Actin Cytoskeleton Regulation in Neuronal Morphogenesis and Structural Plasticity

Rho GTPases and the Actin Cytoskeleton

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

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

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The Molecular Biology of Axon Guidance

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

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Rho GTPases and signaling networksPreprint

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

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The establishment of polarity by hippocampal neurons in culture.

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Neurotrophins as synaptic modulators

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

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A deep-learning framework reveals whole-body perturbations at cell level

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Co-occurrence of rare variants implicates gene pairs in cytoskeletal pathways and is associated with increased severity in autism spectrum disorder

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Plexin B2 in physiology and pathophysiology of the central nervous system

Wang, Q., Zhang, Y., Ma, K., Lin, P., Wang, Y., Wang, R., Li, H., Li, Z., & Wang, G. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.114627 · Cited by 5

The effect of cofilin 1 expression and phosphorylation dynamics on cell fate determination and neuron maturation in neural stem cells

Jiang, X., lv, J., Zhou, R., & Xiang, X. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.136292 · Cited by 5

De Novo Variants Found in Three Distinct Schizophrenia Populations Hit a Common Core Gene Network Related to Microtubule and Actin Cytoskeleton Gene Ontology Classes

Loe-Mie, Y., Plançon, C., Dubertret, C., Yoshikawa, T., Yalcin, B., Collins, S. C., Boland, A., Deleuze, J., Gorwood, P. A. P. M., Benmessaoud, D., et al. (2024) · Life · doi:10.3390/life14020244 · Cited by 5

Beyond Secretases

Medda, F., Smith, B. E., Gokhale, V. M., Shaw, A. Y., Dunckley, T. L., & Hulme, C. (2013) · Annual reports in medicinal chemistry · doi:10.1016/b978-0-12-417150-3.00005-3 · Cited by 5

The persisting effects of electroconvulsive stimulation on the hippocampal proteome

O'Donovan, S. M., O’Mara, S. M., Dunn, M. J., & McLoughlin, D. M. (2014) · Brain Research · doi:10.1016/j.brainres.2014.10.020 · Cited by 5

Neuritic complexity of hippocampal neurons depends on WIP ‐mediated mTORC 1 and Abl family kinases activities

Franco, A. C. G., Wandosell, F. G., & Anton, I. M. (2015) · Brain and Behavior · doi:10.1002/brb3.359 · Cited by 5

Expression and functions of semaphorins in cancer

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Current Topics in Anesthesiology

Erbay, R. H. (2017) · InTech eBooks · doi:10.5772/63140 · Cited by 5

A Stochastic Framework for Neuronal Morphological Comparison: Application to the Study of imp Knockdown Effects in Drosophila Gamma Neurons

Razetti, A., Descombes, X., Médioni, C., & Besse, F. (2017) · Communications in computer and information science · doi:10.1007/978-3-319-54717-6_9 · Cited by 5

Sensory experience controls dendritic structure and behavior by distinct pathways involving degenerins

Inberg, S., Iosilevskii, Y., Calatayud-Sanchez, A., Setty, H., Oren‐Suissa, M., Krieg, M., & Podbilewicz, B. (2025) · eLife · doi:10.7554/elife.83973 · Cited by 6

Recent Research Progress on the Antidepressant-like Effect and Neuropharmacological Potential of Gastrodia elata Blume

Lin, Y., Lu, K., & Sheen, L. (2018) · Current Pharmacology Reports · doi:10.1007/s40495-018-0137-2 · Cited by 5

Anesthetic Neurotoxicity in Pediatric Patients

Özer, A. B., & Özcan, S. (2017) · InTech eBooks · doi:10.5772/65921 · Cited by 5

Dasm1: A Receptor That Shapes Neuronal Dendrites and Turns On Silent Synapses?

Falls, D. L. (2005) · Science s STKE · doi:10.1126/stke.2742005pe10 · Cited by 5

Hereditary Genetics

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Doublecortin-like kinase is required for cnidocyte development in Nematostella vectensis

Kraus, J. E. M., Busengdal, H., Kraus, Y. A., Hausen, H., & Rentzsch, F. (2024) · Neural Development · doi:10.1186/s13064-024-00188-0 · Cited by 5

Twinfilin-1 phosphorylation in reelin signaling regulates actin dynamics and spine development

Dong, G., Mori, D., Matsuzaki, T., Tanaka, R., Itoh, N., Matsui, T., Sato, A., Arioka, Y., Okumura, H., Fukaya, R., et al. (2025) · Pharmacological Research · doi:10.1016/j.phrs.2025.107986 · Cited by 4

