ADF/Cofilin: a functional node in cell biology

Rho GTPases and actin dynamics in membrane protrusions and vesicle trafficking

Ridley, A. J. (2006) · Trends in Cell Biology · doi:10.1016/j.tcb.2006.08.006 · Cited by 1,215

Proteins of the ADF/Cofilin Family: Essential Regulators of Actin Dynamics

Bamburg, J. R. (1999) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.15.1.185 · Cited by 1,015

Rate constants for the reactions of ATP- and ADP-actin with the ends of actin filaments.

Pollard, T. D. (1986) · The Journal of Cell Biology · doi:10.1083/jcb.103.6.2747 · Cited by 890

Mechanism of Actin Filament Turnover by Severing and Nucleation at Different Concentrations of ADF/Cofilin

Andrianantoandro, E., & Pollard, T. D. (2006) · Molecular Cell · doi:10.1016/j.molcel.2006.08.006 · Cited by 710

Crystal Structure of Arp2/3 Complex

Robinson, R. C., Turbedsky, K., Kaiser, D. A., Marchand, J.-B., Higgs, H. N., Choe, S., & Pollard, T. D. (2001) · Science · doi:10.1126/science.1066333 · Cited by 540

Integrin regulation

Ginsberg, M. H., Partridge, A. W., & Shattil, S. J. (2005) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2005.08.010 · Cited by 415

Real-Time Measurements of Actin Filament Polymerization by Total Internal Reflection Fluorescence Microscopy

Kuhn, J. R., & Pollard, T. D. (2004) · Biophysical Journal · doi:10.1529/biophysj.104.047399 · Cited by 399

Neurodegenerative stimuli induce persistent ADF/cofilin–actin rods that disrupt distal neurite function

Minamide, L. S., Striegl, A. M., Boyle, J. A., Meberg, P. J., & Bamburg, J. R. (2000) · Nature Cell Biology · doi:10.1038/35023579 · Cited by 394

Actin-depolymerizing Factor and Cofilin-1 Play Overlapping Roles in Promoting Rapid F-Actin Depolymerization in Mammalian Nonmuscle Cells

Hotulainen, P., Paunola, E., Vartiainen, M. K., & Lappalainen, P. (2004) · Molecular Biology of the Cell · doi:10.1091/mbc.e04-07-0555 · Cited by 384

Cortactin regulates cofilin and N-WASp activities to control the stages of invadopodium assembly and maturation

Oser, M. G., Yamaguchi, H., Mader, C. C., Bravo‐Cordero, J. J., Arias, M., Chen, X., DesMarais, V. M., van Rheenen, J., Koleske, A. J., & Condeelis, J. S. (2009) · The Journal of Cell Biology · doi:10.1083/jcb.200812176 · Cited by 369

Up-regulating methylation of CAP1 promoter can promote apoptosis and inhibit migration and invasion of lung adenocarcinoma cells

Li, G., Gu, Y., Wang, K., Miao, Y., Tan, M., Zhang, J., Zou, J., Li, H., Wang, C., & Xie, S. (2025) · European journal of medical research · doi:10.1186/s40001-025-03135-9 · Cited by 1

Cofilin hyperphosphorylation triggers TDP-43 pathology in sporadic amyotrophic lateral sclerosis

Jagaraj, C. J., Saravanabavan, S., Parakh, S., Jayakumar, M., Kashani, S. A., Shadfar, S., Mehta, P. M., Gautam, S., Farzana, F., Suchowerska, A. K., et al. (2026) · Brain · doi:10.1093/brain/awag096 · Cited by 1

Discovery of actinators, actin-derived bioactive peptides that modulate cytoskeleton and actin-related cellular activities

Yi, F., Guo, J., Vo, T. T., Hetrick, B., Haikerwal, A., Zhou, Z., Sealey, L., He, S., Han, Y., Chilin, L. D., et al. (2026) · Science Advances · doi:10.1126/sciadv.aeb5548 · Cited by 1

Dynamic Remodeling of Plant Cytoskeleton in Response to Environmental Stress

Chen, P., Xia, Z., Wu, H., Zhang, J., Liu, Y., Wang, Q., & Zhong, M. (2026) · Biology · doi:10.3390/biology15100752 · Cited by 1

Changes in ADF/destrin expression in the development of hair cells following Atoh1-induced ectopic regeneration

JIN, K., Ren, D., Chi, F., Yang, J., HUANG, Y.-B., & Li, W. (2013) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2013.1089 · Cited by 1

