Shrinkage of Dendritic Spines Associated with Long-Term Depression of Hippocampal Synapses

Cellular Motility Driven by Assembly and Disassembly of Actin Filaments

Pollard, T. D., & Borisy, G. G. (2003) · Cell · doi:10.1016/s0092-8674(03)00120-x · Cited by 4,334

Structural basis of long-term potentiation in single dendritic spines

Matsuzaki, M., Honkura, N., Ellis-Davies, G. C. R., & Kasai, H. (2004) · Nature · doi:10.1038/nature02617 · Cited by 2,483

Homosynaptic long-term depression in area CA1 of hippocampus and effects of N-methyl-D-aspartate receptor blockade.

Dudek, S. M., & Bear, M. F. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.10.4363 · Cited by 1,708

Dendritic spine changes associated with hippocampal long-term synaptic plasticity

Engert, F., & Bonhoeffer, T. (1999) · Nature · doi:10.1038/19978 · Cited by 1,412

Synaptic plasticity: LTP and LTD

Bear, M. F., & Malenka, R. C. (1994) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(94)90101-5 · Cited by 1,355

Structure and function of dendritic spines

Nimchinsky, E. A., Sabatini, B. L., & Svoboda, K. (2002) · Annual Review of Physiology · doi:10.1146/annurev.physiol.64.081501.160008 · Cited by 1,208

Mechanisms underlying induction of homosynaptic long-term depression in area CA1 of the hippocampus

Mulkey, R. M., & Malenka, R. C. (1992) · Neuron · doi:10.1016/0896-6273(92)90248-c · Cited by 1,113

Involvement of a calcineurin/ inhibitor-1 phosphatase cascade in hippocampal long-term depression

Mulkey, R. M., Endo, S., Shenolikar, S., & Malenka, R. C. (1994) · Nature · doi:10.1038/369486a0 · Cited by 1,083

Dendritic spines of CA 1 pyramidal cells in the rat hippocampus: serial electron microscopy with reference to their biophysical characteristics

Harris, K., & Stevens, J. (1989) · The Journal of Neuroscience · doi:10.1523/jneurosci.09-08-02982.1989 · Cited by 1,073

Abnormal dendritic spines in fragile X knockout mice: Maturation and pruning deficits

Comery, T. A., Harris, J. B., Willems, P. J., Oostra, B. A., Irwin, S. A., Weiler, I. J., & Greenough, W. T. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.10.5401 · Cited by 1,046

The Ins and Outs of miRNA-Mediated Gene Silencing during Neuronal Synaptic Plasticity

Rajgor, D., & Hanley, J. G. (2016) · Non-Coding RNA · doi:10.3390/ncrna2010001 · Cited by 15

PSD-95 in CA1 Area Regulates Spatial Choice Depending on Age

Cały, A., Śliwińska, M. A., Ziółkowska, M., Łukasiewicz, K., Pagano, R., Dzik, J. M., Kalita, K. B., Bernaś, T., Stewart, M. G., Giese, K.-P., et al. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1996-20.2020 · Cited by 17

Water diffusion reveals networks that modulate multiregional morphological plasticity after repetitive brain stimulation

Abe, M., Fukuyama, H., & Mima, T. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1320223111 · Cited by 13

Activity-Dependent Structural Plasticity of Dendritic Spines

Chapleau, C. A., & Pozzo‐Miller, L. D. (2008) · Elsevier eBooks · doi:10.1016/b978-012370509-9.00039-5 · Cited by 14

Myosin II regulates actin rearrangement-related structural synaptic plasticity during conditioned taste aversion memory extinction

Bi, A.-L., Wang, Y., Zhang, S., Li, B., Sun, Z., Bi, H., & Chen, Z.-Y. (2013) · Brain Structure and Function · doi:10.1007/s00429-013-0685-5 · Cited by 13

Polarity proteins: Shaping dendritic spines and memory

Voglewede, M. M., & Zhang, H. (2022) · Developmental Biology · doi:10.1016/j.ydbio.2022.05.007 · Cited by 14

Non-ionotropic signaling through the NMDA receptor GluN2B carboxy-terminal domain drives dendritic spine plasticity and reverses fragile X phenotypes

Barnes, S. A., Thomazeau, A., Finnie, P. S. B., Heinrich, M. J., Heynen, A. J., Komiyama, N. H., Grant, S. G. N., Menniti, F. S., Osterweil, E. K., & Bear, M. F. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115311 · Cited by 14

Network, Cellular, and Molecular Mechanisms Underlying Long-Term Memory Formation

Carasatorre, M., & Ramı́rez-Amaya, V. (2012) · Current topics in behavioral neurosciences · doi:10.1007/7854_2012_229 · Cited by 14

Neuronal Synapses: Microscale Signal Processing Machineries Formed by Phase Separation?

