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 401–500 of 895
Hypothermia-Associated Loss of Dendritic Spines
Roelandse, M., & Matus, A. I. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2872-04.2004 · Cited by 56
Self-citationMolecular mechanisms of synaptogenesis
Qi, C., Luo, L.-D., Feng, I., & Ma, S. (2022) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2022.939793 · Cited by 54
Waltereit, R., Leimer, U., Halbach, O. V. B. U., Panke, J., Hölter, S. M., Garrett, L., Wittig, K., Schneider, M., Schmitt, C., Calzada‐Wack, J., et al. (2012) · The FASEB Journal · doi:10.1096/fj.11-202317 · Cited by 55
Mateos, J. M., Lüthi, A., Savic, N., Stierli, B., Streit, P., Gähwiler, B. H., & McKinney, R. A. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2006.120550 · Cited by 53
Liu, Z.-H., Ding, J.-J., Yang, Q.-Q., Song, H.-Z., Chen, X.-T., Xu, Y., Xiao, G.-R., & Wang, H.-L. (2016) · Scientific Reports · doi:10.1038/srep32492 · Cited by 53
Schmidt, H., & Eilers, J. (2009) · Journal of Computational Neuroscience · doi:10.1007/s10827-009-0139-5 · Cited by 57
Role of Cdk5 in Neuronal Signaling, Plasticity, and Drug Abuse
Bibb, J. A. (2003) · Neurosignals · doi:10.1159/000074620 · Cited by 54
Phalloidin-Eosin Followed by Photo-oxidation
Capani, F., Deerinck, T. J., Ellisman, M. H., Bushong, E. A., Bobik, M., & Martone, M. E. (2001) · Journal of Histochemistry & Cytochemistry · doi:10.1177/002215540104901103 · Cited by 52
Neuronal profilins in health and disease: Relevance for spine plasticity and Fragile X syndrome
Michaelsen‐Preusse, K., Zessin, S., Grigoryan, G., Scharkowski, F., Feuge, J., Remus, A., & Körte, M. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1516697113 · Cited by 56
Calcium dynamics in dendritic spines, modeling and experiments
Holcman, D., Korkotian, E., & Segal, M. (2005) · Cell Calcium · doi:10.1016/j.ceca.2005.01.015 · Cited by 52
Umeda, T., Ebihara, T., & Okabe, S. (2004) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2004.09.010 · Cited by 52
Dendritic and Synaptic Protection: Is It Enough to Save the Retinal Ganglion Cell Body and Axon?
Morquette, J. B., & Di Polo, A. (2008) · Journal of Neuro-Ophthalmology · doi:10.1097/wno.0b013e318177edf0 · Cited by 51
The synaptic cytoskeleton in development and disease
Goellner, B., & Aberle, H. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20892 · Cited by 52
PRG-1 Regulates Synaptic Plasticity via Intracellular PP2A/β1-Integrin Signaling
Liu, X., Huai, J., Endle, H., Schlüter, L., Fan, W., Li, Y., Richers, S., Yurugi, H., Rajalingam, K., Ji, H., et al. (2016) · Developmental Cell · doi:10.1016/j.devcel.2016.06.019 · Cited by 54
Paradoxical signaling regulates structural plasticity in dendritic spines
Rangamani, P., Levy, M. G., Khan, S., & OSTER, G. F. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1610391113 · Cited by 52
Brünig, I., Kaech, S., Brinkhaus, H., Oertner, T. G., & Matus, A. I. (2004) · Neuropharmacology · doi:10.1016/j.neuropharm.2004.07.038 · Cited by 53
Self-citationEffects of N-cadherin disruption on spine morphological dynamics
Mysore, S. P. (2007) · Frontiers in Cellular Neuroscience · doi:10.3389/neuro.03.001.2007 · Cited by 55
Structural basis for developmentally regulated changes in cadherin function at synapses
Elste, A. M., & Benson, D. L. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.20876 · Cited by 50
Phosphorylation of Microtubule-associated Protein STOP by Calmodulin Kinase II
Baratier, J., Peris, L., Brocard, J., Gory‐Fauré, S., Dufour, F., Bosc, C., Fourest‐Lieuvin, A., Blanchoin, L., Salin, P. A., Job, D., et al. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m509602200 · Cited by 58
Richards, D. A., De Paola, V., Caroni, P., Gähwiler, B. H., & McKinney, R. A. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.062091 · Cited by 49
Lin, H., Huganir, R. L., & Liao, D. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.02.086 · Cited by 53
Gisselsson, L., Matus, A. I., & Wieloch, T. W. (2005) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/sj.jcbfm.9600131 · Cited by 49
Self-citationPhosphorylation of spinophilin by ERK and cyclin-dependent PK 5 (Cdk5)
Futter, M., Uematsu, K., Bullock, S. A., Kim, Y. D., Hemmings, H. C., Nishi, A., Greengard, P., & Nairn, A. C. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0409802102 · Cited by 51
Drakew, A., Frotscher, M., & Heimrich, B. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00378-4 · Cited by 49
Spine motility: a means towards an end?
