Sodium butyrate as a selective cognitive enhancer for weak or impaired memory

Translating the Histone Code

Jenuwein, T., & Allis, C. D. (2001) · Science · doi:10.1126/science.1063127 · Cited by 9,756 · 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

HDAC2 negatively regulates memory formation and synaptic plasticity

Guan, J.-S., Haggarty, S. J., Giacometti, E., Dannenberg, J.-H., Joseph, N., Gao, J., Nieland, T. J. F., Zhou, Y., Wang, X., Mazitschek, R., et al. (2009) · Nature · doi:10.1038/nature07925 · Cited by 1,644 · see citing works

Cooperation between Complexes that Regulate Chromatin Structure and Transcription

Narlikar, G. J., Fan, H.-Y., & Kingston, R. E. (2002) · Cell · doi:10.1016/s0092-8674(02)00654-2 · Cited by 1,486 · see citing works

Regulation of histone acetylation during memory formation in the hippocampus

Levenson, J. M., O'Riordan, K. J., Brown, K. D., Trinh, M. A., Molfese, D. L., & Sweatt, J. D. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m402229200 · Cited by 1,131 · 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

Engineering a memory with LTD and LTP

Nabavi, S., Fox, R., Proulx, C. D., Lin, J. Y., Tsien, R. Y., & Malinow, R. (2014) · Nature · doi:10.1038/nature13294 · Cited by 980 · see citing works

Chromatin Acetylation, Memory, and LTP Are Impaired in CBP+/− Mice

Alarcón, J. M., Malleret, G., Touzani, K., Vronskaya, S., Ishii, S., Kandel, E. R., & Barco, A. (2004) · Neuron · doi:10.1016/j.neuron.2004.05.021 · Cited by 892 · 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

Histone Deacetylase Inhibitors Enhance Memory and Synaptic Plasticity via CREB: CBP-Dependent Transcriptional Activation

Vecsey, C. G., Hawk, J. D., Lattal, K. M., Stein, J. M., Fabian, S., Attner, M. A., Cabrera, S. M., McDonough, C. B., Brindle, P. K., Abel, T. G., et al. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0296-07.2007 · Cited by 828 · see citing works

CBP Histone Acetyltransferase Activity Is a Critical Component of Memory Consolidation

Korzus, E., Rosenfeld, M. G., & Mayford, M. (2004) · Neuron · doi:10.1016/j.neuron.2004.06.002 · Cited by 823 · see citing works

Epigenetic mechanisms in memory formation

Levenson, J. M., & Sweatt, J. D. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1604 · Cited by 767 · see citing works

Inhibitors of Class 1 Histone Deacetylases Reverse Contextual Memory Deficits in a Mouse Model of Alzheimer's Disease

Kilgore, M., Miller, C. A., Fass, D. M., Hennig, K. M., Haggarty, S. J., Sweatt, J. D., & Rumbaugh, G. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.197 · Cited by 727 · see citing works

Contextual and temporal modulation of extinction: behavioral and biological mechanisms

Bouton, M. E., Westbrook, R. F., Corcoran, K. A., & Maren, S. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.12.015 · Cited by 671 · see citing works

Histone modifications around individual BDNF gene promoters in prefrontal cortex are associated with extinction of conditioned fear

Bredy, T. W., Wu, H., Crego, C., Zellhoefer, J., Sun, Y. E., & Barad, M. (2007) · Learning & Memory · doi:10.1101/lm.500907 · Cited by 548 · see citing works

Special HATs for special occasions: linking histone acetylation to chromatin assembly and gene activation

Brownell, J. E., & Allis, C. D. (1996) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(96)80048-7 · Cited by 534 · see citing works

Integration of Long-Term-Memory-Related Synaptic Plasticity Involves Bidirectional Regulation of Gene Expression and Chromatin Structure

Guan, Z., Giustetto, M., Lomvardas, S., Kim, J.-H., Miniaci, M. C., Schwartz, J. H., Thanos, D., & Kandel, E. R. (2002) · Cell · doi:10.1016/s0092-8674(02)01074-7 · Cited by 497 · see citing works

Reconsolidation and Extinction of Conditioned Fear: Inhibition and Potentiation

Lee, J. L. C., Milton, A. L., & Everitt, B. J. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.2466-06.2006 · Cited by 479 · 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