Feng, Z., Zeng, M., Chen, X., & Zhang, M. (2018) · Biochemistry · doi:10.1021/acs.biochem.8b00313 · Cited by 13

Neuronal mechanisms mediating pathological reward-related behaviors: A focus on silent synapses in the nucleus accumbens

McDevitt, D. S., & Graziane, N. (2018) · Pharmacological Research · doi:10.1016/j.phrs.2018.08.025 · Cited by 13

Palmitoylated Proteins in Dendritic Spine Remodeling

Albanesi, J. P., Baryłko, B., Demartino, G., & Jameson, D. M. (2020) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2020.00022 · Cited by 13

Connectivity and circuitry in a dish versus in a brain

Chinchalongporn, V., Koppensteiner, P., Prè, D., Thangnipon, W., Bilo, L., & Arancio, O. (2015) · Alzheimer s Research & Therapy · doi:10.1186/s13195-015-0129-y · Cited by 15

Dynamin Superfamily at Pre- and Postsynapses: Master Regulators of Synaptic Transmission and Plasticity in Health and Disease

Arriagada-Díaz, J., Prado‐Vega, L., Cárdenas, A. M., Ardiles, Á. O., & González‐Jamett, A. M. (2020) · The Neuroscientist · doi:10.1177/1073858420974313 · Cited by 12

Nanoscale Sub-Compartmentalization of the Dendritic Spine Compartment

Vallés, A. S., & Barrantes, F. J. (2021) · Biomolecules · doi:10.3390/biom11111697 · Cited by 14

Soluble Oligomers of the Amyloid β-Protein: Impair Synaptic Plasticity and Behavior

Selkoe, D. J. (2008) · Springer eBooks · doi:10.1007/978-3-540-76330-7_8 · Cited by 13

How to Grow a Synapse

Straub, C., & Sabatini, B. L. (2014) · Neuron · doi:10.1016/j.neuron.2014.03.033 · Cited by 12

Calcineurin knockout mice show a selective loss of small spines

Okazaki, H., Hayashi‐Takagi, A., Nagaoka, A., Negishi, M., Ucar, H., Yagishita, S., Ishii, K., Toyoizumi, T., Fox, K. D., & Kasai, H. (2018) · Neuroscience Letters · doi:10.1016/j.neulet.2018.02.006 · Cited by 12

Pathway specificity of dendritic spine morphology in identified synapses onto rat hippocampal CA1 neurons in organotypic slices

Simoni, A. D., & Edwards, F. A. (2006) · Hippocampus · doi:10.1002/hipo.20236 · Cited by 13

Aberrant synaptic PTEN in symptomatic Alzheimer's patients may link synaptic depression to network failure

Díaz González, M., Buberman, A., Morales, M., Ferrer, I., & Knafo, S. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.683290 · Cited by 12

Loss of the actin regulator cyclase-associated protein 1 (CAP1) modestly affects dendritic spine remodeling during synaptic plasticity

Heinze, A., & Rust, M. B. (2023) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2023.151357 · Cited by 12

Nobiletin improves diphenoxylate-induced constipation and the accompanied depressive behavior disorders by regulating gut-SCFAs-brain axis

Kong, X., Zhao, J. W., Gao, H., Wang, W., Wang, J., & Tan, X. (2024) · Food Bioscience · doi:10.1016/j.fbio.2024.103808 · Cited by 12

L-type Ca 2+ channel activation of STIM1–Orai1 signaling remodels the dendritic spine ER to maintain long-term structural plasticity

Dittmer, P. J., & Dell’Acqua, M. L. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2407324121 · Cited by 12

Microglial regulation of white matter development and its disruption in autism spectrum disorder

Canada, K., Evans, T. M., & Pelphrey, K. A. (2025) · Cerebral Cortex · doi:10.1093/cercor/bhaf109 · Cited by 13

Relative input strength rapidly regulates dendritic structure of chick auditory brainstem neurons

Sorensen, S. A., & Rubel, E. W. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22656 · Cited by 12

