The DOI matches its Crossref record; 101 of the 103 references it cites were found in a registry or an index.
Spine Motility
Open accessAbstract
Throughout the history of neuroscience, dendritic spines have been considered stable structures, but in recent years, imaging techniques have revealed that spines are constantly changing shape. Spine motility is difficult to categorize, has different forms, and possibly even represents multiple phenomena. It is influenced by synaptic transmission, intracellular calcium, and a multitude of ions and other molecules. An actin-based cascade mediates this phenomenon, and while the precise signaling pathways are still unclear, the Rho family of GTPases could well be a "common denominator" controlling spine morphology. One role of spine motility might be to enable a searching function during synaptogenesis, allowing for more efficacious neuronal connectivity in the neuronal thicket. This idea revisits concepts originally formulated by Cajal, who proposed over a hundred years ago that spines might help to increase and modify synaptic connections.
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
“Organotypic hippocampal slice cultures are known to undergo key developmental steps similar to those observed in vivo, including synapse maturation28–31, and have been previously used to study ramified microglia function32.”
From Microglia remodel synapses by presynaptic trogocytosis and spine head filopodia induction (2018) · cites this paper as [28]
Citations
Cites
Rho GTPases and the Actin Cytoskeleton
Hall, A. (1998) · Science · doi:10.1126/science.279.5350.509 · Cited by 6,138
The Molecular Biology of Axon Guidance
Tessier‐Lavigne, M., & Goodman, C. S. (1996) · Science · doi:10.1126/science.274.5290.1123 · Cited by 3,311
The Fine Structure of the Nervous System.
Tennyson, V. M. (1970) · Archives of Neurology · doi:10.1001/archneur.1970.00480240094019 · Cited by 1,946
Axo-somatic and axo-dendritic synapses of the cerebral cortex: an electron microscope study.
Eg, G. (1959) · PubMed · Cited by 1,768
Dendritic spine changes associated with hippocampal long-term synaptic plasticity
Engert, F., & Bonhoeffer, T. (1999) · Nature · doi:10.1038/19978 · Cited by 1,412
Self-citationCADHERINS: A MOLECULAR FAMILY IMPORTANT IN SELECTIVE CELL-CELL ADHESION
Takeichi, M. (1990) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.59.070190.001321 · Cited by 1,301
Morphological Changes in Dendritic Spines Associated with Long-Term Synaptic Plasticity
Yuste, R., & Bonhoeffer, T. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.1071 · Cited by 1,269
Self-citationNaturally occurring fluctuation in dendritic spine density on adult hippocampal pyramidal neurons
Woolley, C., Gould, E., Frankfurt, M., & McEwen, B. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-12-04035.1990 · Cited by 1,107
Harris, K., & Stevens, J. (1989) · The Journal of Neuroscience · doi:10.1523/jneurosci.09-08-02982.1989 · Cited by 1,073
Harris, K. M., Jensen, F. E., & Tsao, B. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-07-02685.1992 · Cited by 1,036
Research works printed but not linked: 2
- Gray, 1959, Axo-somatic and axo-dendritic synapses of the cerebral cortex, J. Anat., 83, 420
- Ramón y Cajal, 1891, Significación fisiológica de las expansiones protoplásmicas y nerviosas de la sustancia gris, Revista de Ciencias Médicas de Barcelona, 22, 23
Cited by
Sorted by citations
A brain-specific microRNA regulates dendritic spine development
Schratt, G. M., Tuebing, F., Nigh, E. A., Kane, C. G., Sabatini, M. E., Kiebler, M., & Greenberg, M. E. (2006) · Nature · doi:10.1038/nature04367 · Cited by 1,786
Pyramidal neurons: dendritic structure and synaptic integration
Spruston, N. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2286 · Cited by 1,688
PDZ domain proteins of synapses
