The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
The small GTP-binding protein rho regulates the assembly of focal adhesions and actin stress fibers in response to growth factors
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.
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
Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
LAEMMLI, U. K. (1970) · Nature · doi:10.1038/227680a0 · Cited by 249,961
Greenberg, S., el Khoury, J., di Virgilio, F., Kaplan, E. M., & Silverstein, S. C. (1991) · The Journal of cell biology · doi:10.1083/jcb.113.4.757 · Cited by 171
Cited by
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
Rho GTPases and their effector proteins
BISHOP, A. L., & HALL, A. (2000) · Biochemical Journal · doi:10.1042/bj3480241 · Cited by 2,575
Self-citationFormation of actin stress fibers and focal adhesions enhanced by Rho-kinase
Amano, M., Chihara, K., Kimura, K., Fukata, Y., Nakamura, N., Matsuura, Y., & Kaibuchi, K. (1997) · Science · doi:10.1126/science.275.5304.1308 · Cited by 1,077
Identification of two distinct mechanisms of phagocytosis controlled by different Rho GTPases
Caron, E., & Hall, A. (1998) · Science · doi:10.1126/science.282.5394.1717 · Cited by 1,019
Self-citationCaspase-3-mediated cleavage of ROCK I induces MLC phosphorylation and apoptotic membrane blebbing
Sebbagh, M., Renvoizé, C., Hamelin, J., Riché, N., Bertoglio, J., & Bréard, J. (2001) · Nature Cell Biology · doi:10.1038/35070019 · Cited by 915
Tager, A. M., LaCamera, P., Shea, B. S., Campanella, G. S., Selman, M., Zhao, Z., Polosukhin, V., Wain, J., Karimi-Shah, B. A., Kim, N. D., et al. (2008) · Nature Medicine · doi:10.1038/nm1685 · Cited by 823
Phagocytosis and the actin cytoskeleton
May, R. C., & Machesky, L. M. (2001) · Journal of Cell Science · doi:10.1242/jcs.114.6.1061 · Cited by 715
Activation of Rac1, RhoA, and mitogen-activated protein kinases is required for Ras transformation
Khosravi-Far, R., Solski, P. A., Clark, G. J., Kinch, M. S., & Der, C. J. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.11.6443 · Cited by 683
Differential Localization of Rho Gtpases in Live Cells
Michaelson, D., Silletti, J., Murphy, G., D'Eustachio, P., Rush, M., & Philips, M. R. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.152.1.111 · Cited by 679
Lang, P., Gesbert, F., Delespine‐Carmagnat, M., Stancou, R., Pouchelet, M., & Bertoglio, J. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00383.x · Cited by 558
A role for Rho in Ras transformation
Qiu, R. G., Chen, J., McCormick, F., & Symons, M. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.25.11781 · Cited by 533
Sturgeon, C., & Fasano, A. (2016) · Tissue Barriers · doi:10.1080/21688370.2016.1251384 · Cited by 497
Cerione, R. A., & Zheng, Y. (1996) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(96)80068-8 · Cited by 437
Wound healing recapitulates morphogenesis in Drosophila embryos
Wood, W., Jacinto, A., Grose, R., Woolner, S., Gale, J., Wilson, C., & Martin, P. (2002) · Nature Cell Biology · doi:10.1038/ncb875 · Cited by 435
folded gastrulation , cell shape change and the control of myosin localization
Dawes-Hoang, R. E., Parmar, K. M., Christiansen, A. E., Phelps, C. B., Brand, A. H., & Wieschaus, E. F. (2005) · Development · doi:10.1242/dev.01938 · Cited by 414
Focal adhesions, stress fibers and mechanical tension