Long-Term Potentiation

Lisman, J. E., & Hell, J. W. (2008) · Springer eBooks · doi:10.1007/978-0-387-77232-5_17 · Cited by 12

Flexible Transmitter Network

Zhang, S.-Q., & Zhou, Z. (2021) · Neural Computation · doi:10.1162/neco_a_01431 · Cited by 14

miR-483-5p offsets functional and behavioural effects of stress in male mice through synapse-targeted repression of Pgap2 in the basolateral amygdala

Mucha, M. W., Skrzypiec, A. E., Kolenchery, J. B., Brambilla, V., Patel, S., Labrador-Ramos, A., Kudla, L., Murrall, K., Skene, N., Dymicka-Piekarska, V., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-37688-2 · Cited by 14

Suppression of spreading depolarization and stabilization of dendritic spines by GLYX-13, an NMDA receptor glycine-site functional partial agonist

Zhang, X.-L., Shuttleworth, C. W., Moskal, J. R., & Stanton, P. K. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.07.025 · Cited by 12

Stress influences the dynamics of hippocampal structural remodeling associated with fear memory extinction

Bender, C. L., Giachero, M., Mutis, R. C., Molina, V. A., & Calfa, G. D. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.09.002 · Cited by 12

Tianeptine modulates synaptic vesicle dynamics and favors synaptic mitochondria processes in socially isolated rats

Perić, I., Costina, V., Djordjević, S., Gass, P., Findeisen, P., Inta, D., Borgwardt, S., & Filipović, D. (2021) · Scientific Reports · doi:10.1038/s41598-021-97186-7 · Cited by 13

CREB-Dependent Transcription and Synaptic Plasticity

Barco, Á., Jančić, D., & Kandel, E. R. (2007) · Springer eBooks · doi:10.1007/978-0-387-73609-9_7 · Cited by 12

Chronic calcium imaging in neuronal development and disease

Aramuni, G., & Griesbeck, O. (2012) · Experimental Neurology · doi:10.1016/j.expneurol.2012.02.008 · Cited by 12

Brief sleep disruption alters synaptic structures among hippocampal and neocortical somatostatin-expressing interneurons

Raven, F., Vega-Medina, A., Schmidt, K., He, A., Vankampen, A. A., Balendran, V., & Aton, S. J. (2025) · SLEEP · doi:10.1093/sleep/zsaf064 · Cited by 12

Dendritic Spines and Pain Memory

Benson, C. A., King, J. F., Reimer, M. L., Kauer, S. D., Waxman, S. G., & Tan, A. M. (2022) · The Neuroscientist · doi:10.1177/10738584221138251 · Cited by 13

Involvement of primary somatosensory cortex in motor learning and task execution

Huang, Y., Zhang, X., & Li, W. (2024) · Neuroscience Letters · doi:10.1016/j.neulet.2024.137753 · Cited by 14

Chronic and Acute Manipulation of Cortical Glutamate Transmission Induces Structural and Synaptic Changes in Co-cultured Striatal Neurons

Kuhlmann, N., Valladolid, M. W., Quesada-Ramírez, L., Farrer, M. J., & Milnerwood, A. J. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.569031 · Cited by 14

Estradiol attenuates chronic restraint stress-induced dendrite and dendritic spine loss and cofilin1 activation in ovariectomized mice

Xu, H., Yu, Z.-H., Ge, M.-J., Shen, J., Han, F., Pan, C., Chen, J., Zhu, X.-L., Hou, W.-Y., Hou, Y.-Q., et al. (2021) · Hormones and Behavior · doi:10.1016/j.yhbeh.2021.105040 · Cited by 11

Age-Related Progressive Synaptic Dysfunction: The Critical Role of Presenilin 1

Auffret, A., Mariani, J., & Rovira, C. (2010) · Reviews in the Neurosciences · doi:10.1515/revneuro.2010.21.4.239 · Cited by 11

Drebrin Isoforms Critically Regulate NMDAR- and mGluR-Dependent LTD Induction

Yasuda, H., Kojima, N., Hanamura, K., Yamazaki, H., Sakimura, K., & Shirao, T. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00330 · Cited by 11

Optical interrogation of multi-scale neuronal plasticity underlying behavioral learning

Tsutsumi, S., & Hayashi‐Takagi, A. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.07.002 · Cited by 10

