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Cell Migration: Integrating Signals from Front to Back
Open accessAbstract
Cell migration is a highly integrated multistep process that orchestrates embryonic morphogenesis; contributes to tissue repair and regeneration; and drives disease progression in cancer, mental retardation, atherosclerosis, and arthritis. The migrating cell is highly polarized with complex regulatory pathways that spatially and temporally integrate its component processes. This review describes the mechanisms underlying the major steps of migration and the signaling pathways that regulate them, and outlines recent advances investigating the nature of polarity in migrating cells and the pathways that establish it.
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Cites
Cell Migration: A Physically Integrated Molecular Process
Lauffenburger, D. A., & Horwitz, A. F. (1996) · Cell · doi:10.1016/s0092-8674(00)81280-5 · Cited by 3,915
Self-citationCory, G. O. C., & Ridley, A. J. (2002) · Nature · doi:10.1038/418732a · Cited by 72
Self-citation
Cited by
Comprehensive molecular characterization of gastric adenocarcinoma
The Cancer Genome Atlas Research Network (2014) · Nature · doi:10.1038/nature13480 · Cited by 6,498
Lutolf, M. P., & Hubbell, J. A. (2005) · Nature Biotechnology · doi:10.1038/nbt1055 · Cited by 4,551
RHO GTPASES: Biochemistry and Biology
Jaffe, A. B., & Hall, A. (2005) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.21.020604.150721 · Cited by 3,009
Focal adhesion kinase: in command and control of cell motility.
Mitra, S. K., Hanson, D. A., & Schlaepfer, D. D. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1549 · Cited by 2,335
Cancer Invasion and the Microenvironment: Plasticity and Reciprocity
Friedl, P., & Alexander, S. (2011) · Cell · doi:10.1016/j.cell.2011.11.016 · Cited by 1,940
Deconstructing the third dimension – how 3D culture microenvironments alter cellular cues
Baker, B. M., & Chen, C. S. (2012) · Journal of Cell Science · doi:10.1242/jcs.079509 · Cited by 1,760
Physiology of cell volume regulation in vertebrates
Hoffmann, E. K., Lambert, I. H., & Pedersen, S. F. (2009) · Physiological Reviews · doi:10.1152/physrev.00037.2007 · Cited by 1,441
Wolf, K., te Lindert, M., Krause, M., Alexander, S., te Riet, J., Willis, A. L., Hoffman, R. M., Figdor, C. G., Weiss, S. J., & Friedl, P. (2013) · Journal of Cell Biology · doi:10.1083/jcb.201210152 · Cited by 1,375
In vitro cell migration and invasion assays
Kramer, N., Walzl, A., Unger, C., Rosner, M., Krupitza, G., Hengstschläger, M., & Dolznig, H. (2013) · Mutation Research/Reviews in Mutation Research · doi:10.1016/j.mrrev.2012.08.001 · Cited by 1,170
CDK inhibitors: Cell cycle regulators and beyond
Besson, A., Dowdy, S. F., & Roberts, J. M. (2008) · Developmental Cell · doi:10.1016/j.devcel.2008.01.013 · Cited by 1,152
Actin stress fibers – assembly, dynamics and biological roles
Tojkander, S., Gateva, G., & Lappalainen, P. (2012) · Journal of Cell Science · doi:10.1242/jcs.098087 · Cited by 900
Choi, C. K., Vicente-Manzanares, M., Zareno, J., Whitmore, L. A., Mogilner, A., & Horwitz, A. R. (2008) · Nature Cell Biology · doi:10.1038/ncb1763 · Cited by 797
Self-citationDesigning degradable hydrogels for orthogonal control of cell microenvironments
Kharkar, P. M., Kiick, K. L., & Kloxin, A. M. (2013) · Chem. Soc. Rev. · doi:10.1039/c3cs60040h · Cited by 717
Lillis, A. P., Van Duyn, L. B., Murphy-Ullrich, J. E., & Strickland, D. K. (2008) · Physiological Reviews · doi:10.1152/physrev.00033.2007 · Cited by 669
Neuronal polarity: from extracellular signals to intracellular mechanisms.