Kim, E., & Sheng, M. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1517 · Cited by 1,630
The importance of dendritic mitochondria in the morphogenesis and plasticity of spines and synapses
Li, Z., Okamoto, K.-I., Hayashi, Y., & Sheng, M. (2004) · Cell · doi:10.1016/j.cell.2004.11.003 · Cited by 1,498
Distinct morphological stages of dentate granule neuron maturation in the adult mouse hippocampus
Zhao, C., Teng, E. M., Summers, R. G., Ming, G.-L., & Gage, F. H. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.3648-05.2006 · Cited by 1,257
Transient and persistent dendritic spines in the neocortex in vivo
Holtmaat, A. J. G. D., Trachtenberg, J. T., Wilbrecht, L., Shepherd, G. M., Zhang, X., Knott, G. W., & Svoboda, K. (2005) · Neuron · doi:10.1016/j.neuron.2005.01.003 · Cited by 1,131
The role of the Rho GTPases in neuronal developmentPreprint
Govek, E., Newey, S. E., & Aelst, L. V. (2005) · Genes & Development · doi:10.1101/gad.1256405 · Cited by 1,030
Microglia remodel synapses by presynaptic trogocytosis and spine head filopodia induction
Weinhard, L., di Bartolomei, G., Bolasco, G., Machado, P., Schieber, N. L., Neniskyte, U., Exiga, M., Vadisiute, A., Raggioli, A., Schertel, A., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-03566-5 · Cited by 790
Stress duration modulates the spatiotemporal patterns of spine formation in the basolateral amygdala
Mitra, R., Jadhav, S., McEwen, B. S., Vyas, A., & Chattarji, S. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504011102 · Cited by 663
Genesis of dendritic spines: insights from ultrastructural and imaging studies
Yuste, R., & Bonhoeffer, T. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1300 · Cited by 657
Self-citationMolecular mechanisms of dendritic spine morphogenesis
Tada, T., & Sheng, M. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.12.001 · Cited by 615
Activity-Dependent Regulation of MEF2 Transcription Factors Suppresses Excitatory Synapse Number
Flavell, S. W., Cowan, C. W., Kim, T.-K., Greer, P. L., Lin, Y., Paradis, S., Griffith, E. C., Hu, L. S., Chen, C., & Greenberg, M. E. (2006) · Science · doi:10.1126/science.1122511 · Cited by 573
Regulation of affect by the lateral septum: implications for neuropsychiatry
Sheehan, T. P., Chambers, R. A., & Russell, D. S. (2004) · Brain Research Reviews · doi:10.1016/j.brainresrev.2004.04.009 · Cited by 514
Ropers, H., & Hamel, B. C. J. (2005) · Nature Reviews Genetics · doi:10.1038/nrg1501 · Cited by 523
The Subspine Organization of Actin Fibers Regulates the Structure and Plasticity of Dendritic Spines
Honkura, N., Matsuzaki, M., Noguchi, J., Ellis-Davies, G. C. R., & Kasai, H. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.013 · Cited by 490
Dictenberg, J. B., Swanger, S. A., Antar, L. N., Singer, R. H., & Bassell, G. J. (2008) · Developmental Cell · doi:10.1016/j.devcel.2008.04.003 · Cited by 511
Structural Plasticity and Hippocampal Function
Leuner, B., & Gould, E. (2009) · Annual Review of Psychology · doi:10.1146/annurev.psych.093008.100359 · Cited by 478
Neural activity and the dynamics of central nervous system development
Hua, J. Y., & Smith, S. J. (2004) · Nature Neuroscience · doi:10.1038/nn1218 · Cited by 450
The actin cytoskeleton: integrating form and function at the synapse
Dillon, C., & Goda, Y. (2005) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135757 · Cited by 447
Si, K., Giustetto, M., Etkin, A., Hsu, R., Janisiewicz, A. M., Miniaci, M. C., Kim, J., Zhu, H., & Kandel, E. R. (2003) · Cell · doi:10.1016/s0092-8674(03)01021-3 · Cited by 442
Spine-Neck Geometry Determines NMDA Receptor-Dependent Ca2+ Signaling in Dendrites
Noguchi, J., Matsuzaki, M., Ellis-Davies, G. C. R., & Kasai, H. (2005) · Neuron · doi:10.1016/j.neuron.2005.03.015 · Cited by 419
Structural Components of Synaptic Plasticity and Memory ConsolidationPreprint