Dunaevsky, A., & Mason, C. A. (2003) · Trends in Neurosciences · doi:10.1016/s0166-2236(03)00028-6 · Cited by 50
Radley, J. J., Johnson, L. R., Janssen, W. G. M., Martino, J., Lamprecht, R., Hof, P. R., LeDoux, J. E., & Morrison, J. H. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04962.x · Cited by 48
Sekerková, G., Loomis, P. A., Changyaleket, B., Zheng, L., Eytan, R. I., Chen, B., Mugnaini, E., & Bartles, J. R. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-04-01310.2003 · Cited by 50
BDNF and NT4/5 promote survival and neurite outgrowth of pontocerebellar mossy fiber neurons
Rabacchi, S. A., Kruk, B., Hamilton, J. A., Carney, C., Hoffman, J. R., Meyer, S. L., Springer, J. E., & Baird, D. H. (1999) · Journal of Neurobiology · doi:10.1002/(sici)1097-4695(199908)40:2 · Cited by 48
Rac GEF Dock4 interacts with cortactin to regulate dendritic spine formation.
Ueda, S., Negishi, M., & Katoh, H. (2013) · Molecular Biology of the Cell · doi:10.1091/mbc.e12-11-0782 · Cited by 47
The functional architecture of axonal actin
Papandréou, M., & Leterrier, C. (2018) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2018.05.003 · Cited by 50
Martone, M. E., Deerinck, T. J., Yamada, N., Bushong, E. A., & Ellisman, M. H. (2000) · Journal of Histotechnology · doi:10.1179/his.2000.23.3.261 · Cited by 47
Bausen, M., Fuhrmann, J. C., Betz, H., & O’Sullivan, G. A. (2006) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2005.11.004 · Cited by 47
Role of Rho GTPases in the Morphogenesis and Motility of Dendritic Spines
Tashiro, A., & Yuste, R. (2008) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(07)00421-1 · Cited by 47
Rehberg, K., Bergado-Acosta, J. R., Koch, J. C., & Stork, O. (2010) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2010.04.007 · Cited by 47
Rubio, M. D., Haroutunian, V. H., & Meador‐Woodruff, J. H. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.02.006 · Cited by 47
Jedlička, P., & Deller, T. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.07.023 · Cited by 49
Structural dynamics of dendritic spines: Molecular composition, geometry and functional regulation
Ebrahimi, S., & Okabe, S. (2014) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2014.06.002 · Cited by 51
Learning and Memory: Basic Mechanisms
Brown, T. H., Byrne, J. H., LaBar, K. S., LeDoux, J. E., Lindquist, D. H., Thompson, R. F., & Teyler, T. J. (2004) · Elsevier eBooks · doi:10.1016/b978-012148660-0/50019-6 · Cited by 46
Usui, S., Konno, D., Hori, K., Maruoka, H., Okabe, S., Fujikado, T., Tano, Y., & Sobue, K. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m210802200 · Cited by 46
A converging‐methods approach to fragile X syndrome
Churchill, J. D., Grossman, A. W., Irwin, S. A., Galvez, R., Klintsova, A. Y., Weiler, I. J., & Greenough, W. T. (2002) · Developmental Psychobiology · doi:10.1002/dev.10036 · Cited by 46
Párducz, Á., Hoyk, Z., Kis, Z., & García‐Segura, L. M. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.02127.x · Cited by 46
Eikermann‐Haerter, K., Arbel‐Ornath, M., Yalcin, N., Yu, E. S., Kuchibhotla, K. V., Yuzawa, I., Hudry, E., Willard, C. R., Climov, M., Keles, F., et al. (2015) · Annals of Neurology · doi:10.1002/ana.24449 · Cited by 45
Yamashiro, S., Mizuno, H., Smith, M. B., Ryan, G. L., Kiuchi, T., Vavylonis, D., & Watanabe, N. (2014) · Molecular Biology of the Cell · doi:10.1091/mbc.e13-03-0162 · Cited by 45
All-optical synaptic electrophysiology probes mechanism of ketamine-induced disinhibition