Subcellular distribution of the Rho‐GEF Lfc in primate prefrontal cortex: Effect of neuronal activation

Muly, E. C., Nairn, A. C., Greengard, P., & Rainnie, D. G. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21703 · Cited by 12

Cell-specific expression of calcineurin immunoreactivity within the rat basolateral amygdala complex and colocalization with the neuropeptide Y Y1 receptor

Leitermann, R. J., Sajdyk, T. J., & Urban, J. H. (2012) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2012.07.005 · Cited by 11

Dendritic spine heterogeneity and calcium dynamics in basolateral amygdala principal neurons

Power, J., & Sah, P. (2014) · Journal of Neurophysiology · doi:10.1152/jn.00770.2013 · Cited by 11

Homer proteins shape Xenopus optic tectal cell dendritic arbor development in vivo

Keuren‐Jensen, K. R. V., & Cline, H. T. (2008) · Developmental Neurobiology · doi:10.1002/dneu.20659 · Cited by 12

ADF/Cofilin, Actin Dynamics, and Disease

Maloney, M. T., Kinley, A. W., Pak, C. W., & Bamburg, J. R. (2008) · Springer eBooks · doi:10.1007/978-0-387-71749-4_6 · Cited by 10

Future Perspectives of NMDAR in CNS Disorders

Capó, T., Rebassa, J. B., Raïch, I., Lillo, J., Badia, P., Navarro, G., & Reyes‐Resina, I. (2025) · Molecules · doi:10.3390/molecules30040877 · Cited by 12

Long-Term Treatment with Low Doses of Methamphetamine Promotes Neuronal Differentiation and Strengthens Long-Term Potentiation of Glutamatergic Synapses onto Dentate Granule Neurons

Baptista, S., Lourenço, J., Milhazes, N., Borges, F., Silva, A. P., & Bacci, A. (2016) · eNeuro · doi:10.1523/eneuro.0141-16.2016 · Cited by 10

Primary cultured neuronal networks and type 2 diabetes model mouse fatty liver tissues in aqueous liquid observed by atmospheric SEM (ASEM): Staining preferences of metal solutions

Sato, C., Yamazawa, T., Ohtani, A., Maruyama, Y., Memtily, N., Sato, M., Hatano, Y., Shiga, T., & Ebihara, T. (2018) · Micron · doi:10.1016/j.micron.2018.11.005 · Cited by 11

Methodological approaches to understand the molecular mechanism of structural plasticity of dendritic spines

Mikuni, T., & Uchigashima, M. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14734 · Cited by 11

Dendritic Spines: Similarities with Protrusions and Adhesions in Migrating Cells

Vicente‐Manzanares, M., Hodges, J., & Horwitz, A. R. (2009) · The Open Neuroscience Journal · doi:10.2174/1874082000903020087 · Cited by 12

The Altered Supramolecular Structure of Dopamine D2 Receptors in Disc1-deficient Mice

Onishi, T., Sakamoto, H., Namiki, S., & Hirose, K. (2018) · Scientific Reports · doi:10.1038/s41598-018-20090-0 · Cited by 10

Cofilin: Molecular and Cellular Functions and Its Role in the Functioning of the Nervous System

Kovaleva, T. F., Maksimova, N. S., Жуков, И. Ю., Pershin, V. I., Mukhina, I. V., & Gainullin, M. (2019) · Neurochemical Journal · doi:10.1134/s1819712419010124 · Cited by 10

Defects in syntabulin-mediated synaptic cargo transport associate with autism-like synaptic dysfunction and social behavioral traits

Xiong, G.-J., Cheng, X., Sun, T., Xie, Y., Huang, N., Li, S., Lin, M.-Y., & Sheng, Z. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-0713-9 · Cited by 11

Experimental and computational aspects of signaling mechanisms of spike‐timing‐dependent plasticity

Urakubo, H., Honda, M., Tanaka, K., & Kuroda, S. (2009) · HFSP journal · doi:10.2976/1.3137602 · Cited by 10

Optimal Information Storage: Nonsequential Sources and Neural Channels

Varshney, L. R. (2006) · Cited by 11

Synaptic priming: A framework for pharmacotherapy in depression

Brown, K. A., Ajibola, M. I., Medeiros, G. C., & Gould, T. D. (2025) · Neuron · doi:10.1016/j.neuron.2025.09.010 · Cited by 11

