WASP and WAVE family proteins: key molecules for rapid rearrangement of cortical actin filaments and cell mov

Rho GTPases and the Actin Cytoskeleton

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

Rho GTPases and their effector proteins

Bishop, A. L., & Hall, A. (2000) · Biochemical Journal · doi:10.1042/bj3480241 · Cited by 2,019

The interaction of Arp2/3 complex with actin: Nucleation, high affinity pointed end capping, and formation of branching networks of filaments

Mullins, R. D., Heuser, J. A., & Pollard, T. D. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.11.6181 · Cited by 1,483

The Interaction between N-WASP and the Arp2/3 Complex Links Cdc42-Dependent Signals to Actin Assembly

Rohatgi, R., Ma, L., Miki, H., Lopez, M., Kirchhausen, T. L., Takenawa, T., & Kirschner, M. W. (1999) · Cell · doi:10.1016/s0092-8674(00)80732-1 · Cited by 1,350

Arp2/3 Complex and Actin Depolymerizing Factor/Cofilin in Dendritic Organization and Treadmilling of Actin Filament Array in Lamellipodia

Svitkina, T., & Borisy, G. G. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.145.5.1009 · Cited by 1,191

Isolation of a novel gene mutated in Wiskott-Aldrich syndrome

Derry, J. M. J., Ochs, H. D., & Francke, U. (1994) · Cell · doi:10.1016/0092-8674(94)90528-2 · Cited by 1,048

Wiskott–Aldrich Syndrome Protein, a Novel Effector for the GTPase CDC42Hs, Is Implicated in Actin Polymerization

Symons, M. H., Derry, J. M. J., Karlak, B., Jiang, S., Lemahieu, V., McCormick, F. P., Francke, U., & Abo, A. (1996) · Cell · doi:10.1016/s0092-8674(00)81050-8 · Cited by 830

Scar, a WASp-related protein, activates nucleation of actin filaments by the Arp2/3 complex

Machesky, L. M., Mullins, R. D., Higgs, H. N., Kaiser, D. A., Blanchoin, L., May, R. C., Hall, M. E., & Pollard, T. D. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.7.3739 · Cited by 773

Autoinhibition and activation mechanisms of the Wiskott–Aldrich syndrome protein

Kim, A. S., Kakalis, L. T., Abdul-Manan, N., Liu, G. A., & Rosen, M. K. (2000) · Nature · doi:10.1038/35004513 · Cited by 765

WAVE, a novel WASP‐family protein involved in actin reorganization induced by Rac

Miki, H., Suetsugu, S., & Takenawa, T. (1998) · The EMBO Journal · doi:10.1093/emboj/17.23.6932 · Cited by 705

Migration of F9 parietal endoderm cells is regulated by the ERK pathway

Hong, T., & Grabel, L. B. (2005) · Journal of Cellular Biochemistry · doi:10.1002/jcb.20728 · Cited by 24

PGE2 mediates cytoskeletal rearrangement of hemocytes via Cdc42, a small G protein, to activate actin‐remodeling factors in Spodoptera exigua (Lepidoptera: Noctuidae)

Ahmed, S., & Kim, Y. (2019) · Archives of Insect Biochemistry and Physiology · doi:10.1002/arch.21607 · Cited by 23

Lamellipodia Protrusion: Moving Interactions of Vinculin and Arp2/3

Craig, S. W., & Chen, H. A. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00160-x · Cited by 23

Analysis of conformational changes in WASP using a split YFP

Lim, R. P. Z., Misra, A., Wu, Z., & Thanabalu, T. (2007) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.08.124 · Cited by 23

Actin Engine in Immunological Synapse

Piragyte, I., & Jun, C. (2012) · Immune Network · doi:10.4110/in.2012.12.3.71 · Cited by 22

Suppression of Breast Cancer Metastasis Using Stapled Peptides Targeting the WASF Regulatory Complex

Cowell, J. K., Teng, Y., Bendzunas, N. G., Ara, R., Arbab, A. S., & Kennedy, E. J. (2017) · Cancer Growth and Metastasis · doi:10.1177/1179064417713197 · Cited by 24

Rac1 Promotes Cell Motility by Controlling Cell Mechanics in Human Glioblastoma

Xu, J., Galvanetto, N., Nie, J., Yang, Y., & Torre, V. (2020) · Cancers · doi:10.3390/cancers12061667 · Cited by 22