Nck1 activity in lateral amygdala regulates long-term fear memory formation

Ilovich, O., Dines, M., Paul, B. K., Barkai, E., & Lamprecht, R. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-02244-x · Cited by 4

Hippocampal Nogo66‐ NgR1 signaling activation restricts postsynaptic assembly in aged mice with postoperative neurocognitive disorders

Jia, M., Li, G., Chen, J., Tang, X., Zang, Y., Yang, G., Shi, Y. S., Ma, D., Ji, M., & Yang, J. (2024) · Aging Cell · doi:10.1111/acel.14366 · Cited by 5

Loss of neuronal βPix isoforms impairs neuronal morphology in the hippocampus and causes behavioral defects

Kwon, Y., Lee, S. J., Shin, Y. K., Choi, J.-S., Park, D. E., & Shin, J. E. (2025) · Animal Cells and Systems · doi:10.1080/19768354.2024.2448999 · Cited by 4

Cytoskeletal Organization: Actin

Abouelezz, A. M., Minkeviciene, R., & Hotulainen, P. (2016) · Springer eBooks · doi:10.1007/978-4-431-56050-0_2 · Cited by 4

Quantitative trait loci for morphometric traits in multiple families of common carp (Cyprinus carpio)

Zheng, X., Kuang, Y., Lv, W., Cao, D., Sun, Z., Wu, J., & Sun, X. (2016) · Science China Life Sciences · doi:10.1007/s11427-016-0182-5 · Cited by 4

Role of the Cytoskeleton and Membrane Trafficking in Axon–Dendrite Morphogenesis

Flynn, K. C., Stieß, M., & Bradke, F. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397266-8.00124-1 · Cited by 5

Not Just for Muscle Anymore: Activity and Calcium Regulation of MEF2-Dependent Transcription in Neuronal Survival and Differentiation

Shalizi, A., & Bonni, A. (2007) · Springer eBooks · doi:10.1007/978-0-387-73609-9_12 · Cited by 4

Brain-derived neurotrophic factor : generation and characterization of adult mice lacking BDNF in the adult brain

Rauskolb, S. (2008) · edoc (University of Basel) · doi:10.5451/unibas-004587325 · Cited by 4

Dysfunctional S1P/S1PR1 signaling in the dentate gyrus drives vulnerability of chronic pain-related memory impairmentPreprint

Cui, M., Pan, X., Fan, Z., Wu, S., Ji, R., Wang, X., Kong, X., Wu, Z., Song, L., Song, W., et al. (2024) · eLife · doi:10.7554/elife.99862 · Cited by 4

Dysfunctional S1P/S1PR1 signaling in the dentate gyrus drives vulnerability of chronic pain-related memory impairment

Cui, M., Pan, X., Fan, Z., Wu, S., Ji, R., Wang, X., Kong, X., Wu, Z., Song, L., Song, W., et al. (2024) · eLife · doi:10.7554/elife.99862.3 · Cited by 7

Disentangling the role of tau pathology in autism spectrum disorders

Villavicencio-Tejo, F., Olesen, M. A., Moya, M. L., & Quintanilla, R. A. (2025) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2025.111496 · Cited by 4

Refinement of synaptic connections

Sanes, D. H., Reh, T. A., & Harris, W. A. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-374539-2.00013-6 · Cited by 3

The RNA-Binding Protein SBR (Dm NXF1) Is Required for the Constitution of Medulla Boundaries in Drosophila melanogaster Optic Lobes

Мамон, Л. А., Yakimova, A. O., Kopytova, D. V., & Golubkova, E. V. (2021) · Cells · doi:10.3390/cells10051144 · Cited by 3

Deciphering the Nanoscale Architecture of Presynaptic Actin Using a Micropatterned Presynapse-on-Glass Model

Tumminia, S., Mezache, L., Wiesner, T., Boroni-Rueda, F., Parperis, C., Vianay, B., Théry, M., Papandréou, M., & Leterrier, C. (2026) · Journal of Neuroscience · doi:10.1523/jneurosci.1741-24.2026 · Cited by 3

Axon Growth and Branching

Ma, L., & Gibson, D. A. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397266-8.00001-6 · Cited by 3

Cloning and expression analysis of porcine ACTA2 gene and its association with production traits

Huang, J., & Deng, C. (2009) · Hereditas (Beijing) · doi:10.3724/sp.j.1005.2009.00489 · Cited by 3

Waves in Excitable Neural Fields

Bressloff, P. C. (2013) · Lecture notes on mathematical modelling in the life sciences · doi:10.1007/978-1-4614-8866-8_7 · Cited by 3