Epigenetic regulation of memory formation and maintenancePreprint

Zovkic, I. B., Karlsson, M. G., & Sweatt, J. D. (2013) · Learning & Memory · doi:10.1101/lm.026575.112 · Cited by 362 · see citing works

Epigenetic Priming of Memory Updating during Reconsolidation to Attenuate Remote Fear Memories

Gräff, J., Joseph, N. F., Horn, M. E., Samiei, A., Meng, J., Seo, J., Rei, D., Bero, A. W., Phan, T. X., Wagner, F., et al. (2014) · Cell · doi:10.1016/j.cell.2013.12.020 · Cited by 357 · see citing works

Transgenic mice expressing a truncated form of CREB-binding protein (CBP) exhibit deficits in hippocampal synaptic plasticity and memory storagePreprint

Wood, M. A., Kaplan, M. P., Park, A., Blanchard, E. J., Oliveira, A. M. M., Lombardi, T. L., & Abel, T. G. (2005) · Learning & Memory · doi:10.1101/lm.86605 · Cited by 333 · see citing works

Drug Insight: histone deacetylase inhibitors—development of the new targeted anticancer agent suberoylanilide hydroxamic acid

Kelly, W. K., & Marks, P. A. (2005) · Nature Clinical Practice Oncology · doi:10.1038/ncponc0106 · Cited by 330 · see citing works

Histone deacetylase inhibitors: discovery and development as anticancer agents

Marks, P. A., & Dokmanovic, M. (2005) · Expert Opinion on Investigational Drugs · doi:10.1517/13543784.14.12.1497 · Cited by 318 · see citing works

Memory Suppressor Genes: Inhibitory Constraints on the Storage of Long-Term Memory

Abel, T. G., Martin, K. C., Bartsch, D., & Kandel, E. R. (1998) · Science · doi:10.1126/science.279.5349.338 · Cited by 316 · see citing works

Truncated CBP protein leads to classical Rubinstein-Taybi syndrome phenotypes in mice: implications for a dominant-negative mechanism

Oike, Y. (1999) · Human Molecular Genetics · doi:10.1093/hmg/8.3.387 · Cited by 306 · see citing works

Retrieval of memory for fear-motivated training initiates extinction requiring protein synthesis in the rat hippocampus

Vianna, M., Szapiro, G., McGaugh, J. D., Medina, J., & Izquierdo, I. (2001) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.211433298 · Cited by 301 · see citing works

Positive and negative regulatory mechanisms that mediate long-term memory storage

Abel, T. G., & Kandel, E. R. (1998) · Brain Research Reviews · doi:10.1016/s0165-0173(97)00050-7 · Cited by 265 · see citing works

Stability of recent and remote contextual fear memory

Frankland, P. W., Ding, H.-K., Takahashi, E., Suzuki, A., Kida, S., & Silva, A. J. (2006) · Learning & Memory · doi:10.1101/lm.183406 · Cited by 259 · see citing works

The histone deacetylase inhibitor valproic acid enhances acquisition, extinction, and reconsolidation of conditioned fearPreprint

Bredy, T. W., & Barad, M. (2008) · Learning & Memory · doi:10.1101/lm.801108 · Cited by 248 · see citing works

Systemic or intrahippocampal delivery of histone deacetylase inhibitors facilitates fear extinction.

Lattal, K. M., Barrett, R. M., & Wood, M. A. (2007) · Behavioral Neuroscience · doi:10.1037/0735-7044.121.5.1125 · Cited by 236 · see citing works

The IκB Kinase Regulates Chromatin Structure during Reconsolidation of Conditioned Fear Memories

Lubin, F. D., & Sweatt, J. D. (2007) · Neuron · doi:10.1016/j.neuron.2007.07.039 · Cited by 234 · see citing works

Acetylation of Nuclear Factor-κB in Rat Amygdala Improves Long-Term but not Short-Term Retention of Fear Memory

Yeh, S.-H., Lin, C.-H., & Gean, P. (2004) · Molecular Pharmacology · doi:10.1124/mol.65.5.1286 · Cited by 198 · see citing works

