Dendritic Spines: The Locus of Structural and Functional Plasticity

Synapses and Dendritic Spines as Pathogenic Targets in Alzheimer’s Disease

Yu, W., & Lu, B. (2012) · Neural Plasticity · doi:10.1155/2012/247150 · Cited by 123

The X-Linked Intellectual Disability Protein TSPAN7 Regulates Excitatory Synapse Development and AMPAR Trafficking

Bassani, S., Cingolani, L. A., Valnegri, P., Folci, A., Zapata, J., Gianfelice, A., Sala, C., Goda, Y., & Passafaro, M. (2012) · Neuron · doi:10.1016/j.neuron.2012.01.021 · Cited by 120

Structural Modulation of Dendritic Spines during Synaptic Plasticity

Fortin, D. A., Srivastava, T., & Soderling, T. R. (2011) · The Neuroscientist · doi:10.1177/1073858411407206 · Cited by 119

Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene

Bacchelli, E., Blasi, F., Biondolillo, M., Lamb, J. A., Bonora, E., Barnby, G., Parr, J., Beyer, K. S., Klauck, S. M., Poustka, A., et al. (2003) · Molecular Psychiatry · doi:10.1038/sj.mp.4001340 · Cited by 117

Brain-derived neurotrophic factor regulates AMPA receptor trafficking to post-synaptic densities via IP3R and TRPC calcium signaling

Nakata, H., & Nakamura, S. (2007) · FEBS Letters · doi:10.1016/j.febslet.2007.04.041 · Cited by 117

Cofilin-mediated neurodegeneration in alzheimer’s disease and other amyloidopathies

Maloney, M. T., & Bamburg, J. R. (2007) · Molecular Neurobiology · doi:10.1007/bf02700622 · Cited by 117

WAVE1 controls neuronal activity-induced mitochondrial distribution in dendritic spines

Sung, J. Y., Engmann, O., Teylan, M. A., Nairn, A. C., Greengard, P., & Kim, Y. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0712180105 · Cited by 117

Two-photon Na + imaging in spines and fine dendrites of central neurons

Rose, C. R., Kovalchuk, Y., Eilers, J., & Konnerth, A. (1999) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s004249900123 · Cited by 116

The X-linked intellectual disability protein IL1RAPL1 regulates excitatory synapse formation by binding PTPδ and RhoGAP2

Valnegri, P., Montrasio, C., Brambilla, D., Ko, J., Passafaro, M., & Sala, C. (2011) · Human Molecular Genetics · doi:10.1093/hmg/ddr418 · Cited by 116

Synaptic Dysfunction in Alzheimer’s Disease

Marcello, E. E., Epis, R., Saraceno, C., & Luca, M. D. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-3-7091-0932-8_25 · Cited by 115

Anatomical Plasticity of Adult Brain Is Titrated by Nogo Receptor 1

Akbik, F. V., Bhagat, S. M., Patel, P. R., Cafferty, W. B. J., & Strittmatter, S. M. (2013) · Neuron · doi:10.1016/j.neuron.2012.12.027 · Cited by 115

Microtubule-associated Protein 1B (MAP1B) Is Required for Dendritic Spine Development and Synaptic Maturation

Tortosa, E., Montenegro‐Venegas, C., Benoist, M., Härtel, S., González-Billault, C. E., Esteban, J. A., & Ávila, J. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.271320 · Cited by 115

Role of Numb in Dendritic Spine Development with a Cdc42 GEF Intersectin and EphB2

Nishimura, T., Yamaguchi, T., Tokunaga, A., Hara, A., Hamaguchi, T., Kato, K., Iwamatsu, A., Okano, H., & Kaibuchi, K. (2006) · Molecular Biology of the Cell · doi:10.1091/mbc.e05-07-0700 · Cited by 114

