The DOI matches its Crossref record; 111 of the 111 references it cites were found in a registry or an index.
Targeting and transport: How microtubules control focal adhesion dynamics
Open accessAbstract
Directional cell migration requires force generation that relies on the coordinated remodeling of interactions with the extracellular matrix (ECM), which is mediated by integrin-based focal adhesions (FAs). Normal FA turnover requires dynamic microtubules, and three members of the diverse group of microtubule plus-end-tracking proteins are principally involved in mediating microtubule interactions with FAs. Microtubules also alter the assembly state of FAs by modulating Rho GTPase signaling, and recent evidence suggests that microtubule-mediated clathrin-dependent and -independent endocytosis regulates FA dynamics. In addition, FA-associated microtubules may provide a polarized microtubule track for localized secretion of matrix metalloproteases (MMPs). Thus, different aspects of the molecular mechanisms by which microtubules control FA turnover in migrating cells are beginning to emerge.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source doesn’t support the claim as written.
In the citing paper
“Furthermore, local stabilization and expansion of microtubules in the vicinity of focal adhesions 32,74 can potentially trigger GEF-H1 release and RhoA-dependent focal adhesion disassembly during cell movement.”
From Taxane-induced conformational changes in the microtubule lattice activate GEF-H1-dependent RhoA signalling (2026) · cites this paper as [74]
Checked by a reasoning model — may be wrong.
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Matrix Metalloproteinases: Regulators of the Tumor Microenvironment
Kessenbrock, K., Plaks, V., & Werb, Z. (2010) · Cell · doi:10.1016/j.cell.2010.03.015 · Cited by 5,151
Cell adhesion: integrating cytoskeletal dynamics and cellular tension
Parsons, J. T., Horwitz, A. R., & Schwartz, M. A. (2010) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2957 · Cited by 2,081
Regulation of the small GTP‐binding protein Rho by cell adhesion and the cytoskeleton
Ren, X. D., Kiosses, W. B., & Schwartz, M. A. (1999) · The EMBO Journal · doi:10.1093/emboj/18.3.578 · Cited by 1,575
Nanoscale architecture of integrin-based cell adhesions
Kanchanawong, P., Shtengel, G. E., Pasapera, A. M., Ramko, E. B., Davidson, M. W., Hess, H. F., & Waterman, C. M. (2010) · Nature · doi:10.1038/nature09621 · Cited by 1,572
Beyond self-assembly: From microtubules to morphogenesis
Kirschner, M. W. (1986) · Cell · doi:10.1016/0092-8674(86)90318-1 · Cited by 1,382
Coordination of Rho GTPase activities during cell protrusion
Machacek, M., Hodgson, L., Welch, C. M., Elliott, H. L., Pertz, O. C., Nalbant, P., Abell, A. N., Johnson, G. L., Hahn, K. M., & Danuser, G. M. (2009) · Nature · doi:10.1038/nature08242 · Cited by 1,049
Tracking the ends: a dynamic protein network controls the fate of microtubule tips
Akhmanova, A., & Steinmetz, M. O. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2369 · Cited by 1,047
Dynamin, a membrane-remodelling GTPase
Ferguson, S. M., & Camilli, P. V. D. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3266 · Cited by 1,027
Conserved microtubule–actin interactions in cell movement and morphogenesis