Histone deacetylases in memory and cognition

Penney, J., & Tsai, L. (2014) · Science Signaling · doi:10.1126/scisignal.aaa0069 · Cited by 192 · see citing works

HDAC1 Regulates Fear Extinction in Mice

Bahari‐Javan, S., Maddalena, A., Kerimoglu, C., Wittnam, J. L., Held, T., Bähr, M., Burkhardt, S., Delalle, I., Kügler, S., Fischer, A., et al. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0079-12.2012 · Cited by 186 · see citing works

Increasing Histone Acetylation in the Hippocampus-Infralimbic Network Enhances Fear Extinction

Stafford, J. M., Raybuck, J. D., Ryabinin, A. E., & Lattal, K. M. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.12.012 · Cited by 157 · see citing works

Reinstatement of long-term memory following erasure of its behavioral and synaptic expression in Aplysia

Chen, S., Cai, D., Pearce, K. C., Sun, P. Y., Roberts, A. C., & Glanzman, D. L. (2014) · eLife · doi:10.7554/elife.03896 · Cited by 150 · see citing works

Deacetylase Activity Is Required for cAMP Activation of a Subset of CREB Target Genes

Fass, D. M., Butler, J. E. F., & Goodman, R. H. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m305905200 · Cited by 136 · see citing works

Epigenetic alterations in the lateral amygdala are required for reconsolidation of a Pavlovian fear memoryPreprint

Maddox, S. A., & Schafe, G. E. (2011) · Learning & Memory · doi:10.1101/lm.2243411 · Cited by 130 · see citing works

Sodium Butyrate Prevents Memory Impairment by Re-Establishing BDNF and GDNF Expression in Experimental Pneumococcal Meningitis

Barichello, T., Generoso, J. S., Simões, L. R., Faller, C. J., Ceretta, R. A., Petronilho, F., Lopes-Borges, J., Valvassori, S. S., & Quevedo, J. (2015) · Molecular Neurobiology · doi:10.1007/s12035-014-8914-3 · Cited by 125 · see citing works

Posttraining systemic administration of the histone deacetylase inhibitor sodium butyrate ameliorates aging-related memory decline in rats

Reolon, G. K., Maurmann, N., Werenicz, A., Garcia, V. A., Schröder, N., Wood, M. A., & Roesler, R. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.03.033 · Cited by 94 · see citing works

Histone acetylation is recruited in consolidation as a molecular feature of stronger memoriesPreprint

Federman, N., Fustiñana, M. S., & Romano, A. G. (2009) · Learning & Memory · doi:10.1101/lm.1537009 · Cited by 89 · see citing works

Role of protein synthesis and DNA methylation in the consolidation and maintenance of long-term memory in Aplysia

Pearce, K. C., Cai, D., Roberts, A. C., & Glanzman, D. L. (2017) · eLife · doi:10.7554/elife.18299 · Cited by 77 · see citing works

HDAC inhibition promotes both initial consolidation and reconsolidation of spatial memory in mice

Villain, H., Florian, C., & Roullet, P. (2016) · Scientific Reports · doi:10.1038/srep27015 · Cited by 54 · see citing works

Activation of NF-κB in Basolateral Amygdala Is Required for Memory Reconsolidation in Auditory Fear Conditioning

Si, J., Yang, J., Xue, L., Yang, C., Luo, Y., Shi, H., & Lü, L. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043973 · Cited by 45 · see citing works

Bridging Synaptic and Epigenetic Maintenance Mechanisms of the Engram

Kyrke‐Smith, M., & Williams, J. M. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00369 · Cited by 40 · see citing works

Basolateral amygdala activity is required for enhancement of memory consolidation produced by histone deacetylase inhibition in the hippocampus

Blank, M., Dornelles, A. D. S., Werenicz, A., Velho, L. A., Pinto, D. F., Fedi, A. C., Schröder, N., & Roesler, R. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.02.009 · Cited by 39 · see citing works

Reconsolidation and extinction: Using epigenetic signatures to challenge conventional wisdom

Hemstedt, T. J., Lattal, K. M., & Wood, M. A. (2017) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2017.01.007 · Cited by 30 · see citing works

Enhancement of memory consolidation by the histone deacetylase inhibitor sodium butyrate in aged rats