Fan, L. Z., Nehme, R., Adam, Y., Jung, E. S., Wu, H., Eggan, K. C., Arnold, D. B., & Cohen, A. E. (2018) · Nature Methods · doi:10.1038/s41592-018-0142-8 · Cited by 45
Release of the Styryl Dyes from Single Synaptic Vesicles in Hippocampal Neurons
Chen, X., Barg, S., & Almers, W. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.4518-07.2008 · Cited by 45
Distribution of Rho family GTPases in the adult rat hippocampus and cerebellum
O'Kane, E. M., Stone, T. W., & MORRIS, B. J. (2003) · Molecular Brain Research · doi:10.1016/s0169-328x(03)00121-9 · Cited by 45
Ferhat, L., Esclapez, M., Represa, A., Fattoum, A., Shirao, T., & Ben‐Ari, Y. (2003) · Hippocampus · doi:10.1002/hipo.10136 · Cited by 48
Molecular mechanisms of dendritic spine development and maintenance [Review]
Sala, C., Cambianica, I., & Rossi, F. (2008) · Acta Neurobiologiae Experimentalis · doi:10.55782/ane-2008-1696 · Cited by 45
Dendritic spine plasticity in hippocampus
Gazzaley, A. H., Kay, S., & Benson, D. L. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00021-0 · Cited by 45
Glial glutamate transport modulates dendritic spine head protrusions in the hippocampus
Verbich, D., Prenosil, G., Chang, P. K. ‐., Murai, K. K., & McKinney, R. A. (2012) · Glia · doi:10.1002/glia.22335 · Cited by 48
Yu, H., Majewska, A. K., & Sur, M. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1108270109 · Cited by 44
Measuring F-actin properties in dendritic spines
Koskinen, M., & Hotulainen, P. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00074 · Cited by 48
The actin-modulating protein synaptopodin mediates long-term survival of dendritic spines
Yap, K. A. F., Drakew, A., Smilović, D., Rietsche, M., Paul, M. H., Vukšić, M., Turco, D. D., & Deller, T. (2020) · eLife · doi:10.7554/elife.62944 · Cited by 47
Lin, W., Nebhan, C. A., Anderson, B., & Webb, D. J. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.129841 · Cited by 47
Image-Based Profiling of Synaptic Connectivity in Primary Neuronal Cell Culture
Verstraelen, P., Dyck, M. V., Verschuuren, M., Kashikar, N. D., Nuydens, R., Timmermans, J., & Vos, W. H. D. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00389 · Cited by 48
Dendritic spine density is increased on nucleus accumbens D2 neurons after chronic social defeat
Fox, M. E., Figueiredo, A. M. P. D., Menken, M. S., & Lobo, M. K. (2020) · Scientific Reports · doi:10.1038/s41598-020-69339-7 · Cited by 47
Roles of palmitoylation in structural long-term synaptic plasticity
Ji, B., & Skup, M. (2021) · Molecular Brain · doi:10.1186/s13041-020-00717-y · Cited by 44
The Culture of Chick Forebrain Neurons
Heidemann, S. R., Reynolds, M., Ngo, K., & Lamoureux, P. L. (2003) · Methods in cell biology · doi:10.1016/s0091-679x(03)01004-5 · Cited by 43
De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures
Ito, Y., Carss, K. J., Duarte, S. T., Hartley, T., Keren, B., Kurian, M. A., Marey, I., Charles, P., Mendonça, C., Nava, C., et al. (2018) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2018.06.001 · Cited by 41
The Position of the GFP Tag on Actin Affects the Filament Formation in Mammalian Cells
Nagasaki, A., Kijima, S. T., Yumoto, T., Imaizumi, M., Yamagishi, A., Kim, H., Nakamura, C., & Uyeda, T. Q. P. (2017) · Cell Structure and Function · doi:10.1247/csf.17016 · Cited by 42
Chazeau, A., Garcia, M., Czöndör, K., Perrais, D., Tessier, B., Giannone, G., & Thoumine, O. R. (2015) · Molecular Biology of the Cell · doi:10.1091/mbc.e14-06-1086 · Cited by 42
Deng, J., & Dunaevsky, A. (2004) · Developmental Biology · doi:10.1016/j.ydbio.2004.09.028 · Cited by 43