New sites of action for GIRK and SK channels

Luján, R., Maylie, J., & Adelman, J. P. (2009) · Nature reviews. Neuroscience · doi:10.1038/nrn2668 · Cited by 113

EphB Receptors Regulate Dendritic Spine Morphogenesis through the Recruitment/Phosphorylation of Focal Adhesion Kinase and RhoA Activation

Moeller, M. L., Shi, Y., Reichardt, L. F., & Ethell, I. M. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m511756200 · Cited by 111

Structural Dynamics of Dendritic Spines are Influenced by an Environmental Enrichment: An In Vivo Imaging Study

Jung, C. K. E., & Herms, J. W. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs317 · Cited by 111

Activity-Dependent Dendritic Spine Structural Plasticity Is Regulated by Small GTPase Rap1 and Its Target AF-6

Xie, Z., Huganir, R. L., & Penzes, P. (2005) · Neuron · doi:10.1016/j.neuron.2005.09.027 · Cited by 110

SUMOylation of the MAGUK protein CASK regulates dendritic spinogenesis

Chao, H., Hong, C., Huang, T., Lin, Y., & Hsueh, Y. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200712094 · Cited by 110

The p21-activated Kinase 3 Implicated in Mental Retardation Regulates Spine Morphogenesis through a Cdc42-dependent Pathway

Kreis, P., Thévenot, E., Rousseau, V., Boda, B., Muller, D., & Barnier, J.-V. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m703298200 · Cited by 109

Fear conditioning drives profilin into amygdala dendritic spines

Lamprecht, R., Farb, C. R., Rodrigues, S. M., & LeDoux, J. E. (2006) · Nature Neuroscience · doi:10.1038/nn1672 · Cited by 108

Dysregulation of Rho GTPases in the αPix/Arhgef6 mouse model of X-linked intellectual disability is paralleled by impaired structural and synaptic plasticity and cognitive deficits

Ramakers, G. J. A., Wolfer, D. P., Rosenberger, G., Kuchenbecker, K., Kreienkamp, H., Prange‐Kiel, J., Rune, G. M., Richter, K., Langnaese, K., Masneuf, S., et al. (2011) · Human Molecular Genetics · doi:10.1093/hmg/ddr457 · Cited by 108

Estrogen up-regulates estrogen receptor α and synaptophysin in slice cultures of rat hippocampus

Rune, G. M., Wehrenberg, U., Prange‐Kiel, J., Zhou, L., Adelmann, G., & Frotscher, M. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00152-5 · Cited by 107

Estrogen Receptor β Activity Modulates Synaptic Signaling and Structure

Srivastava, D. P., Woolfrey, K. M., Liu, F., Brandon, N. J., & Penzes, P. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.3264-10.2010 · Cited by 107

Intersectin Regulates Dendritic Spine Development and Somatodendritic Endocytosis but Not Synaptic Vesicle Recycling in Hippocampal Neurons

Thomas, S., Ritter, B., Verbich, D., Sanson, C., Bourbonnière, L., McKinney, R. A., & McPherson, P. S. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m809746200 · Cited by 106

Estrogen-regulated synaptogenesis in the hippocampus: Sexual dimorphism in vivo but not in vitro

Fester, L., Prange‐Kiel, J., Zhou, L., von Blittersdorff, B., Böhm, J. W., Jarry, H., Schumacher, M., & Rune, G. M. (2011) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2011.11.010 · Cited by 106

Requirement for Plk2 in Orchestrated Ras and Rap Signaling, Homeostatic Structural Plasticity, and Memory

Lee, K. J., Lee, Y., Rozeboom, A. M., Lee, J.-Y., Udagawa, N., Hoe, H., & Pak, D. T. S. (2011) · Neuron · doi:10.1016/j.neuron.2011.02.004 · Cited by 105

A critical role for the PAR-1/MARK-tau axis in mediating the toxic effects of Aβ on synapses and dendritic spines