Neural Wiskott-Aldrich syndrome protein (nWASP) is implicated in human lung cancer invasion

Frugtniet, B. A., Martin, T. A., Zhang, L., & Jiang, W. G. (2017) · BMC Cancer · doi:10.1186/s12885-017-3219-3 · Cited by 22

FBP11 regulates nuclear localization of N-WASP and inhibits N-WASP-dependent microspike formation

Mizutani, K., Suetsugu, S., & Takenawa, T. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2003.11.139 · Cited by 22

Phagocytosis of Aspergillus fumigatus by Human Bronchial Epithelial Cells Is Mediated by the Arp2/3 Complex and WIPF2

Culibrk, L., Croft, C. A., Toor, A., Yang, S. J., Singhera, G. K., Dorscheid, D. R., Moore, M. M., & Tebbutt, S. J. (2019) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2019.00016 · Cited by 20

Targeting the WASF3 complex to suppress metastasis

Limaye, A. J., Whittaker, M. K., Bendzunas, G. N., Cowell, J. K., & Kennedy, E. J. (2022) · Pharmacological Research · doi:10.1016/j.phrs.2022.106302 · Cited by 23

The microtubule-associated protein EB1 maintains cell polarity through activation of protein kinase C

Schober, J. M., Kwon, G., Jayne, D., & Cain, J. M. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.11.056 · Cited by 21

p190A RhoGAP is involved in EGFR pathways and promotes proliferation, invasion and migration in lung adenocarcinoma cells

Notsuda, H., Sakurada, A., Endo, C., Okada, Y., Horii, A., Shima, H., & Kondo, T. (2013) · International Journal of Oncology · doi:10.3892/ijo.2013.2096 · Cited by 21

PIP2 and septin control STIM1/Orai1 assembly by regulating cytoskeletal remodeling via a CDC42-WASP/WAVE-ARP2/3 protein complex

de Souza, L. B., Ong, H. L., Liu, X., & Ambudkar, I. S. (2021) · Cell Calcium · doi:10.1016/j.ceca.2021.102475 · Cited by 21

Gene expression analyses in X-linked myotubular myopathy

Noguchi, S., Fujita, M., Murayama, K., Kurokawa, R., & Nishino, I. (2005) · Neurology · doi:10.1212/01.wnl.0000174625.67484.4d · Cited by 25

WAVE3 phosphorylation regulates the interplay between PI3K, TGF-β, and EGF signaling pathways in breast cancer

Wang, W., Kansakar, U., Marković, V. G., Wang, B., & Sossey‐Alaoui, K. (2020) · Oncogenesis · doi:10.1038/s41389-020-00272-0 · Cited by 20

Collective cell migration driven by filopodia—New insights from the social behavior of myotubes

Bischoff, M. C., & Bogdan, S. (2021) · BioEssays · doi:10.1002/bies.202100124 · Cited by 20

Relationship of p21‐activated kinase (PAK) and filopodia to persistence and oncogenic transformation

Heckman, C. A., DeMuth, J. G., Deters, D., Malwade, S. R., Cayer, M. L., Monfries, C. A. L., & Mamais, A. (2009) · Journal of Cellular Physiology · doi:10.1002/jcp.21788 · Cited by 20

Wiskott-Aldrich Syndrome Protein Is Needed for Vaccinia Virus Pathogenesis

Guerra, S., Aracil, M., Conde-Álvarez, R., Bernad, A., & Estéban, M. (2005) · Journal of Virology · doi:10.1128/jvi.79.4.2133-2140.2005 · Cited by 20

The acidic regions of WASp and N‐WASP can synergize with CDC42Hs and Rac1 to induce filopodia and lamellipodia

Hüfner, K., Schell, B., Aepfelbacher, M., & Linder, S. (2002) · FEBS Letters · doi:10.1016/s0014-5793(02)02358-x · Cited by 20

Microfilament regulatory protein MENA increases activity of RhoA and promotes metastasis of hepatocellular carcinoma

Lin, L., Yang, X., Li, J., Zhang, Y., Qin, W., & Zhang, Z. (2014) · Experimental Cell Research · doi:10.1016/j.yexcr.2014.05.010 · Cited by 19

Predicting and preventing melanoma invasiveness: advances in clarifying E2F1 function

Pützer, B. M., Steder, M., & Alla, V. (2010) · Expert Review of Anticancer Therapy · doi:10.1586/era.10.153 · Cited by 19