Distribution of p120 catenin during rat brain development:
Chauvet, N., Prieto, M., Fabre, C., Hooten, N. N., & Privat, A. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(03)00030-7 · Cited by 42
Grossman, S. D., Hsieh‐Wilson, L. C., Allen, P. B., Nairn, A. C., & Greengard, P. (2002) · NeuroMolecular Medicine · doi:10.1385/nmm:2:1:61 · Cited by 42
Synapse adhesion: a dynamic equilibrium conferring stability and flexibility
Benson, D. L., & Huntley, G. W. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.09.011 · Cited by 43
Vukovic, N., Hansen, B., Lund, T. E., Jespersen, S. N., & Юрьевич, Ш. Ю. (2021) · PLoS Biology · doi:10.1371/journal.pbio.3001290 · Cited by 43
Song, C., Perides, G., Wang, D., & Liu, Y. F. (2002) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2002.01182.x · Cited by 41
Neurorepair versus Neuroprotection in Stroke
Hurtado, O., Pradillo, J. M., Alonso‐Escolano, D., Lorenzo, P., Sobrino, T., Castillo, J., Lizasoaín, I., & Moro, M. Á. (2006) · Cerebrovascular Diseases · doi:10.1159/000091704 · Cited by 41
Marchetti, C., Tafi, E., Middei, S., Rubinacci, M. A., Restivo, L., Ammassari‐Teule, M., & Marie, H. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.09.017 · Cited by 42
The small GTPase ADP‐ribosylation factor 6 negatively regulates dendritic spine formation
Miyazaki, H., Yamazaki, M., Watanabe, H., Maehama, T., Yokozeki, T., & Kanaho, Y. (2005) · FEBS Letters · doi:10.1016/j.febslet.2005.11.022 · Cited by 43
Rho kinase inhibition protects CA1 cells in organotypic hippocampal slices during in vitro ischemia
Gisselsson, L., Toresson, H., Ruscher, K., & Wieloch, T. W. (2009) · Brain Research · doi:10.1016/j.brainres.2009.11.087 · Cited by 40
Actin and Actin-Binding Proteins: Masters of Dendritic Spine Formation, Morphology, and Function
Lin, W., & Webb, D. J. (2009) · The Open Neuroscience Journal · doi:10.2174/1874082000903020054 · Cited by 42
Kanjhan, R., Noakes, P. G., & Bellingham, M. C. (2015) · Neural Plasticity · doi:10.1155/2016/3423267 · Cited by 42
Scharkowski, F., Frotscher, M., Lutz, D., Körte, M., & Michaelsen‐Preusse, K. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw408 · Cited by 40
Capani, F., Ellisman, M. H., & Martone, M. E. (2001) · Brain Research · doi:10.1016/s0006-8993(01)03189-4 · Cited by 40
Bourne, J. N., Morgan, J. R., & Pieribone, V. A. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.21006 · Cited by 43
Focal motility determines the geometry of dendritic spines☆
Roelandse, M., Welman, A., Wagner, U., Hagmann, J., & Matus, A. I. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00405-6 · Cited by 41
Self-citationPresynaptic and Postsynaptic Scaffolds
Ziv, N. E., & Fisher-Lavie, A. (2014) · The Neuroscientist · doi:10.1177/1073858414523321 · Cited by 39
Dendritic spine dysgenesis in neuropathic pain
Tan, A. M., & Waxman, S. G. (2014) · Neuroscience Letters · doi:10.1016/j.neulet.2014.11.024 · Cited by 40
EPHB receptor signaling in dendritic spine development
Irie, F. (2004) · Frontiers in bioscience · doi:10.2741/1325 · Cited by 40
Functionally distinct pools of actin in secretory cells
Ammar, D. A., Nguyen, P. N. B., & Forte, J. G. (2001) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.2001.281.2.c407 · Cited by 39
Differential expression of thymosins β4 and β10 during rat cerebellum postnatal development
Anadón, R., Rodríguez‐Moldes, I., Carpintero, P., Evangelatos, G. P., Livianou, E., Leondiadis, L., Quintela, I., Cerviño, M. C., & Gómez‐Márquez, J. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02024-8 · Cited by 39