CELF4 regulates spine formation and depression-like behaviors of mice

Shen, Y., Zhang, C., Xiao, K., Liu, D., & Xie, G. (2022) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2022.03.067 · Cited by 9

Cognitive decline in diabetic mice predisposed to Alzheimer’s disease is greater than in wild type

Carús-Cadavieco, M., Berenguer, I., Canelo, A. M., Serrano-Lope, M. A., la Fuente, S. G., Aguado, B., Fernández‐Rodrigo, A., Saido, T. C., Frank, A., Venero, C., et al. (2023) · Life Science Alliance · doi:10.26508/lsa.202201789 · Cited by 9

A novel function of the cell polarity-regulating kinase PAR-1/MARK in dendritic spines

Hayashi, K., Suzuki, A., & Ohno, S. (2011) · BioArchitecture · doi:10.4161/bioa.1.6.19199 · Cited by 9

Using Inspiration from Synaptic Plasticity Rules to Optimize Traffic Flow in Distributed Engineered Networks

Suen, J. Y., & Navlakha, S. (2017) · Neural Computation · doi:10.1162/neco_a_00945 · Cited by 9

Drebrin and Spine Formation

Takahashi, H., & Naito, Y. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-4-431-56550-5_10 · Cited by 10

Modulation of dendritic spines by protein phosphatase-1

Platholi, J., & Hemmings, H. C. (2020) · Advances in pharmacology · doi:10.1016/bs.apha.2020.10.001 · Cited by 8

Abnormal dendritic morphology in the cerebellum of cyclooxygenase‐2 − knockin mice

Kissoondoyal, A., Rai‐Bhogal, R., & Crawford, D. A. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.15454 · Cited by 10

Toward a Brain-Inspired Developmental Neural Network Based on Dendritic Spine Dynamics

Zhao, F., Zeng, Y., & Bai, J. (2021) · Neural Computation · doi:10.1162/neco_a_01448 · Cited by 9

Neurotransmissão glutamatérgica e plasticidade sináptica: aspectos moleculares, clínicos e filogenéticos

Ruggiero, R. N., Bueno-Júnior, L. S., Ross, J. B. D., Fachim, H., Padovan‐Neto, F. E., Merlo, S., Rohner, C. J. S., Ikeda, E. T., Brusco, J., & Moreira, J. E. (2011) · Medicina (Ribeirão Preto) · doi:10.11606/issn.2176-7262.v44i2p143-156 · Cited by 9

Dendritic spine plasticity as an underlying mechanism of neuropathic pain: Commentary on Tan et al.

Melemedjian, O. K., & Price, T. J. (2011) · Experimental Neurology · doi:10.1016/j.expneurol.2011.11.016 · Cited by 10

Behaviorally evoked transient reorganization of hippocampal spines

Kitanishi, T., Ikegaya, Y., & Matsuki, N. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06860.x · Cited by 8

Sam68 Enables Metabotropic Glutamate Receptor-Dependent LTD in Distal Dendritic Regions of CA1 Hippocampal Neurons

Klein, M. E., Younts, T. J., Freire‐Cobo, C., Buxbaum, A. R., Aow, J., Erdjument‐Bromage, H., Richard, S., Malinow, R., Neubert, T. A., Singer, R. H., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.10.030 · Cited by 10

Dynamics underlying synaptic gain between pairs of cortical pyramidal neurons

Pratt, K. G., Taft, C. E., Burbea, M., & Turrigiano, G. G. (2007) · Developmental Neurobiology · doi:10.1002/dneu.20577 · Cited by 10

Loss of synaptopodin impairs mGluR5 and protein synthesis–dependent mGluR-LTD at CA3-CA1 synapses

Wu, P. Y., Ji, L., Sanctis, C. D., Francesconi, A., Inglebert, Y., & McKinney, R. A. (2024) · PNAS Nexus · doi:10.1093/pnasnexus/pgae062 · Cited by 8

Repetitive magnetic stimulation with iTBS600 induces persistent structural and functional plasticity in mouse organotypic slice cultures

Lu, H., Garg, S., Lenz, M., & Vlachos, A. (2025) · Brain stimulation · doi:10.1016/j.brs.2025.07.008 · Cited by 12

Spontaneous activity of astrocytes is a stochastic functional signal for memory consolidation

Losi, G., Vignoli, B., Granata, R., Lia, A., Zonta, M., Sansevero, G., Pischedda, F., Chiavegato, A., Santi, S., Zentilin, L., et al. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2500511122 · Cited by 8

