The DOI matches its Crossref record; 40 of the 40 references it cites were found in a registry or an index.
Rapid Actin-Based Plasticity in Dendritic Spines
Open accessAbstract
Dendritic spines have been proposed as primary sites of synaptic plasticity in the brain. Consistent with this hypothesis, spines contain high concentrations of actin, suggesting that they might be motile. To investigate this possibility, we made video recordings from hippocampal neurons expressing actin tagged with green fluorescent protein (GFP-actin). This reagent incorporates into actin-containing structures and allows the visualization of actin dynamics in living neurons. In mature neurons, recordings of GFP fluorescence revealed large actin-dependent changes in dendritic spine shape, similar to those inferred from previous studies using fixed tissues. Visible changes occurred within seconds, suggesting that anatomical plasticity at synapses can be extremely rapid. As well as providing a molecular basis for structural plasticity, the presence of motile actin in dendritic spines implicates the postsynaptic element as a primary site of this phenomenon.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“A recent study demonstrated that, in cultured hippocampal neurons, actin distribution in spines changes on a time scale of seconds to minutes in a manner that is perturbed by latrunculin A (Fischer et al., 1998).”
From Regulation of F-Actin Stability in Dendritic Spines by Glutamate Receptors and Calcineurin (1998) · cites this paper as Fischer et al., 1998
In the citing paper
“Morphological alterations of dendritic spines have been shown to have profound effects on the efficacy of synaptic transmission43.”
In the citing paper
“The concentrations of latrunculin A and cytochalasins used here (0.01–1 μM) are similar to those that have been shown previously to alter actin filament organization in cultured cells, prevent lamellipodial ruffling in fibroblasts, inhibit motility and retrograde flow in neuronal growth cones, and arrest dendritic spine motility in hippocampal neurons (3, 4, 7, 10).”
From Dynamic actin filaments are required for stable long-term potentiation (LTP) in area CA1 of the hippocampus (2000) · cites this paper as [10]
Citations
Cites
The Fine Structure of the Nervous System.
Tennyson, V. M. (1970) · Archives of Neurology · doi:10.1001/archneur.1970.00480240094019 · Cited by 1,946
Gonadal steroids regulate dendritic spine density in hippocampal pyramidal cells in adulthood
Gould, E., Woolley, C., Frankfurt, M., & McEwen, B. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-04-01286.1990 · Cited by 1,406
Harris, K. M., & Kater, S. B. (1994) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.17.030194.002013 · Cited by 1,020
Dendritic spines as basic functional units of neuronal integration
Yuste, R., & Denk, W. (1995) · Nature · doi:10.1038/375682a0 · Cited by 950
Evidence for a Role of Dendritic Filopodia in Synaptogenesis and Spine Formation
Ziv, N. E., & Smith, S. J. (1996) · Neuron · doi:10.1016/s0896-6273(00)80283-4 · Cited by 882
Forscher, P., & Smith, S. J. (1988) · The Journal of cell biology · doi:10.1083/jcb.107.4.1505 · Cited by 854
fine structure of the nervous system
Peters, A., Palay, S. L., & Webster, H. D. (1976) · Cited by 796
Moser, M., Trommald, M., & Andersen, P. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.26.12673 · Cited by 617
The Dynamics of Dendritic Structure in Developing Hippocampal Slices