Bailey, C. H., Kandel, E. R., & Harris, K. M. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a021758 · Cited by 419
Antar, L. N., Afroz, R., Dictenberg, J. B., Carroll, R. C., & Bassell, G. J. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.0099-04.2004 · Cited by 411
Bhatt, D. H., Zhang, S., & Gan, W.-B. (2009) · Annual Review of Physiology · doi:10.1146/annurev.physiol.010908.163140 · Cited by 380
Yamagata, M., Sanes, J. R., & Weiner, J. A. (2003) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(03)00107-8 · Cited by 374
Genetics of Early Onset Cognitive Impairment
Ropers, H. (2010) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-082509-141640 · Cited by 398
Tolias, K. F., Bikoff, J. B., Burette, A., Paradis, S., Harrar, D., Tavazoie, S., Weinberg, R. J., & Greenberg, M. E. (2005) · Neuron · doi:10.1016/j.neuron.2005.01.024 · Cited by 365
Delayed Stabilization of Dendritic Spines in Fragile X Mice
Cruz-Martin, A., Crespo, M., & Portera-Cailliau, C. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0577-10.2010 · Cited by 321
Rho GTPases, dendritic structure, and mental retardation
Newey, S. E., Velamoor, V., Govek, E., & Van Aelst, L. (2005) · Journal of Neurobiology · doi:10.1002/neu.20153 · Cited by 351
The Control of Dendrite Development
Jan, Y. N., & Jan, L. Y. (2003) · Neuron · doi:10.1016/s0896-6273(03)00631-7 · Cited by 311
Reviews: BDNF and Memory Formation and Storage
Bekinschtein, P., Cammarota, M., Izquierdo, I., & Medina, J. H. (2007) · The Neuroscientist · doi:10.1177/1073858407305850 · Cited by 309
Cellular and molecular mechanisms of presynaptic assembly
Ziv, N. E., & Garner, C. C. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1370 · Cited by 312
Dendritic Spine Dynamics Are Regulated by Monocular Deprivation and Extracellular Matrix Degradation
Oray, S., Majewska, A., & Sur, M. (2004) · Neuron · doi:10.1016/j.neuron.2004.12.001 · Cited by 296
Calcium Signaling in Neuronal Motility
Zheng, J. Q., & Poo, M.-M. (2007) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.23.090506.123221 · Cited by 292
Rapid functional maturation of nascent dendritic spines
Zito, K., Scheuss, V., Knott, G., Hill, T., & Svoboda, K. (2009) · Neuron · doi:10.1016/j.neuron.2008.10.054 · Cited by 272
Multiple roles of ephrins in morphogenesis, neuronal networking, and brain functionPreprint
Palmer, A., & Klein, R. (2003) · Genes & Development · doi:10.1101/gad.1093703 · Cited by 272
Rapid Reversible Changes in Dendritic Spine Structure In Vivo Gated by the Degree of Ischemia
Zhang, S., Boyd, J., Delaney, K., & Murphy, T. H. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.1085-05.2005 · Cited by 267
Activity-dependent modulation of the BDNF receptor TrkB: mechanisms and implications
Nagappan, G., & Lu, B. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.07.003 · Cited by 273
Development and Regulation of Dendritic Spine Synapses
Calabrese, B., Wilson, M. S., & Halpain, S. (2006) · Physiology · doi:10.1152/physiol.00042.2005 · Cited by 287
Axon pruning: An essential step underlying the developmental plasticity of neuronal connections
Low, L. K., & Cheng, H.-J. (2006) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2006.1883 · Cited by 258
Tashiro, A., & Yuste, R. (2004) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2004.04.001 · Cited by 265
Self-citationRemodeling of Synaptic Structure in Sensory Cortical AreasIn Vivo
Majewska, A. K., Newton, J. R., & Sur, M. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4454-05.2006 · Cited by 258
Lang, C., Barco, A., Zablow, L., Kandel, E. R., Siegelbaum, S. A., & Zakharenko, S. S. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407581101 · Cited by 245
Saneyoshi, T., Wayman, G. A., Fortin, D. A., Davare, M. A., Hoshi, N., Nozaki, N., Natsume, T., & Soderling, T. R. (2008) · Neuron · doi:10.1016/j.neuron.2007.11.016 · Cited by 234