Neural Field Model of Binocular Rivalry Waves

Bressloff, P. C. (2013) · Lecture notes on mathematical modelling in the life sciences · doi:10.1007/978-1-4614-8866-8_8 · Cited by 3

Comparative analysis of protein-protein interaction networks in neural differentiation mechanisms

Moazeny, M., Salari, A., Hojati, Z., & Esmaeili, F. (2022) · Differentiation · doi:10.1016/j.diff.2022.05.003 · Cited by 3

Guidance of Axons to Targets in Development and in Disease

Witte, H., & Bradke, F. (2005) · Elsevier eBooks · doi:10.1016/b978-0-7216-9491-7.50024-7 · Cited by 3

Axon growth and branching

Ma, L., & Tymanskyj, S. R. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814407-7.00003-1 · Cited by 2

Reducing polypyrimidine tract‑binding protein 1 fails to promote neuronal transdifferentiation on HT22 and mouse astrocyte cells under physiological conditions

Li, Q., Zhang, W., Qiao, X.-Y., Liu, C., Dao, J.-J., Qiao, C.-M., Cui, C., Shen, Y., & Zhao, W. (2023) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2023.12360 · Cited by 2

VSOT: volume-surface optimization for accurate ultrastructure analysis of dendritic spines

Lyu, B., Wang, J., Risher, W. C., & Yu, G. (2025) · Bioinformatics · doi:10.1093/bioinformatics/btaf220 · Cited by 3

Wat gebeurt er in het hoofdje van een baby? Over hersenontwikkeling en intelligentie

Ramakers, G. J. A. (2005) · Neuropraxis · doi:10.1007/bf03079059 · Cited by 2

Nootropic benzothiazoles promote dendritic spine formation by targeting fascin-1

Shivkumar, A., Berg, K. R., Sibucao, K. C. A., Leriche, G., Dozier, L. E., Espinoza, C. A., Patrick, G. N., Gaieb, Z., Seitz, C., Amaro, R. E., et al. (2025) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2025.110572 · Cited by 2

Role of integrin in influencing differentiation of PC12 cell grown on PLLA-aligned nanofiber: a mRNA–microRNA–protein integrative study

Lü, X., Yang, F., Huang, Y., & Yu, Y. (2016) · Regenerative Biomaterials · doi:10.1093/rb/rbw040 · Cited by 2

Gap Junctions Underlying Labile Memory

Shih, M.-F. M., & Wu, C. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-803471-2.00003-5 · Cited by 2

A high-throughput screen to identify novel compounds to promote neurite outgrowth.

Wong, J. W. J., Brastianos, H., Andersen, R., & O'Connor, T. (2008) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2007.11.013 · Cited by 3

Methods to Study the Roles of Rho GTPases in Dendritic Tree Complexity

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Role of the cytoskeleton and membrane trafficking in axon–dendrite morphogenesis

Flynn, K. C., & Bradke, F. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814407-7.00002-x · Cited by 2

Growth Cones

Raper, J. A. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.00340-5 · Cited by 2

Genetic and Molecular Approaches to Study Neuronal Migration in the Developing Cerebral Cortex

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The Central Role of Actin in Creutzfeldt-Jakob Disease: Unlocking Therapeutic Pathways

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A dendritic guidance receptor functions in both ligand dependent and independent modes

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Research progress on biomarkers of traumatic brain injury

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To Be or Not To Be a Protrusion: Unraveling the Determinants of Protrusion Formation

Varghese, M. (2012) · OhioLink ETD Center (Ohio Library and Information Network) · Cited by 1

Compartmentalization of Synaptic Tagging and Capture

Alarcón, J. M. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1761-7_2 · Cited by 1

Calcium Waves and Sparks

Bressloff, P. C. (2013) · Lecture notes on mathematical modelling in the life sciences · doi:10.1007/978-1-4614-8866-8_4 · Cited by 1

Muscle-associated Drosophila adducin regulates larval neuromuscular junction development and the localization of Draper to the synapse

Wang, M. (2013) · Summit (Simon Fraser University) · Cited by 1

Regulation of Hippocampal mGluR-Dependent Long-Term Depression by GluA2-Dependent Cofilin-Mediated Actin Remodeling

Jia, Z., & Collingridge, G. L. (2017) · Springer eBooks · doi:10.1007/978-3-319-56170-7_12 · Cited by 1

Exercise Training Enhances Expression of Tropomedulin-2 and ADP-Ribosylation Factor 6 in the Cerebellum of Male Wistar Rats

