Actin Cytoskeleton Regulation in Neuronal Morphogenesis and Structural Plasticity

Rho GTPases and the Actin Cytoskeleton

Hall, A. (1998) · Science · doi:10.1126/science.279.5350.509 · Cited by 6,138

Rho, Rac, and Cdc42 GTPases regulate the assembly of multimolecular focal complexes associated with actin stress fibers, lamellipodia, and filopodia

Nobes, C. D., & Hall, A. (1995) · Cell · doi:10.1016/0092-8674(95)90370-4 · Cited by 4,414

The small GTP-binding protein rac regulates growth factor-induced membrane ruffling

Ridley, A. J., Paterson, H. F., Johnston, C. L., Diekmann, D., & Hall, A. (1992) · Cell · doi:10.1016/0092-8674(92)90164-8 · Cited by 3,616

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

Calcium sensitization of smooth muscle mediated by a Rho-associated protein kinase in hypertension

Uehata, M., Ishizaki, T., Satoh, H., Ono, T., Kawahara, T., Morishita, T., Tamakawa, H., Yamagami, K., Inui, J., Maekawa, M., et al. (1997) · Nature · doi:10.1038/40187 · Cited by 2,862

Rho GTPases and signaling networksPreprint

Aelst, L. V., & D’Souza‐Schorey, C. (1997) · Genes & Development · doi:10.1101/gad.11.18.2295 · Cited by 2,358

Phosphorylation and Activation of Myosin by Rho-associated Kinase (Rho-kinase)

Amano, M., Ito, M., Kimura, K., Fukata, Y., Chihara, K., Nakano, T., Matsuura, Y., & Kaibuchi, K. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.34.20246 · Cited by 2,009

The establishment of polarity by hippocampal neurons in culture.

Dotti, C., Sullivan, C., & Banker, G. (1988) · The Journal of Neuroscience · doi:10.1523/jneurosci.08-04-01454.1988 · Cited by 1,862

Neurotrophins as synaptic modulators

Poo, M.-M. (2001) · Nature Reviews Neuroscience · doi:10.1038/35049004 · Cited by 1,775

Signaling from Rho to the Actin Cytoskeleton Through Protein Kinases ROCK and LIM-kinase

Maekawa, M., Ishizaki, T., Boku, S., Watanabe, N., Fujita, A., Iwamatsu, A., Obinata, T., Ohashi, K., Mizuno, K., & Narumiya, S. (1999) · Science · doi:10.1126/science.285.5429.895 · Cited by 1,640

Phenotypes ofDrosophilaBrain Neurons in Primary Culture Reveal a Role for Fascin in Neurite Shape and Trajectory

Kraft, R., Escobar, M., Narro, M. L., Kurtis, J. L., Efrat, A., Barnard, K., & Restifo, L. L. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2106-06.2006 · Cited by 58

Multiple functions for the cadherin/catenin complex during neuronal development

Yu, X., & Malenka, R. C. (2004) · Neuropharmacology · doi:10.1016/j.neuropharm.2004.07.031 · Cited by 57

Sra-1 interacts with Kette and Wasp and is required for neuronal and bristle development inDrosophila

Bogdan, S., Grewe, O., Strunk, M., Mertens, A., & Klämbt, C. (2004) · Development · doi:10.1242/dev.01274 · Cited by 59

Retrograde Signaling That Regulates Synaptic Development and Function at the Drosophila Neuromuscular Junction

Marqués, G., & Zhang, B. (2006) · International review of neurobiology · doi:10.1016/s0074-7742(06)75012-7 · Cited by 56

Mechanisms of TSC-mediated Control of Synapse Assembly and Axon Guidance

Knox, S. M., Ge, H., Dimitroff, B. D., Ren, Y., Howe, K. A., Arsham, A. M., Easterday, M. C., Neufeld, T. P., O’Connor, M. B., & Selleck, S. B. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000375 · Cited by 56