Caprice/ MISP is a novel F ‐actin bundling protein critical for actin‐based cytoskeletal reorganizations

Kumeta, M., Gilmore, J. L., Umeshima, H., Ishikawa, M.-A., Kitajiri, S., Horigome, T., Kengaku, M., & Takeyasu, K. (2014) · Genes to Cells · doi:10.1111/gtc.12131 · Cited by 19

Expression and subcellular localization of WAVE isoforms in the megakaryocyte/platelet lineage

Kashiwagi, H., Shiraga, M., Kato, H., Honda, S., Sako, M., Kurata, Y., Kanakura, Y., & Tomiyama, Y. (2005) · Journal of Thrombosis and Haemostasis · doi:10.1111/j.1538-7836.2004.01082.x · Cited by 19

In vitro fluorescence assay to measure GDP/GTP exchange of guanine nucleotide exchange factors of Rho family GTPases

Blaise, A. M., Corcoran, E. E., Wattenberg, E. S., Zhang, Y.-L., Cottrell, J. R., & Koleske, A. J. (2021) · Biology Methods and Protocols · doi:10.1093/biomethods/bpab024 · Cited by 18

CED-10-WASP-Arp2/3 signaling axis regulates apoptotic cell corpse engulfment in C. elegans

Wu, D., Chai, Y., Zhu, Z., Li, W., Ou, G., & Li, W. (2017) · Developmental Biology · doi:10.1016/j.ydbio.2017.06.005 · Cited by 18

WAVE2 is associated with poor prognosis in pancreatic cancers and promotes cell motility and invasiveness via binding to ACTN4

Taniuchi, K., Furihata, M., Naganuma, S., & Saibara, T. (2018) · Cancer Medicine · doi:10.1002/cam4.1837 · Cited by 18

Pronounced Alterations of Cellular Metabolism and Structure Due to Hyper- or Hypo-Osmosis

Mao, L., Hartl, D., Nolden, T., Koppelstaetter, A., Klose, J., Himmelbauer, H., & Zabel, C. (2008) · Journal of Proteome Research · doi:10.1021/pr800245x · Cited by 18

Two verprolin homology domains increase the Arp2/3 complex-mediated actin polymerization activities of N-WASP and WAVE1 C-terminal regions

Yamaguchi, H., Miki, H., & Takenawa, T. (2002) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(02)02137-x · Cited by 18

Modifying PCDH19 levels affects cortical interneuron migration

Pancho, A., Mitsogiannis, M. D., Aerts, T., Vecchia, M. D., Ebert, L. K., Geenen, L., Noterdaeme, L., Vanlaer, R., Stulens, A., Hulpiau, P., et al. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.887478 · Cited by 19

Ataxin-7 and Non-stop coordinate SCAR protein levels, subcellular localization, and actin cytoskeleton organization

Cloud, V. J., Thapa, A., Morales‐Sosa, P., Miller, T. M., Miller, S., Holsapple, D., Gerhart, P. M., Momtahan, E., Jack, J. L., Leiva, E., et al. (2019) · eLife · doi:10.7554/elife.49677 · Cited by 16

High level of WAVE1 expression is associated with tumor aggressiveness and unfavorable prognosis of epithelial ovarian cancer

Zhang, J., Tang, L., Shen, L., Zhou, S., Duan, Z., Xiao, L., Cao, Y. L., Mu, X., Zha, L., & Wang, H. (2012) · Gynecologic Oncology · doi:10.1016/j.ygyno.2012.06.008 · Cited by 17

The Rac1 inhibitor, NSC23766, depolarizes adhesive secretion, endomembrane cycling, and tip growth in the fucoid alga, Silvetia compressa

Hable, W. E., Reddy, S., & Julien, L. (2008) · Planta · doi:10.1007/s00425-007-0673-1 · Cited by 16

Crosstalk of cell polarity signaling pathways

Mazel, T. (2017) · PROTOPLASMA · doi:10.1007/s00709-017-1075-2 · Cited by 18

Tristetraprolin Down-Regulation Contributes to Persistent TNF-Alpha Expression Induced by Cigarette Smoke Extract through a Post-Transcriptional Mechanism

Zhao, X., Che, P., Cheng, M.-L., Zhang, Q., Mu, M., Li, H., Luo, Y., Liang, Y., Luo, X.-H., Gao, C., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0167451 · Cited by 16