Arimura, N., & Kaibuchi, K. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2056 · Cited by 655
Membrane potential and cancer progression
Yang, M., & Brackenbury, W. J. (2013) · Frontiers in Physiology · doi:10.3389/fphys.2013.00185 · Cited by 614
Mechanical compression drives cancer cells toward invasive phenotype
Tse, J. M., Cheng, G., Tyrrell, J. A., Wilcox-Adelman, S. A., Boucher, Y., Jain, R. K., & Munn, L. L. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1118910109 · Cited by 631
The extracellular matrix in tumor progression and metastasis
Eble, J. A., & Niland, S. (2019) · Clinical & Experimental Metastasis · doi:10.1007/s10585-019-09966-1 · Cited by 613
Calcium flickers steer cell migration
Wei, C., Wang, X., Chen, M., Ouyang, K., Song, L.-S., & Cheng, H. (2009) · Nature · doi:10.1038/nature07577 · Cited by 611
Verhey, K. J., & Gaertig, J. (2007) · Cell Cycle · doi:10.4161/cc.6.17.4633 · Cited by 558
Signalling through Class I PI3Ks in mammalian cells
Hawkins, P. T., Anderson, K. E., Davidson, K., & Stephens, L. R. (2006) · Biochemical Society Transactions · doi:10.1042/bst0340647 · Cited by 540
Rho signaling, ROCK and mDia1, in transformation, metastasis and invasion
Narumiya, S., Tanji, M., & Ishizaki, T. (2009) · Cancer and Metastasis Reviews · doi:10.1007/s10555-008-9170-7 · Cited by 530
Watanabe, T., Wang, S., Noritake, J., Sato, K., Fukata, M., Takefuji, M., Nakagawa, M., Izumi, N., Akiyama, T., & Kaibuchi, K. (2004) · Developmental Cell · doi:10.1016/j.devcel.2004.10.017 · Cited by 480
Saharinen, P., Eklund, L., Miettinen, J., Wirkkala, R., Anisimov, A., Winderlich, M., Nottebaum, A., Vestweber, D., Deutsch, U., Koh, G. Y., et al. (2008) · Nature Cell Biology · doi:10.1038/ncb1715 · Cited by 471
Integrins: masters and slaves of endocytic transport
Caswell, P. T., Vadrevu, S., & Norman, J. C. (2009) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2799 · Cited by 460
Crosstalk between small GTPases and polarity proteins in cell polarization
Iden, S., & Collard, J. G. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2521 · Cited by 451
The Molecular Basis of Filamin Binding to Integrins and Competition with Talin
Kiema, T., Lad, Y., Jiang, P., Oxley, C. L., Baldassarre, M., Wegener, K. L., Campbell, I. D., Ylänne, J., & Calderwood, D. A. (2006) · Molecular Cell · doi:10.1016/j.molcel.2006.01.011 · Cited by 434
Role of Ion Channels and Transporters in Cell Migration
Schwab, A., Fabian, A., Hanley, P. J., & Stock, C. (2012) · Physiological Reviews · doi:10.1152/physrev.00018.2011 · Cited by 420
Matrix remodeling by MMPs during wound repair
Rohani, M. G., & Parks, W. C. (2015) · Matrix Biology · doi:10.1016/j.matbio.2015.03.002 · Cited by 407
Semaphorin Regulation of Cellular Morphology
Tran, T. S., Kolodkin, A. L., & Bharadwaj, R. (2007) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.22.010605.093554 · Cited by 388
Extracellular matrix regulation of fibroblast function: redefining our perspective on skin aging
Cole, M. A., Quan, T., Voorhees, J. J., & Fisher, G. J. (2018) · Journal of Cell Communication and Signaling · doi:10.1007/s12079-018-0459-1 · Cited by 365
Endocytosis and signaling: Cell logistics shape the eukaryotic cell plan
Sigismund, S., Confalonieri, S., Ciliberto, A., Polo, S., Scita, G., & Di Fiore, P. P. (2012) · Physiological Reviews · doi:10.1152/physrev.00005.2011 · Cited by 338
Rac1 GTPase: A “Rac” of All Trades
Bosco, E. E., Mulloy, J. C., & Zheng, Y. (2009) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-008-8552-x · Cited by 350
The urokinase plasminogen activator system: a target for anti-cancer therapy
