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 501–600 of 895
Ganglioside/calmodulin kinase ii signal inducing cdc42-mediated neuronal actin reorganization
Chen, N., Furuya, S., Doi, H., Hashimoto, Y., Kudo, Y., & Higashi, H. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00259-8 · Cited by 35
Postnatal development of synaptopodin expression in the rodent hippocampus
LaFaver, K., Haas, C. A., Orth, C. B., Deller, T., & Frotscher, M. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20651 · Cited by 37
Optimizing the spatial resolution of Channelrhodopsin-2 activation
Schoenenberger, P., Grunditz, Å., Rose, T., & Oertner, T. G. (2008) · Journal of Neurocytology · doi:10.1007/s11068-008-9025-8 · Cited by 38
Imbalance of synaptic actin dynamics as a key to fragile X syndrome?
Michaelsen‐Preusse, K., Feuge, J., & Körte, M. (2018) · The Journal of Physiology · doi:10.1113/jp275571 · Cited by 36
Burns, J. C., & Corwin, J. T. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4355-13.2014 · Cited by 34
Local Ca2+ signaling in neurons
Llinás, R., & Moreno, H. (1998) · Cell Calcium · doi:10.1016/s0143-4160(98)90059-8 · Cited by 34
Drought-induced changes in the actin cytoskeleton of barley (Hordeum vulgare L.) leaves
Śniegowska-Świerk, K., Dubas, E., & Rapacz, M. (2015) · Acta Physiologiae Plantarum · doi:10.1007/s11738-015-1820-0 · Cited by 34
Catenins: playing both sides of the synapse
Kwiatkowski, A. V., Weis, W. I., & Nelson, W. J. (2007) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2007.08.005 · Cited by 35
Rami, G., Caillard, O., Medina, I., Pellegrino, C., Fattoum, A., Ben‐Ari, Y., & Ferhat, L. (2005) · Hippocampus · doi:10.1002/hipo.20145 · Cited by 36
Modeling Calcium Dynamics in Dendritic Spines
Holcman, D., & Schuss, Z. (2005) · SIAM Journal on Applied Mathematics · doi:10.1137/s003613990342894x · Cited by 33
Zhong, H., Ceballos, C. C., Massengill, C. I., Muniak, M. A., Ma, L., Qin, M., Kaech, S., & Mao, T. (2021) · eLife · doi:10.7554/elife.64911 · Cited by 33
Self-citationSmith, B. A., Roy, H., Koninck, P. D., Grütter, P., & Koninck, Y. D. (2006) · Biophysical Journal · doi:10.1529/biophysj.106.092361 · Cited by 32
Imaging T‐cell antigen recognition and comparing immunological and neuronal synapses
Donnadieu, E., Revy, P., & Trautmann, A. (2001) · Immunology · doi:10.1046/j.1365-2567.2001.01268.x · Cited by 33
Molecular Regulation of Dendritic Spine Shape and Function
Sala, C. (2002) · Neurosignals · doi:10.1159/000065433 · Cited by 32
Dendritic spines: elementary structural units of neuronal plasticity
Segal, M. (2002) · Progress in brain research · doi:10.1016/s0079-6123(02)38070-1 · Cited by 32
A Pictorial History of the Neuronal Cytoskeleton
Leterrier, C. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2872-20.2020 · Cited by 31
The regulation and function of inositol 1,4,5-trisphosphate 3-kinases
Irvine, R. F., Lloyd-Burton, S. M., Yu, J. C. H., Letcher, A. J., & Schell, M. J. (2006) · Advances in Enzyme Regulation · doi:10.1016/j.advenzreg.2006.01.009 · Cited by 31
Evans, J. C., Robinson, C. M., Shi, M., & Webb, D. J. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.605543 · Cited by 31