Taherabadi, S. J., & Rahmati, M. (2019) · Zahedan Journal of Research in Medical Sciences · doi:10.5812/zjrms.89902 · Cited by 1

Dendritic Development

Cline, H. T., Ghosh, A., Jan, Y. N., & Sanes, J. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-385870-2.00020-2 · Cited by 1

Role of Cytoskeletal Protein, Actin in Various Diseases

Pathak, S., Kale, A., Kumar, C. M. S., & Mansoor, S. (2021) · Springer eBooks · doi:10.1007/978-3-030-72999-8_6 · Cited by 1

The Wingless planar cell polarity pathway is essential for optimal activity-dependent synaptic plasticity

Dominicci-Cotto, C., Vázquez, M., & Marie, B. (2024) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2024.1322771 · Cited by 1

Altered expression of the Plexin-B2 system in tuberous sclerosis complex and focal cortical dysplasia IIb lesions.

Dai, L., Huang, J., Shen, K., Yang, X.-L., Zhu, G., Zhang, L., Wang, Z.-K., Liu, S., Liao, X., Xu, S., et al. (2024) · PubMed · doi:10.14670/hh-18-707 · Cited by 1

Nature and Nurture Converge in the Nucleus to Regulate Activity-Dependent Neuronal Development

Thompson, J. R., & Lin, Y. (2024) · Springer eBooks · doi:10.1007/978-3-031-68550-7_10 · Cited by 1

Regulation of Actin Filaments During Neurite Extension and Guidance

Letourneau, P. C. (2010) · Advances in neurobiology · doi:10.1007/978-1-4419-7368-9_3 · Cited by 1

Screening, cloning and sequence analysis of the differential expression genes in Longissimus dorsi of Yanbian Yellow Cattle

Tian, W., Shou-fa, Z., Xiang-Zi, L. I., Gao, Q., Xin, J. I. N., & Yan, C. (2011) · Hereditas (Beijing) · doi:10.3724/sp.j.1005.2011.01219 · Cited by 1

Cytoskeleton in Plasticity

Ferrari, A., & Goda, Y. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.00791-9 · Cited by 1

Actin Cytoskeleton in Growth Cones, Nerve Terminals, and Dendritic Spines

Halpain, S., Calabrese, B., & Dehmelt, L. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.00729-4 · Cited by 1

The Molecular Basis of Directional Cell Migration

Mannherz, H. G. (2005) · doi:10.1002/9783527619689.ch9 · Cited by 1

Actin Reorganization in Nerve Morphogenesis

Singh, A. P., Rodrigues, V., & VijayRaghavan, K. (2010) · Wiley eBooks · doi:10.1002/9780470015902.a0021850 · Cited by 1

MOLECULAR GENETICS OF ACTIVITY-DEPENDENT STRUCTURAL CHANGES AT THE SYNAPSE

Devaud, J., & Ferrús, A. (2003) · Journal of Neurogenetics · doi:10.1080/01677060390441840 · Cited by 2

Preliminarily Investigating the Polymorphism of Self-organized Actin Filament in Vitro by Atomic Force Microscope

Zhang, J., Wang, Y., Chen, X., He, C., Cheng, C., & Cao, Y. (2004) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/36.9.637 · Cited by 1

El neurocitoesqueleto: un nuevo blanco terapéutico para el tratamiento de la depresión

Jiménez-Rubio, G., Bellon, A., Ortíz‐López, L., Ramírez-Rodríguez, G. B., Ortega-Soto, H. A., & Benítez‐King, G. (2007) · Redalyc (Universidad Autónoma del Estado de México) · Cited by 1

The role of filopodia in the formation of spine synapses

Arstikaitis, P. (2011) · cIRcle (University of British Columbia) · doi:10.14288/1.0071638 · Cited by 1

Changing the Intrinsic Growth Capacity of motor and sensory neurons to promote axonal growth after injury

Allodi, I. (2012) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) · Cited by 1

Sound encoding in mutant mice with disrupted action potential generation

Yamanbaeva, G. (2018) · doi:10.53846/goediss-7005 · Cited by 1

C9orf72 - derived proline:arginine poly-dipeptides disturb cytoskeletal architecturePreprint

Shiota, T., Nagata, R., Kikuchi, S., Nanaura, H., Matsubayashi, M., Nakanishi, M., Kobashigawa, S., NAGAYAMA, K., Sugie, K., Yamashiro, Y., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.10.14.338566 · Cited by 1