Burridge, K., & Guilluy, C. (2016) · Experimental Cell Research · doi:10.1016/j.yexcr.2015.10.029 · Cited by 409
Fc-receptor-mediated phagocytosis is regulated by mechanical properties of the target
Beningo, K. A., & Wang, Y.-L. (2002) · Journal of Cell Science · doi:10.1242/jcs.115.4.849 · Cited by 389
Mitogenic signaling via G protein-coupled receptors
van BIESEN, T., LUTTRELL, L. M., HAWES, B. E., & LEFKOWITZ, R. J. (1996) · Endocrine Reviews · doi:10.1210/edrv-17-6-698 · Cited by 361
Tight junction modulation and its relationship to drug delivery
SALAMA, N., EDDINGTON, N., & FASANO, A. (2006) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2006.01.003 · Cited by 357
Intracellular signaling in M‐CSF‐induced microglia activation: Role of Iba1
Imai, Y., & Kohsaka, S. (2002) · Glia · doi:10.1002/glia.10149 · Cited by 359
Ehrlich, J. S., Hansen, M. D. H., & Nelson, W. J. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00216-2 · Cited by 358
Structural and Functional Regulation of Tight Junctions by RhoA and Rac1 Small GTPases
Jou, T.-S., Schneeberger, E. E., & James Nelson, W. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.142.1.101 · Cited by 354
Vaezi, A., Bauer, C., Vasioukhin, V., & Fuchs, E. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00259-9 · Cited by 349
Bridging Ral GTPase to Rho Pathways
Jullien-Flores, V., Dorseuil, O., Romero, F., Letourneur, F., Saragosti, S., Berger, R., Tavitian, A., Gacon, G., & Camonis, J. H. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.38.22473 · Cited by 338
Shutes, A., Onesto, C., Picard, V., Leblond, B., Schweighoffer, F., & Der, C. J. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m703571200 · Cited by 336
α-Smooth Muscle Actin Is Crucial for Focal Adhesion Maturation in Myofibroblasts
Hinz, B., Dugina, V., Ballestrem, C., Wehrle-Haller, B., & Chaponnier, C. (2003) · Molecular Biology of the Cell · doi:10.1091/mbc.e02-11-0729 · Cited by 322
Serra‐Pagès, C., Kedersha, N. L., Fazikas, L., Medley, Q., Debant, A., & Streuli, M. (1995) · The EMBO Journal · doi:10.1002/j.1460-2075.1995.tb07282.x · Cited by 321
Dynamic actin-based epithelial adhesion and cell matching during Drosophila dorsal closure
Jacinto, A., Wood, W., Balayo, T., Turmaine, M., Martinez-Arias, A., & Martin, P. (2000) · Current Biology · doi:10.1016/s0960-9822(00)00796-x · Cited by 315
Cantor, S. B., Urano, T., & Feig, L. A. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.8.4578 · Cited by 310
Ren, Y., Li, R., Zheng, Y., & Busch, H. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.52.34954 · Cited by 295
Hepatic stellate cells: role in microcirculation and pathophysiology of portal hypertension
Reynaert, H., Thompson, M. G., Thomas, T., & Geerts, A. (2002) · Gut · doi:10.1136/gut.50.4.571 · Cited by 289
Davis, M. J., Earley, S., Li, Y.-S., & Chien, S. (2023) · Physiological Reviews · doi:10.1152/physrev.00053.2021 · Cited by 273
Ridley, A. J., Self, A. J., Kasmi, F., Paterson, H. F., Hall, A., Marshall, C. J., & Ellis, C. (1993) · The EMBO Journal · doi:10.1002/j.1460-2075.1993.tb06210.x · Cited by 238
Self-citationβ-Actin Messenger RNA Localization and Protein Synthesis Augment Cell Motility
Kislauskis, E. H., Zhu, X.-C., & Singer, R. H. (1997) · The Journal of Cell Biology · doi:10.1083/jcb.136.6.1263 · Cited by 230
RGS-containing RhoGEFs: the missing link between transforming G proteins and Rho?