Saalfrank, D., Konduri, A. K., Latifi, S., Habibey, R., Golabchi, A., Martiniuc, A. V., Knoll, A., Ingebrandt, S., & Blau, A. W. (2015) · Royal Society Open Science · doi:10.1098/rsos.150031 · Cited by 31
Kijima, S. T., Staiger, C. J., Katoh, K., Nagasaki, A., Ito, K., & Uyeda, T. Q. P. (2018) · Scientific Reports · doi:10.1038/s41598-018-22707-w · Cited by 31
Lendvai, B., Zelles, T., Rózsa, B. J., & Vizi, E. S. (2002) · Brain Research Bulletin · doi:10.1016/s0361-9230(02)00873-0 · Cited by 31
Verzi, D. W., Rheuben, M. B., & Baer, S. M. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00373.2004 · Cited by 31
Metabotropic glutamate receptor type 1α and tubulin assemble into dynamic interacting complexes
Ciruela, F., & McIlhinney, R. A. J. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00099.x · Cited by 31
Ofer, N., Benavides‐Piccione, R., DeFelipe, J., & Yuste, R. (2022) · eNeuro · doi:10.1523/eneuro.0039-22.2022 · Cited by 30
Hypoxia-Induced MicroRNA-210 Targets Neurodegenerative Pathways
Watts, M. E., Williams, S., Nithianantharajah, J., & Claudianos, C. (2018) · Non-Coding RNA · doi:10.3390/ncrna4020010 · Cited by 30
Three-dimensional real time imaging of amyloid β aggregation on living cells
Kuragano, M., Yamashita, R., Chikai, Y., Kitamura, R., & Tokuraku, K. (2020) · Scientific Reports · doi:10.1038/s41598-020-66129-z · Cited by 30
Sex Steroids and Neuronal Growth in Adulthood
Woolley, C. S., & Cohen, R. S. (2002) · Elsevier eBooks · doi:10.1016/b978-012532104-4/50079-2 · Cited by 30
Crimins, J. L., Wang, A. C., Yuk, F., Puri, R., Janssen, W. G. M., Hara, Y., Rapp, P. R., & Morrison, J. H. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw050 · Cited by 29
Shen, W., Jin, L., Zhu, A., Lin, Y., Pan, G., Zhou, S., Cheng, J., Zhang, J., Tu, F., Liu, C., et al. (2021) · Life Sciences · doi:10.1016/j.lfs.2021.119033 · Cited by 29
Presynaptic AMPA Receptors in Health and Disease
Zanetti, L., Regoni, M., Ratti, E., Valtorta, F., & Sassone, J. (2021) · Cells · doi:10.3390/cells10092260 · Cited by 29
Lin, W., Hurley, J. T., Raines, A. N., Cheney, R. E., & Webb, D. J. (2013) · Journal of Cell Science · doi:10.1242/jcs.132969 · Cited by 30
Dombert, B., Balk, S., Lüningschrör, P., Moradi, M., Sivadasan, R., Saal-Bauernschubert, L., & Jablonka, S. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00346 · Cited by 32
Physiological roles of spine motility: development, plasticity and disorders
McKinney, R. A. (2005) · Biochemical Society Transactions · doi:10.1042/bst20051299 · Cited by 29
Beta- and Gamma-Cytoplasmic Actins Are Required for Meiosis in Mouse Oocytes1
Brockmann, C., Huarte, J., Dugina, V. B., Challet, L., Rey, E., Conne, B., Swetloff, A., Nef, S., Chaponnier, C., & Vassalli, J. (2011) · Biology of Reproduction · doi:10.1095/biolreprod.111.091736 · Cited by 28
Feuge, J., Scharkowski, F., Michaelsen‐Preusse, K., & Körte, M. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz059 · Cited by 28
Depolarization gates spine calcium transients and spike-timing-dependent potentiation