Signaling Mechanisms in Cortical Axon Growth, Guidance, and Branching

Kalil, K., Li, L., & Hutchins, B. I. (2011) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2011.00062 · Cited by 56

Kinetic-structural analysis of neuronal growth cone veil motility

Mongiu, A. K., Weitzke, E. L., Chaga, O. Y., & Borisy, G. G. (2007) · Journal of Cell Science · doi:10.1242/jcs.03384 · Cited by 56

Proteomic analysis of rat hippocampus and frontal cortex after chronic treatment with fluoxetine or putative novel antidepressants: CRF1 and NK1 receptor antagonists

Carboni, L., Vighini, M., Piubelli, C., Castelletti, L., Milli, A., & Domenici, E. (2006) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2006.01.007 · Cited by 56

Drosophila, a genetic model system to study cocaine-related behaviors: A review with focus on LIM-only proteins

Heberlein, U., Tsai, L. T.-Y., Kapfhamer, D., & Lasek, A. W. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.07.023 · Cited by 57

Roles of LIM kinases in central nervous system function and dysfunction

Cuberos, H., Vallée, B., Vourc'h, P., Tastet, J., Andres, C. R., & Bénédetti, H. (2015) · FEBS Letters · doi:10.1016/j.febslet.2015.10.032 · Cited by 54

Association of N‐cadherin levels and downstream effectors of Rho GTPases with dendritic spine loss induced by chronic stress in rat hippocampal neurons

Castañeda, P., Muñoz, M., García‐Rojo, G., Ulloa, J. L., Bravo, J. A., Márquez, R., García-Pérez, M. A., Arancibia, D., Araneda, K., Rojas, P. S., et al. (2015) · Journal of Neuroscience Research · doi:10.1002/jnr.23602 · Cited by 56

The C-terminal Basic Tail of RhoG Assists the Guanine Nucleotide Exchange Factor Trio in Binding to Phospholipids

Skowronek, K., Guo, F., Zheng, Y., & Nassar, N. N. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m312677200 · Cited by 56

The autism-associated MET receptor tyrosine kinase engages early neuronal growth mechanism and controls glutamatergic circuits development in the forebrain

Peng, Y. W., Lu, Z., Li, G., Piechowicz, M., Anderson, M. J., Uddin, Y., Wu, J., & Qiu, S. (2016) · Molecular Psychiatry · doi:10.1038/mp.2015.182 · Cited by 55

Role of Cdk5 in Neuronal Signaling, Plasticity, and Drug Abuse

Bibb, J. A. (2003) · Neurosignals · doi:10.1159/000074620 · Cited by 54

Ionising Radiation Immediately Impairs Synaptic Plasticity-Associated Cytoskeletal Signalling Pathways in HT22 Cells and in Mouse Brain: An In Vitro/In Vivo Comparison Study

Kempf, S. J., Buratovic, S., von Toerne, C., Moertl, S., Stenerlöw, B., Hauck, S. M., Atkinson, M. J., Eriksson, P., & Tapio, S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0110464 · Cited by 52

Protein tyrosine phosphatase PTPRT as a regulator of synaptic formation and neuronal development

Lee, J.-R. (2015) · BMB Reports · doi:10.5483/bmbrep.2015.48.5.037 · Cited by 51

Understanding Myelination Through Studying Its Evolution

Schweigreiter, R., Roots, B. I., Bandtlow, C. E., & Gould, R. M. (2006) · International review of neurobiology · doi:10.1016/s0074-7742(06)73007-0 · Cited by 51

Serotonin 5-HT4 receptor boosts functional maturation of dendritic spines via RhoA-dependent control of F-actin

Schill, Y., Bijata, M., Kopach, O., Cherkas, V., Galil, D. A., Böhm, K., Schwab, M. H., Matsuda, M., Compan, V., Basu, S., et al. (2020) · Communications Biology · doi:10.1038/s42003-020-0791-x · Cited by 50