Yu, W., Polepalli, J., Wagh, D., Rajadas, J., Malenka, R., & Lu, B. (2012) · Human Molecular Genetics · doi:10.1093/hmg/ddr576 · Cited by 103

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

Functional Plasticity Triggers Formation and Pruning of Dendritic Spines in Cultured Hippocampal Networks

Goldin, M. M., Segal, M., & Avignone, E. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-01-00186.2001 · Cited by 102

Elimination of Dendritic Spines with Long-Term Memory Is Specific to Active Circuits

Sanders, J. D., Cowansage, K. K., Baumgärtel, K., & Mayford, M. R. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1131-12.2012 · Cited by 102

ARF6 and EFA6A Regulate the Development and Maintenance of Dendritic Spines

Choi, S., Ko, J., Lee, J.-R., Lee, H. W., Kim, K., Chung, H. S., Kim, H., & Kim, E. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.4182-05.2006 · Cited by 101

Chemically induced long‐term potentiation increases the number of perforated and complex postsynaptic densities but does not alter dendritic spine volume in CA1 of adult mouse hippocampal slices

Stewart, M. G., Medvedev, N. I., Popov, V. I., Schoepfer, R., Davies, H. A., Murphy, K., Dallérac, G. M., Kraev, I., & Rodríguez, J. J. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04174.x · Cited by 101

Inhibition of RhoA pathway rescues the endocytosis defects in Oligophrenin1 mouse model of mental retardation

Khelfaoui, M., Pavlowsky, A., Powell, A. D., Valnegri, P., Cheong, K. W., Blandin, Y., Passafaro, M., Jefferys, J. G. R., Chelly, J., & Billuart, P. (2009) · Human Molecular Genetics · doi:10.1093/hmg/ddp189 · Cited by 100

The Spine Apparatus, Synaptopodin, and Dendritic Spine Plasticity

Segal, M., Vlachos, A., & Korkotian, E. (2010) · The Neuroscientist · doi:10.1177/1073858409355829 · Cited by 100

Deletion of α‐neurexins does not cause a major impairment of axonal pathfinding or synapse formation

Dudanova, I., Tabuchi, K., Rohlmann, A., Südhof, T. C., & Missler, M. (2007) · Journal of Comparative Neurology · doi:10.1002/cne.21305 · Cited by 98

PICK1 inhibition of the Arp2/3 complex controls dendritic spine size and synaptic plasticity

Nakamura, Y., Wood, C. L., Patton, A. P., Jaafari, N., Henley, J. M., Mellor, J. R., & Hanley, J. G. (2011) · The EMBO Journal · doi:10.1038/emboj.2010.357 · Cited by 97

Alterations of cortical pyramidal neurons in mice lacking high-affinity nicotinic receptors

Ballesteros-Yáñez, I., Benavides-Piccione, R., Bourgeois, J.-P., Changeux, J.-P., & DeFelipe, J. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1006269107 · Cited by 96

Alterations in dendritic morphology of the prefrontal cortical and striatum neurons in the unilateral 6‐OHDA‐rat model of Parkinson's disease

Solís, Ó., Limón, I. D., Flores‐Hernández, J., & Flores, G. (2007) · Synapse · doi:10.1002/syn.20381 · Cited by 96

Rescue of dendritic spine phenotype in Fmr1 KO mice with the mGluR5 antagonist AFQ056/Mavoglurant

Pop, A. S., Levenga, J., de Esch, C. E. F., Buijsen, R. A. M., Nieuwenhuizen, I. M., Li, T., Isaacs, A., Gasparini, F., Oostra, B. A., & Willemsen, R. (2014) · Psychopharmacology · doi:10.1007/s00213-012-2947-y · Cited by 93

The Insulin Receptor Substrate IRSp53 Links Postsynaptic shank1 to the Small G-Protein cdc42

Soltau, M., Richter, D., & Kreienkamp, H.-J. (2002) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2002.1201 · Cited by 93