Ulisse, S., Baldini, E., Sorrenti, S., & D'Armiento, M. (2009) · Current Cancer Drug Targets · doi:10.2174/156800909787314002 · Cited by 312
Ray, A., Lee, O., Win, Z., Edwards, R. M., Alford, P. W., Kim, D.-H., & Provenzano, P. P. (2017) · Nature Communications · doi:10.1038/ncomms14923 · Cited by 293
Alexandrova, A. Y., Arnold, K., Schaub, S., Vasiliev, J. M., Meister, J.-J., Bershadsky, A. D., & Verkhovsky, A. B. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003234 · Cited by 275
Ji, H., Wang, J., Nika, H., Hawke, D., Keezer, S., Ge, Q., Fang, B., Fang, X., Fang, D., Litchfield, D. W., et al. (2009) · Molecular Cell · doi:10.1016/j.molcel.2009.09.034 · Cited by 270
CD98hc (SLC3A2) mediates integrin signaling
Feral, C. C., Nishiya, N., Fenczik, C. A., Stuhlmann, H., Slepak, M., & Ginsberg, M. H. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0404852102 · Cited by 264
Self-citationRedox regulation of cell migration and adhesion
Hurd, T. R., DeGennaro, M., & Lehmann, R. (2012) · Trends in Cell Biology · doi:10.1016/j.tcb.2011.11.002 · Cited by 263
Integrin modulation and signaling in leukocyte adhesion and migration
Rose, D. M., Alon, R., & Ginsberg, M. H. (2007) · Immunological Reviews · doi:10.1111/j.1600-065x.2007.00536.x · Cited by 243
Self-citation‘See-saw’ expression of microRNA-198 and FSTL1 from a single transcript in wound healing
Sundaram, G. M., Common, J. E. A., Gopal, F. E., Srikanta, S., Lakshman, K., Lunny, D. P., Lim, T. C., Tanavde, V., Lane, E. B., & Sampath, P. (2013) · Nature · doi:10.1038/nature11890 · Cited by 231
Integrin-driven actin polymerization consolidates long-term potentiation
Kramár, E. A., Lin, B., Rex, C. S., Gall, C. M., & Lynch, G. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0601354103 · Cited by 221
Development and dynamics of cell polarity at a glance
Campanale, J. P., Sun, T. Y., & Montell, D. J. (2017) · Journal of Cell Science · doi:10.1242/jcs.188599 · Cited by 198
Nanoscale Surveillance of the Brain by Microglia via cAMP-Regulated Filopodia
Bernier, L.-P., Bohlen, C. J., York, E. M., Choi, H. B., Kamyabi, A., Dissing-Olesen, L., Hefendehl, J. K., Collins, H. Y., Stevens, B., Barres, B. A., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.05.010 · Cited by 211
Neutrophil morphology and migration are affected by substrate elasticity
Oakes, P. W., Patel, D. C., Morin, N. A., Zitterbart, D. P., Fabry, B., Reichner, J. S., & Tang, J. X. (2009) · Blood · doi:10.1182/blood-2008-11-191445 · Cited by 208
Roles of the Rac1 and Rac3 GTPases in human tumor cell invasion
Chan, A. Y., Coniglio, S. J., Chuang, Y.-Y., Michaelson, D., Knaus, U. G., Philips, M. R., & Symons, M. (2005) · Oncogene · doi:10.1038/sj.onc.1208909 · Cited by 202
Chemotaxis of human articular chondrocytes and mesenchymal stem cells
Mishima, Y., & Lotz, M. (2008) · Journal of Orthopaedic Research · doi:10.1002/jor.20668 · Cited by 192
ERK regulates Golgi and centrosome orientation towards the leading edge through GRASP65
Bisel, B., Wang, Y., Wei, J.-H., Xiang, Y., Tang, D., Miron-Mendoza, M., Yoshimura, S.-I., Nakamura, N., & Seemann, J. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200805045 · Cited by 184
Integrins control motile strategy through a Rho–cofilin pathway
Danen, E. H. J., van Rheenen, J., Franken, W., Huveneers, S., Sonneveld, P., Jalink, K., & Sonnenberg, A. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200412081 · Cited by 185
Gilkes, D. M., Xiang, L., Lee, S. J., Chaturvedi, P., Hubbi, M. E., Wirtz, D., & Semenza, G. L. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1321510111 · Cited by 184
RetractedMYC suppresses cancer metastasis by direct transcriptional silencing of αv and β3 integrin subunits