CpG DNA enhances macrophage cell spreading by promoting the Src-family kinase-mediated phosphorylation of paxillin

Achuthan, A. A., Elsegood, C. L., Masendycz, P. J., Hamilton, J. A., & Scholz, G. M. (2006) · Cellular Signalling · doi:10.1016/j.cellsig.2006.05.007 · Cited by 16

Ribosomal protein L10 interacts with the SH3 domain and regulates GDNF‐induced neurite growth in SH‐SY‐5y cells

Park, S., & Jeong, D. (2006) · Journal of Cellular Biochemistry · doi:10.1002/jcb.20888 · Cited by 16

Evidence for the involvement of FAM110C protein in cell spreading and migration

Hauge, H., Fjelland, K. E., Sioud, M., & Aasheim, H. (2009) · Cellular Signalling · doi:10.1016/j.cellsig.2009.08.001 · Cited by 15

Directional control of WAVE2 membrane targeting by EB1 and phosphatidylinositol 3,4,5-triphosphate

Takahashi, K., Tanaka, T., & Suzuki, K. (2009) · Cellular Signalling · doi:10.1016/j.cellsig.2009.11.005 · Cited by 16

NKG2D- and CD28-mediated costimulation regulate CD8+ T cell chemotaxis through different mechanisms: the role of Cdc42/N-WASp

Serrano‐Pertierra, E., Cernuda‐Morollón, E., & López‐Larrea, C. (2013) · Journal of Leukocyte Biology · doi:10.1189/jlb.0613316 · Cited by 15

Rho GTPases in Hematopoietic Cells

van Hennik, P. B., & Hordijk, P. L. (2005) · Antioxidants and Redox Signaling · doi:10.1089/ars.2005.7.1440 · Cited by 15

Neuronal Wiskott‐Aldrich syndrome protein regulates TGF‐β1‐mediated lung vascular permeability

Wagener, B. M., Hu, M., Zheng, A., Zhao, X., Che, P., Brandon, A. P., Anjum, N., Snapper, S. B., Creighton, J. R., Guan, J., et al. (2016) · The FASEB Journal · doi:10.1096/fj.201600102r · Cited by 15

Multiscale Modeling of Cell Shape from the Actin Cytoskeleton

Rangamani, P., Xiong, G. Y., & Iyengar, R. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-397897-4.00002-4 · Cited by 15

Oncogenic KRas-induced Increase in Fluid-phase Endocytosis is Dependent on N-WASP and is Required for the Formation of Pancreatic Preneoplastic Lesions

Lubeseder–Martellato, C., Alexandrow, K., Hidalgo‐Sastre, A., Heid, I., Boos, S. L., von Briel, T., Schmid, R. M., & Siveke, J. T. (2016) · EBioMedicine · doi:10.1016/j.ebiom.2016.12.013 · Cited by 15

Wasf3 Deficiency Reveals Involvement in Metastasis in a Mouse Model of Breast Cancer

Qin, H., Lu, S., Thangaraju, M., & Cowell, J. K. (2019) · American Journal Of Pathology · doi:10.1016/j.ajpath.2019.08.012 · Cited by 15

The Polybasic Region of Rac1 Modulates Bacterial Uptake Independently of Self-association and Membrane Targeting

Wong, K., Mohammadi, S., & Isberg, R. R. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m804717200 · Cited by 15

Exposure of human fetal penile cells to different PCB mixtures: transcriptome analysis points to diverse modes of interference on external genitalia programming

Tait, S., Rocca, C. L., & Mantovani, A. (2011) · Reproductive Toxicology · doi:10.1016/j.reprotox.2011.02.001 · Cited by 14

Dicer suppresses cytoskeleton remodeling and tumorigenesis of colorectal epithelium by miR-324-5p mediated suppression of HMGXB3 and WASF-2

Sun, L. N., Cheng, X., Zhi, Z., Liu, Y., Chen, L., Shen, T., Zhou, Q. Y., Liu, Y. H., Gan, W. J., Wang, J., et al. (2017) · Oncotarget · doi:10.18632/oncotarget.18218 · Cited by 15

Zebrafish diras1 Promoted Neurite Outgrowth in Neuro-2a Cells and Maintained Trigeminal Ganglion Neurons In Vivo via Rac1-Dependent Pathway

Yeh, C., & Hsu, L. (2015) · Molecular Neurobiology · doi:10.1007/s12035-015-9550-2 · Cited by 14

Podosomal proteins as causes of human syndromes: A role in craniofacial development?