The short-time structural plasticity of dendritic spines is altered in a model of Rett syndrome

Landi, S., Putignano, E., Boggio, E. M., Giustetto, M., Pizzorusso, T., & Ratto, G. M. (2011) · Scientific Reports · doi:10.1038/srep00045 · Cited by 93

Resequencing and Association Analysis of the KALRN and EPHB1 Genes And Their Contribution to Schizophrenia Susceptibility

Kushima, I., Nakamura, Y., Aleksic, B., Ikeda, M., Ito, Y., Shiino, T., Okochi, T., Fukuo, Y., Ujike, H., Suzuki, M., et al. (2012) · Schizophrenia Bulletin · doi:10.1093/schbul/sbq118 · Cited by 92

Cadherins and catenins in synapse development

Salinas, P. C., & Price, S. R. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.01.001 · Cited by 92

Remodeling of hippocampal synapses after hippocampus-dependent associative learning

Geinisman, Y., Disterhoft, J. F., Gundersen, H. J. G., McEchron, M. D., Persina, I. S., Power, J., van der Zee, E. A., & West, M. J. (2000) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(20000131)417:1<49::aid-cne4>3.0.co;2-3 · Cited by 92

Modulation of dendritic spines and synaptic function by Rac1: A possible link to Fragile X syndrome pathology

Bongmba, O. Y. N., Martinez, L. A., Elhardt, M. E., Butler, K., & Tejada-Simon, M. V. (2011) · Brain Research · doi:10.1016/j.brainres.2011.05.020 · Cited by 91

Dynamic regulation of spine–dendrite coupling in cultured hippocampal neurons

Korkotian, E., Holcman, D., & Segal, M. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03691.x · Cited by 91

Cortactin-Binding Protein 2 Modulates the Mobility of Cortactin and Regulates Dendritic Spine Formation and Maintenance

Chen, Y.-K., & Hsueh, Y.-P. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.4405-11.2012 · Cited by 90

Satb1 Ablation Alters Temporal Expression of Immediate Early Genes and Reduces Dendritic Spine Density during Postnatal Brain Development

Balamotis, M. A., Tamberg, N., Woo, Y. J., Li, J., Davy, B., Kohwi-shigematsu, T., & Kohwi, Y. (2011) · Molecular and Cellular Biology · doi:10.1128/mcb.05917-11 · Cited by 90

EphA4 Signaling Regulates Phospholipase Cγ1 Activation, Cofilin Membrane Association, and Dendritic Spine Morphology

Zhou, L., Martinez, S. J., Haber, M., Jones, E. V., Bouvier, D. S., Doucet, G., Corera, A. T., Fon, E. A., Zisch, A. H., & Murai, K. K. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1170-07.2007 · Cited by 89

Disassembly of Shank and Homer Synaptic Clusters Is Driven by Soluble β-Amyloid1-40 through Divergent NMDAR-Dependent Signalling Pathways

Roselli, F., Hutzler, P., Wegerich, Y., Livrea, P., & Almeida, O. F. X. (2009) · PLoS ONE · doi:10.1371/journal.pone.0006011 · Cited by 88

Hippocampal Drebrin Loss in Mild Cognitive Impairment

Counts, S., He, B., Nadeem, M., Wuu, J., Scheff, S. W., & Mufson, E. J. (2012) · Neurodegenerative Diseases · doi:10.1159/000333122 · Cited by 88

The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations

Schumacher, J., Laje, G., Jamra, R. A., Becker, T., Mühleisen, T. W., Vasilescu, C., Mattheisen, M., Herms, S., Hoffmann, P., Hillmer, A. M., et al. (2009) · Human Molecular Genetics · doi:10.1093/hmg/ddp204 · Cited by 86

Rapid Signaling of Estrogen to WAVE1 and Moesin Controls Neuronal Spine Formation via the Actin Cytoskeleton