Fukuhara, S., Chikumi, H., & Gutkind, J. S. (2001) · Oncogene · doi:10.1038/sj.onc.1204182 · Cited by 219
Overexpression of the rhoC gene correlates with progression of ductal adenocarcinoma of the pancreas
Suwa, H., Ohshio, G., Imamura, T., Watanabe, G., Arii, S., Imamura, M., Narumiya, S., Hiai, H., & Fukumoto, M. (1998) · British Journal of Cancer · doi:10.1038/bjc.1998.23 · Cited by 218
Direct Activation of RhoA by Reactive Oxygen Species Requires a Redox-Sensitive Motif
Aghajanian, A., Wittchen, E. S., Campbell, S. L., & Burridge, K. (2009) · PLoS ONE · doi:10.1371/journal.pone.0008045 · Cited by 208
Li, H., Wu, G., Ware, D., Davis, K. R., & Yang, Z. (1998) · Plant Physiology · doi:10.1104/pp.118.2.407 · Cited by 194
Interactions between the bud emergence proteins Bem1p and Bem2p and Rho-type GTPases in yeast.
Peterson, J., Zheng, Y., Bender, L., Myers, A., Cerione, R., & Bender, A. (1994) · The Journal of cell biology · doi:10.1083/jcb.127.5.1395 · Cited by 197
Lamarche, N., & Hall, A. (1994) · Trends in Genetics · doi:10.1016/0168-9525(94)90114-7 · Cited by 196
Self-citationRho family GTPases: more than simple switches
Symons, M., & Settleman, J. (2000) · Trends in Cell Biology · doi:10.1016/s0962-8924(00)01832-8 · Cited by 195
Inhibition of bone resorption by alendronate and risedronate does not require osteoclast apoptosis.
Halasy-Nagy, J. M., Rodan, G. A., & Reszka, A. A. (2001) · Bone · doi:10.1016/s8756-3282(01)00615-9 · Cited by 190
Angiopoietin-2 Is Critical for Cytokine-Induced Vascular Leakage
Benest, A. V., Kruse, K., Savant, S., Thomas, M., Laib, A. M., Loos, E. K., Fiedler, U., & Augustin, H. G. (2013) · PLoS ONE · doi:10.1371/journal.pone.0070459 · Cited by 178
van Horck, F. P. G., Ahmadian, M. R., Haeusler, L. C., Moolenaar, W. H., & Kranenburg, O. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m003839200 · Cited by 174
Wnt4 from the Niche Controls the Mechano-Properties and Quiescent State of Muscle Stem Cells
Eliazer, S., Muncie, J. M., Christensen, J., Sun, X., D’Urso, R. S., Weaver, V. M., & Brack, A. S. (2019) · Cell Stem Cell · doi:10.1016/j.stem.2019.08.007 · Cited by 171
“Rho regulates the formation of stress fibers and focal adhesions (Ridley and Hall, 1992).”
BackgroundFASANO, A. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb05244.x · Cited by 169
PAK4 mediates morphological changes through the regulation of GEF-H1
Callow, M. G., Zozulya, S., Gishizky, M. L., Jallal, B., & Smeal, T. (2005) · Journal of Cell Science · doi:10.1242/jcs.02313 · Cited by 169
Protein prenylation: more than just glue?
