA Receptors

Yao, Y., Kelly, M. T., Sajikumar, S., Serrano, P. A., Tian, D., Bergold, P. J., Frey, J. U., & Sacktor, T. C. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0223-08.2008 · Cited by 272

PKMζ Maintains Remote Contextual Fear Memory by Inhibiting GluA2-Dependent AMPA Receptor Endocytosis in the Prelimbic Cortex

Marcondes, L. A., Myskiw, J. D. C., Nachtigall, E. G., Narvaes, R. F., Izquierdo, I., & Furini, C. R. G. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.12.028 · Cited by 3

Increased PKMζ activity impedes lateral movement of GluA2-containing AMPA receptors

Yu, N., Uhm, H., Shim, J.-H., Choi, J., Bae, S., Sacktor, T. C., Hohng, S., & Kaang, B. (2017) · Molecular Brain · doi:10.1186/s13041-017-0334-7 · Cited by 18

Protein kinase Mzeta maintains fear memory in the amygdala but not in the hippocampus.

Kwapis, J. L., Jarome, T. J., Lonergan, M. E., & Helmstetter, F. J. (2009) · Behavioral Neuroscience · doi:10.1037/a0016343 · Cited by 86

The role of PKMζ in the maintenance of long-term memory: a review

Patel, H., & Zamani, R. (2021) · Reviews in the Neurosciences · doi:10.1515/revneuro-2020-0105 · Cited by 23