Liu, H., Radisky, D. C., Yang, D., Xu, R., Radisky, E. S., Bissell, M. J., & Bishop, J. M. (2012) · Nature Cell Biology · doi:10.1038/ncb2491 · Cited by 181
Wilson, P. M., Fryer, R. H., Fang, Y., & Hatten, M. E. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0032-10.2010 · Cited by 169
Microtubules Regulate Migratory Polarity through Rho/ROCK Signaling in T Cells
Takesono, A., Heasman, S. J., Wojciak-Stothard, B., Garg, R., & Ridley, A. J. (2010) · PLoS ONE · doi:10.1371/journal.pone.0008774 · Cited by 170
Self-citationNalbant, P., Chang, Y.-C., Birkenfeld, J., Chang, Z.-F., & Bokoch, G. M. (2009) · Molecular Biology of the Cell · doi:10.1091/mbc.e09-01-0041 · Cited by 148
Partida-Sanchez, S., Gasser, A., Fliegert, R., Siebrands, C. C., Dammermann, W., Shi, G., Mousseau, B. J., Sumoza-Toledo, A., Bhagat, H., Walseth, T. F., et al. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.11.7827 · Cited by 144
Su, S.-C., Lin, C.-W., Yang, W.-E., Fan, W.-L., & Yang, S.-F. (2016) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.2016.1113260 · Cited by 145
Tsai, F.-C., & Meyer, T. (2012) · Current Biology · doi:10.1016/j.cub.2012.03.037 · Cited by 141
RalA and RalB: Antagonistic Relatives in Cancer Cell Migration
Oxford, G., Owens, C. R., Titus, B. J., Foreman, T. L., Herlevsen, M. C., Smith, S. C., & Theodorescu, D. (2005) · Cancer Research · doi:10.1158/0008-5472.can-04-1957 · Cited by 139
Thurnherr, T., Benninger, Y., Wu, X., Chrostek, A., Krause, S. M., Nave, K.-A., Franklin, R. J. M., Brakebusch, C., Suter, U., & Relvas, J. B. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.2158-06.2006 · Cited by 142
Cabrero, J. R., Serrador, J. M., Barreiro, O., Mittelbrunn, M., Naranjo-Suárez, S., Martín-Cófreces, N., Vicente-Manzanares, M., Mazitschek, R., Bradner, J. E., Ávila, J., et al. (2006) · Molecular Biology of the Cell · doi:10.1091/mbc.e06-01-0008 · Cited by 95
Schneider, L., Stock, C.-M., Dieterich, P., Jensen, B. H., Pedersen, L. B., Satir, P., Schwab, A., Christensen, S. T., & Pedersen, S. F. (2009) · Journal of Cell Biology · doi:10.1083/jcb.200806019 · Cited by 94
A Novel Mammalian Retromer Component, Vps26B
Kerr, M. C., Bennetts, J. S., Simpson, F., Thomas, E. C., Flegg, C., Gleeson, P. A., Wicking, C., & Teasdale, R. D. (2005) · Traffic · doi:10.1111/j.1600-0854.2005.00328.x · Cited by 93
Rab5 Activation Promotes Focal Adhesion Disassembly, Migration and Invasiveness of Tumor Cells
Mendoza, P., Ortiz, R., Díaz, J., Quest, A. F. G., Leyton, L., Stupack, D., & Torres, V. A. (2013) · Journal of Cell Science · doi:10.1242/jcs.119727 · Cited by 92
Huang, B., Lu, M., Jolly, M. K., Tsarfaty, I., Onuchic, J., & Ben-Jacob, E. (2014) · Scientific Reports · doi:10.1038/srep06449 · Cited by 91
TOR kinase complexes and cell migration
Liu, L., & Parent, C. A. (2011) · Journal of Cell Biology · doi:10.1083/jcb.201102090 · Cited by 87
Echarri, A., Lai, M. J., Robinson, M. R., & Pendergast, A. M. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.11.4979-4993.2004 · Cited by 88
Lee, J. G., & Kay, E. P. (2006) · Investigative Opthalmology & Visual Science · doi:10.1167/iovs.05-1223 · Cited by 79
Goldfinger, L. E., Ptak, C., Jeffery, E. D., Shabanowitz, J., Hunt, D. F., & Ginsberg, M. H. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200603111 · Cited by 78
Self-citationPIP kinases define PI4,5P2 signaling specificity by association with effectors
Choi, S., Thapa, N., Tan, X., Hedman, A. C., & Anderson, R. A. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2015.01.009 · Cited by 75
Neurons in motion: same principles for different shapes?