Jiang, H., & Oertner, T. G. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.10.004 · Cited by 29
Guillery, R. W. (2000) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01635-0 · Cited by 32
Collaboration of PSD-Zip70 with Its Binding Partner, SPAR, in Dendritic Spine Maturity
Maruoka, H., Konno, D., Hori, K., & Sobue, K. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3920-04.2005 · Cited by 28
Popp, R. L., & Dertien, J. S. (2008) · Alcohol · doi:10.1016/j.alcohol.2008.06.006 · Cited by 28
Ca2+‐dependent regulation of synaptic δ2 glutamate receptor density in cultured rat Purkinje neurons
Hirai, H. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01630.x · Cited by 28
Chapter 9 Changing views of Cajal's neuron: the case of the dendritic spine
Segal, M. (2002) · Progress in brain research · doi:10.1016/s0079-6123(02)36011-4 · Cited by 28
General Considerations for Live Imaging of Developing Hippocampal Neurons in CulturePreprint
Kaech, S., Huang, C.-F., & Banker, G. A. (2012) · Cold Spring Harbor Protocols · doi:10.1101/pdb.ip068221 · Cited by 28
Self-citationDendritic Spine Dysgenesis in Neuropathic Pain
Tan, A. M. (2015) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2014.12.001 · Cited by 27
Fine structure of synapses on dendritic spines
Frotscher, M., Studer, D., Graber, W. A., Chai, X., Nestel, S., & Zhao, S. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00094 · Cited by 29
Kopec, C. D., & Malinow, R. (2006) · Science · doi:10.1126/science.1137595 · Cited by 28
He, S., Jin, Z., & Masland, R. H. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-18-08049.1999 · Cited by 27
Timofeeva, Y., Lord, G. J., & Coombes, S. (2006) · Journal of Computational Neuroscience · doi:10.1007/s10827-006-8776-4 · Cited by 26
The Dendritic Cytoskeleton as a Computational Device: An Hypothesis
Priel, A., Tuszyński, J. A., & Cantiello, H. F. (2006) · Springer eBooks · doi:10.1007/3-540-36723-3_8 · Cited by 26
N-cadherin, spine dynamics, and synaptic function
Mysore, S. P. (2008) · Frontiers in Neuroscience · doi:10.3389/neuro.01.035.2008 · Cited by 26
Effects of GSM 1800 MHz on dendritic development of cultured hippo-campal neurons
Wei, N., Xu, S., Chiang, H., Xu, Z., Zhou, S., Yang, W., & Luo, J. (2007) · Acta Pharmacologica Sinica · doi:10.1111/j.1745-7254.2007.00668.x · Cited by 26
Richards, B. A., & Frankland, P. W. (2013) · Hippocampus · doi:10.1002/hipo.22089 · Cited by 26
Tominaga, M., Kurihara, H., Honda, S., Amakawa, G., Sakai, T., & Tomooka, Y. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03554.x · Cited by 26
A GFP-based System to Uncouple mRNA Transport from Translation in a Single Living Neuron
Macchi, P., Hemraj, I., Goetze, B., Grunewald, B., Mallardo, M., & Kiebler, M. A. (2003) · Molecular Biology of the Cell · doi:10.1091/mbc.e02-08-0505 · Cited by 26
Gerisch, G., & Müller‐Taubenberger, A. (2003) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(03)61017-7 · Cited by 26
Waller, J. A., Chen, F., & Sánchez, C. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.12.012 · Cited by 25
Retinal Ganglion Cell Death Postponed: Giving Apoptosis a Break?