Breast Cancer Proteomics

Pucci‐Minafra, I. (2014) · Springer eBooks · doi:10.1007/978-81-322-0843-3_9 · Cited by 1

Redundant and Non-Redundant Functions of Actin Depolymerizing Factor (ADF) and Cofilin in Metastasis- Review

Tahtamouni, L. H., & Bamburg, J. R. (2011) · Cited by 1

Actin Organizing Proteins in Regulation of Osteoclast Function

McMichael, B. K., & Lee, B. S. (2015) · Springer eBooks · doi:10.1007/978-1-4939-2904-7_14 · 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

LIM-kinase 1 in regulation of cognitive and locomotor functions of Drosophila melanogaster

Kaminskaya, A. N., & Медведева, А. В. (2013) · Ecological genetics · doi:10.17816/ecogen11363-78 · Cited by 1

Inka2 expression in smooth muscle cells and its involvement in cell migration

Yamada, S., Tokunaga, A., & Sakakibara, S. (2022) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2022.12.068 · Cited by 1

Is Alzheimer's disease a manifestation of brain quantum decoherence resulting from mitochondrial and microtubular deterioration?

Nichols, T. W. (2023) · Journal of Multiscale Neuroscience · doi:10.56280/1564010613 · Cited by 2

Deciphering the Cofilin Oligomers via Intermolecular Disulfide Bond Formation: A Coarse-Grained Molecular Dynamics Approach to Understanding Cofilin’s Regulation on Actin Filaments

Li, C., Wei, T.-Y., Cheung, M. S., & Tsai, M.-Y. (2024) · The Journal of Physical Chemistry B · doi:10.1021/acs.jpcb.3c07938 · Cited by 1

Sequence and structural Analysis of β- actin Protein of fishes, using Bioinformatics Tools and techniques

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Multifunctional role of the ubiquitin proteasome pathway in phagocytosis

Lalnunthangi, A., Dakpa, G., & Tiwari, S. (2022) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2022.06.023 · Cited by 1

Actin Assembly Dynamics and Its Regulation in Motile and Morphogenetic Processes

Pernier, J., Montaville, P., & Carlier, M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-394447-4.20055-2 · Cited by 1

The Large Maf Transcription Factor Traffic Jam Regulates Collective Cell Migration During Drosophila Oogenesis

Gunawan, F. (2015) · TSpace (University of Toronto) · Cited by 1

ESAT-6 of Mycobacterium tuberculosis downregulates cofilin1, leads to filamentous actin enrichment and reduces the phagosome acidification in infected macrophages, which are partially reversed by a single methionine mutationPreprint

Mahesh, P., Retnakumar, R. J., C, S. K., & Mundayoor, S. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.05.04.076976 · Cited by 1

Extracellular | Tension and Tissue Morphogenesis

Camuglia, J. M., Yeh, A. R., & Martin, A. C. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819460-7.00068-2 · Cited by 1

DSTN hypomethylation promotes radiotherapy resistance of rectal cancer by activating Wnt/β-catenin signaling pathwayPreprint

Wen, R., Zhou, L., Jiang, S., Fan, H., Zheng, K., Yu, Y., Gao, X., Hao, L., Lou, Z., Yu, G., et al. (2022) · Research Square · doi:10.21203/rs.3.rs-2084750/v1 · Cited by 1

Spontaneous cell morphogenesis via self-propelled actin filamentsPreprint

Yagami, K., Baba, K., Minegishi, T., Misu, S., Katsuno‐Kambe, H., Okano, K., Sakumura, Y., Hosokawa, Y., & Inagaki, N. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.02.28.582450 · Cited by 1

Neuronal expression of S100B triggered by oligomeric Aβ peptide protects against cytoskeletal damage and synaptic lossPreprint

Saavedra, J., Nascimento, M., Figueira, A. J., da Silva, M. I. O., Gião, T., Oliveira, J. F., Liz, M. A., Gomes, C. M., & Cardoso, I. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.04.647260 · Cited by 1

Environmentally relevant depleted uranium exposure damages mitochondria, decreases cytosolic reductive capacity, and increases global DNA damage accumulation through a ROS-independent mechanism involving slingshot protein phosphatase 1b enrichmentPreprint

Kalaniopio, P. H., Gibbons, L. B., Allen, R. S., Matthews, S. M., Lujan, O. R., Gaaloul, E., Allen, C. M., Wilbanks, J., Chassman, C., Traustadóttir, T., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.07.02.736169 · Cited by 1