Sanchez, A. M., Flamini, M. I., Fu, X.-D., Mannella, P., Giretti, M. S., Goglia, L., Genazzani, A. R., & Simoncini, T. (2009) · Molecular Endocrinology · doi:10.1210/me.2008-0408 · Cited by 86

α5 Integrin Signaling Regulates the Formation of Spines and Synapses in Hippocampal Neurons

Webb, D. J., Zhang, H., Majumdar, D., & Horwitz, A. F. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m610981200 · Cited by 86

IQGAP1 regulates NR2A signaling, spine density, and cognitive processes

Gao, C., Frausto, S. F., Guedea, A. L., Tronson, N. C., Jovasevic, V., Leaderbrand, K., Corcoran, K. A., Guzman, Y. F., Swanson, G. T., & Radulovic, J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.1300-11.2011 · Cited by 85

GEFT, A Rho Family Guanine Nucleotide Exchange Factor, Regulates Neurite Outgrowth and Dendritic Spine Formation

Bryan, B. A., Kumar, V., Stafford, L. J., Cai, Y., Wu, G., & Liu, M. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m406216200 · Cited by 85

Constitutively Active Rap2 Transgenic Mice Display Fewer Dendritic Spines, Reduced Extracellular Signal-Regulated Kinase Signaling, Enhanced Long-Term Depression, and Impaired Spatial Learning and Fear Extinction

Ryu, J., Futai, K., Feliú-Mójer, M. I., Weinberg, R. J., & Sheng, M. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1944-08.2008 · Cited by 84

Stage-Specific Functions of the Small Rho GTPases Cdc42 and Rac1 for Adult Hippocampal Neurogenesis

Vadodaria, K. C., Brakebusch, C., Suter, U., & Jessberger, S. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2103-12.2013 · Cited by 84

Rac1-regulated dendritic spine remodeling contributes to neuropathic pain after peripheral nerve injury

Tan, A. M., Chang, Y.-W., Zhao, P., Hains, B. C., & Waxman, S. G. (2011) · Experimental Neurology · doi:10.1016/j.expneurol.2011.08.028 · Cited by 84

Comparison between basal and apical dendritic spines in estrogen-induced rapid spinogenesis of CA1 principal neurons in the adult hippocampus

Murakami, G., Tsurugizawa, T., Hatanaka, Y., Komatsuzaki, Y., Tanabe, N., Mukai, H., Hojo, Y., Kominami, S. A. J., Yamazaki, T., Kimoto, T., et al. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.10.066 · Cited by 84

Myosin IIB Activity and Phosphorylation Status Determines Dendritic Spine and Post-Synaptic Density Morphology

Hodges, J., Litwa, K., Asmussen, H., Vicente‐Manzanares, M., & Horwitz, A. R. (2011) · PLoS ONE · doi:10.1371/journal.pone.0024149 · Cited by 84

Dopamine Depletion of the Prefrontal Cortex Induces Dendritic Spine Loss: Reversal by Atypical Antipsychotic Drug Treatment

Wang, H.-D., & Deutch, A. Y. (2007) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301521 · Cited by 83

Overexpression of drebrin A in immature neurons induces the accumulation of F-actin and PSD-95 into dendritic filopodia, and the formation of large abnormal protrusions

Mizui, T., Takahashi, H., Sekino, Y., & Shirao, T. (2005) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2005.06.008 · Cited by 83

AMPA receptor and GEF-H1/Lfc complex regulates dendritic spine development through RhoA signaling cascade

Kang, M.-G., Guo, Y., & Huganir, R. L. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0812861106 · Cited by 82

Sequential implication of the mental retardation proteins ARHGEF6 and PAK3 in spine morphogenesis

Nodé-Langlois, R., Müller, D., & Boda, B. (2006) · Journal of Cell Science · doi:10.1242/jcs.03273 · Cited by 82