Cox, A. D., & Der, C. J. (1992) · Current Opinion in Cell Biology · doi:10.1016/0955-0674(92)90133-w · Cited by 169
Distinct functions of Rho and Rac are required for convergent extension during Xenopus gastrulation
Tahinci, E., & Symes, K. (2003) · Developmental Biology · doi:10.1016/s0012-1606(03)00206-9 · Cited by 162
CMS: An adapter molecule involved in cytoskeletal rearrangements
Kirsch, K. H., Georgescu, M.-M., Ishimaru, S., & Hanafusa, H. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.11.6211 · Cited by 162
Autophagy is required for ectoplasmic specialization assembly in sertoli cells
Liu, C., Wang, H., Shang, Y., Liu, W., Song, Z., Zhao, H., Wang, L., Jia, P., Gao, F., Xu, Z., et al. (2016) · Autophagy · doi:10.1080/15548627.2016.1159377 · Cited by 154
Fibroblast migration is mediated by CD44-dependent TGFβ activation
Acharya, P. S., Majumdar, S., Jacob, M., Hayden, J., Mrass, P., Weninger, W., Assoian, R. K., & Puré, E. (2008) · Journal of Cell Science · doi:10.1242/jcs.021683 · Cited by 157
Autophagy regulates spermatid differentiation via degradation of PDLIM1
Shang, Y., Wang, H., Jia, P., Zhao, H., Liu, C., Liu, W., Song, Z., Xu, Z., Yang, L., Wang, Y., et al. (2016) · Autophagy · doi:10.1080/15548627.2016.1192750 · Cited by 154
Li, X., Bu, X., Lu, B., Avraham, H., Flavell, R. A., & Lim, B. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.4.1158-1171.2002 · Cited by 153
Cucurbitacin E-induced disruption of the actin and vimentin cytoskeleton in prostate carcinoma cells
Duncan, K. L. K., Duncan, M. D., Alley, M. C., & Sausville, E. A. (1996) · Biochemical Pharmacology · doi:10.1016/s0006-2952(96)00557-6 · Cited by 151
Barcia, C., Ros, C. M., Annese, V., Carrillo-de Sauvage, M. A., Ros-Bernal, F., Gómez, A., Yuste, J. E., Campuzano, C. M., de Pablos, V., Fernandez-Villalba, E., et al. (2012) · Scientific Reports · doi:10.1038/srep00809 · Cited by 150
Structure and mutagenesis of the Dbl homology domain
Aghazadeh, B., Zhu, K., Kubiseski, T. J., Liu, G. A., Pawson, T., Zheng, Y., & Rosen, M. K. (1998) · Nature Structural Biology · doi:10.1038/4209 · Cited by 145
Polarized Distribution of Endogenous Rac1 and RhoA at the Cell Surface
Michaely, P. A., Mineo, C., Ying, Y.-S., & Anderson, R. G. W. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.30.21430 · Cited by 139
RHO GTPases: from new partners to complex immune syndromes
El Masri, R., & Delon, J. (2021) · Nature Reviews Immunology · doi:10.1038/s41577-021-00500-7 · Cited by 131
A GDP Dissociation Inhibitor That Serves as a GTPase Inhibitor for the Ras-Like Protein CDC42Hs
Hart, M. J., Maru, Y., Leonard, D., Witte, O. N., Evans, T., & Cerione, R. A. (1992) · Science · doi:10.1126/science.1439791 · Cited by 130
The endothelial cytoskeleton as a target of electroporation-based therapies
Kanthou, C., Kranjc, S., Sersa, G., Tozer, G., Zupanic, A., & Cemazar, M. (2006) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-06-0410 · Cited by 129
Critical Role of Actin in Modulating BBB Permeability
Lai, C.-H., Kuo, K.-H., & Leo, J. M. (2005) · Brain Research Reviews · doi:10.1016/j.brainresrev.2005.03.007 · Cited by 129
Luchsinger, L. L., Patenaude, C. A., Smith, B. D., & Layne, M. D. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.276931 · Cited by 127
Characterization of EHT 1864, a novel small molecule inhibitor of Rac family small GTPases
(2008) · Methods in Enzymology · doi:10.1016/s0076-6879(07)00409-0 · Cited by 126
Rac GTPase interacts with GAPs and target proteins through multiple effector sites.