Lee, C.-C., Huang, C., & Hsu, K. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.06.003 · Cited by 231
The trouble with spines in fragile X syndrome: density, maturity and plasticity
He, C. X., & Portera‐Cailliau, C. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.03.049 · Cited by 217
Cortical area and species differences in dendritic spine morphology
Benavides-Piccione, R., Ballesteros-Yáñez, I., DeFelipe, J., & Yuste, R. (2002) · Journal of Neurocytology · doi:10.1023/a:1024134312173 · Cited by 207
Self-citationHourcade, B., Muenz, T. S., Sandoz, J., Rößler, W., & Devaud, J. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0841-10.2010 · Cited by 201
MicroRNA function in neuronal development, plasticity and disease
Fiore, R., Siegel, G., & Schratt, G. M. (2007) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2007.12.006 · Cited by 206
The neocortical microcircuit as a tabula rasa
Kalisman, N., Silberberg, G., & Markram, H. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407088102 · Cited by 203
Sprouting, regeneration and circuit formation in the injured spinal cord: factors and activity
Maier, I. C., & Schwab, M. E. (2006) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2006.1890 · Cited by 197
Meng, J., Meng, Y., Hanna, A., Janus, C., & Jia, Z. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0028-05.2005 · Cited by 202
Induction of Spine Growth and Synapse Formation by Regulation of the Spine Actin Cytoskeleton
Zito, K., Knott, G. W., Shepherd, G. M., Shenolikar, S., & Svoboda, K. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.022 · Cited by 202
Dendritic pathology in mental retardation: from molecular genetics to neurobiology
Dierssen, M., & Ramakers, G. J. A. (2006) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2006.00224.x · Cited by 191
Ji, Y., Gong, Y., Gan, W., Beach, T., Holtzman, D. M., & Wisniewski, T. (2003) · Neuroscience · doi:10.1016/j.neuroscience.2003.08.007 · Cited by 189
Post-translational protein modification as the substrate for long-lasting memory
Routtenberg, A., & Rekart, J. L. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.11.006 · Cited by 186
Alsin Is a Rab5 and Rac1 Guanine Nucleotide Exchange Factor
Topp, J. D., Gray, N. W., Gerard, R. D., & Horazdovsky, B. F. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m313504200 · Cited by 191
Electrical compartmentalization in dendritic spines
Yuste, R. (2013) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150455 · Cited by 180
Self-citationA Critical Role for Myosin IIB in Dendritic Spine Morphology and Synaptic Function
Ryu, J., Liu, L., Wong, T. P., Wu, D., Burette, A., Weinberg, R. J., Wang, Y. T., & Sheng, M. (2006) · Neuron · doi:10.1016/j.neuron.2005.12.017 · Cited by 179
Perez-Cruz, C., Nolte, M. W., van Gaalen, M. M., Rustay, N. R., Termont, A., Tanghe, A., Kirchhoff, F., & Ebert, U. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.6142-10.2011 · Cited by 172
Benavides‐Piccione, R., Fernaud-Espinosa, I., Robles, V., Yuste, R., & DeFelipe, J. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs154 · Cited by 180
Self-citationX-linked mental retardation: many genes for a complex disorder
Ropers, H. (2006) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2006.04.017 · Cited by 177
Non-synaptic dendritic spines in neocortex
Arellano, J. I., Espinosa, A., Fairén, A. G., Yuste, R., & DeFelipe, J. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.12.015 · Cited by 179
Self-citationSynaptic contact dynamics controlled by cadherin and catenins
Takeichi, M., & Abe, K. (2005) · Trends in Cell Biology · doi:10.1016/j.tcb.2005.02.002 · Cited by 176
A Requirement for Nuclear Factor-κB in Developmental and Plasticity-Associated Synaptogenesis
Boersma, M. C. H., Dresselhaus, E. C., De Biase, L. M., Mihalas, A. B., Bergles, D. E., & Meffert, M. K. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.2456-10.2011 · Cited by 168