Signal transduction mechanisms in commissural axon guidance: The role of intracellular tyrosine kinases in Netrin-DCC/frazzled axon attraction

O’Donnell, M. P. (2012) · ScholarlyCommons (University of Pennsylvania)

Thyroid hormone mediates fibroblast growth factor receptor expression, which both alter cell surface mechanical properties of the mammalian cochlea

Szarama, K. B. (2012) · Figshare

Stress-induced changes in gene transcriptions and translations related to Alzheimer’s disease

Sántha, P. (2014) · SZTE Repository of Dissertations (University of Szeged) · doi:10.14232/phd.2358

LIM-kinase 1 in regulation of cognitive and locomotor functions of Drosophila melanogaster

Kaminskaya, A. N., & Медведева, А. В. (2014) · Russian Journal of Genetics Applied Research · doi:10.1134/s2079059714050050

Cofilin navigates cellular cytoskeleton and invasion responses to TGF-beta towards prostate cancer metastasis

Collazo, J. (2013)

Molecular evolution and functional characterization of the Arabidopsis thaliana actin-depolymerizing factor gene family

Roy-Zokan, E. M. (2012)

Establishment of human lymphoma cell lines with different thiopurine S-methyltransferase (TPMT) activities and differential proteome analysis after thiopurine exposure.

Misdaq, M. (2013) · doi:10.53846/goediss-3790

Form follows function: actin-binding proteins as critical regulators of excitatory synapses

Rust, M. B., & Michaelsen‐Preusse, K. (2016) · e-Neuroforum · doi:10.1007/s13295-015-0019-6

Role of the Slingshot-Cofilin and RanBP9 pathways in Alzheimer's Disease Pathogenesis

Woo, J. A. (2015) · Digital Commons - University of South Florida (University of South Florida)

Dynamic Src Tyrosine Kinase Signaling Directs Invadopodia Formation and Function in Head and Neck Cancer: Novel Insights into the Original Oncogene

Kelley, L. C. (2010) · The Research Repository @ WVU (West Virginia University) · doi:10.33915/etd.3258

Why Cytoskeletal Gel?

Osada, Y., Kawamura, R., & Sano, K. (2016) · Springer eBooks · doi:10.1007/978-3-319-27377-8_2

STRESS - INDUCED CHANGES IN GENE TRANSCRIPTIONS AND TRANSLATIONS RELATED TO ALZHEIMER'S DISEASE

Szent, A. (2014)

Profilin : From the Cell Edge into the Nucleus

Sadi, S. (2014) · KTH Publication Database DiVA (KTH Royal Institute of Technology)

cofilinndent inhibition of Cdc42 and activation of Neocortical dendritic complexity is controlled during development

Simó, S., & Cooper, J. A. (2012)

Identification of biomarkers for bone union promoted by mechanical stimulation

Yu, X. (2015) · Frontiers in bioscience · doi:10.2741/4356

Role of EPAC in axon determination

Muñoz-LLancao, P. (2015)

Abelson Kinase Based Regulation of Tumor Cell Invasion in HNSCC

Hayes, K. E. (2013) · The Research Repository @ WVU (West Virginia University) · doi:10.33915/etd.472

Investigating the Glial Contribution to Persistent Neuropathic Pain

Whitley, S. T. (2012) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/szj3-5t06

Chapter 17 Role of Dynamic and Cooperative Conformational Changes in Actin Filaments

Uyeda, T. Q. P. (2016) · Pan Stanford Publishing Pte. Ltd. eBooks · doi:10.1201/9781315364674-18

The dynamic nature and functions of actin in Toxoplasma gondii

Whitelaw, J. (2017) · Enlighten: Theses (The University of Glasgow)

PAPEL DA PROTEÍNA COFILINA-1 NA RESISTÊNCIA À CISPLATINA EM CÂNCER DE PULMÃO DE NÃO-PEQUENAS CÉLULAS

Freitas, M. B. (2010) · Americanae (AECID Library)

Immune responses against tumors controlled by the actin cytoskeleton : lessons from primary immunodeficiencies

Kritikou, J. S. (2017) · Figshare

Transient Receptor Potential Melastatin 7 Channels Regulate Neuronal Cytoskeletal Dynamics

Bent, R. (2011) · TSpace (University of Toronto)

Identificação e caracterização de proteínas que se ligam a actina (ABPs) no apicomplexa Neospora caninum