Afadin, A Ras/Rap Effector That Controls Cadherin Function, Promotes Spine and Excitatory Synapse Density in the Hippocampus

Beaudoin, G. M. J., Schofield, C. M., Nuwal, T., Zang, K., Ullian, E. M., Huang, B., & Reichardt, L. F. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.4565-11.2012 · Cited by 81

The Muscarinic Long-Term Enhancement of NMDA and AMPA Receptor-Mediated Transmission at Schaffer Collateral Synapses Develop through Different Intracellular Mechanisms

de Sevilla, D. F., & Buño, W. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1848-10.2010 · Cited by 81

Neurone specific regulation of dendritic spines in vivo by post synaptic density 95 protein (PSD-95)

Vickers, C. A., Stephens, B., Bowen, J., Arbuthnott, G. W., Grant, S. G. N., & Ingham, C. A. (2006) · Brain Research · doi:10.1016/j.brainres.2006.03.075 · Cited by 81

Postsynaptic TrkB signaling has distinct roles in spine maintenance in adult visual cortex and hippocampus

Chakravarthy, S., Saiepour, M. H., Bence, M., Perry, S., Hartman, R., Couey, J. J., Mansvelder, H. D., & Levelt, C. N. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0506305103 · Cited by 81

Sodium channels amplify spine potentials

Araya, R., Nikolenko, V., Eisenthal, K. B., & Yuste, R. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705282104 · Cited by 80

Differential subcellular targeting of glutamate receptor subtypes during homeostatic synaptic plasticity

Soares, C., Lee, K. F. H., Nassrallah, W., & Béïque, J.-C. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.1873-13.2013 · Cited by 80

A Role of Rnd1 GTPase in Dendritic Spine Formation in Hippocampal Neurons

Ishikawa, Y., Katoh, H., & Negishi, M. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-35-11065.2003 · Cited by 79

The Insulin Receptor Substrate of 53 kDa (IRSp53) Limits Hippocampal Synaptic Plasticity

Sawallisch, C., Berhörster, K., Disanza, A., Mantoani, S., Kintscher, M., Stoenica, L., Dityatev, A. E., Sieber, S., Kindler, S., Morellini, F., et al. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m808425200 · Cited by 79

Spike-Associated Fast Contraction of Dendritic Spines in Cultured Hippocampal Neurons

Korkotian, E., & Segal, M. (2001) · Neuron · doi:10.1016/s0896-6273(01)00314-2 · Cited by 79

Direct ovarian effects and safety aspects of GnRH agonists and antagonists

Janssens, R. M. J. (2000) · Human Reproduction Update · doi:10.1093/humupd/6.5.505 · Cited by 79

Dendritic Spine Dynamics Regulate the Long-Term Stability of Synaptic Plasticity

O’Donnell, C., Nolan, M. F., & van Rossum, M. C. W. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2520-11.2011 · Cited by 79

Kalirin is Under-Expressed in Alzheimer's Disease Hippocampus

Youn, H., Jeoung, M., Koo, Y., Ji, H., Markesbery, W. R., Ji, I., & Ji, T. H. (2007) · Journal of Alzheimer's Disease · doi:10.3233/jad-2007-11314 · Cited by 77

Regulation of Dendritic Spines, Spatial Memory, and Embryonic Development by the TANC Family of PSD-95-Interacting Proteins

Han, S., Nam, J., Li, Y., Kim, S.-H., Cho, S., Cho, Y. S., Choi, S. Y., Choi, J., Han, K., Kim, Y., et al. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.3128-10.2010 · Cited by 77

Fine-tuning of neuronal architecture requires two profilin isoforms

Michaelsen, K., Murk, K., Zagrebelsky, M., Dreznjak, A., Jockusch, B. M., Rothkegel, M., & Körte, M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1004406107 · Cited by 76