Comer, A. L., Jinadasa, T., Sriram, B., Phadke, R. A., Kretsge, L. N., Nguyen, T. P. H., Antognetti, G., Gilbert, J. P., Lee, J., Newmark, E., et al. (2020) · PLoS Biology · doi:10.1371/journal.pbio.3000604 · Cited by 163
Bidirectional Regulation of Hippocampal Mossy Fiber Filopodial Motility by Kainate Receptors
Tashiro, A., Dunaevsky, A., Blazeski, R., Mason, C. A., & Yuste, R. (2003) · Neuron · doi:10.1016/s0896-6273(03)00299-x · Cited by 165
Self-citationFMRP interferes with the Rac1 pathway and controls actin cytoskeleton dynamics in murine fibroblasts
Castets, M., Schaeffer, C., Bechara, E., Schenck, A., Khandjian, E. W., Luche, S., Moine, H., Rabilloud, T., Mandel, J.-L., & Bardoni, B. (2005) · Human Molecular Genetics · doi:10.1093/hmg/ddi077 · Cited by 162
Karpova, A., Mikhaylova, M., Thomas, U., Knöpfel, T., & Behnisch, T. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4573-05.2006 · Cited by 162
Signaling mechanisms underlying dendrite formation
Miller, F. D., & Kaplan, D. R. (2003) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(03)00072-2 · Cited by 160
Eph receptors in the adult brain
Yamaguchi, Y., & Pasquale, E. B. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.04.003 · Cited by 162
BDNF signaling during the lifetime of dendritic spines
Zagrebelsky, M., Tacke, C., & Korte, M. (2020) · Cell and Tissue Research · doi:10.1007/s00441-020-03226-5 · Cited by 147
The EphA4 receptor regulates dendritic spine remodeling by affecting β1-integrin signaling pathways
Bourgin, C., Murai, K. K., Richter, M., & Pasquale, E. B. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200610139 · Cited by 136
A hippocampal Cdk5 pathway regulates extinction of contextual fear
Sananbenesi, F., Fischer, A., Wang, X., Schrick, C., Neve, R. L., Radulović, J., & Tsai, L. (2007) · Nature Neuroscience · doi:10.1038/nn1943 · Cited by 143
Dendritic spine morphogenesis and plasticity
Lippman, J., & Dunaevsky, A. (2005) · Journal of Neurobiology · doi:10.1002/neu.20149 · Cited by 142
Insights into Rapid Modulation of Neuroplasticity by Brain Estrogens
Srivastava, D. P., Woolfrey, K. M., & Penzes, P. (2013) · Pharmacological Reviews · doi:10.1124/pr.111.005272 · Cited by 146
Leuner, B., & Shors, T. J. (2004) · Molecular Neurobiology · doi:10.1385/mn:29:2:117 · Cited by 143
A central role for the small GTPase Rac1 in hippocampal plasticity and spatial learning and memory
Haditsch, U., Leone, D. P., Farinelli, M., Chrostek‐Grashoff, A., Brakebusch, C., Mansuy, I. M., McConnell, S. K., & Palmer, T. D. (2009) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2009.04.005 · Cited by 144
Small GTPase Cdc42 Is Required for Multiple Aspects of Dendritic Morphogenesis
Scott, E. K., Reuter, J. E., & Luo, L. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-08-03118.2003 · Cited by 134
Ryan, X. P., Alldritt, J., Svenningsson, P., Allen, P. B., Wu, G.-Y., Nairn, A. C., & Greengard, P. (2005) · Neuron · doi:10.1016/j.neuron.2005.05.013 · Cited by 142
Tsubouchi, A., Caldwell, J. C., & Tracey, W. D. (2012) · Current Biology · doi:10.1016/j.cub.2012.09.019 · Cited by 127
Huang, F., Chotiner, J. K., & Steward, O. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2410-07.2007 · Cited by 127
Cell adhesion in development: a complex signaling network
Thiery, J. P. (2003) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(03)00088-1 · Cited by 124
Distinct Behavioral Responses to Ethanol Are Regulated by Alternate RhoGAP18B Isoforms
Rothenfluh, A., Threlkeld, R. J., Bainton, R. J., Tsai, L. T.-Y., Lasek, A. W., & Heberlein, U. (2006) · Cell · doi:10.1016/j.cell.2006.09.010 · Cited by 121
Aoki, C. J., Sekino, Y., Hanamura, K., Fujisawa, S., Mahadomrongkul, V., Ren, Y., & Shirao, T. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20449 · Cited by 119