The Arp2/3 complex is essential at multiple stages of neural development
Chou, F., & Wang, P. (2016) · Neurogenesis · doi:10.1080/23262133.2016.1261653 · Cited by 38
Zhang, W., & Benson, D. L. (2002) · Journal of Neuroscience Research · doi:10.1002/jnr.10313 · Cited by 38
Synaptic Metaplasticity through NMDA Receptor Lateral Diffusion
Zhao, J., Peng, Y., Xu, Z., Chen, R., Gu, Q., Chen, Z., & Lü, W. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.5450-07.2008 · Cited by 38
RetractedChandler, L. J., Carpenter‐Hyland, E. P., Hendricson, A. W., Maldve, R. E., Morrisett, R. A., Zhou, F., Sari, Y., Bell, R. L., & Szumlinski, K. K. (2006) · Alcoholism Clinical and Experimental Research · doi:10.1111/j.1530-0277.2006.00041.x · Cited by 38
Seizures Induced by in Vivo Latrunculin A and Jasplakinolide Microperfusion in the Rat Hippocampus
Sierra‐Paredes, G., Oreiro-García, T., Núñez-Rodriguez, A., Vázquez-López, A., & Sierra‐Marcuño, G. (2006) · Journal of Molecular Neuroscience · doi:10.1385/jmn:28:2:151 · Cited by 38
Ruan, Y., Lei, Z., Fan, Y., Zou, B., & Xu, Z. C. (2008) · Journal of Neuroscience Research · doi:10.1002/jnr.21816 · Cited by 39
Turvey, M. R., Fogarty, K. E., & Thorn, P. (2005) · Journal of Cell Science · doi:10.1242/jcs.01693 · Cited by 38
Structural plasticity of spines at giant mossy fiber synapses
Zhao, S., Studer, D., Chai, X., Graber, W. A., Brose, N., Nestel, S., Young, C. C., Rodriguez, E., Saetzler, K., & Frotscher, M. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00103 · Cited by 40
Magnetic resonance microscopy of human and porcine neurons and cellular processes
Flint, J. J., Hansen, B., Portnoy, S., Lee, C.-H., King, M. A., Fey, M., Vincent, F., Stanisz, G. J., Vestergaard‐Poulsen, P., & Blackband, S. J. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.050 · Cited by 37
Roles of phosphoinositide-specific phospholipase Cγ1 in brain development
Kang, D., Yang, Y. R., Lee, C., Kim, S., Ryu, S. H., & Suh, P. (2015) · Advances in Biological Regulation · doi:10.1016/j.jbior.2015.10.002 · Cited by 38
Sema4D-plexin-B1 implicated in regulation of dendritic spine density through RhoA/ROCK pathway
Lin, X., Ogiya, M., Takahara, M., Yamaguchi, W., Furuyama, T., Tanaka, H., Tohyama, M., & Inagaki, S. (2007) · Neuroscience Letters · doi:10.1016/j.neulet.2007.09.045 · Cited by 37
Role of Dendritic Spines in Action Potential Backpropagation: A Numerical Simulation Study
Tsay, D., & Yuste, R. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00781.2001 · Cited by 37
Roth, S. U., Sommer, C., Mundel, P. H., & Kiessling, M. (2001) · Brain Pathology · doi:10.1111/j.1750-3639.2001.tb00389.x · Cited by 37
Spine loss and other dendritic abnormalities in epilepsy
Swann, J. W., Al‐Noori, S., Jiang, M., & Lee, C. L. (2000) · Hippocampus · doi:10.1002/1098-1063(2000)10:5 · Cited by 268
Bock, J., Thode, C., Hannemann, O., Braun, K., & Darlison, M. G. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.02.048 · Cited by 36
EphA Signaling Promotes Actin-based Dendritic Spine Remodeling through Slingshot Phosphatase
Zhou, L., Jones, E. V., & Murai, K. K. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.302802 · Cited by 38
Tanokashira, D., Morita, T., Hayashi, K., Mayanagi, T., Fukumoto, K., Kubota, Y., Yamashita, T., & Sobue, K. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2380-12.2012 · Cited by 36
Nestor, M. W., Cai, X., Stone, M. R., Bloch, R. J., & Thompson, S. M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016197 · Cited by 37
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