Cejudo–Martín, P., & Courtneidge, S. A. (2011) · genesis · doi:10.1002/dvg.20732 · Cited by 13

A novel role for 14-kDa phosphohistidine phosphatase in lamellipodia formation

Xu, A., Li, X., Li, S., Sun, L., Wu, S., Zhang, B., & Huang, J. (2016) · Cell Adhesion & Migration · doi:10.1080/19336918.2016.1268319 · Cited by 13

Elucidating the molecular signaling pathways of WAVE3

Kansakar, U., Wang, W., Marković, V. G., & Sossey‐Alaoui, K. (2020) · Annals of Translational Medicine · doi:10.21037/atm.2020.02.16 · Cited by 14

F-actin Binding Region of SPIN90 C-terminus Is Essential for Actin Polymerization and Lamellipodia Formation

Kim, D. J., Kim, S. H., Kim, S.-M., Bae, J., Ahnn, J., & Song, W. K. (2007) · Cell Communication & Adhesion · doi:10.1080/15419060701225010 · Cited by 13

WAVE2 Protein Complex Coupled to Membrane and Microtubules

Takahashi, K. (2012) · Journal of Oncology · doi:10.1155/2012/590531 · Cited by 13

Automated profiling of growth cone heterogeneity defines relations between morphology and motility

Bagonis, M. M., Fusco, L., Pertz, O. C., & Danuser, G. M. (2018) · The Journal of Cell Biology · doi:10.1083/jcb.201711023 · Cited by 13

Intracellular Calcium

Kramer, I. M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-394803-8.00006-1 · Cited by 13

Phosphorylation of the proline-rich domain of WAVE3 drives its oncogenic activity in breast cancer

Kansakar, U., Wang, W., Marković, V. G., & Sossey‐Alaoui, K. (2021) · Scientific Reports · doi:10.1038/s41598-021-83479-4 · Cited by 13

Cooperative function of oncogenic MAPK signaling and the loss of Pten for melanoma migration through the formation of lamellipodia

Yasuta, Y., Kaminaka, R., Nagai, S., Mouri, S., Ishida, K., Tanaka, A., Zhou, Y., Sakurai, H., & Yokoyama, S. (2024) · Scientific Reports · doi:10.1038/s41598-024-52020-8 · Cited by 12

Actin polymerization counteracts prewetting of N-WASP on supported lipid bilayers

Wiegand, T., Liu, J., Vogeley, L., LuValle-Burke, I., Geisler, J., Fritsch, A. W., Hyman, A. A., & Grill, S. W. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2407497121 · Cited by 12

Biochemical characterization of distinct regions of SPEC molecules and their role in phagocytosis

Ching, K. H., Kisailus, A. E., & Burbelo, P. D. (2006) · Experimental Cell Research · doi:10.1016/j.yexcr.2006.09.011 · Cited by 11

Differentially up‐regulated genes in proliferating porcine neonatal pancreas cells caused by epidermal growth factor

Jeon, S. Y., Baek, K., Kim, Y., Park, C., Kwon, H. S., Ko, S., Song, K., Yoo, S. J., Son, H. S., Cha, B. Y., et al. (2003) · Journal of Cellular Biochemistry · doi:10.1002/jcb.10752 · Cited by 11

Oocyte-specific deletion ofN-WASPdoes not affect oocyte polarity, but causes failure of meiosis II completion

Wang, Z., Ma, X., Hu, M., Jiang, Z., Meng, T., Dong, M., Fan, L., Ouyang, Y., Snapper, S. B., Schatten, H., et al. (2016) · Molecular Human Reproduction · doi:10.1093/molehr/gaw046 · Cited by 11

Ignition of a cellular machine

Kreishman-Deitrick, M., & Rosen, M. K. (2002) · Nature Cell Biology · doi:10.1038/ncb0202-e31 · Cited by 9

Other Well-Defined Immunodeficiencies

Yeganeh, M., Gambineri, E., Abolmaali, K., Tamizifar, B., & Español, T. (2008) · Springer eBooks · doi:10.1007/978-3-540-78936-9_9 · Cited by 10

Copy number variation analysis in 83 children with early-onset developmental and epileptic encephalopathy after targeted resequencing of a 109-epilepsy gene panel