Huang, Z. J. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2008.168211 · Cited by 117
Cheadle, L., & Biederer, T. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201205041 · Cited by 118
Schubert, V., Silva, J. S. D., & Dotti, C. G. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200506136 · Cited by 117
Lowe syndrome protein OCRL1 interacts with Rac GTPase in the trans-Golgi network
Faucherre, A. (2003) · Human Molecular Genetics · doi:10.1093/hmg/ddg250 · Cited by 112
Fauchereau, F. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(03)00078-2 · Cited by 109
MicroRNA-9 controls dendritic development by targeting REST
Giusti, S. A., Vogl, A. M., Brockmann, M. M., Vercelli, C. A., Rein, M. L., Trümbach, D., Wurst, W., Cazalla, D., Stein, V., Deussing, J. M., et al. (2014) · eLife · doi:10.7554/elife.02755 · Cited by 113
Synaptic organization in the adult Drosophila mushroom body calyx
Leiss, F., Groh, C., Butcher, N. J., Meinertzhagen, I. A., & Tavosanis, G. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22184 · Cited by 106
The dynamic cytoskeleton: backbone of dendritic spine plasticity
Dent, E. W., Merriam, E. B., & Hu, X. (2010) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2010.08.013 · Cited by 116
On the electrical function of dendritic spines
Tsay, D., & Yuste, R. (2003) · Trends in Neurosciences · doi:10.1016/j.tins.2003.11.008 · Cited by 103
Self-citationRegulation of Spine Morphology and Synaptic Function by LIMK and the Actin Cytoskeleton
Meng, Y., Zhang, Y., Tregoubov, V., Falls, D. L., & Jia, Z. (2003) · Reviews in the Neurosciences · doi:10.1515/revneuro.2003.14.3.233 · Cited by 101
Pilpel, Y., & Segal, M. (2004) · European Journal of Neuroscience · doi:10.1111/j.0953-816x.2004.03380.x · Cited by 102
Huang, Z. J., & Scheiffele, P. (2008) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2008.05.008 · Cited by 101
KCC2 regulates actin dynamics in dendritic spines via interaction with β-PIX
Llano, O., Sv, S., Soni, S., Golubtsov, A., Guillemin, I., Hotulainen, P., Medina, I., Nothwang, H. G., Rivera, C., & Ludwig, A. (2015) · The Journal of Cell Biology · doi:10.1083/jcb.201411008 · Cited by 101
Regulation of the Actin Cytoskeleton in Dendritic Spines
Penzes, P., & Rafalovich, I. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-3-7091-0932-8_4 · Cited by 102
Villalba, R. M., & Smith, Y. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.07.011 · Cited by 97
Metadata
- Authors
- Bonhoeffer, T., & Yuste, R.
- Affiliations
- Max Planck Institute of Neurobiology (DE)
- Max Planck Society (DE)
- Corresponding author
- Bonhoeffer, Tobias
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2002-09
- Volume
- 35
- Issue
- 6
- Pages
- 1019-1027
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W151176851
- Cited by
- 337
- References
- 103
- Citations by year
- 2025: 6 · 2024: 5 · 2023: 10 · 2022: 7 · 2021: 10 · 2020: 11 · 2019: 9 · 2018: 10 · 2017: 2 · 2016: 9 · 2015: 16 · 2014: 12 · 2013: 12 · 2012: 18
- FWCI
- 2.72
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 3972 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- Max Planck Institute for Plasma Physics (submittedVersion)
- Max Planck Digital Library (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Funders
- National Eye Institute (R01EY013237, EY 13237)
- National Institute of Neurological Disorders and Stroke (NS 40726, R01NS040726)
- 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 › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
- Keywords
- dendritic spines, spine motility, dendritic spine morphology, synaptic transmission, intracellular calcium, actin cytoskeleton, Rho GTPases, synaptogenesis, neuronal connectivity, Santiago Ramón y Cajal
- MeSH terms
- Animals, Central Nervous System, Dendrites, Humans, Synaptic Transmission, Neuronal Plasticity, Synapses
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