Dailey, M. E., & Smith, S. J. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-09-02983.1996 · Cited by 611
Competitive binding of α-actinin and calmodulin to the NMDA receptor
Wyszynski, M., Lin, J., Rao, A., Nigh, E., Beggs, A. H., Craig, A. M., & Sheng, M. (1997) · Nature · doi:10.1038/385439a0 · Cited by 596
Cited by
Sorted by citations
Items 701–800 of 895
Wehrle‐Haller, B., & Bastmeyer, M. (2014) · Progress in brain research · doi:10.1016/b978-0-444-63486-3.00018-9 · Cited by 9
Genetics and Genomics of Neurobehavioral Disorders
Fisch, G. S. (2003) · Humana Press eBooks · doi:10.1385/1592593534 · Cited by 9
Redell, J. B., Xue‐Bian, J., Bubb, M., & Crow, T. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.06.023 · Cited by 9
RNA Transport and Local Protein Synthesis in the Dendritic Compartment
Gardiol, A., Racca, C., & Triller, A. (2001) · Results and problems in cell differentiation · doi:10.1007/978-3-540-40025-7_7 · Cited by 9
Popov, V. I., Деев, А. Д., Klimenko, O. A., Kraev, I., Kuz’minykh, S. B., Medvedev, N. I., Patrushev, I. V., Rv, P., Rogachevskii, V. V., Khutsiyan, S. S., et al. (2005) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-005-0030-4 · Cited by 9
Regulation of Dendritic Filopodial Interactions by ZO-1 and Implications for Dendrite Morphogenesis
Komaki, R., Togashi, H., & Takai, Y. (2013) · PLoS ONE · doi:10.1371/journal.pone.0076201 · Cited by 8
MARCKS for Maintenance in Dendritic Spines
Matus, A. I. (2005) · Neuron · doi:10.1016/j.neuron.2005.09.013 · Cited by 8
Self-citationImaging of Molecular Dynamics Regulated by Electrical Activities in Neural Circuits and in Synapses
Fujii, R., Ichikawa, M., & Ozaki, M. (2008) · Neurosignals · doi:10.1159/000123037 · Cited by 8
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
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
Endogenous ion channel complexes: the NMDA receptor
Frank, R. (2011) · Biochemical Society Transactions · doi:10.1042/bst0390707 · Cited by 8
DeBello, W., & Zito, K. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-803784-3.00014-7 · Cited by 9
Hirooka, Y. (2003) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2003.11.008 · Cited by 8
Neural Analysis of Learning in Simple Systems
Krasne, F. (2002) · Wiley eBooks · doi:10.1002/0471214426.pas0304 · Cited by 8
Bonilla-Quintana, M., & Rangamani, P. (2022) · Physical Biology · doi:10.1088/1478-3975/ac6cbe · Cited by 7
Analysis of Actin Turnover and Spine Dynamics in Hippocampal Slice Cultures
Michaelsen‐Preusse, K., Kellner, Y., Körte, M., & Zagrebelsky, M. (2014) · Neuromethods · doi:10.1007/978-1-4939-0381-8_9 · Cited by 7
Vázquez-Hernández, N., Martínez-Torres, N. I., & González‐Burgos, I. (2020) · Behavioural Brain Research · doi:10.1016/j.bbr.2020.113014 · Cited by 7
Rudolf, M. A., Andreeva, A. Y., Kim, C. E., DeNovio, A. C.-J., Koshar, A. N., Baker, W., Cartagena‐Rivera, A. X., & Corwin, J. T. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.859882 · Cited by 7
Ca 2+ -independent spine dynamics in cultured hippocampal neurons
Zhang, S., & Murphy, T. H. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2003.10.017 · Cited by 7
The small GTPase Arf6 is dysregulated in a mouse model for fragile X syndrome
Briševac, D., Scholz, R., Du, D., Elagabani, M. N., Köhr, G., & Kornau, H. (2020) · Journal of Neurochemistry · doi:10.1111/jnc.15230 · Cited by 7