Blank, M., Werenicz, A., Velho, L. A., Pinto, D. F., Fedi, A. C., Lopes, M. W., Peres, T. V., Leal, R. B., Dornelles, A. D. S., & Roesler, R. (2015) · Neuroscience Letters · doi:10.1016/j.neulet.2015.03.059 · Cited by 28 · see citing works

Cued memory reconsolidation in rats requires nitric oxide

Bal, N. V., Rysakova, M. P., Vinarskaya, A. K., Ivanova, V. O., Zuzina, A. B., & Balaban, P. M. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13503 · Cited by 24 · see citing works

Histone deacetylase inhibitor treatment restores memory‐related gene expression and learning ability in neonicotinoid‐treated Apis mellifera

Hu, Y. ‐., Tang, C.-K., Wu, C. ‐., Wu, P., Yang, E., Tai, C. ‐., & Wu, Y. ‐. (2018) · Insect Molecular Biology · doi:10.1111/imb.12390 · Cited by 24 · see citing works

Epigenetic Regulation as a Basis for Long-Term Changes in the Nervous System: In Search of Specificity Mechanisms

Borodinova, A. A., & Balaban, P. M. (2020) · Biochemistry (Moscow) · doi:10.1134/s0006297920090023 · Cited by 24 · see citing works

TrkB blockade in the hippocampus after training or retrieval impairs memory: protection from consolidation impairment by histone deacetylase inhibition

Blank, M., Petry, F. D. S., Lichtenfels, M., Valiati, F. E., Dornelles, A. D. S., & Roesler, R. (2015) · Journal of Neural Transmission · doi:10.1007/s00702-015-1464-7 · Cited by 20 · see citing works

The role of nuclear PKMζ in memory maintenance

Ko, H., Kim, J., Sim, S.-E., Kim, T., Yoo, J., Choi, S.-L., Baek, S. H., Yu, W.-J., Yoon, J., Sacktor, T. C., et al. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.06.010 · Cited by 20 · see citing works

Histone deacetylase inhibitors rescue the impaired memory in terrestrial snails

Zuzina, A. B., Vinarskaya, A. K., & Balaban, P. M. (2020) · Journal of Comparative Physiology A · doi:10.1007/s00359-020-01422-w · Cited by 18 · see citing works

Effects of Systemic Administration of Histone Deacetylase Inhibitor on Memory Formation and Immediate Early Gene Expression in Chick Brain

Тиунова, А. А., Toropova, K. A., Коновалова, Е. В., & Anokhin, K. V. (2012) · Bulletin of Experimental Biology and Medicine · doi:10.1007/s10517-012-1815-4 · Cited by 4 · see citing works

Epigenetic regulation in major depression and other stress-related disorders: molecular mechanisms, clinical relevance and therapeutic potential

Yuan, M., Yang, B., Rothschild, G., Mann, J. J., Sanford, L. D., Tang, X., Huang, C., Wang, C., & Zhang, W. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01519-z · Cited by 246 · see citing works

Epigenetic Targeting of Histone Deacetylases in Diagnostics and Treatment of Depression

Park, H., Kim, J., Ahn, S. H., & Ryu, H. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22105398 · Cited by 50 · see citing works

SCFAs Ameliorate Chronic Postsurgical Pain–Related Cognition Dysfunction via the ACSS2-HDAC2 Axis in Rats

Li, Z., Sun, T., He, Z., Li, Z., Zhang, W., Wang, J., & Xiang, H. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-02971-8 · Cited by 32 · see citing works

On making (and turning adaptive to) maladaptive aversive memories in laboratory rodents

Gazarini, L., Stern, C. A. J., & Bertoglio, L. J. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105101 · Cited by 25 · see citing works

The effect of phenobarbital treatment on behavioral comorbidities and on the composition and function of the fecal microbiome in dogs with idiopathic epilepsy

Watanangura, A., Meller, S., Suchodolski, J. S., Pilla, R., Khattab, M. R., Loderstedt, S., Becker, L. F., Bathen‐Nöthen, A., Mazzuoli‐Weber, G., & Volk, H. A. (2022) · Frontiers in Veterinary Science · doi:10.3389/fvets.2022.933905 · Cited by 20 · see citing works