Increased Dendrite Branching in AβPP/PS1 Mice and Elongation of Dendrite Arbors by Fasudil Administration

Couch, B. A., DeMarco, G. J., Gourley, S. L., & Koleske, A. J. (2010) · Journal of Alzheimer s Disease · doi:10.3233/jad-2010-091114 · Cited by 50

Unique Transcriptome Patterns of the White and Grey Matter Corroborate Structural and Functional Heterogeneity in the Human Frontal Lobe

Mills, J. D., Kavanagh, T., Kim, W. S., Chen, B. J., Kawahara, Y., Halliday, G. M., & Janitz, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0078480 · Cited by 49

The ROCK Inhibitor Fasudil Prevents Chronic Restraint Stress-Induced Depressive-Like Behaviors and Dendritic Spine Loss in Rat Hippocampus

García‐Rojo, G., Fresno, C., Vilches, N., Díaz‐Véliz, G., Mora, S., Aguayo, F. I., Pacheco, A., Parra-Fiedler, N. A., Parra, C. S., Rojas, P. S., et al. (2016) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyw108 · Cited by 51

Systematic reconstruction of autism biology from massive genetic mutation profiles

Luo, W., Zhang, C., Jiang, Y., & Brouwer, C. (2018) · Science Advances · doi:10.1126/sciadv.1701799 · Cited by 49

Inhibitory effect of SLIT2 on granulosa cell proliferation mediated by the CDC42-PAKs-ERK1/2 MAPK pathway in the prehierarchical follicles of the chicken ovary

Xu, R., Qin, N., Xu, X., Sun, X. K., Chen, X., & Zhao, J. (2018) · Scientific Reports · doi:10.1038/s41598-018-27601-z · Cited by 50

Involvement of advillin in somatosensory neuron subtype-specific axon regeneration and neuropathic pain

Chuang, Y.-C., Lee, C., Sun, W., & Chen, C. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1716470115 · Cited by 49

Journal of NeuroVirology

(2013) · Journal of NeuroVirology · doi:10.1007/13365.1538-2443 · Cited by 50

Bisphenol A promotes dendritic morphogenesis of hippocampal neurons through estrogen receptor-mediated ERK1/2 signal pathway

Xu, X., Lu, Y., Zhang, G., Chen, L., Tian, D., Shen, X., Yang, Y., & Dong, F. (2014) · Chemosphere · doi:10.1016/j.chemosphere.2013.09.063 · Cited by 49

Synaptic Plasticity, a Symphony in GEF

Kiraly, D. D., Eipper-Mains, J. E., Mains, R. E., & Eipper, B. A. (2010) · ACS Chemical Neuroscience · doi:10.1021/cn100012x · Cited by 52

A 29‐amino acid fragment of Clostridium botulinum C3 protein enhances neuronal outgrowth, connectivity, and reinnervation

Höltje, M., Djalali, S., Hofmann, F., Münster‐Wandowski, A., Hendrix, S., Boato, F., Dreger, S. C., Grosse, G., Henneberger, C., Grantyn, R., et al. (2008) · The FASEB Journal · doi:10.1096/fj.08-116855 · Cited by 49

TrkB-mediated activation of geranylgeranyltransferase I promotes dendritic morphogenesis

Zhou, X., Wu, K.-Y., Liang, B., Fu, X.-Q., & Luo, Z. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0800846105 · Cited by 49

Phosphoinositide 3-kinase signalling events controlling axonal morphogenesis

Cosker, K., & Eickholt, B. J. (2007) · Biochemical Society Transactions · doi:10.1042/bst0350207 · Cited by 49

Melatonin induces neuritogenesis at early stages in N1E‐115 cells through actin rearrangements via activation of protein kinase C and Rho‐associated kinase

Bellon, A., Ortíz‐López, L., Ramírez-Rodríguez, G. B., Antón‐Tay, F., & Benítez‐King, G. (2006) · Journal of Pineal Research · doi:10.1111/j.1600-079x.2006.00408.x · Cited by 49