Diekmann, D., Nobes, C. D., Burbelo, P. D., Abo, A., & Hall, A. (1995) · The EMBO Journal · doi:10.1002/j.1460-2075.1995.tb00214.x · Cited by 123
Self-citationHinchliffe (1998) · doi:10.1016/s0005-2760(98)00140-4 · Cited by 110
A selective ROCK inhibitor, Y27632, prevents dimethylnitrosamine-induced hepatic fibrosis in rats
Tada, S., Iwamoto, H., Nakamuta, M., Sugimoto, R., Enjoji, M., Nakashima, Y., & Nawata, H. (2001) · Journal of Hepatology · doi:10.1016/s0168-8278(00)00059-3 · Cited by 102
Regulation of mitochondria distribution by RhoA and formins
Minin, A. A., Kulik, A. V., Gyoeva, F. K., Li, Y., Goshima, G., & Gelfand, V. I. (2006) · Journal of Cell Science · doi:10.1242/jcs.02762 · Cited by 102
Nakazawa, T., Watabe, A. M., Tezuka, T., Yoshida, Y., Yokoyama, K., Umemori, H., Inoue, A., Okabe, S., Manabe, T., & Yamamoto, T. (2003) · Molecular Biology of the Cell · doi:10.1091/mbc.e02-09-0623 · Cited by 100
Meiri, D., Marshall, C. B., Greeve, M. A., Kim, B., Balan, M., Suarez, F., Bakal, C., Wu, C., LaRose, J., Fine, N., et al. (2012) · Molecular Cell · doi:10.1016/j.molcel.2012.01.027 · Cited by 98
Adra, C. N., Manor, D., Ko, J. L., Zhu, S., Horiuchi, T., Van Aelst, L., Cerione, R. A., & Lim, B. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.9.4279 · Cited by 97
The RhoA/ROCK-I/MLC pathway is involved in the ethanol-induced apoptosis by anoikis in astrocytes
Miñambres, R., Guasch, R. M., Perez-Aragó, A., & Guerri, C. (2006) · Journal of Cell Science · doi:10.1242/jcs.02723 · Cited by 94
Role of Rho GTPase in astrocyte morphology and migratory response during in vitro wound healing
Höltje, M., Hoffmann, A., Hofmann, F., Mucke, C., Große, G., Van Rooijen, N., Kettenmann, H., Just, I., & Ahnert‐Hilger, G. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03443.x · Cited by 94
The Rho GTPases in Macrophage Motility and Chemotaxis
Jones, G. E., Allen, W. E., & Ridley, A. J. (1998) · Cell Adhesion and Communication · doi:10.3109/15419069809004479 · Cited by 89
Self-citationBabbin, B. A., Parkos, C. A., Mandell, K. J., Winfree, L. M., Laur, O., Ivanov, A. I., & Nusrat, A. (2007) · The American Journal of Pathology · doi:10.2353/ajpath.2007.060647 · Cited by 89
Role of transglutaminase II in retinoic acid-induced activation of RhoA-associated kinase-2
Singh, U. S., Kunar, M. T., Kao, Y., & Baker, K. M. (2001) · The EMBO Journal · doi:10.1093/emboj/20.10.2413 · Cited by 88
Scott, G., Leopardi, S., Parker, L., Babiarz, L., Seiberg, M., & Han, R. (2003) · Journal of Investigative Dermatology · doi:10.1046/j.1523-1747.2003.12427.x · Cited by 87
Hansen, S. H., Zegers, M. M. P., Woodrow, M., Rodriguez-Viciana, P., Chardin, P., Mostov, K. E., & McMahon, M. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.24.9364-9375.2000 · Cited by 85
HDAC6 and RhoA are novel players in Abeta-driven disruption of neuronal polarity
Tsushima, H., Emanuele, M., Polenghi, A., Esposito, A., Vassalli, M., Barberis, A., Difato, F., & Chieregatti, E. (2015) · Nature Communications · doi:10.1038/ncomms8781 · Cited by 71
Fine Tuning Muscarinic Acetylcholine Receptor Signaling Through Allostery and Bias
van der Westhuizen, E. T., Choy, K. H. C., Valant, C., McKenzie-Nickson, S., Bradley, S. J., Tobin, A. B., Sexton, P. M., & Christopoulos, A. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.606656 · Cited by 63
Seipel, K., Medley, Q. G., Kedersha, N. L., Zhang, X. A., O’Brien, S. P., Serra-Pages, C., Hemler, M. E., & Streuli, M. (1999) · Journal of Cell Science · doi:10.1242/jcs.112.12.1825 · Cited by 62