Functional recovery outcomes following acute stroke is associated with abundance of gut microbiota related to inflammation, butyrate and secondary bile acid

Hammond, T. C., Powell, E. S., Green, S. J., Chlipala, G. E., Frank, J. A., Yackzan, A. T., Yanckello, L. M., Chang, Y., Xing, X., Heil, S. D., et al. (2022) · Frontiers in Rehabilitation Sciences · doi:10.3389/fresc.2022.1017180 · Cited by 23 · see citing works

A high‐salt diet induces synaptic loss and memory impairment via gut microbiota and butyrate in mice

Lei, C., Liu, C., Peng, Y., Zhan, Y., Zhang, X., Liu, T., & Liu, Z. (2023) · iMeta · doi:10.1002/imt2.97 · Cited by 15 · see citing works

Histone Deacetylase 2-Mediated Epigenetic Regulation is Involved in the Early Isoflurane Exposure-Related Increase in Susceptibility to Anxiety-Like Behaviour Evoked by Chronic Variable Stress in Mice

Peng, L., Liu, X., Yang, Y., Guo, Q., & Zhong, T. (2021) · Neurochemical Research · doi:10.1007/s11064-021-03368-0 · Cited by 16 · see citing works

The immunomodulatory effects of ethosuximide and sodium butyrate on experimentally induced fibromyalgia: The interaction between IL-4, synaptophysin, and TGF-β1/NF-κB signaling

Elmaaboud, M. A. A., Awad, M. M., El‐Shaer, R. A. A., & Kabel, A. M. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.110061 · Cited by 11 · see citing works

Epigenetic changes caused by early life stress in the pathogenesis of depression

Bi, H., Jin, J., Sun, M., Chen, M., Li, X., & Wang, Y. (2025) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2025.177671 · Cited by 10 · see citing works

Acetylome analyses provide novel insights into the effects of chronic intermittent hypoxia on hippocampus-dependent cognitive impairment

Liu, F., Yan, W., Chen, C., Zeng, Y., Kong, Y., He, X., Pei, P., Wang, S., & Zhang, T. (2024) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2024.1324458 · Cited by 7 · see citing works

Increased histone acetylation levels or a serotonin precursor reinstate the context memory impaired by the serotonin receptor blocker methiothepin

Zuzina, A. B., & Vinarskaya, A. K. (2022) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-022-01303-6 · Cited by 7 · see citing works

Remember the gut: The emerging role of microbial SCFAs in cognitive health

de Paiva, I. H. R., Duarte-Silva, E. P., & Peixoto, C. A. (2025) · Food Bioscience · doi:10.1016/j.fbio.2025.107838 · Cited by 7 · see citing works

Microbiome‐derived metabolites in substance use disorders: Mechanisms and implications

Koperska, M., & Kiraly, D. D. (2025) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.15416 · Cited by 4 · see citing works

Contribution of histone acetylation to the serotonin-mediated long-term synaptic plasticity in terrestrial snails

Zuzina, A. B., & Balaban, P. M. (2022) · Journal of Comparative Physiology A · doi:10.1007/s00359-022-01562-1 · Cited by 4 · see citing works

DNA Methylation Inhibition Reversibly Impairs the Long-Term Context Memory Maintenance in Helix

Zuzina, A. B., Vinarskaya, A. K., & Balaban, P. M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241814068 · Cited by 4 · see citing works

Ginkgo Biloba as a niche theme cognitive enhancer agent, 1420 dokumen of Scopus database. A bibliometric study from 1988 to 2024

Saleh, A. Y., Saputra, D. A. Y., Valentina, R., & Susanto, T. D. (2025) · F1000Research · doi:10.12688/f1000research.160416.3 · Cited by 1 · see citing works

Influence of histone deacetylases inhibitor sodium butyrate on hippocampal neuronal activity in vivo

Roshchina, M. A., Borodinova, A. A., & Roshchin, M. V. (2022) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-022-01240-4 · Cited by 2 · see citing works

Modulation of Murine Hippocampal Synaptic Plasticity by Microbial Metabolites: Sex‐Specific Effects of the Short‐Chain Fatty Acid Butyrate