Wnt5a evokes cortical axon outgrowth and repulsive guidance by tau mediated reorganization of dynamic microtubules

Li, L., Fothergill, T., Hutchins, B. I., Dent, E. W., & Kalil, K. (2013) · Developmental Neurobiology · doi:10.1002/dneu.22102 · Cited by 52

Cdo promotes neuronal differentiation via activation of the p38 mitogen‐activated protein kinase pathway

Oh, J., Bae, G., Yang, Y.-J., Yi, M.-J., Lee, H., Kim, B.-G., Krauss, R. S., & Kang, J. (2009) · The FASEB Journal · doi:10.1096/fj.08-119255 · Cited by 48

Cortactin binding protein 2 increases microtubule stability and regulates dendritic arborization

Shih, P.-Y., Lee, S., Chen, Y., & Hsueh, Y. (2014) · Journal of Cell Science · doi:10.1242/jcs.149476 · Cited by 47

C3G is required for c-Abl-induced filopodia and its overexpression promotes filopodia formation

Radha, V., Rajanna, A., Mitra, A., Rangaraj, N., & Swarup, G. (2007) · Experimental Cell Research · doi:10.1016/j.yexcr.2007.03.019 · Cited by 47

Cytoskeleton changes following differentiation of N1E-115 neuroblastoma cell line

Oh, J., Raja, K. K., Shin, J., Pollak, A. J., Hengstschläger, M., & Lübec, G. (2006) · Amino Acids · doi:10.1007/s00726-005-0256-z · Cited by 47

Transmembrane agrin regulates filopodia in rat hippocampal neurons in culture

McCroskery, S., Chaudhry, A., Lin, L., & Daniels, M. P. (2006) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2006.06.004 · Cited by 47

BDNF, via truncated TrkB receptor, modulates GlyT1 and GlyT2 in astrocytes

Aroeira, R. I., Sebastião, A. M., & Valente, C. A. (2015) · Glia · doi:10.1002/glia.22884 · Cited by 45

Bidirectional influence of sodium channel activation on NMDA receptor–dependent cerebrocortical neuron structural plasticity

George, J., Baden, D. G., Gerwick, W. H., & Murray, T. F. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1212584109 · Cited by 45

The Role of Ephs and Ephrins in Memory Formation

Dines, M., & Lamprecht, R. (2016) · International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyv106 · Cited by 47

Memory Deficits in Aging and Neurological Diseases

Khan, Z. U., Martín‐Montañez, E., Navarro‐Lobato, I., & Muly, E. C. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-420170-5.00001-5 · Cited by 48

Cell Volume Regulatory Ion Transport in the Regulation of Cell Migration

Jakab, M., & Ritter, M. (2006) · KARGER eBooks · doi:10.1159/000096322 · Cited by 46

TGFβ signals regulate axonal development through distinct Smad-independent mechanisms

Ng, J. (2008) · Development · doi:10.1242/dev.028209 · Cited by 46

Inositol 1,4,5-Trisphosphate 3-Kinase A Functions As a Scaffold for Synaptic Rac Signaling

Kim, I. H., Park, S. K., Hong, S. T., Jo, Y. S., Kim, E. J., Park, E., Han, S. B., Shin, H., Sun, W., Kim, H. T., et al. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2483-09.2009 · Cited by 42

MR Diffusion Tensor Imaging Detects Rapid Microstructural Changes in Amygdala and Hippocampus Following Fear Conditioning in Mice

Ding, A. Y., Li, Q., Zhou, I. Y., Ma, S. J., Tong, G., McAlonan, G. M., & Wu, E. X. (2013) · PLoS ONE · doi:10.1371/journal.pone.0051704 · Cited by 47

Anti-Ganglioside Antibody-Mediated Activation of RhoA Induces Inhibition of Neurite Outgrowth