Rodriguez, O. C., Schaefer, A. W., Mandato, C. A., Forscher, P., Bement, W. M., & Waterman-Storer, C. M. (2003) · Nature Cell Biology · doi:10.1038/ncb0703-599 · Cited by 844
Dishevelled: The hub of Wnt signaling
Gao, C., & Chen, Y. (2009) · Cellular Signalling · doi:10.1016/j.cellsig.2009.11.021 · Cited by 780
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–200 of 241
Tuntithavornwat, S., Shea, D. J., Wong, B. S., Guardia, T., Lee, S. J., Yankaskas, C. L., Zheng, L., Kontrogianni‐Konstantopoulos, A., & Κωνσταντόπουλος, Κ. (2021) · Cancer Letters · doi:10.1016/j.canlet.2021.11.016 · Cited by 30
Medicinal Plants: A Potential Source of Compounds for Targeting Cell Division
Zulkipli, I. N., David, S. R. N., Rajabalaya, R., & Idris, A. (2015) · Drug Target Insights · doi:10.4137/dti.s24946 · Cited by 36
Cortical dynamics during cell motility are regulated by CRL3KLHL21 E3 ubiquitin ligase
Courthéoux, T., Enchev, R. I., Lampert, F., Gerez, J., Beck, J., Picotti, P., Sumara, I., & Peter, M. (2016) · Nature Communications · doi:10.1038/ncomms12810 · Cited by 30
Li, Y., Wu, M., Zhang, Z., Xia, J., Wang, Z., Chen, X., Xiao, X., Lu, F., & Dong, Z. (2019) · Tissue Engineering Part A · doi:10.1089/ten.tea.2019.0046 · Cited by 29
Mutation-specific non-canonical pathway of PTEN as a distinct therapeutic target for glioblastoma
Choi, S. W., Lee, Y., Shin, K., Koo, H., Kim, D., Sa, J. K., Cho, H. J., Shin, H.-M., Lee, S. J., Kim, H., et al. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-03657-0 · Cited by 29
Trogden, K. P., Lee, J., Bracey, K. M., Ho, K.-H., McKinney, H., Zhu, X.-D., Arpağ, G., Folland, T., Osipovich, A. B., Magnuson, M. A., et al. (2021) · eLife · doi:10.7554/elife.59912 · Cited by 20
On the Role of Rab5 in Cell Migration
Mendoza, P., Díaz, J., & Torres, V. A. (2014) · Current Molecular Medicine · doi:10.2174/1566524014666140128111347 · Cited by 29
Li, N., Mruk, D. D., Tang, E. I., Lee, W. M., Wong, C. K. C., & Cheng, C. Y. (2016) · Endocrinology · doi:10.1210/en.2016-1133 · Cited by 29
Guo, K., Zhang, J., Huang, P., Xu, Y., Pan, W., Li, K., Chen, L., Luo, L., Yu, W., Chen, S., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113321 · Cited by 28
Bachmann, A., & Straube, A. (2015) · Biochemical Society Transactions · doi:10.1042/bst20140280 · Cited by 27
An ELMO2-RhoG-ILK network modulates microtubule dynamics
Jackson, B. C., Ivanova, I. A., & Dagnino, L. (2015) · Molecular Biology of the Cell · doi:10.1091/mbc.e14-10-1444 · Cited by 26
TRIM15 is a focal adhesion protein that regulates focal adhesion disassembly
Uchil, P. D., Pawliczek, T., Reynolds, T. D., Ding, S., Hinz, A., Munro, J. B., Huang, F., Floyd, R. W., Yang, H., Hamilton, W., et al. (2014) · Journal of Cell Science · doi:10.1242/jcs.143537 · Cited by 27
Zhang, Y., Luo, Y., Lyu, R., Chen, J., Liu, R., Li, D., Liu, M., & Zhou, J. (2016) · Theranostics · doi:10.7150/thno.16356 · Cited by 26
Weng, Z., Shang, Y., Yao, D., Zhu, J., & Zhang, R. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.816017 · Cited by 25
Centrosome guides spatial activation of Rac to control cell polarization and directed cell migration
Cheng, H., Hsiao, C.-T., Chen, Y., Huang, C.-M., Chan, S.-I., Chiou, A. E. T., & Kuo, J. (2019) · Life Science Alliance · doi:10.26508/lsa.201800135 · Cited by 29
Autophagy suppresses cell migration by degrading GEF-H1, a RhoA GEF