Johansson, B. B., & Belichenko, P. V. (2001) · Springer eBooks · doi:10.1007/978-3-642-59446-5_10 · Cited by 7
Glutamate and Alcohol-Induced Neurotoxicity
Crews, F. T., Rudolph, J. G., & Chandler, L. J. (2002) · Humana Press eBooks · doi:10.1007/978-1-59259-306-4_24 · Cited by 7
Neuromechanics: The Role of Tension in Neuronal Growth and Memory
Ahmed, W., Rajagopalan, J., Tofangchi, A., & Saif, T. A. (2012) · Wiley eBooks · doi:10.1002/9781118482568.ch3 · Cited by 7
Johansson, B. B. (2008) · European Journal of Neurology · doi:10.1111/j.1468-1331.2008.02287.x · Cited by 7
F-dynamics: Automated quantification of dendrite filopodia dynamics in living neurons
Hendricusdottir, R., & Bergmann, J. (2014) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2014.08.016 · Cited by 6
Urban, P., Tabar, V. R., Denkiewicz, M., Bokota, G., Das, N., Basu, S., & Plewczyński, D. (2020) · Journal of Computational Biology · doi:10.1089/cmb.2019.0383 · Cited by 6
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
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
Wang, J., Wang, Y., Sun, W., Yu, Y., Wei, N., Du, R., Yang, Y. L., Liang, T., Wang, X., Ou, C., et al. (2021) · Neurobiology of Disease · doi:10.1016/j.nbd.2021.105302 · Cited by 6
Chapter 11 Neurones as physical objects: Structure, dynamics and function
Meunier, C., & Segev, I. (2001) · Handbook of biological physics · doi:10.1016/s1383-8121(01)80014-2 · Cited by 6
Yamazaki, H., Koganezawa, N., Yokoo, H., Sekino, Y., & Shirao, T. (2023) · Neurosciences research · doi:10.1016/j.neures.2023.08.002 · Cited by 5
Using ALS to understand profilin 1's diverse roles in cellular physiology
Lindamood, H. L., Liu, T. M., Read, T., & Vitriol, E. A. (2024) · Cytoskeleton · doi:10.1002/cm.21896 · Cited by 5
Chemical Stimulation of Rodent and Human Cortical Synaptosomes: Implications in Neurodegeneration
Ahmad, F., Yu, J. H., Lladó, A., & Liu, P. (2021) · Cells · doi:10.3390/cells10051174 · Cited by 6
Plasticity of Dendritic Spines Underlies Fear Memory
Choi, J. E., & Kaang, B. (2023) · The Neuroscientist · doi:10.1177/10738584231185530 · Cited by 5
Neuroanatomical Considerations Specific to the Study of Neurogenetics
Galaburda, A. M., & Schmitt, J. E. (2003) · Humana Press eBooks · doi:10.1007/978-1-59259-353-8_2 · Cited by 5
Long-Term Potentiation: A Candidate Cellular Mechanism for Information Storage in the CNS ☆
Hawkins, K. E., Gavin, C. F., & Sweatt, J. D. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21103-6 · Cited by 7
Forrest, C. M., Addae, J. I., Murthy, S. S., Darlington, L. G., MORRIS, B. J., & Stone, T. W. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07853.x · Cited by 5
Balanced GABAergic and glutamatergic synapse development in hippocampal neurons
Zhao, X., Shoji, S., & Lau, P.-M. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.03.083 · Cited by 5
Lordkipanidze, T. G., Bikashvili, T., Japaridze, N. J., & Zhvania, M. G. (2013) · Micron · doi:10.1016/j.micron.2013.02.009 · Cited by 5
Penzes, P. (2007) · Neuron · doi:10.1016/j.neuron.2007.12.006 · Cited by 6
Dynamic Stabilization: Structural Plasticity at Inhibitory Postsynaptic Sites
Kneussel, M. (2006) · Traffic · doi:10.1111/j.1600-0854.2006.00501.x · Cited by 5
Lin, V., Matta, S. M., Dallman, J. E., Hosie, S., Moreau, M., Franks, A. E., Bourgeron, T., & Hill‐Yardin, E. L. (2025) · Autism Research · doi:10.1002/aur.70112 · Cited by 5
Wiest, M. C., & Puniani, A. S. (2025) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2025.09.016 · Cited by 7