Zhang, G., Lehmann, H., Manoharan, S., Hashmi, M., Shim, S., Ming, G., Schnaar, R., López, P., Bogdanova, N., & Sheikh, K. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3829-10.2011 · Cited by 49

Mechanisms that regulate morphogenesis of a highly branched neuron in C. elegans

Sundararajan, L., Stern, J. L., & Miller, D. M. (2019) · Developmental Biology · doi:10.1016/j.ydbio.2019.04.002 · Cited by 43

Neuritogenesis and neuronal differentiation promoted by 2,4‐dinitrophenol, a novel anti‐amyloidogenic compound

Wasilewska‐Sampaio, A. P., Silveira, M. S., Holub, O., Goecking, R., Gomes, F. C. A., Moura‐Neto, V., Linden, R., Ferreira, S. T., & Felice, F. G. D. (2005) · The FASEB Journal · doi:10.1096/fj.05-3812com · Cited by 45

P-Rex1 – a multidomain protein that regulates neurite differentiation

Waters, J. E., Astle, M. V., Ooms, L. M., Balamatsias, D., Gurung, R., & Mitchell, C. A. (2008) · Journal of Cell Science · doi:10.1242/jcs.030353 · Cited by 45

Neuroplasticity and Multilevel System of Connections Determine the Integrative Role of Nucleus Accumbens in the Brain Reward System

Bayassi-Jakowicka, M., Lietzau, G., Czuba, E., Steliga, A., Waśkow, M., & Kowiański, P. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22189806 · Cited by 43

Gamma-1-Syntrophin Mediates Trafficking of Gamma-Enolase towards the Plasma Membrane and Enhances Its Neurotrophic Activity

Pišlar, A. H., Obermajer, N., & Kos, J. (2010) · Neurosignals · doi:10.1159/000324292 · Cited by 44

Aβ Influences Cytoskeletal Signaling Cascades with Consequences to Alzheimer’s Disease

Henriques, A. G., Oliveira, J. M., Carvalho, L., & Silva, O. A. B. D. C. E. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8913-4 · Cited by 45

p116Rip Targets Myosin Phosphatase to the Actin Cytoskeleton and Is Essential for RhoA/ROCK-regulated Neuritogenesis

Mulder, J., Ariaens, A., van den Boomen, D. J. H., & Moolenaar, W. H. (2004) · Molecular Biology of the Cell · doi:10.1091/mbc.e04-04-0275 · Cited by 44

Changes in the Number and Morphology of Dendritic Spines in the Hippocampus and Prefrontal Cortex of the C58/J Mouse Model of Autism

Barón-Mendoza, I., Maqueda-Martínez, E., Martínez‐Marcial, M., Fuente, M. D. L., Gómez-Chavarı́n, M., & González‐Arenas, A. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.726501 · Cited by 43

Diabetic complications in pregnancy: is resveratrol a solution?

Singh, C. K., Kumar, A., LaVoie, H. A., DiPette, D. J., & Singh, U. S. (2013) · Experimental Biology and Medicine · doi:10.1177/1535370212473704 · Cited by 44

Super-Resolution Three-Dimensional Imaging of Actin Filaments in Cultured Cells and the Brain via Expansion Microscopy

Park, C. E., Cho, Y., Cho, I., Jung, H., Kim, B., Shin, J. H., Choi, S., Kwon, S., Hahn, Y. K., & Chang, J. (2020) · ACS Nano · doi:10.1021/acsnano.0c04915 · Cited by 38

Direct interaction of myosin regulatory light chain with the NMDA receptor

Amparan, D., Avram, D., Thomas, C. G., Lindahl, M. G., Yang, J., Bajaj, G., & Ishmael, J. E. (2004) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2004.02869.x · Cited by 42

Oxytocin Increases Neurite Length and Expression of Cytoskeletal Proteins Associated with Neuronal Growth

Lestanova, Z., Bačová, Z., Kiss, A., Havránek, T., Štrbák, V., & Bakoš, J. (2015) · Journal of Molecular Neuroscience · doi:10.1007/s12031-015-0664-9 · Cited by 43