Yoshida, T., Tsujioka, M., Honda, S., Tanaka, M., & Shimizu, S. (2016) · Oncotarget · doi:10.18632/oncotarget.8883 · Cited by 26
In-situ coupling between kinase activities and protein dynamics within single focal adhesions
Wu, Y., Zhang, K., Seong, J., Fan, J., Chien, S., Wang, Y., & Lu, S. (2016) · Scientific Reports · doi:10.1038/srep29377 · Cited by 26
Adams, G., Zhou, J., Wang, W., Wu, H., Quan, J., Liu, Y., Xia, P., Wang, Z., Zhou, S. F., Jiang, J., et al. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.732719 · Cited by 25
Front-to-Rear Polarity in Migrating Cells
Llense, F., & Etienne‐Manneville, S. (2015) · Springer eBooks · doi:10.1007/978-3-319-14463-4_5 · Cited by 27
The emerging role of microtubules in invasion plasticity
Legátová, A., Pelantová, M., Rösel, D., Brábek, J., & Škarková, A. (2023) · Frontiers in Oncology · doi:10.3389/fonc.2023.1118171 · Cited by 25
Microtubule control of migration: Coordination in confinement
Schmidt, C. J., & Stehbens, S. J. (2023) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2023.102289 · Cited by 23
Self-citationFOCAD loss impacts microtubule assembly, G2/M progression and patient survival in astrocytic gliomas
Brand, F. J., Förster, A., Christians, A., Bucher, M., Thomé, C. M., Raab, M. S., Westphal, M., Pietsch, T., von Deimling, A., Reifenberger, G., et al. (2019) · Acta Neuropathologica · doi:10.1007/s00401-019-02067-z · Cited by 22
Plestant, C., Strale, P., Seddiki, R., Nguyen, E., Ladoux, B., & Mège, R. (2014) · Journal of Cell Science · doi:10.1242/jcs.131284 · Cited by 25
Park, S. Y., Park, J., Lee, G. W., Li, L., & Chun, Y. (2018) · BMC Cancer · doi:10.1186/s12885-017-3942-9 · Cited by 21
Protein tyrosine phosphatase PTP1B in cell adhesion and migration
Arregui, C. O., González, Á., Burdisso, J. E., & Wusener, A. E. G. (2013) · Cell Adhesion & Migration · doi:10.4161/cam.26375 · Cited by 21
Microtubule dynamics regulation contributes to endothelial morphogenesis
Lyle, K. S., Corleto, J. A., & Wittmann, T. (2012) · BioArchitecture · doi:10.4161/bioa.22335 · Cited by 21
Self-citationItou, J., Tanaka, S., Li, W., Iida, A., Sehara‐Fujisawa, A., Sato, F., & Toi, M. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2016.10.012 · Cited by 21
Vimentin supports cell polarization by enhancing centrosome function and microtubule acetylation
Saldanha, R., Thanh, M. T. H., Krishnan, N., Hehnly, H., & Patteson, A. (2024) · Journal of The Royal Society Interface · doi:10.1098/rsif.2023.0641 · Cited by 19
Erdoğan, B., Cammarata, G. M., Lee, E. J., Pratt, B. C., Francl, A. F., Rutherford, E. L., & Lowery, L. A. (2017) · Neural Development · doi:10.1186/s13064-017-0080-7 · Cited by 19
Hernandez, S. J., Fote, G., Reyes-Ortiz, A. M., Steffan, J. S., & Thompson, L. M. (2021) · Matrix Biology Plus · doi:10.1016/j.mbplus.2021.100089 · Cited by 17
Quantitative imaging of focal adhesion dynamics and their regulation by HGF and Rap1 signaling
Spanjaard, E., Smal, I., Angelopoulos, N., Verlaan-Klink, I., Matov, A., Meijering, E. H. W., Wessels, L. F. A., Bos, H., & de Rooij, J. (2014) · Experimental Cell Research · doi:10.1016/j.yexcr.2014.10.012 · Cited by 18
Rho family GTPases: Making it to the third dimension
Riching, K. M., & Keely, P. J. (2014) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2014.11.007 · Cited by 17
Zong, H., Hazelbaker, M. A., Moe, C., Ems-McClung, S. C., Hu, K., & Walczak, C. (2021) · Molecular Biology of the Cell · doi:10.1091/mbc.e20-05-0301 · Cited by 17