Collins, M., Rosell‐Cardona, C., Golubeva, A. V., McDermott, M. M., Cronin, A. M., Clarke, G., O'Riordan, K. J., & Cryan, J. F. (2024) · Neuroscience Applied · doi:10.1016/j.nsa.2024.105058 · Cited by 2 · see citing works

Pancreas-brain axis: exploring the pathogenic mechanisms of pancreatic encephalopathy

Dai, N., Geng, Z., Wang, J., Bu, X., Gong, M.-Y., Qin, C., Zhang, Y., Fu, X.-Y., & Fu, B. (2026) · International Immunopharmacology · doi:10.1016/j.intimp.2026.116332 · Cited by 2 · see citing works

Contribution of Epigenetic Mechanisms to the Formation, Maintenance, and Reconsolidation of a Long-Term Food-Related Aversive Memory in Terrestrial Snails

Zuzina, A. B., & Balaban, P. M. (2024) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-024-01576-z · Cited by 2 · see citing works

The HDAC inhibitor sodium butyrate moderately enhances long-term fear extinction memory retrieval in humans

Ribbens, C., Peeters, L., Oudenhove, L. V., Vervliet, B., & Dalile, B. (2026) · Molecular Psychiatry · doi:10.1038/s41380-026-03802-1 · Cited by 2 · see citing works

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 · see citing works

Ginkgo Biloba as a niche theme cognitive enhancer agent, 1420 dokumen of Scopus database. A bibliometric study from 1988 to 2024

Saleh, A. Y., Saputra, D. A. Y., Valentina, R., & Susanto, T. D. (2025) · F1000Research · doi:10.12688/f1000research.160416.2 · Cited by 1 · see citing works

Epigenetics of Memory Processes

Pulya, S., & Ghosh, B. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-91909-8.00018-9 · Cited by 1 · see citing works

THE CONTRIBUTION OF EPIGENETIC MECHANISMS TO THE FORMATION, MAINTENANCE AND RECONSOLIDATION OF THE LONG-TERM FOOD AVERSIVE MEMORY IN TERRESTRIAL SNAIL

Zuzina, A. B., & Balaban, P. M. (2023) · Журнал высшей нервной деятельности им И П Павлова · doi:10.31857/s0044467723050118

Increase in histone acetylation rescues a weak remote fear memory in rats

Vinarskaya, A. K., Balaban, P. M., & Zuzina, A. B. (2023) · Журнал высшей нервной деятельности им И П Павлова · doi:10.31857/s0044467723060138

Ginkgo Biloba as a niche theme cognitive enhancer agent, 1420 dokumen of Scopus database. A bibliometric study from 1988 to 2024

Saleh, A. Y., Saputra, D. A. Y., Valentina, R., & Susanto, T. D. (2025) · F1000Research · doi:10.12688/f1000research.160416.1 · Cited by 1 · see citing works

Epigenetics and epilepsy

Bhasin, J., PETER-OKAKA, U., & BOISON, D. (2026) · Handbook of clinical neurology · doi:10.1016/b978-0-443-19043-8.00006-2

Histone acetylation increase rescues a weak remote fear memory in rats

Vinarskaya, A. K., Zuzina, A. B., & Balaban, P. M. (2023) · Genes and Cells · doi:10.17816/gc623277 · Cited by 3 · see citing works

Enhancement of memory consolidation by the histone deacetylase inhibitor sodium butyrate in aged rats

Blank, M., Werenicz, A., Velho, L. A., Pinto, D. F., Fedi, A. C., Lopes, M. W., Peres, T. V., Leal, R. B., Dornelles, A. D. S., & Roesler, R. (2015) · Neuroscience Letters · doi:10.1016/j.neulet.2015.03.059 · Cited by 28 · see citing works

Increase in histone acetylation rescues a weak remote fear memory in rats

Vinarskaya, A. K., Balaban, P. M., & Zuzina, A. B. (2023) · Журнал высшей нервной деятельности им И П Павлова · doi:10.31857/s0044467723060138

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 · see citing works

Histone deacetylase inhibitors rescue the impaired memory in terrestrial snails

Zuzina, A. B., Vinarskaya, A. K., & Balaban, P. M. (2020) · Journal of Comparative Physiology A · doi:10.1007/s00359-020-01422-w · Cited by 18 · see citing works