Hirabayashi, K., Uehara, D. T., Abe, H., Ishii, A., Moriyama, K., Hirose, S., & Inazawa, J. (2019) · Journal of Human Genetics · doi:10.1038/s10038-019-0661-x · Cited by 10

Developmental expression of neural Wiskott–Aldrich syndrome protein (N-WASP) and WASP family verprolin-homologous protein (WAVE)-related proteins in postnatal rat cerebral cortex and hippocampus

Tsuchiya, D., Kitamura, Y., Takata, K., Sugisaki, T., Taniguchi, T., Uemura, K., Miki, H., Takenawa, T., & Shimohama, S. (2006) · Neuroscience Research · doi:10.1016/j.neures.2006.09.007 · Cited by 10

Proteolytic events are relevant cellular responses during nervous system regeneration of the starfish Marthasterias glacialis

Franco, C., Santos, R., & Coelho, A. V. (2014) · Journal of Proteomics · doi:10.1016/j.jprot.2013.12.012 · Cited by 11

The actin filament architecture: tightly regulated by the cells, manipulated by pathogens: International Titisee Conference on the actin cytoskeleton: from signalling to bacterial pathogenesis

Ahmadian, M. R., Wittinghofer, A., & Schmidt, G. (2002) · The EMBO Reports · doi:10.1093/embo-reports/kvf057 · Cited by 10

Module 4: Sensors and Effectors

Berridge, M. J. (2012) · Cell Signalling Biology · doi:10.1042/csb0001004 · Cited by 11

ARP2 /3 complex affects myofibroblast differentiation and migration in pancreatic ductal adenocarcinoma

Sun, Y., Qiao, Y., Niu, Y., Madhavan, B. K., Fang, C., Hu, J., Schuck, K., Traub, B., Frieß, H., Herr, I., et al. (2024) · International Journal of Cancer · doi:10.1002/ijc.35246 · Cited by 9

Prominosomes - a particular class of extracellular vesicles containing prominin-1/CD133?

Karbanová, J., Thamm, K., Fargeas, C. A., Deniz, I. A., Lorico, A., & Corbeil, D. (2025) · Journal of Nanobiotechnology · doi:10.1186/s12951-025-03102-w · Cited by 10

Las17p–Vrp1p but not Las17p–Arp2/3 interaction is important for actin patch polarization in yeast

Rajamuthiah, R., Wong, M. H., Meng, L., Munn, A. L., & Thanabalu, T. (2009) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2009.02.012 · Cited by 9

Wasp and WAVE Family Proteins

Frittoli, E., Disanza, A., & Scita, G. (2008) · Springer eBooks · doi:10.1007/978-0-387-46407-7_8 · Cited by 9

Molecular basis of actin reorganization promoted by binding of enterohaemorrhagic Escherichia coli EspB to α‐catenin

Hamaguchi, M., Hamada, D., Suzuki, K. N., Sakata, I., & Yanagihara, I. (2008) · FEBS Journal · doi:10.1111/j.1742-4658.2008.06750.x · Cited by 9

Small GTPase RBJ promotes cancer progression by mobilizing MDSCs via IL-6

Liu, Q., Zhu, H., Zhang, C., Chen, T., & Cao, X. (2016) · OncoImmunology · doi:10.1080/2162402x.2016.1245265 · Cited by 9

The WAVE complex in developmental and adulthood brain disorders

Kim, H.-G., Berdasco, C., Nairn, A. C., & Kim, Y. (2025) · Experimental & Molecular Medicine · doi:10.1038/s12276-024-01386-w · Cited by 8

Neuronal Wiskott‐Aldrich syndrome protein regulates Pseudomonas aeruginosa ‐induced lung vascular permeability through the modulation of actin cytoskeletal dynamics

Che, P., Wagener, B. M., Zhao, X., Brandon, A. P., Evans, C. A., Cai, G., Zhao, R., Xu, Z., Han, X., Pittet, J., et al. (2020) · The FASEB Journal · doi:10.1096/fj.201902915r · Cited by 8

Characterization of porcine SKIP gene in skeletal muscle development: Polymorphisms, association analysis, expression and regulation of cell growth in C2C12 cells

Xiong, Q., Chai, J., Deng, C., Jiang, S., Liu, Y., Huang, T., Suo, X., Zhang, N., Li, X., Yang, Q., et al. (2012) · Meat Science · doi:10.1016/j.meatsci.2012.05.016 · Cited by 8