Targeting Microtubules for Wound Repair
Charafeddine, R. A., Nosanchuk, J. D., & Sharp, D. J. (2015) · Advances in Wound Care · doi:10.1089/wound.2015.0658 · Cited by 15
Role of microtubule cytoskeleton in regulation of endothelial barrier function
Alieva, I. B. (2014) · Biochemistry (Moscow) · doi:10.1134/s0006297914090119 · Cited by 16
Spindly is required for rapid migration of human cells
Conte, C., Baird, M. A., Davidson, M. W., & Griffis, E. R. (2018) · Biology Open · doi:10.1242/bio.033233 · Cited by 16
EB1 Restricts Breast Cancer Cell Invadopodia Formation and Matrix Proteolysis via FAK
Chanez, B., Ostacolo, K., Badache, A., & Thuault, S. (2021) · Cells · doi:10.3390/cells10020388 · Cited by 15
Actomyosin dynamics modulate microtubule deformation and growth during T-cell activation
Rey‐Suarez, I., Rogers, N., Kerr, S., Shroff, H., & Upadhyaya, A. (2021) · Molecular Biology of the Cell · doi:10.1091/mbc.e20-10-0685 · Cited by 15
RITA modulates cell migration and invasion by affecting focal adhesion dynamics
Hoock, S. C., Ritter, A., Steinhäuser, K., Roth, S., Behrends, C., Oswald, F., Solbach, C., Louwen, F., Kreis, N., & Yuan, J. (2019) · Molecular Oncology · doi:10.1002/1878-0261.12551 · Cited by 15
Microtubules and motor proteins support zebrafish neuronal migration by directing cargo
Theisen, U., Ernst, A., Heyne, R. L. S., Ring, T. P., Thorn‐Seshold, O., & Köster, R. W. (2020) · The Journal of Cell Biology · doi:10.1083/jcb.201908040 · Cited by 15
Dynamic interplay of microtubule and actomyosin forces drive tissue extension
Singh, A., Thale, S., Leibner, T., Lamparter, L., Ricker, A., Nüsse, H., Klingauf, J., Galic, M., Ohlberger, M., & Matis, M. (2024) · Nature Communications · doi:10.1038/s41467-024-47596-8 · Cited by 14
Cytoskeleton systems contribute differently to the functional intrinsic properties of chondrospheres
Gryadunova, A. A., Koudan, E. V., Rodionov, S. A., Pereira, F. D. A. S., Meteleva, N. Y., Kasyanov, V. A., Parfenov, V. A., Av, K., Khesuani, Y. D., Mironov, V. A., et al. (2020) · Acta Biomaterialia · doi:10.1016/j.actbio.2020.10.007 · Cited by 14
Sharma, R., Chen, K., & Sharma, R. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1134712 · Cited by 13
Center or periphery? Modeling the effects of focal adhesion placement during cell spreading
Stolarska, M., & Rammohan, A. R. (2017) · PLoS ONE · doi:10.1371/journal.pone.0171430 · Cited by 13
ERRα coordinates actin and focal adhesion dynamics
Tribollet, V., Cerutti, C., Géloën, A., Berger, E., Mets, R. D. M. D., Balland, M., Courchet, J., Vanacker, J.-M., & Forcet, C. (2022) · Cancer Gene Therapy · doi:10.1038/s41417-022-00461-6 · Cited by 13
Kosinski, J. R., Sechi, A. S., Hain, J., Villwock, S., Ha, S. A., Hauschulz, M., Rose, M., Steib, F., Ortiz‐Brüchle, N., Heij, L. R., et al. (2024) · Molecular Oncology · doi:10.1002/1878-0261.13609 · Cited by 13
A cell surface display fluorescent biosensor for measuring MMP14 activity in real-time
Braun, A., Farber, M. J., Klase, Z. A., Berget, P. B., & Myers, K. A. (2018) · Scientific Reports · doi:10.1038/s41598-018-24080-0 · Cited by 12
Low-dose eribulin reduces lung metastasis of osteosarcoma in vitro and in vivo
Watanabe, K., Yui, Y., Sasagawa, S., Suzuki, K., Kanamori, M., Yasuda, T., & Kimura, T. (2019) · Oncotarget · doi:10.18632/oncotarget.26536 · Cited by 12