Ras-related GTPase RhoB Represses NF-κB Signaling
Fritz, G., & Kaina, B. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m005058200 · Cited by 57
Scaffold-Mediated Immunoengineering as Innovative Strategy for Tendon Regeneration
Russo, V., El Khatib, M., Prencipe, G., Cerveró-Varona, A., Citeroni, M. R., Mauro, A., Berardinelli, P., Faydaver, M., Haidar-Montes, A. A., Turriani, M., et al. (2022) · Cells · doi:10.3390/cells11020266 · Cited by 49
Controlling Major Cellular Processes of Human Mesenchymal Stem Cells using Microwell Structures
Xu, X., Wang, W., Kratz, K., Fang, L., Li, Z., Kurtz, A., Ma, N., & Lendlein, A. (2014) · Advanced Healthcare Materials · doi:10.1002/adhm.201400415 · Cited by 49
GRAMD1B regulates cell migration in breast cancer cells through JAK/STAT and Akt signaling
Khanna, P., Lee, J. S., Sereemaspun, A., Lee, H., & Baeg, G. H. (2018) · Scientific Reports · doi:10.1038/s41598-018-27864-6 · Cited by 48
Matsui, A., Okigaki, M., Amano, K., Adachi, Y., Jin, D., Takai, S., Yamashita, T., Kawashima, S., Kurihara, T., Miyazaki, M., et al. (2007) · Circulation · doi:10.1161/circulationaha.106.645416 · Cited by 47
Rho GTPases in neurodegeneration diseases
DeGeer, J., & Lamarche-Vane, N. (2013) · Experimental Cell Research · doi:10.1016/j.yexcr.2013.06.016 · Cited by 46
Prestress and Adhesion Site Dynamics Control Cell Sensitivity to Extracellular Stiffness
Féréol, S., Fodil, R., Laurent, V. M., Balland, M., Louis, B., Pelle, G., Hénon, S., Planus, E., & Isabey, D. (2009) · Biophysical Journal · doi:10.1016/j.bpj.2008.10.072 · Cited by 43
Dual Roles for RHOA/RHO-Kinase In the Regulated Trafficking of a Voltage-sensitive Potassium Channel
Stirling, L., Williams, M. R., & Morielli, A. D. (2009) · Molecular Biology of the Cell · doi:10.1091/mbc.e08-10-1074 · Cited by 45
Nicolaou, F., Teodoridis, J. M., Park, H., Georgakis, A., Farokhzad, O. C., Böttinger, E. P., Da Silva, N., Rousselot, P., Chomienne, C., Ferenczi, K., et al. (2003) · Blood · doi:10.1182/blood-2002-01-0324 · Cited by 39
Amado-Azevedo, J., Valent, E. T., & Van Nieuw Amerongen, G. P. (2014) · Cell and Tissue Research · doi:10.1007/s00441-014-1828-6 · Cited by 36
Dock2 participates in bone marrow lympho-hematopoiesis
Kikuchi, T., Kubonishi, S., Shibakura, M., Namba, N., Matsui, T., Fukui, Y., Tanimoto, M., & Katayama, Y. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.12.093 · Cited by 16
Gαz Inhibits Serum Response Factor-Dependent Transcription by Inhibiting Rho Signaling
Dutt, P., Jaffe, A. B., Merdek, K. D., Hall, A., & Toksoz, D. (2004) · Molecular Pharmacology · doi:10.1124/mol.104.002949 · Cited by 13
Self-citationCarrizales, M. G., Boulton, A. D., & Koleske, A. J. (2025) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2025.110429 · Cited by 2
Meiring, J. C. M., Mahapatra, V., Liu, R., Gravett, M. S. C., Morren, D., Saunders, H. A. J., Choi, S. R., Pelster José, A., Karhanova, A., Metallidou, I., et al. (2026) · Nature Cell Biology · doi:10.1038/s41556-026-02079-4
Metadata
- Authors
- Ridley, A. J., & Hall, A.
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 1992-08
- Volume
- 70
- Issue
- 3
- Pages
- 389-399
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W2007660746
- Cited by
- 4,468
- References
- 2
- FWCI
- 61.33
- Type
- journal article
- Language
- en
- Open access
- closed
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
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.