Baroni, L. (2017) · doi:10.11606/t.60.2017.tde-03072017-082155

Lamellipodia in Stationary and Fluctuating States

Holz, D., McMillen, L. M., Ryan, G. L., & Vavylonis, D. (2018) · Modeling and simulation in science, engineering & technology · doi:10.1007/978-3-319-96842-1_8

Mecanismos moleculares envolvidos no fenótipo endotelial em resposta a estímulos físicos e químicos

da Silva, T. G. (2018) · doi:10.11606/t.5.2018.tde-22102018-104726

COFILIN AND ACTIN DEPOLYMERIZING FACTOR PLAY DIFFERENT ROLES IN THE REGULATION OF INTESTINAL BRUSH BORDER STRUCTURE AND SODIUM-HYDROGEN EXCHANGER 3 ACTIVITY

Gao, L. (2015)

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Cofilin, Trafficking

Wu, Y. (2013) · Springer eBooks · doi:10.1007/978-1-4614-9610-6_69-1

Molecular insights into the Tau-actin interaction

Fontela, Y. C. (2018) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-6842

Marine Polysaccharides

Laurienzo, P. (2018) · MDPI eBooks · doi:10.3390/books978-3-03842-900-5 · Cited by 1

Axotomy induce an increase in the expression of Pink1, Parkin and Сofilin in rat dorsal root ganglia

Pitinova, M., Kalyuzhnaya, Y. N., & Demyanenko, S. V. (2022) · Saratov Fall Meeting: Optical and Nanotechnologies for Biology and Medicine (SFM) · doi:10.1117/12.2623566

CFL1

Lopes, F. M., Coelho, J. C., Leal, M. H., Parsons, R. B., & Klamt, F. (2017) · Springer eBooks · doi:10.1007/978-3-319-67199-4_101634

Faculty Opinions recommendation of ADF/cofilin promotes invadopodial membrane recycling during cell invasion in vivo.

Carlier, M. (2014) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.718323464.793493207

Faculty Opinions recommendation of Yorkie controls tube length and apical barrier integrity during airway development.

Chisholm, A. D. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.736217766.793580467

CFL1

Lopes, F. M., Coelho, J. C., Leal, M. H., Parsons, R. B., & Klamt, F. (2016) · Springer eBooks · doi:10.1007/978-1-4614-6438-9_101634-1

Cytoskeletal Elements in Neurotoxicity

Pyle, S. J., & Meberg, P. J. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.65380-1

Dynamin2 - a Novel Regulator of Lamellipodial and Lamellar Actin Networks in Non-muscle Cells

Menon, M. (2013) · doi:10.18130/v3922j

Faculty Opinions recommendation of Torsional stress generated by ADF/cofilin on cross-linked actin filaments boosts their severing.

Egelman, E. H. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.734944292.793555906

Cofilin, Trafficking

Wu, Y. (2018) · Springer eBooks · doi:10.1007/978-1-4939-7101-5_69

Faculty Opinions recommendation of Torsional stress generated by ADF/cofilin on cross-linked actin filaments boosts their severing.

Lappalainen, P. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.734944292.793556131

Form follows function: actin-binding proteins as critical regulators of excitatory synapses

Rust, M. B., & Michaelsen‐Preusse, K. (2016) · e-Neuroforum · doi:10.1515/s13295-015-0019-6

Deletion of a Putative GPI-Anchored Protein-Encoding Gene Aog185 Impedes the Growth and Nematode-Trapping Efficiency of Arthrobotrys oligospora by Disrupting Transmembrane Transport Homeostasis

Peng, H., Lu, H., Dong, X., Liang, X. H., Sheng, K., Wang, J., Kong, X., Zha, X., & Wang, Y. (2022) · Cellular Microbiology · doi:10.1155/2022/8738290

Actin Assembly Dynamics and Its Regulation in Motile and Morphogenetic Processes

Pernier, J., Montaville, P., & Carlier, M. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-821618-7.20055-2

Abnormal hypo-methylation of CAP1 (adenylate cyclase associated protein 1) gene enhances biological characteristics of lung adenocarcinoma cellsPreprint

Li, G., Xie, S., Wang, K., Tan, M., Zhou, G.-L., Zhan, J., Zou, J., Fan, L., & Wang, C. (2023) · Research Square · doi:10.21203/rs.3.rs-2632990/v1

Identifizierung von In-vivo Interaktionspartnern von PMP22 im peripheren Nerven der Ratte

Arlt, F. A. (2023) · doi:10.53846/goediss-9795

Quantitative Multicolour Nanoscopy for the Investigation of the Postsynaptic Actin Cytoskeleton