Cell adhesion and spreading on fluid membranes through microtubules-dependent mechanotransduction
Mikhajlov, O., Adar, R. M., Tătulea-Codrean, M., Macé, A., Manzi, J., Tabarin, F., Battistella, A., Federico, F. D., Joanny, J., Nhieu, G. T. V., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-56343-6 · Cited by 11
Mechanobiology, tissue development, and tissue engineering
Li, D., & Wang, Y. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-818422-6.00015-0 · Cited by 11
Fidgetin-like 2 depletion enhances cell migration by regulating GEF-H1, RhoA, and FAK
Smart, K., Kramer, A. H., Smart, S., Hodgson, L., & Sharp, D. J. (2022) · Biophysical Journal · doi:10.1016/j.bpj.2022.12.018 · Cited by 12
Role of dynamin 2 in the disassembly of focal adhesions
Briñas, L., Vassilopoulos, S., Bonne, G., Guicheney, P., & Bitoun, M. (2013) · Journal of Molecular Medicine · doi:10.1007/s00109-013-1040-2 · Cited by 15
LGN Directs Interphase Endothelial Cell Behavior via the Microtubule Network
Wright, C. E., Kushner, E. J., Du, Q., & Bautch, V. L. (2015) · PLoS ONE · doi:10.1371/journal.pone.0138763 · Cited by 11
Collective dynamics of actin and microtubule and its crosstalk mediated by FHDC1
Tong, C. S., Su, M., Sun, H. Q., Chua, X. L., Xiong, D., Guo, S., Raj, R., Ong, N. W. P., Lee, A. G., Miao, Y., et al. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1261117 · Cited by 9
Microtubules and mechanosensing: key players in endothelial responses to mechanical stimuli
Mohammed, D., Hamid, I., Vanhollebeke, B., & Martin, M. (2025) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-025-05828-0 · Cited by 11
Nanni, S. B., Pratt, J., Beauchemin, D., Haidara, K., & Annabi, B. (2016) · Biomarkers in Cancer · doi:10.4137/bic.s38894 · Cited by 8
FAK regulates dynein localisation and cell polarity in migrating mouse fibroblasts
Fructuoso, M., Legrand, M., Mousson, A., Steffan, T., Vauchelles, R., Mey, J. D., Sick, É., Rondé, P., & Dujardin, D. (2019) · Biology of the Cell · doi:10.1111/boc.201900041 · Cited by 10
Guo, S. S., Seiwert, A., Szeto, I. Y. Y., & Fässler, R. (2020) · Experimental Cell Research · doi:10.1016/j.yexcr.2020.112391 · Cited by 9
Novel interactions between erythroblast macrophage protein and cell migration
Javan, G. T., Can, İ., Yeboah, F., Lee, Y., & Soni, S. (2016) · Blood Cells Molecules and Diseases · doi:10.1016/j.bcmd.2016.06.004 · Cited by 9
Cdc42 is essential for the polarized movement and adhesion of human dental pulp stem cells
Li, M., Ma, L., Song, B., Yu, D., Min, X., Mei, X., Guo, H., & Yu, Q. (2017) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2017.09.036 · Cited by 9
How does the tubulin code facilitate directed cell migration?
Simoes-da-Silva, M. M., & Barišić, M. (2025) · Biochemical Society Transactions · doi:10.1042/bst20240841 · Cited by 9
TTL-Expression Modulates Epithelial Morphogenesis
Müller, M., Ringer, K., Hub, F., Kamm, N., Worzfeld, T., & Jacob, R. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.635723 · Cited by 8
Spatial distribution of filament elasticity determines the migratory behaviors of a cell
Harn, H. I., Hsu, C., Wang, Y.-K., Huang, Y.-W., Chiu, W., Lin, H., Cheng, C., & Tang, M. (2016) · Cell Adhesion & Migration · doi:10.1080/19336918.2016.1156825 · Cited by 8
Estrogens—Origin of Centrosome Defects in Human Cancer?