Metabolic dysfunction–associated steatotic liver disease alters brain function and behavior: Insights from liver-targeted siRNA therapy

Delgado, T. C., Martín-Cuevas, C., Sánchez-Hidalgo, A. C., Gil-Gómez, A., Rejano-Gordillo, C. M., Landa, J., Gallego-Duran, R., Goikoetxea-Usandizaga, N., González-Recio, I., Gil-Pitarch, C., et al. (2025) · Science Advances · doi:10.1126/sciadv.ady9758 · Cited by 8

SPIN90 Modulates Long-Term Depression and Behavioral Flexibility in the Hippocampus

Kim, D. H., Kang, M., Kim, C., Huh, Y. H., Cho, I. H., Ryu, H.-H., Chung, K. H., Park, C., Rhee, S., Lee, Y., et al. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00295 · Cited by 8

Shedding light on learning and memory: optical interrogation of the synaptic circuitry

Lu, J., & Zuo, Y. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.10.015 · Cited by 8

A Systems Biology Approach for Hypothesizing the Effect of Genetic Variants on Neuroimaging Features in Alzheimer’s Disease

Khatami, S. G., Domingo‐Fernándéz, D., Mubeen, S., Hoyt, C. T., Robinson, C., Karki, R., Iyappan, A., Kodamullil, A. T., & Hofmann‐Apitius, M. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-201397 · Cited by 8

Pre-synaptic control of remote fear extinction in the neocortex

Vetere, G., Restivo, L., & Ammassari‐Teule, M. (2012) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2012.00034 · Cited by 8

Synaptic Mechanisms of Activity-Dependent Remodeling in Visual Cortex during Monocular Deprivation

Rittenhouse, C. D., & Majewska, A. K. (2009) · Journal of Experimental Neuroscience · doi:10.4137/jen.s2559 · Cited by 9

Hippocampal Dendritic Spines Are Segregated Depending on Their Actin Polymerization

Domıńguez-Iturza, N., Calvo, M., Benoist, M., Esteban, J. A., & Morales, M. (2016) · Neural Plasticity · doi:10.1155/2016/2819107 · Cited by 8

Remodeling of Actin Filaments by Drebrin A and Its Implications

Grintsevich, E. E. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-4-431-56550-5_5 · Cited by 8

Chemical LTD, but not LTP, induces transient accumulation of gelsolin in dendritic spines

Hlushchenko, I., & Hotulainen, P. (2019) · Biological Chemistry · doi:10.1515/hsz-2019-0110 · Cited by 8

Can biophysical models of dendritic spines be used to explore synaptic changes associated with addiction?

Bonilla-Quintana, M., & Rangamani, P. (2022) · Physical Biology · doi:10.1088/1478-3975/ac6cbe · Cited by 7

Experience-dependent plasticity in visual cortex

Tropea, D., Sur, M., & Majewska, A. K. (2011) · Communicative & Integrative Biology · doi:10.4161/cib.4.2.14505 · Cited by 7

Structural plasticity of dendritic spines

Zhang, S., Wang, J., & Wang, L. (2010) · Frontiers in Biology · doi:10.1007/s11515-010-0011-z · Cited by 7

The Role of Tau in the Post-synapse

Regan, P. L., & Cho, K. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-981-32-9358-8_10 · Cited by 7

Abnormal chromatin remodeling caused by ARID1A deletion leads to malformation of the dentate gyrus

Liu, P., Lu, S.-P., Li, X., Tang, G.-B., Liu, X., Dai, S., Jiao, L., Lin, X., Li, X., Hu, B., et al. (2023) · Cell Death and Differentiation · doi:10.1038/s41418-023-01199-w · Cited by 7

Rapid hippocampal network adaptation to recurring synchronous activity – a role for calcineurin

Casanova, J. R., Nishimura, M., Le, J. P., Lam, T. T., & Swann, J. W. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12315 · Cited by 7

Increased Expression of Phospho-Cofilin in CA1 and Subiculum Areas after Theta-Burst Stimulation of Schaffer Collateral-Commissural Fibers in Rat Hippocampal Slices

Zhang, L. (2010) · The Chinese Journal of Physiology · doi:10.4077/cjp.2010.amk054 · Cited by 6

Correlative Ultrastructural Analysis of Functionally Modulated Synapses Using Automatic Tape-Collecting Ultramicrotome - SEM Array Tomography