Delgado, A. R. C. (2023) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-9960

Dysregulated actin dynamics and cofilin correlate with TDP-43 pathology in sporadic amyotrophic lateral sclerosisPreprint

Jagaraj, C. J., Mehta, P. M., Parakh, S., Shadfar, S., Jamali, S., Suchowerska, A. K., Sultana, J., Fath, T., & Atkin, J. D. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.08.28.555209 · Cited by 1

Comparative Proteomics: Assessing the Variation in Molecular Physiology Within the Adductor Muscle Between Mytilus Galloprovincialis and Mytilus Trossulus in Response to Acute Heat Stress

Mier, J. S. (2018) · doi:10.15368/theses.2018.161

La rigenerazione del miocardio nello scompenso cardiaco: ieri, oggi e domani

(2024) · il Diabete · doi:10.30682/ildia2304f

CFL1 is Implicated in Chronic Myeloid Leukemia Response during Imatinib Therapy

Yin, X., Li, X., Jiang, H., Lin, X., Ma, Z., Chen, X., Teng, Q., Zhang, J. C., & Jin, J. (2024) · Journal of Cancer · doi:10.7150/jca.92202

Relationship Among the Biophysical Characteristics, Cytoskeletal Structure, and Functions of Dendritic Cells at Different Stages of Differentiation

Long, J., Xu, X., Wang, Y., Long, S., Xiong, H., Gong, M., & Zeng, Z. (2024) · Springer eBooks · doi:10.1007/978-981-97-6246-0_4

Computational Insights into the Effect of Mutation on Actin-Actin Dimer and Actin Related Binding Proteins InteractionsPreprint

Sedighpour, D., Ghalichi, F., & Oskui, I. Z. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5240515

Genome-wide identification and comprehensive characterization of the ADF gene family in Triticum monococcum L. subsp. aegilopoides with insights into structure, evolution and cold stress response

Liu, X., Zhang, M., Su, J. Q., Wu, L., Shen, M., Wang, Q., Zhuang, Y., Zhang, L., Li, H., & Chen, G. (2025) · Frontiers in Plant Science · doi:10.3389/fpls.2025.1649202

ESAT-6 of Mycobacterium tuberculosis downregulates cofilin1, leads to filamentous actin enrichment and reduces the phagosome acidification in infected macrophages, which are partially reversed by a single methionine mutation

Mahesh, P., Retnakumar, R. J., Sivakumar, K. C., & Mundayoor, S. (2025) · Tuberculosis · doi:10.1016/j.tube.2025.102680

Molecular pathology of Birt-Hogg-Dubé Syndrome

Fenton, J. C. (2014) · University of Birmingham Institutional Research Archive (University of Birmingham)

Water Fluxes and Cell Migration : How Aquaporin 9 Controls Cell Shape and Motility

Karlsson, T. (2013) · DiVA (Linkoping University)

Cytoskeleton: How three proteins collude to break actin filaments

Romet‐Lemonne, G. (2026) · Current Biology · doi:10.1016/j.cub.2025.11.027

Marine medaka PKCα promotes red-spotted grouper nervous necrosis virus entry by orchestrating MYL3-mediated macropinocytosis and cofilin-dependent actin remodeling

Yao, L., XiaoGang, Y., Li, H., Xiong, X., Yi, M., & Jia, K. (2026) · Journal of Virology · doi:10.1128/jvi.02064-25

Cancer-Associated Actin Mutations Enhance Cofilin Binding Affinity: Insights from Steered Molecular Dynamics Simulations

Sedighpour, D., Ghalichi, F., & Oskui, I. Z. (2025) · National and International Iranian Conference on Biomedical Engineering (ICBME) · doi:10.1109/icbme68496.2025.11392316

c-Myc transactivates CFL1 to induce senescence-like phenotype and potentiate the bystander effects for the migration and proliferation in lung cancer cells

Chou, Y.-T., Leu, J., Yang, W.-Y., Li, C., Lin, M.-Y., Kao, C.-W., Chang, Y.-C., Hsiao, M., & Lee, Y. (2026) · Cell Death Discovery · doi:10.1038/s41420-026-03065-3

A duo implication of miR-134 microRNA and LIM Kinase1 protein in neuropathic pain modulation of the rat spinal cord

Mohamed, S. A. S. I. (2012) · theses.fr (ABES) · doi:10.70675/1cc9e154z7031z4330z9d3dze6199606f242