Bühler, M., & Stolz, A. (2022) · Cells · doi:10.3390/cells11030432 · Cited by 7
Cho, W., Kim, H., Lee, J., Hong, S. H., & Choe, J. (2013) · Immune Network · doi:10.4110/in.2013.13.5.199 · Cited by 8
Piazzi, M., Bavelloni, A., Greco, S., Focaccia, E., Orsini, A., Benini, S., Gambarotti, M., Faenza, I., & Blalock, W. L. (2019) · Journal of Cellular Physiology · doi:10.1002/jcp.29024 · Cited by 8
Erdoğan, B., Clair, R. M. S., Cammarata, G. M., Zaccaro, T., Ballif, B. A., & Lowery, L. A. (2020) · Cytoskeleton · doi:10.1002/cm.21622 · Cited by 8
Hax1 regulate focal adhesion dynamics through IQGAP1
Ren, X., Guo, X., Liang, Z., Guo, R., Liang, S., & Liu, H. (2023) · Cell Communication and Signaling · doi:10.1186/s12964-023-01189-y · Cited by 7
Molika, P., Leetanaporn, K., Chiangjong, W., Choochuen, P., & Navakanitworakul, R. (2024) · Cells · doi:10.3390/cells13232004 · Cited by 9
CLASP1 regulates endothelial cell branching morphology and directed migration
Myer, N. M., & Myers, K. A. (2017) · Biology Open · doi:10.1242/bio.028571 · Cited by 7
Dynamic microtubules drive fibroblast spreading
Tvorogova, A. V., Saidova, A. A., Смирнова, Т. А., & Vorobjev, I. A. (2018) · Biology Open · doi:10.1242/bio.038968 · Cited by 7
Dupas, S. J., Parada, G. E., Li, J. D., Brown, K. R., Moffat, J., & Blencowe, B. J. (2026) · Nature Communications · doi:10.1038/s41467-025-67931-x · Cited by 7
Awakening the stalled axon — Surprises in CSPG gradients
Lee, S. J., Kalinski, A. L., & Twiss, J. L. (2014) · Experimental Neurology · doi:10.1016/j.expneurol.2013.12.025 · Cited by 6
The βI domain promotes active β1 integrin clustering into mature adhesion sites
Mana, G., Valdembri, D., Askari, J. A., Li, Z., Caswell, P. T., Zhu, C., Humphries, M. J., Ballestrem, C., & Serini, G. (2022) · Life Science Alliance · doi:10.26508/lsa.202201388 · Cited by 6
Expression of Nucleolin Affects Microtubule Dynamics
Gaume, X., Place, C., Delage, H., Mongélard, F., Monier, K., & Bouvet, P. (2016) · PLoS ONE · doi:10.1371/journal.pone.0157534 · Cited by 6
Microtubules keep large cells in shape
Meiring, J. C. M., & Akhmanova, A. S. (2020) · The Journal of Cell Biology · doi:10.1083/jcb.202004031 · Cited by 5
Effects of the interaction between hydroxyapatite nanoparticles and hepatoma cells
Yin, M., Xu, W., Cui, B., Dai, H., Han, Y., Yin, Y., & Li, S. (2014) · Journal of Wuhan University of Technology-Mater Sci Ed · doi:10.1007/s11595-014-0970-z · Cited by 6
McNiven, M. A., & Razidlo, G. L. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-394447-4.30030-x · Cited by 6
Braun, A., Caesar, N. M., Dang, K., & Myers, K. A. (2016) · Journal of Visualized Experiments · doi:10.3791/54265 · Cited by 5
Ouzounidis, V. R., Green, M., van Capelle, C. D. C., Gebhardt, C., Crellin, H. A., Finlayson, C., Prevo, B., & Cheerambathur, D. K. (2024) · Molecular Biology of the Cell · doi:10.1091/mbc.e23-08-0325 · Cited by 4
Njangiru, I. K., Bózsity, N., Resch, V. E., Paragi, G., Frank, É., Balogh, G. T., Zupkó, I., & Minorics, R. (2024) · Pharmaceutics · doi:10.3390/pharmaceutics16050622 · Cited by 5
Itou, J., Tsukihara, H., Nukatsuka, M., Toi, M., & Takechi, T. (2018) · Cancer Medicine · doi:10.1002/cam4.1265 · Cited by 4
The Actin Cytoskeleton and the Regulation of Cell Migration
Lee, J. M. (2013) · Colloquium Series on Building Blocks of the Cell Cell Structure and Function · doi:10.4199/c00083ed1v01y201305bbc005 · Cited by 3
Rab11-Mediated Focal Adhesion Turnover in Sarcoma Cell Migration
Kao, L.-Y., & Chao, W. (2021) · The Chinese Journal of Physiology · doi:10.4103/cjp.cjp_90_20 · Cited by 3
Peng, P., Sun, J., Li, M., Cheng, R.-X., Liu, S., Qin, M., Zhang, J., & Huang, J.-A. (2025) · World Journal of Gastrointestinal Oncology · doi:10.4251/wjgo.v17.i5.104686 · Cited by 2
Park, S., Lee, S. S., Kim, S., Lee, Y. G., Park, G., Kim, J. O., & Choi, J. H. (2025) · Molecular Oncology · doi:10.1002/1878-0261.13779 · Cited by 2