Structural Transformations of Synaptic Partners During Growth and Competition of the Giant Nerve Terminal, the Calyx of Held, in the Medial Nucleus of the Trapezoid Body in the Developing Postnatal Mouse

Jackson, D. (2020) · The Research Repository @ WVU (West Virginia University) · doi:10.33915/etd.7835 · Cited by 1

Regulation of Axon Branching

Kalil, K., Dent, E. W., & Tang, F. (2007) · Springer eBooks · doi:10.1007/978-0-387-68561-8_12 · Cited by 1

Deep Learning and 3D Imaging Reveal Whole-Body Alterations in ObesityPreprint

Kaltenecker, D., Horvath, I., Al-Maskari, R., Kolabas, Z. I., Chen, Y., Hoeher, L., Todorov, M. I., Kapoor, S., Ali, M., Kofler, F., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.18.608300 · Cited by 1

Self-Organization in Cells II: Reaction-Diffusion Models

Bressloff, P. C. (2014) · Interdisciplinary applied mathematics · doi:10.1007/978-3-319-08488-6_9

Polybrominated Diphenyl Ethers Disturb Neural Development in Mice and Men

Schreiber, T. (2010) · Univ. Duesseldorf: Duesseldorfer Dokumenten- und Publikationsserver

p116Rip : a new player in RhoA signalling

Mulder, J. (2005) · Leiden Repository (Leiden University)

GTPases Rho e o potencial regenerativo da retina de mamíferos

Debbio, C. B. D. (2010) · doi:10.11606/t.42.2010.tde-25032010-150345

REDOX PROTEOMICS IDENTIFICATION OF OXIDATIVELY MODIFIED PROTEINS AND THEIR PHARMACOLOGICAL MODULATION: INSIGHT INTO OXIDATIVE STRESS IN BRAIN AGING, AGE-RELATED COGNITIVE IMPAIRMENT

Poon, H. F. (2005) · UKnowledge (University of Kentucky)

mTORC2 controls neuron size and Purkinje cell morphology independent of mTORC1

Thomanetz, V. (2012) · edoc (University of Basel) · doi:10.5451/unibas-005976915

Waves in the Developing and the Diseased Brain

Bressloff, P. C. (2013) · Lecture notes on mathematical modelling in the life sciences · doi:10.1007/978-1-4614-8866-8_9

Localisation of Protein Kinase C in Apoptosis and Neurite Outgrowth

Schultz, A. R. (2005)

Cooperation between integrin and growth factor receptor signalling in the regulation of neurite growth from rat sensory neurons

Tucker, B. A. (2006) · Memorial University Research Repository (Memorial University)

Differentiation of dendrites and the analysis of spine- like structures on Lobula Plate Tangential Cells in Drosophila melanogaster

Koper, E. (2007) · Electronic Theses of LMU Munich (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.6924

Population Models and Neural Fields

Bressloff, P. C. (2013) · Lecture notes on mathematical modelling in the life sciences · doi:10.1007/978-1-4614-8866-8_6

Actin Isoforms in Neuronal Structure and Function

Cheever, T. R. (2011) · University of Minnesota Digital Conservancy (University of Minnesota)

Molecular Mechanisms Underlying Morphological Effects of Protein Kinase C Under Normal Conditions and Cellular Stress

Sunesson, L. (2008) · Lund University Publications (Lund University)

Waves in Synaptically Coupled Spiking Networks

Bressloff, P. C. (2013) · Lecture notes on mathematical modelling in the life sciences · doi:10.1007/978-1-4614-8866-8_5

The neural cell adhesion molecule associates with and signals through p21-activated kinase 1 to regulate neuronal growth cone morphology in mice (Mus musculus Linnaeus, 1758)

Li, S. (2009)

Molecular Regulation of Synaptogenesis in Drosophila

Walla, D. A. (2014) · Scholars' Bank (University of Oregon)

Systematic Reconstruction of Autism Biology with Multi-Level Whole Exome AnalysisPreprint

Luo, W., Zhang, C., & Brouwer, C. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/052878

One-hit Stochastic Decline in a Mechanochemical Model of Cytoskeleton-induced Neuron Death

Lomasko, T. (2009) · TSpace (University of Toronto)

Genes and Neurons

Kaang, B. (2009) · Springer eBooks · doi:10.1007/978-0-387-75269-3_1

Understanding the Function of Tuberous Sclerosis Complex Genes in Neural Development: Roles in Synapse Assembly and Axon Guidance

Selleck, S. B. (2012) · doi:10.21236/ada603854

RHO GTPASES in neuronal morphogenesis

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The role of small GTPases in neuronal morphogenesis and polarity

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