Marín, O., Valdeolmillos, M., & Moya, F. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.10.001 · Cited by 71
Fan, Y., Gong, Y., Ghosh, P. K., Graham, L. M., & Fox, P. L. (2009) · Developmental Cell · doi:10.1016/j.devcel.2009.03.009 · Cited by 68
Phosphorylation of WAVE2 by MAP kinases regulates persistent cell migration and polarity
Danson, C. M., Pocha, S. M., Bloomberg, G. B., & Cory, G. O. (2007) · Journal of Cell Science · doi:10.1242/jcs.013714 · Cited by 66
Actin dynamics associated with focal adhesions
Ciobanasu, C., Faivre, B., & Le Clainche, C. (2012) · International Journal of Cell Biology · doi:10.1155/2012/941292 · Cited by 63
Datla, S. R., McGrail, D. J., Vukelic, S., Huff, L. P., Lyle, A. N., Pounkova, L., Lee, M., Seidel-Rogol, B., Khalil, M. K., Hilenski, L. L., et al. (2014) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00918.2013 · Cited by 60
Easley, C. A., Brown, C. M., Horwitz, A. F., & Tombes, R. M. (2008) · Cell Motility · doi:10.1002/cm.20294 · Cited by 56
Self-citationRegulation and functions of the RhoA regulatory guanine nucleotide exchange factor GEF-H1
Joo, E., & Olson, M. F. (2021) · Small GTPases · doi:10.1080/21541248.2020.1840889 · Cited by 56
Troeger, A., Johnson, A. J., Wood, J., Blum, W. G., Andritsos, L. A., Byrd, J. C., & Williams, D. A. (2012) · Blood · doi:10.1182/blood-2011-12-395939 · Cited by 55
Feng, P., Wang, B., & Ren, E. C. (2008) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2007.06.020 · Cited by 51
Zou, H., Yue, W., Yu, W.-K., Liu, D., Fong, C.-C., Zhao, J., & Yang, M. (2015) · Analytical Chemistry · doi:10.1021/acs.analchem.5b00873 · Cited by 47
Kong, M., Bui, T. V., Ditsworth, D., Gruber, J. J., Goncharov, D., Krymskaya, V. P., Lindsten, T., & Thompson, C. B. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m703159200 · Cited by 43
RNA localization and co‐translational interactions control RAB13 GTPase function and cell migration
Moissoglu, K., Stueland, M., Gasparski, A. N., Wang, T., Jenkins, L. M., Hastings, M. L., & Mili, S. (2020) · The EMBO Journal · doi:10.15252/embj.2020104958 · Cited by 43
Moran, D. M., & Maki, C. G. (2010) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-09-1220 · Cited by 35
Globular Adiponectin Activates Motility and Regenerative Traits of Muscle Satellite Cells
Fiaschi, T., Giannoni, E., Taddei, M. L., & Chiarugi, P. (2012) · PLoS ONE · doi:10.1371/journal.pone.0034782 · Cited by 37
Rho A and Rac1: Antagonists moving forward
Salloum, G., Jaafar, L., & El-Sibai, M. (2020) · Tissue and Cell · doi:10.1016/j.tice.2020.101364 · Cited by 36
Fuhler, G. M., Drayer, A. L., Olthof, S. G. M., Schuringa, J. J., Coffer, P. J., & Vellenga, E. (2008) · Blood · doi:10.1182/blood-2006-11-060632 · Cited by 36