Pak1 regulates dendritic branching and spine formation

Hayashi, K., Ohshima, T., Hashimoto, M., & Mikoshiba, K. (2007) · Developmental Neurobiology · doi:10.1002/dneu.20363 · Cited by 75

A prospective longitudinal volumetric MRI study of superior temporal gyrus gray matter and amygdala–hippocampal complex in chronic schizophrenia

Yoshida, T., McCarley, R. W., Nakamura, M., Lee, K., Koo, M.-S., Bouix, S., Salisbury, D. F., Morra, L., Shenton, M. E., & Niznikiewicz, M. A. (2009) · Schizophrenia Research · doi:10.1016/j.schres.2009.05.004 · Cited by 74

Intrinsic Control of Precise Dendritic Targeting by an Ensemble of Transcription Factors

Komiyama, T., & Luo, L. (2007) · Current Biology · doi:10.1016/j.cub.2006.11.067 · Cited by 73

Subcellular distribution of L-type calcium channel subtypes in rat hippocampal neurons

Leitch, B., Szostek, A., Lin, R. C. S., & Shevtsova, O. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.08.006 · Cited by 73

A role for synaptopodin and the spine apparatus in hippocampal synaptic plasticity

Deller, T., Orth, C. B., Turco, D. D., Vlachos, A., Burbach, G. J., Drakew, A., Chabanis, S., Körte, M., Schwegler, H., Haas, C. A., et al. (2006) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/j.aanat.2006.06.013 · Cited by 72

Synaptic removal of diacylglycerol by DGKζ and PSD‐95 regulates dendritic spine maintenance

Kim, K., Yang, J., Zhong, X.-P., Kim, M., Kim, Y., Lee, H. W., Han, S., Choi, J., Han, K., Seo, J., et al. (2009) · The EMBO Journal · doi:10.1038/emboj.2009.44 · Cited by 72

Calcium from internal stores modifies dendritic spine shape

Harris, K. M. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.22.12213 · Cited by 72

Social, Communication, and Cortical Structural Impairments in Epac2-Deficient Mice

Srivastava, D. P., Jones, K. A., Woolfrey, K. M., Burgdorf, J. S., Russell, T. A., Kalmbach, A., Lee, H., Yang, C., Bradberry, M. M., Wokosin, D. L., et al. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1349-12.2012 · Cited by 71

Phosphorylation of Rap1GAP, a striatally enriched protein, by protein kinase A controls Rap1 activity and dendritic spine morphology

McAvoy, T., Zhou, M., Greengard, P., & Nairn, A. C. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0813263106 · Cited by 71

Altered synaptic and non‐synaptic properties of CA1 pyramidal neurons in Kv4.2 knockout mice

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The GTPase Rem2 regulates synapse development and dendritic morphology

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Heterogeneous Nuclear Ribonucleoprotein K Interacts with Abi-1 at Postsynaptic Sites and Modulates Dendritic Spine Morphology

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Molecular Dynamics of the Excitatory Synapse

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SPIN90 Phosphorylation Modulates Spine Structure and Synaptic Function

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Age-dependent glutamate induction of synaptic plasticity in cultured hippocampal neuronsPreprint

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Distinct regional and subcellular localization of the actin‐binding protein filamin a in the mature rat brain

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The postsynaptic density proteins homer and shank form a polymeric network structure

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Region-specific changes in the microanatomy of single dendritic spines over time might account for selective memory alterations in ageing hAPPsweTg2576 mice, a mouse model for Alzheimer disease

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Preferential Control of Basal Dendritic Protrusions by EphB2

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Untitled work

Irwin (2001) · doi:10.1002/1096-8628(20010115)98:2<161::aid-ajmg1025>3.0.co;2-b

Principles of Neural Design

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The role of sleep in regulating structural plasticity and synaptic strength: implications for memory and cognitive function

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Dendrite and spine modifications in autism and related neurodevelopmental disorders in patients and animal models

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MMPs in learning and memory and neuropsychiatric disorders

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