La fonction de résorption des ostéoclastes : mécanismes cellulaires et implication au cours du développement osseux

Touaitahuata, H. (2012) · theses.fr (ABES) · doi:10.70675/5d98385ezeff6z4f0cz84c7z28cc535f0c39

Dynamics of controlled actin network's architecture

Reymann, A.-C. (2011) · doi:10.70675/d0ac905ez4343z4b0dz85c4z881f2dc1d2c4

Apports de la protéomique quantitative différentielle haut-débit à l'étude des mécanismes de modification du cytosquelette de cellules tubulaires proximales induits par les Inhibiteurs de la Calcineurine

Burat, B. (2017) · theses.fr (ABES) · doi:10.70675/c5cb9700z1ff5z4f4fz88f7z394da094ef6a

Signalisation des GTPases de la famille Rho dans les phénotypes migratoires induits par les différentes formes de Bcr-Abl

Rochelle, T. (2012) · theses.fr (ABES) · doi:10.70675/e67b5851za9c2z4fdbzb085zbbf123e60ef2

Conception rationnelle, synthèse et évaluation biologique d'inhibiteurs de la voie de signalisation LIMK/ROCK

Champiré, A. (2018) · doi:10.70675/4df51917z148fz4ddeza41dze073e9e31573

Biochemical and structural study of the functional specificities of a new family of bacterial nucleotidyl cyclase toxins, called ExoY-like toxins, activated by actin in host cells

Nunes, M. T. (2022) · doi:10.70675/3203498cz5c7bz4c71z82bbzfe65afdd443a

Disulfidptosis-related gene DSTN predicts prognosis and promotes malignant progression in head and neck squamous cell carcinoma

Peng, X., Chen, L., Zhang, J., Yang, L., & Wu, X. (2026) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-026-05559-1

Sirtuin 2 Regulates Dorsal Hippocampal Actin Polymerization and Microtubule Acetylation-Dependent EB3 Activation to Modulate Opioid Withdrawal–Induced Aversive Memory and Associative Learning

Long, J.-D., Yao, S.-Y., Wu, W., Zan, G., Wang, Z.-W., Wei, X., Shu, X., Chen, Y., Ju, Y., Chen, J., et al. (2026) · Biological Psychiatry · doi:10.1016/j.biopsych.2026.06.001

Spontaneous membrane protrusion and cell morphogenesis via self-propelled actin filaments

Yagami, K., Minegishi, T., Baba, K., Misu, S., Katsuno‐Kambe, H., Okano, K., Sakumura, Y., Hosokawa, Y., & Inagaki, N. (2026) · EMBO Reports · doi:10.1038/s44319-026-00804-6

USP14 promotes head and neck squamous cell carcinoma progression via deubiquitinating and stabilizing CFL2

Liu, Y., Wang, Z., Liu, W., Li, P., Chen, J., Shi, Z., & Ye, J. (2026) · Future Science OA · doi:10.1080/20565623.2026.2702980

Alterations of actin in aging

Averbukh, M., Wang, T., Garcia, G., & Higuchi‐Sanabria, R. (2026) · Journal of Cell Science · doi:10.1242/jcs.264775

From molecular markers to architectural control: cytoskeletal checkpoints as the decisive state-access layer of the aging microglial targetome

Pinto, I. M., Beça, P., Correia, M., Moreira, J. T., Galvão, J., Portugal, C. C., Relvas, J. B., & Socodato, R. (2026) · Targetome · doi:10.48130/targetome-0026-0035

Label-free proteomic profiling identifies ECM-related alterations across regeneration states in human peripheral axonal neuropathies

Damato, M., Aboulouard, S., Pesa, V. L., Gentile, F., Lunghi, G., Perrone, M., Pranzo, B., Chiricozzi, E., Riva, N., Fournier, I., et al. (2026) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-026-01219-6

Cofilin 1 overexpression in the ventral hippocampus partially alleviates depressive-like behaviors in postmenopausal depression model mice through the dynamics of dendrites/dendritic spines in relevant brain regions

Yu, Z.-H., Chen, G., Ge, M.-J., Zhang, Z., Shen, J.-X., Pan, C., Han, F., Lu, Y.-P., & Xu, H. (2026) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2026.174261

Dosage-sensitive regulation of Cofilin-1 and LIMK signaling controls myoblast differentiation and fusion

Gjirlić, D., Weber, A., Posern, G., & Singh, A. K. (2026) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-026-06437-1

Białka kompleksu ADF/kofilina: regulacja dynamiki filamentów aktynowych

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