Tech: a RhoA GEF selectively expressed in hippocampal and cortical neurons

Marx, R., Henderson, J., Wang, J., & Baraban, J. M. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2004.02930.x · Cited by 42

Impaired spine formation and learning in GPCR kinase 2 interacting protein-1 (GIT1) knockout mice

Menon, P., Deane, R., Sagare, A. P., Lane, S. M., Zarcone, T. J., O’Dell, M. R., Chen, Y., Zloković, B. V., & Berk, B. C. (2010) · Brain Research · doi:10.1016/j.brainres.2009.11.084 · Cited by 45

Rho/ROCK pathway is essential to the expansion, differentiation, and morphological rearrangements of human neural stem/progenitor cells induced by lysophosphatidic acid

Frisca, F., Crombie, D. E., Dottori, M., Goldshmit, Y., & Pébay, A. (2013) · Journal of Lipid Research · doi:10.1194/jlr.m032284 · Cited by 43

Alphaherpesviruses and the Cytoskeleton in Neuronal Infections

Zaichick, S., Bohannon, K. P., & Smith, G. A. (2011) · Viruses · doi:10.3390/v3070941 · Cited by 46

The Cell Death Pathway Regulates Synapse Elimination through Cleavage of Gelsolin in Caenorhabditis elegans Neurons

Meng, L., Mulcahy, B., Cook, S. J., Neubauer, M., Wan, A., Jin, Y., & Yan, D. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.05.031 · Cited by 41

Light-Induced Photoreceptor Degeneration in the Mouse Involves Activation of the Small GTPase Rac1

Belmonte, M. A., dos Santos, M. F., Kihara, A. H., Yan, C. Y. I., & Hamassaki‐Britto, D. E. (2006) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.05-0446 · Cited by 41

Actin Filament Assembly by Myristoylated, Alanine-rich C Kinase Substrate–Phosphatidylinositol-4,5-diphosphate Signaling Is Critical for Dendrite Branching

Li, H., Chen, G., Zhou, B., & Duan, S. (2008) · Molecular Biology of the Cell · doi:10.1091/mbc.e08-03-0294 · Cited by 43

Phosphatidylinositol 3,4-bisphosphate regulates neurite initiation and dendrite morphogenesis via actin aggregation

Zhang, S.-X., Duan, L., He, S., Zhuang, G., & Yu, X. (2017) · Cell Research · doi:10.1038/cr.2017.13 · Cited by 40

Serotonin receptor 1A modulates actin dynamics and restricts dendritic growth in hippocampal neurons

Ferreira, T., Iacono, L. L., & Gross, C. T. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07283.x · Cited by 43

The neuronal Arf GAP centaurin α1 modulates dendritic differentiation

Moore, C. D., Thacker, E. E., Larimore, J., Gaston, D., Underwood, A., Kearns, B., Patterson, S. I., Jackson, T., Chapleau, C., Pozzo-Miller, L., et al. (2007) · Journal of Cell Science · doi:10.1242/jcs.006346 · Cited by 40

Actin in development

Jacinto, A., & Baum, B. (2003) · Mechanisms of Development · doi:10.1016/j.mod.2003.06.006 · Cited by 41

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

Histone demethylase KDM6B has an anti-tumorigenic function in neuroblastoma by promoting differentiation

Yang, L., Zha, Y., Ding, J., Ye, B., Liu, M., Yan, C., Dong, Z., Cui, H., & Ding, H. (2019) · Oncogenesis · doi:10.1038/s41389-018-0112-0 · Cited by 40

Actin Filament-Stabilizing Protein Tropomyosin Regulates the Size of Dendritic Fields

Li, W.-J., & Gao, F. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-15-06171.2003 · Cited by 40

Rac-GTPases Regulate Microtubule Stability and Axon Growth of Cortical GABAergic Interneurons