Renner, J., Rasia‐Filho, A. A., González-Tapia, D., & González‐Burgos, I. (2026) · Journal of Anatomy · doi:10.1111/joa.70124 · Cited by 4
Argunşah, A. Ö., & Israely, I. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1253446 · Cited by 4
Kwon, Y., Lee, S. J., Shin, Y. K., Choi, J.-S., Park, D. E., & Shin, J. E. (2025) · Animal Cells and Systems · doi:10.1080/19768354.2024.2448999 · Cited by 4
Dendritic Elaboration: Morphology and Chemistry
Rollenhagen, A., & Lübke, J. H. R. (2016) · Springer eBooks · doi:10.1007/978-1-4939-3474-4_11 · Cited by 4
FAK family kinases in brain health and disease
Srikanth, K. D., Meirson, T., Sams, D. S., & Gil-Henn, H. (2018) · Journal of Molecular and Clinical Medicine · doi:10.31083/j.jmcm.2018.03.007 · Cited by 5
Xie, M.-J., Yagi, H., Iguchi, T., Yamazaki, H., Hanamura, K., Matsuzaki, H., Shirao, T., & Sato, M. (2022) · Neuroscience Research · doi:10.1016/j.neures.2022.09.010 · Cited by 4
Agassandian, K., & Cassell, M. D. (2008) · Brain Research · doi:10.1016/j.brainres.2008.05.082 · Cited by 4
Advanced Neuroscience Technologies
Ahmed, B., Driver, J., Friston, K. J., Matus, A. I., Morris, R., & Rolls, E. T. (2006) · Elsevier eBooks · doi:10.1016/b978-012088566-4/50017-9 · Cited by 4
Self-citationInsights into GABA functions in the developing cerebellum
Fiszman, M. L. (2005) · International review of neurobiology · doi:10.1016/s0074-7742(05)71004-7 · Cited by 4
Sun, M., Nelson, T. J., & Alkon, D. L. (2010) · Research and perspectives in Alzheimer's disease · doi:10.1007/978-3-642-04300-0_10 · Cited by 3
Tyler, W. J. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-812952-4.00011-8 · Cited by 4
Synapses immunologiques et synapses neuronales
Trautmann, A., Revy, P., Donnadieu, E., & Bismuth, G. (2003) · médecine/sciences · doi:10.1051/medsci/2003194429 · Cited by 4
Falk, T., Strazdas, L. A., Borders, R. S., Kilani, R. K., Yool, A. J., & Sherman, S. J. (2001) · PubMed · Cited by 3
Dendritic spines of developing rat cortical neurons in culture.
Huang, Z., Wu, H., Yeh, C.-C., Chou, Y., & Chang, Y. (2006) · PubMed · Cited by 3
Paradoxical Signaling Regulates Structural Plasticity in Dendritic Spines
Rangamani, P., Levy, M., Khan, S., & OSTER, G. F. (2016) · Biophysical Journal · doi:10.1016/j.bpj.2015.11.2003 · Cited by 3
Long-Term Potentiation: A Candidate Cellular Mechanism for Information Storage in the CNS
Sweatt, J. D. (2008) · Elsevier eBooks · doi:10.1016/b978-012370509-9.00016-4 · Cited by 4
Martinez, S. J., & Jones, E. (2007) · Cited by 3
Morphological Characteristics of Glutamatergic Synapses in the Hippocampus
Frotscher, M., Mews, K., & Adelmann, G. (1999) · Handbook of experimental pharmacology · doi:10.1007/978-3-662-08022-1_10 · Cited by 3
USP48/USP31 Is a Nuclear Deubiquitinase that Potently Regulates Synapse RemodelingPreprint
Ma, Q., Ruan, H., Dai, H., & Yao, W. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.19.558317 · Cited by 3
CDKL5 modulates the plasticity of excitatory synapses via liquid–liquid phase separation
Li, M., Zhu, Z., Li, D., Wang, J., Zhang, M., Xu, Q.-W., Zhang, Y., Zhu, Y., Zhu, J., & Xiong, Z. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2511123123 · Cited by 2
(2015) · Molecular & Cellular Epilepsy · doi:10.14800/mce.608 · Cited by 2
The Role of Drebrin-Binding Stable Actin Filaments in Dendritic Spine Morphogenesis
Shirao, T., & Koganezawa, N. (2015) · Springer eBooks · doi:10.1007/978-1-4939-2904-7_15 · Cited by 2