Identification of a Hydrophobic Domain of HA2 Essential to Morphogenesis of Helicoverpa armigera Nucleopolyhedrovirus

Wang, Q., Wang, Y., Liang, C., Song, J., & Chen, X. (2008) · Journal of Virology · doi:10.1128/jvi.02319-07 · Cited by 8

Dedicator of cytokinesis 2 regulates cytoskeletal actin dynamics and is essential for platelet biogenesis and functions

Ji, J., Xu, X., Zhang, L., Liu, S., Chen, J., Gao, H., Xiang, L., Li, Y., Xu, H., Chen, Y., et al. (2025) · Cardiovascular Research · doi:10.1093/cvr/cvaf009 · Cited by 7

MyoD control of SKIP expression during pig skeletal muscle development

Xiong, Q., Chai, J., Zhang, P. P., Jian Xin, W. U., Jiang, S. W., Zheng, R., & Deng, C. Y. (2010) · Molecular Biology Reports · doi:10.1007/s11033-010-0104-4 · Cited by 7

Role of PTEN in modulation of ADP-dependent signaling pathways in vascular endothelial cells

Bretón‐Romero, R., Kalwa, H., Lamas, S., & Michel, T. M. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2013.06.009 · Cited by 7

Proteomic analysis of kidneys from selenoprotein M transgenic rats in response to increased bioability of selenium

Goo, J. S., Kim, Y. N., Choi, K. M., Hwang, I. S., Kim, J. E., Lee, Y. J., Kwak, M. H., Shim, S. B., Jee, S. W., Lim, C. J., et al. (2013) · Clinical Proteomics · doi:10.1186/1559-0275-10-10 · Cited by 7

Promotion of invasion by mutant RAS is dependent on activation of the WASF3 metastasis promoter gene

Teng, Y., Ngoka, L. C. M., & Cowell, J. K. (2017) · Genes Chromosomes and Cancer · doi:10.1002/gcc.22453 · Cited by 7

Pathway Analysis Hints Towards Beneficial Effects of Long-Term Vibration on Human Chondrocytes

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P85 regulates neuronal migration through affecting neuronal morphology during mouse corticogenesis

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Bacterial toxins and virulence factors targeting the actin cytoskeleton and intercellular junctions

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Roles of Nectins in Cell Adhesion, Signaling and Polarization

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SOX4 induces cytoskeleton remodeling and promotes cell motility via N-wasp/ARP2/3 pathway in colorectal cancer cells

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Analysis for Carom complex signaling and function by database mining

Wang, H. (2015) · Frontiers in bioscience · doi:10.2741/4424 · Cited by 6

Assays for Functional Properties of Rab34 in Macropinosome Formation

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Regulation of WAVE1 expression in macrophages at multiple levels

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N-WASP Attenuates Cell Proliferation and Migration through ERK2-Dependent Enhanced Expression of TXNIP

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Cell morphology and gene expression: tracking changes and complementarity across time and cell lines

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WAVEs: A Novel and Promising Weapon in the Cancer Therapy Tool Box

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Lipid Interactions of Cytoskeletal Proteins

Niggli, V. (2006) · Advances in molecular and cell biology · doi:10.1016/s1569-2558(06)37011-7 · Cited by 5

Methods of Cell Propulsion through the Local Stroma in Breast Cancer

Davies, K. J. (2014) · International Journal of Breast Cancer · doi:10.1155/2014/197480 · Cited by 5

Stochastic simulation of biological reactions, and its applications for studying actin polymerization

Ichikawa, K., Suzuki, T., & Murata, N. (2010) · Physical Biology · doi:10.1088/1478-3975/7/4/046010 · Cited by 5

Transfection Microarrays for High-Throughput Phenotypic Screening of Genes Involved in Cell Migration

Onuki-Nagasaki, R., Nagasaki, A., Hakamada, K., Uyeda, T. Q. P., Fujita, S., Miyake, M., & Miyake, J. (2010) · Methods in molecular biology · doi:10.1007/978-1-60761-657-3_13 · Cited by 5

COMMENTARY Signal Transduction and Cellular Organization

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Regulation of actin dynamics by WASP and WAVE family proteins q

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Regulation of Actin Dynamics by WASP Family Proteins

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Regulation of actin dynamics by WASP and WAVE family proteins

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N-WASP, WAVE and Mena play different roles in the organization of actin cytoskeleton in lamellipodia

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