Rodríguez‐Fernández, J. L., & de Lacoba, M. G. (2015) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2015.05.029 · Cited by 2
Chen, C., Huang, H.-P., Jang, L., & Wang, M.-H. (2021) · Electrochimica Acta · doi:10.1016/j.electacta.2021.139009 · Cited by 2
In vitro studies of actin-microtubule coordination
López, M. P. (2015) · Digital Academic REpository of VU University Amsterdam (Vrije Universiteit Amsterdam) · Cited by 2
Rafiq, N. M., Nishimura, Y., Plotnikov, S. V., Thiagarajan, V., Zhang, Z., Natarajan, M., Shi, S., Viasnoff, V., Jones, G. E., Kanchanawong, P., et al. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/195495 · Cited by 2
MACF1 Facilitates SMAD7 Nuclear Translocation to Drive Bone Formation in MicePreprint
Zhao, F., Ma, X., Qiu, W., Wang, P., Zhang, R., Chen, Z., Su, P., Zhang, Y., Li, D., Ma, J., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/743930 · Cited by 2
Eisenberg, S. C., Dey, A., Birnbaum, R., & Sharp, D. J. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.09.04.282657 · Cited by 2
Membrane tension spatially organizes lysosomal exocytosisPreprint
Lachuer, H., Le, L., Lévêque‐Fort, S., Goud, B., & Schauer, K. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.04.22.489160 · Cited by 2
McNiven, M. A., & Razidlo, G. L. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-821618-7.30030-x · Cited by 2
Specialized actin nanoscale layers control focal adhesion turnoverPreprint
Kumari, R., Ven, K., Chastney, M. R., Peränen, J., Aaron, J., Almeida-Souza, L., Kremneva, E., Poincloux, R., Chew, T., Gunning, P. W., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.15.528622 · Cited by 2
Engagement, Reception and Breakup: Three Steps of Cell Motility regulated by HPIP signaling
(2015) · Cancer Cell & Microenvironment · doi:10.14800/ccm.660 · Cited by 1
Bioimaging with photonic crystal enhanced microscopy
Zhuo, Y. (2014) · Illinois Digital Environment for Access to Learning and Scholarship (University of Illinois at Urbana-Champaign) · Cited by 1
Shakhov, A. S., & Alieva, I. B. (2020) · IntechOpen eBooks · doi:10.5772/intechopen.93524 · Cited by 1
Armitage, S. K., & Plotnikov, S. V. (2016) · eLife · doi:10.7554/elife.19733 · Cited by 1
Microtubule Plus‐End‐Tracking Proteins
Pereira, A. L., & Maiato, H. (2015) · Wiley eBooks · doi:10.1002/9780470015902.a0025979 · Cited by 2
Metadata
- Authors
- Stehbens, S., & Wittmann, T.
- Affiliations
- University of California, San Francisco (US)
- Corresponding author
- Wittmann, Torsten
- Venue
- Journal of Cell Biology
- Publisher
- Rockefeller University Press
- Published
- 2012-08-20
- Volume
- 198
- Issue
- 4
- Pages
- 481-489
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- PMC
- PMC3514042
- OpenAlex
- W2102283558
- Cited by
- 244
- References
- 111
- Citations by year
- 2026: 8 · 2025: 9 · 2024: 9 · 2023: 12 · 2022: 12 · 2021: 15 · 2020: 19 · 2019: 25 · 2018: 21 · 2017: 16 · 2016: 30 · 2015: 20 · 2014: 28 · 2013: 18 · 2012: 2
- FWCI
- 2.00
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- The Journal of Cell Biology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- National Institute of General Medical Sciences (R01GM079139)
- National Center for Research Resources (C06RR16490, C06RR016490, S10RR026758)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Health Sciences › Medicine › Immunology and Allergy › Cell Adhesion Molecules Research
- Keywords
- microtubules, focal adhesions, cell migration, integrins, extracellular matrix, microtubule plus-end tracking proteins, Rho GTPase signaling, endocytosis, clathrin, matrix metalloproteinases, focal adhesion turnover, cell polarity
- MeSH terms
- Animals, Endocytosis, Extracellular Matrix, Humans, Microtubules, Signal Transduction, Focal Adhesions
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review