Löhmann, C. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397266-8.00140-x · Cited by 2
Activity-induced synaptic structural modifications by Akt
Kim, Y.-J. (2022) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2022.06.093 · Cited by 2
Molecular Mechanisms of Dendritic Spine Plasticity in Development and Aging
Kreutz, M. R., König, I., Mikhaylova, M., Spilker, C., & Zuschratter, W. (2008) · Springer eBooks · doi:10.1007/978-0-387-32671-9_10 · Cited by 2
Danbolt, N. C. (2000) · Handbook of chemical neuroanatomy · doi:10.1016/s0924-8196(00)80049-4 · Cited by 2
Defects in Rho GTPase Signaling to the Spine Actin Cytoskeleton in FMR1 Knockout Mice
Lauterborn, J. C., & Gall, C. M. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-804461-2.00014-7 · Cited by 2
Müller, D., & Nikonenko, I. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397267-5.00145-x · Cited by 4
Ishii, K., Hayashida, T., Hashikawa, T., & Tsuji, S. (2004) · PubMed · doi:10.5603/4659 · Cited by 2
Neurotrophins and neuronal plasticity in the action of antidepressants and morphine
Sairanen, M. (2007) · Työväentutkimus Vuosikirja · Cited by 2
Creation of long-term mental representations using the dimension of fractal dendrites
Gagne, R., & Gagné, S. (2006) · International Joint Conference on Neural Networks (IJCNN) · doi:10.1109/ijcnn.2005.1556229 · Cited by 2
Automated detection and time lapse analysis of dendritic spines in laser scanning microscopy images
Cheng, J. (2009) · Digital Repository Service (Northeastern University) · doi:10.17760/d10019303 · Cited by 2
Development and plasticity of neuromuscular innervation
Ribchester, R. R. (2005) · ERA · Cited by 2
Shaft versus spine localization affects the structural plasticity of glutamatergic synapsesPreprint
Fanutza, T., Popp, Y., Brueckner, A. M., Hertrich, N., von Sivers, J., Larkum, M. E., Shoichet, S. A., & Mikhaylova, M. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.05.692591 · Cited by 4
Brownian Models of Chemical Reactions in Microdomains
Schuss, Z. (2013) · Applied mathematical sciences · doi:10.1007/978-1-4614-7687-0_5 · Cited by 1
Neuromechanobiology of the brain
Mueller, J., & Tyler, W. J. (2015) · Cambridge University Press eBooks · doi:10.1017/cbo9781139939751.020 · Cited by 2
Coupled shape priors for dynamic segmentation of dendritic spines
Atabakilachini, N., Erdil, E., Argunşah, A. Ö., Rada, L., Ünay, D., & Çetin, M. (2017) · Signal Processing and Communications Applications Conference (SIU) · doi:10.1109/siu.2017.7960599 · Cited by 1
Modulation of the Core Neural Network in Stress: The Role of Endocannabinoids and LTD
Bennett, M. R., & Lagopoulos, J. (2018) · Springer eBooks · doi:10.1007/978-3-319-91116-8_5 · Cited by 1
Poberezhnyi, V. I., Marchuk, O., Shvidyuk, O. S., Petrik, I., & Logvinov, O. S. (2019) · Pain medicine · doi:10.31636/pmjua.v3i4.1 · Cited by 1
Working with Actin: Methodological Approaches for the Study of Actin in Neurons
Dent, E. W. (2010) · Advances in neurobiology · doi:10.1007/978-1-4419-7368-9_6 · Cited by 1
Imaging of Experience-Dependent Structural Plasticity in the Mouse Neocortex in vivo
Holtmaat, A., Paola, V. D., Wilbrecht, L., & Knott, G. W. (2008) · Research and perspectives in Alzheimer's disease · doi:10.1007/978-3-540-76330-7_3 · Cited by 1
Dunaevsky, A. (2004) · Neuron · doi:10.1016/j.neuron.2004.10.003 · Cited by 1
Cellular Biology of AMPA Receptor Trafficking and Synaptic Plasticity