Kamasawa, N., Sun, Y., Mikuni, T., Guerrero‐Given, D., & Yasuda, R. (2015) · Microscopy and Microanalysis · doi:10.1017/s143192761500714x · Cited by 6

Deafferentation-induced alterations in mitral cell dendritic morphology in the adult zebrafish olfactory bulb

Pozzuto, J. M., Fuller, C. L., & Byrd-Jacobs, C. A. (2018) · Journal of Bioenergetics and Biomembranes · doi:10.1007/s10863-018-9772-x · Cited by 7

Statistical Traces of Long-Term Memories Stored in Strengths and Patterns of Synaptic Connections

Stepanyants, A., & Escobar, G. M. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0255-11.2011 · Cited by 7

Making room for new memories

Draguhn, A. (2018) · Science · doi:10.1126/science.aat1493 · Cited by 8

Long-term synaptic depression triggers local biogenesis of autophagic vesicles in dendrites and requires autophagic degradationPreprint

Kallergi, E., Daskalaki, A.-D., Ioannou, E., Kolaxi, A., Plataki, M. E., Haberkant, P., Stein, F., Savitski, M. M., Sidiropoulou, K., Dalezios, Y., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.03.12.983965 · Cited by 7

Perisynaptic Astroglial Response to In Vivo Long-Term Potentiation and Concurrent Long-Term Depression in the Hippocampal Dentate Gyrus

Nam, A. J., Kuwajima, M., Parker, P. H., Bowden, J. B., Abraham, W. C., & Harris, K. M. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.0943-25.2025 · Cited by 6

The role of miRNA134 in pathogenesis and treatment of intractable epilepsy: a review article

Kasaiyan, M., Basiri, M., & Pajouhanfar‎, S. (2024) · Nucleosides Nucleotides & Nucleic Acids · doi:10.1080/15257770.2024.2331046 · Cited by 6

Stress enhances expression of calcium‐binding proteins and NMDAR subunit genes in the rat hippocampus

Parthasarathy, A., Hanumanthappa, R., Bulbule, S. R., Kiran, P. C., Nanjaiah, H., Gopinath, G., Siddaiah, B. M., David, M., & Devaraju, K. S. (2024) · Neuroprotection/Neuroprotection (Chichester, England. Print) · doi:10.1002/nep3.35 · Cited by 6

Changes in dendritic spine density in the nucleus accumbens do not underlie ethanol sensitization

Nona, C. N., Bermejo, M. K., Ramsey, A. J., & Nóbrega, J. N. (2015) · Synapse · doi:10.1002/syn.21862 · Cited by 6

Dendrites: A Key Structural Element of Neurons

Rollenhagen, A., & Lübke, J. H. R. (2012) · Springer eBooks · doi:10.1007/978-1-4614-1997-6_11 · 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

Synaptosomal Actin Dynamics in the Developmental Visual Cortex Regulate Behavioral Visual Acuity in Rats

Bi, A.-L., Zhang, Y., Lu, Z.-Y., Tang, H., Zhang, X., Zhang, Z., Li, B., Guo, D., Gong, S., Li, Q., et al. (2021) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.62.7.20 · Cited by 6

Analysis of activity-dependent morphological plasticity of dendritic spines on hippocampal neurons

Rösch, J. H. (2003) · Electronic Theses of LMU Munich (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.991

Independent Expression of Synaptic and Morphological Plasticity Associated with Long-Term Depression

Wang, X.-B., Yang, Y., & Zhou, Q. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.2015-07.2007 · Cited by 100

Synapse elimination accompanies functional plasticity in hippocampal neurons

Bastrikova, N., Gardner, G. A., Reece, J. M., Jeromin, A., & Dudek, S. M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0800027105 · Cited by 202

Dendritic spines: Revisiting the physiological role

Chidambaram, S. B., Rathipriya, A. G., Bolla, S. R., Bhat, A., Ray, B., Mahalakshmi, A. M., Manivasagam, T., Thenmozhi, A. J., Essa, M. M., Guillemin, G. J., et al. (2019) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2019.01.005 · Cited by 266

Long Lasting Protein Synthesis- and Activity-Dependent Spine Shrinkage and Elimination after Synaptic Depression

Ramiro‐Cortés, Y., & Israely, I. (2013) · PLoS ONE · doi:10.1371/journal.pone.0071155 · Cited by 39