Wu, W., Zhou, Z., Sun, G., Liu, Y., Zhang, A., & Chen, X. (2021) · Materials Science and Engineering: C · doi:10.1016/j.msec.2021.111919 · Cited by 33
Meller, J., Chen, Z., Dudiki, T., Cull, R. M., Murtazina, R., Bal, S. K., Pluskota, E., Stefl, S., Plow, E. F., Trapp, B. D., et al. (2017) · JCI Insight · doi:10.1172/jci.insight.93002 · Cited by 27
Li, M., Kim, Y.-M., Koh, J. H., Park, J., Kwon, H. M., Park, J.-H., Jin, J., Park, Y., Kim, D., & Kim, W.-U. (2024) · Journal of Clinical Investigation · doi:10.1172/jci167835 · Cited by 25
Micro RNA Let‐7b inhibits keratinocyte migration in cutaneous wound healing by targeting IGF 2 BP 2
Wu, Y., Zhong, J. L., Hou, N., Sun, Y., Ma, B., Nisar, M. F., Teng, Y., Tan, Z., Chen, K., Wang, Y., et al. (2017) · Experimental Dermatology · doi:10.1111/exd.13164 · Cited by 25
Chen, Y., Liu, Z., Gong, P., Zhang, H., Chen, Y., Yao, S., Li, W., Zhang, Y., & Yu, Y. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23169041 · Cited by 25
Marshall-Burghardt, S., Migueles-Ramírez, R. A., Lin, Q., El Baba, N., Saada, R., Umar, M., Mavalwala, K., & Hayer, A. (2024) · Science Advances · doi:10.1126/sciadv.adn6858 · Cited by 23
Mechanisms involved in the anti-tumor effects of Toosendanin in glioma cells
Zhang, C., Gao, H., Liu, Z., Lai, J., Zhan, Z., Chen, Y., & Huang, H. (2021) · Cancer Cell International · doi:10.1186/s12935-021-02186-2 · Cited by 21
(2022) · doi:10.1371/journal.pgen.1010384 · Cited by 18
RhoH plays distinct roles in T-cell migrations induced by different doses of SDF1α
Wang, H., Zeng, X., Fan, Z., & Lim, B. (2010) · Cellular Signalling · doi:10.1016/j.cellsig.2010.02.005 · Cited by 16
Multiparametric Analysis of Focal Adhesions in Bidimensional Substrates
Talayero, V. C., & Vicente-Manzanares, M. (2021) · Methods in Molecular Biology · doi:10.1007/978-1-0716-0962-0_3 · Cited by 7
Deb Roy, A., Saez Gonzalez, C., Shahid, F., Yadav, E., & Inoue, T. (2024) · doi:10.1101/2024.12.01.626286 · Cited by 4
Strategy to replace animal-derived ECM by a modular and highly defined matrix
Nesterenko, Y. (2020) · ALTEX · doi:10.14573/altex.2003181 · Cited by 3
OptoTAT reveals microtubule acetylation as a rapid trigger for GEF-H1–mediated cell migration
Deb Roy, A., Gonzalez, C. S., Stanislauskas, M., Shahid, F., Yadav, E., Rezek, J., & Inoue, T. (2026) · Journal of Cell Biology · doi:10.1083/jcb.202508095 · Cited by 2
Metadata
- Authors
- Ridley, A. J., Schwartz, M. A., Burridge, K., Firtel, R. A., Ginsberg, M. H., Borisy, G., Parsons, J. T., & Horwitz, A. R.
- Venue
- Science
- Published
- 2003-12-05
- Volume
- 302
- Issue
- 5651
- Pages
- 1704-1709
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2063220206
- Cited by
- 4,978
- References
- 2
- FWCI
- 54.49
- Type
- journal article
- Language
- en
- Open access
- green
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