Kisiswa, L., Dervan, A. G., Albon, J., Morgan, J. E., & Wride, M. A. (2009) · Ophthalmic Research · doi:10.1159/000247591 · Cited by 25
Hugel, S., Abegg, M. H., Paola, V. D., Caroni, P., Gähwiler, B. H., & McKinney, R. A. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn118 · Cited by 25
Calcium‐triggered exit of F‐actin and IP3 3‐kinase A from dendritic spines is rapid and reversible
Schell, M. J., & Irvine, R. F. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05125.x · Cited by 25
Neuronal LRP4 regulates synapse formation in the developing CNS
Karakatsani, A., Marichal, N., Urban, S., Kalamakis, G., Ghanem, A., Schick, A., Zhang, Y., Conzelmann, K., Rüegg, M. A., Berninger, B., et al. (2017) · Development · doi:10.1242/dev.150110 · Cited by 25
Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neurons
Haq, N., Schmidt‐Hieber, C., Sialana, F. J., Ciani, L., Heller, J. P., Stewart, M. E., Bentley, L., Wells, S. E., Rodenburg, R. J., Nolan, P. M., et al. (2019) · PLoS Biology · doi:10.1371/journal.pbio.3000414 · Cited by 26
Modeling the Shape of Synaptic Spines by Their Actin Dynamics
Bonilla-Quintana, M., Wörgötter, F., Tetzlaff, C., & Fauth, M. J. (2020) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2020.00009 · Cited by 25
Dynamic presynaptic varicosities: a role in activity-dependent synaptogenesis
Müller, D., & Nikonenko, I. (2003) · Trends in Neurosciences · doi:10.1016/j.tins.2003.08.010 · Cited by 25
Brask, J., Owe‐Larsson, B., Hill, R. H., & Kristensson, K. (2001) · Brain Research Bulletin · doi:10.1016/s0361-9230(01)00536-6 · Cited by 25
Diabetes, Insulin and Alzheimer's Disease
Craft, S., & Christen, Y. (2010) · Research and perspectives in Alzheimer's disease · doi:10.1007/978-3-642-04300-0 · Cited by 24
Stereological Assessments of Neuronal Pathology in Auditory Cortex in Schizophrenia
Parker, E. M., & Sweet, R. A. (2018) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00131 · Cited by 25
Multifunctional Roles of Activins in the Brain
Ageta, H., & Tsuchida, K. (2011) · Vitamins and hormones · doi:10.1016/b978-0-12-385961-7.00009-3 · Cited by 25
Reversible, activity-dependent targeting of profilin to neuronal nuclei
Birbach, A., Verkuyl, J. M., & Matus, A. I. (2006) · Experimental Cell Research · doi:10.1016/j.yexcr.2006.03.026 · Cited by 25
Self-citationHonjo, Y., Nakagawa, S., & Takeichi, M. (2000) · Genes to Cells · doi:10.1046/j.1365-2443.2000.00327.x · Cited by 24
In vivo dynamics of the F-actin-binding protein neurabin-II
Stephens, D. J., & Banting, G. S. (2000) · Biochemical Journal · doi:10.1042/bj3450185 · Cited by 24
Intracellular machinery for the transport of AMPA receptors.
Esteban, J. A. (2008) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0707525 · Cited by 29
Kasai, H. (2023) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.99.018 · Cited by 25
Petanjek, Z., Banovac, I., Sedmak, D., & Hladnik, A. (2023) · Advances in neurobiology · doi:10.1007/978-3-031-36159-3_4 · Cited by 34
A Modeling Environment With Three-Dimensional Morphology, A-Cell-3D, and Ca2+ Dynamics in a Spine
Ichikawa, K. (2005) · Neuroinformatics · doi:10.1385/ni:3:1:049 · Cited by 23
Iannella, N. L. (2010) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2010.00021 · Cited by 23
Mita, N., He, X., Sasamoto, K., Mishiba, T., & Ohshima, T. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu264 · Cited by 23
Profilin, an Essential Control Element for Actin Polymerization
Karlsson, R., & Lindberg, U. (2008) · Springer eBooks · doi:10.1007/978-0-387-46407-7_3 · Cited by 23
Overview of Image Analysis, Image Importing, and Image Processing using Freeware
Bearer, E. L. (2003) · Current Protocols in Molecular Biology · doi:10.1002/0471142727.mb1415s63 · Cited by 23
Bearer, E. L., & Satpute‐Krishnan, P. (2002) · Current Drug Targets - Infectious Disorders · doi:10.2174/1568005023342407 · Cited by 23
Characteristics of EYFP-actin and visualization of actin dynamics during ATP depletion and repletion