Tivodar, S., Kalemaki, K., Kounoupa, Z., Vidaki, M., Theodorakis, Κ., Denaxa, M., Kessaris, N., de Curtis, I., Pachnis, V., & Karagogeos, D. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu037 · Cited by 41

Down-regulation of Slit–Robo Pathway Mediating Neuronal Cytoskeletal Remodeling Processes Facilitates the Antidepressive-like Activity of Gastrodia elata Blume

Lin, S.-H., Chen, W., Lu, K., Chen, P., Hsieh, S., Pan, T., Chen, S., & Sheen, L. (2014) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf503132c · Cited by 39

Role of Non-coding RNAs in Axon Regeneration after Peripheral Nerve Injury

Liu, M., Li, P., Jia, Y., Cui, Q., Zhang, K., & Jiang, J. (2022) · International Journal of Biological Sciences · doi:10.7150/ijbs.70290 · Cited by 38

Expression and localization of Cayman ataxia-related protein, Caytaxin, is regulated in a developmental- and spatial-dependent manner

Hayakawa, Y., Itoh, M., Yamada, A., Mitsuda, T., & Nakagawa, T. (2006) · Brain Research · doi:10.1016/j.brainres.2006.10.068 · Cited by 38

Genetic dissection of active forgetting in labile and consolidated memories in Drosophila

Gao, Y., Shuai, Y., Zhang, X., Peng, Y., Wang, L., He, J., Zhong, Y., & Li, Q. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1903763116 · Cited by 40

Formation of Hirano Bodies Induced by Expression of an Actin Cross-Linking Protein with a Gain-of-Function Mutation

Maselli, A. G., Furukawa, R., Thomson, S. A. M., Davis, R. C., & Fechheimer, M. (2003) · Eukaryotic Cell · doi:10.1128/ec.2.4.778-787.2003 · Cited by 38

Very-KIND, a KIND domain–containing RasGEF, controls dendrite growth by linking Ras small GTPases and MAP2

Huang, J., Furuya, A., & Furuichi, T. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200702036 · Cited by 37

Molecular Mechanisms of Axonal Growth

Bouquet, C., & Nothias, F. (2008) · Advances in experimental medicine and biology · doi:10.1007/978-0-387-76715-4_1 · Cited by 37

Myosin-Va-interacting protein, RILPL2, controls cell shape and neuronal morphogenesis via Rac signaling

Lisé, M.-F., Srivastava, D. P., Arstikaitis, P., Lett, R. L., Sheta, R., Viswanathan, V., Penzes, P., O’Connor, T. P., & El-Husseini, A. (2009) · Journal of Cell Science · doi:10.1242/jcs.050344 · Cited by 35

Isoform-specific palmitoylation of JNK regulates axonal development

Yang, G., Liu, Y., Yang, K., Liu, R., Zhu, S., Coquinco, A., Wen, W., Kojic, L. D., Jia, W. W.-G., & Cynader, M. (2011) · Cell Death and Differentiation · doi:10.1038/cdd.2011.124 · Cited by 38

FE65 interacts with ADP-ribosylation factor 6 to promote neurite outgrowth

Cheung, H. N. M., Dunbar, C., Mórotz, G. M., Cheng, W. H., Chan, H. Y. E., Miller, C. C. J., & Lau, K. (2014) · The FASEB Journal · doi:10.1096/fj.13-232694 · Cited by 37

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Detera‐Wadleigh, S. D., Liu, C., Maheshwari, M., Cardona, I., Corona, W., Akula, N., Steele, C. J. M., Badner, J. A., Kundu, M., Kassem, L., et al. (2007) · Psychiatric Genetics · doi:10.1097/ypg.0b013e328133f352 · Cited by 37

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Brocco, M. A., Fernández, M. E., & Frasch, A. C. C. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.07064.x · Cited by 36

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Li, X., Chen, Y., Liu, Y., Gao, J., Gao, F., Bartlam, M. G., Wu, J. Y., & Rao, Z. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m604135200 · Cited by 33

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