Esteban, J. A. (2008) · Springer eBooks · doi:10.1007/978-0-387-77232-5_10 · Cited by 1
Activity-Mediated Structural Plasticity of Dendritic Spines
Müller, D., Roo, M. D., & Nikonenko, I. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-418675-0.00012-2 · Cited by 1
Molecular imaging of the cytoskeleton using GFP-actin fluorescence microscopy
Yan, Y., & Marriott, G. (2002) · Progress in biotechnology · doi:10.1016/s0921-0423(02)80040-5 · Cited by 1
Deng, H., Ma, C., Han, H., Xie, Q., & Shen, L. (2019) · Applied Sciences · doi:10.3390/app9132591 · Cited by 1
Estrogenic Regulation of Synaptic Health and Cognition in Aging Rhesus Monkeys
Crimins, J. L., Hara, Y., & Morrison, J. H. (2020) · Oxford University Press eBooks · doi:10.1093/oso/9780190645908.003.0018 · Cited by 1
(2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-01-00001.2003 · Cited by 1
Piperazine Derivative Stabilizes Actin Filaments in Primary Fibroblasts and Binds G-Actin In Silico
Zernov, N., Ghamaryan, V., Makichyan, A. T., Melenteva, D., Hunanyan, L. S., & Александровна, П. Е. (2022) · Current Issues in Molecular Biology · doi:10.3390/cimb44110353 · Cited by 1
Dendritic Elaboration: Morphology and Chemistry
Rollenhagen, A., & Lübke, J. H. R. (2022) · Springer eBooks · doi:10.1007/978-3-030-88832-9_11 · Cited by 1
Ferrari, A., & Goda, Y. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.00791-9 · Cited by 1
Form and Function: A Neuronal Dialog
Rocha, M., Furtado, D. A., Menezes, J. R. L., & Hedin‐Pereira, C. (2003) · Brain and Mind · doi:10.1023/a:1024156030989 · Cited by 1
Regulation of dendritic spine morphogenesis and synapse formation by copines
Galic, M. (2006) · edoc (University of Basel) · doi:10.5451/unibas-004198769 · Cited by 1
Gelsolin : a regulator of postsynaptic actin assembly and AMPA receptor expression
Zhao, P. (2003) · edoc (University of Basel) · doi:10.5451/unibas-003354194 · Cited by 1
Calcium Dynamics in Neuronal Microdomains: Modeling, Stochastic Simulations, and Data Analysis
Guerrier, C., Korkotian, E., & Holcman, D. (2014) · Springer eBooks · doi:10.1007/978-1-4614-7320-6_179-1 · Cited by 1
Zur Rolle des Calciums bei Estrogen-vermittelter synaptischer Plastizität
Voets, C. (2009) · Cited by 1
Metadata
- Authors
- Fischer, M., Kaech, S., Knutti, D., & Matus, A.
- Affiliations
- Friedrich Miescher Institute (CH)
- Corresponding author
- Matus, Andrew
- ORCID
- Kaech, Stefanie
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 1998-05
- Volume
- 20
- Issue
- 5
- Pages
- 847-854
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W2111916392
- Cited by
- 905
- References
- 40
- Citations by year
- 2026: 4 · 2025: 7 · 2024: 5 · 2023: 12 · 2022: 16 · 2021: 21 · 2020: 18 · 2019: 17 · 2018: 22 · 2017: 17 · 2016: 33 · 2015: 28 · 2014: 31 · 2013: 30 · 2012: 34
- FWCI
- 20.16
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- dendritic spines, actin dynamics, synaptic plasticity, structural plasticity, hippocampal neurons, spine motility, postsynaptic elements
- MeSH terms
- Actins, Animals, Cell Line, Dendrites, Fibroblasts, Hippocampus, Indicators and Reagents, Luminescent Proteins, Neuronal Plasticity, Neurons, Synapses, Thiazoles, Cytochalasin D, Microscopy, Video, Bridged Bicyclo Compounds, Heterocyclic, Nucleic Acid Synthesis Inhibitors, Cell Size, Green Fluorescent Proteins, Rats, Thiazolidines
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review