Herget‐Rosenthal, S., Hosford, M. A., Kribben, A., Atkinson, S. J., Sandoval, R. M., & Molitoris, B. A. (2001) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.2001.281.6.c1858 · Cited by 23
de Bartolomeis, A., Vellucci, L., Simone, G. D., Mazza, B., Barone, A., & Ciccarelli, M. (2023) · Cells · doi:10.3390/cells12040574 · Cited by 22
Molecular Dynamics of the Excitatory Synapse
Okabe, S. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-3-7091-0932-8_6 · Cited by 22
Expansion Microscopy: Toward Nanoscale Imaging of a Diverse Range of Biomolecules
Klimas, A., & Zhao, Y. (2020) · ACS Nano · doi:10.1021/acsnano.0c04374 · Cited by 22
Primary Cilia and Dendritic Spines: Different but Similar Signaling Compartments
Nechipurenko, I. V., Doroquez, D. B., & Sengupta, P. (2013) · Molecules and Cells · doi:10.1007/s10059-013-0246-z · Cited by 23
Jeanneret, V., & Yepes, M. (2016) · Translational Stroke Research · doi:10.1007/s12975-016-0454-x · Cited by 22
Bennett, M. R., Arnold, J. C., Hatton, S. N., & Lagopoulos, J. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.11.029 · Cited by 22
Role of Drebrin in Synaptic Plasticity
Sekino, Y., Koganezawa, N., Mizui, T., & Shirao, T. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-4-431-56550-5_11 · Cited by 22
Nwabuisi‐Heath, E., LaDu, M. J., & Yu, C. (2012) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2012.04.003 · Cited by 26
A regulatory role for actin in dendritic spine proliferation
Johnson, O. L., & Ouimet, C. C. (2006) · Brain Research · doi:10.1016/j.brainres.2006.06.116 · Cited by 23
Trujillo‐Estrada, L., Vanderklish, P. W., Nguyen, M. M. T., Kuang, R. R., Nguyen, C., Huynh, E., da Cunha, C., Javonillo, D. I., Forner, S., Martini, A. C., et al. (2021) · Neurotherapeutics · doi:10.1007/s13311-021-01143-1 · Cited by 22
Dendritic Spines in Learning and Memory: From First Discoveries to Current Insights
Heck, N., & Santos, M. D. (2023) · Advances in neurobiology · doi:10.1007/978-3-031-36159-3_7 · Cited by 24
Phocein: A potential actor in vesicular trafficking at Purkinje cell dendritic spines
Bailly, Y. J. R., & Castets, F. (2007) · The Cerebellum · doi:10.1080/14734220701225912 · Cited by 21
Regulation of dendritic spine morphology by SPIN90, a novel Shank binding partner
Kim, S., Choi, K. Y., Cho, I. H., Rhy, J. H., Kim, S. H., Park, C., Kim, E., & Song, W. K. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06039.x · Cited by 22
Interleukin‐2 Enhances Dendritic Development and Spinogenesis in Cultured Hippocampal Neurons
Shen, Y., Liu, S., Zhan, M., Luo, J., & Zhu, L. (2010) · The Anatomical Record · doi:10.1002/ar.21118 · Cited by 21
The role of dendritic spine morphology in the compartmentalization and delivery of surface receptors
Simon, C. M., Hepburn, I., Chen, W., & Schutter, E. D. (2013) · Journal of Computational Neuroscience · doi:10.1007/s10827-013-0482-4 · Cited by 21
Human Rho Guanine Nucleotide Exchange Factor 11 (ARHGEF11) Regulates Dendritic Morphogenesis
Mizuki, Y., Takaki, M., Sakamoto, S., Okamoto, S., Kishimoto, M., Okahisa, Y., Itoh, M., & Yamada, N. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms18010067 · Cited by 21
Time course of recovery of the somatosensory map following hindpaw sensory deprivation in the rat
Dupont, E., Canu, M., Langlet, C., & Falempin, M. (2001) · Neuroscience Letters · doi:10.1016/s0304-3940(01)02050-x · Cited by 21
Studying Cytoskeletal Dynamics in Living Cells Using Green Fluorescent Protein
Yoon, Y., Pitts, K. R., & McNiven, M. A. (2002) · Molecular Biotechnology · doi:10.1385/mb:21:3:241 · Cited by 21
Schätzle, P., Ster, J., Verbich, D., McKinney, R. A., Gerber, U., Sonderegger, P., & María Mateos, J. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2010.204446 · Cited by 20
Roy, A., Sharma, S., Nag, T. C., Katyal, J., Gupta, Y. K., & Jain, S. (2022) · Neurotoxicity Research · doi:10.1007/s12640-022-00563-x · Cited by 20
Kuriu, T., Yanagawa, Y., & Konishi, S. (2011) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2011.11.002 · Cited by 20
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