The DOI matches its Crossref record; 31 of the 31 references it cites were found in a registry or an index.
Silberblick/Wnt11 mediates convergent extension movements during zebrafish gastrulation
Abstract
Vertebrate gastrulation involves the specification and coordinated movement of large populations of cells that give rise to the ectodermal, mesodermal and endodermal germ layers. Although many of the genes involved in the specification of cell identity during this process have been identified, little is known of the genes that coordinate cell movement. Here we show that the zebrafish silberblick (slb) locus encodes Wnt11 and that Slb/Wnt11 activity is required for cells to undergo correct convergent extension movements during gastrulation. In the absence of Slb/Wnt11 function, abnormal extension of axial tissue results in cyclopia and other midline defects in the head. The requirement for Slb/Wnt11 is cell non-autonomous, and our results indicate that the correct extension of axial tissue is at least partly dependent on medio-lateral cell intercalation in paraxial tissue. We also show that the slb phenotype is rescued by a truncated form of Dishevelled that does not signal through the canonical Wnt pathway, suggesting that, as in flies, Wnt signalling might mediate morphogenetic events through a divergent signal transduction cascade. Our results provide genetic and experimental evidence that Wnt activity in lateral tissues has a crucial role in driving the convergent extension movements underlying vertebrate gastrulation.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“The evidence in zebrafish demonstrated that injection of Wnt11 RNA into the two-cell stage embryo was sufficient to rescue the gastrulation defects observed in the silberblick mutant, indicating that localized expression of Wnt11 was not required and thus its role was permissive.89”
From Wnt signal transduction pathways (2008) · cites this paper as [89]
Citations
Cites
Wnt signaling: a common theme in animal development
Cadigan, K. M., & Nusse, R. (1997) · Genes & Development · doi:10.1101/gad.11.24.3286 · Cited by 2,567
XTcf-3 Transcription Factor Mediates β-Catenin-Induced Axis Formation in Xenopus Embryos
Molenaar, M., van de Wetering, M., Oosterwegel, M., Peterson-Maduro, J., Godsave, S., Korinek, V., Roose, J., Destrée, O., & Clevers, H. (1996) · Cell · doi:10.1016/s0092-8674(00)80112-9 · Cited by 1,824
Boutros, M., Paricio, N., Strutt, D. I., & Mlodzik, M. (1998) · Cell · doi:10.1016/s0092-8674(00)81226-x · Cited by 801
Tada, M., & Smith, J. C. (2000) · Development · doi:10.1242/dev.127.10.2227 · Cited by 675
Self-citationAxelrod, J. D., Miller, J. R., Shulman, J. M., Moon, R. T., & Perrimon, N. (1998) · Genes & Development · doi:10.1101/gad.12.16.2610 · Cited by 659
Cell movements during epiboly and gastrulation in zebrafish
Warga, R. M., & Kimmel, C. B. (1990) · Development · doi:10.1242/dev.108.4.569 · Cited by 562
Molecular mechanisms of male germ cell differentiation
Hecht, N. B. (1998) · BioEssays · doi:10.1002/(sici)1521-1878(199807)20:7 · Cited by 434
Head induction by simultaneous repression of Bmp and Wnt signalling in Xenopus
Glinka, A., Wu, W., Onichtchouk, D., Blumenstock, C., & Niehrs, C. (1997) · Nature · doi:10.1038/39092 · Cited by 350
Barth, K. A., & Wilson, S. W. (1995) · Development · doi:10.1242/dev.121.6.1755 · Cited by 332
Self-citationMoon, R. T., Campbell, R. M., Christian, J. L., McGrew, L. L., Shih, J., & Fraser, S. E. (1993) · Development · doi:10.1242/dev.119.1.97 · Cited by 330
Cited by
Sorted by citations
Items 201–300 of 1,000
Canonical WNT/β-catenin signaling is required for ureteric branching
Bridgewater, D. J., Cox, B., Cain, J. E., Lau, A., Athaide, V., Gill, P. S., Kuure, S., Sainio, K., & Rosenblum, N. D. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2008.02.010 · Cited by 150
Reconciling different models of forebrain induction and patterning: a dual role for the hypoblast
Foley, A. C., Skromne, I., & Stern, C. D. (2000) · Development · doi:10.1242/dev.127.17.3839 · Cited by 150
Caneparo, L., Huang, Y., Staudt, N. D., Tada, M., Ahrendt, R., Kazanskaya, O., Niehrs, C., & Houart, C. (2007) · Genes & Development · doi:10.1101/gad.406007 · Cited by 150
Self-citationYu, H. M., Ye, X., Guo, N., & Nathans, J. (2012) · Development · doi:10.1242/dev.083352 · Cited by 146
Ikeya, M., & Takada, S. (2001) · Mechanisms of Development · doi:10.1016/s0925-4773(01)00338-0 · Cited by 149
Manil-Ségalen, M., Johnston, C. A., Martin, C. A., Dumortier, J. G., Prehoda, K. E., David, N. B., Doe, C. Q., & Bellaı̈che, Y. (2010) · Developmental Cell · doi:10.1016/j.devcel.2010.10.004 · Cited by 156
The chordate amphioxus: an emerging model organism for developmental biology
Holland, L. Z., Laudet, V., & Schubert, M. (2004) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-004-4075-2 · Cited by 148
Jülich, D., Lim, C. H., Round, J. E., Nicolaije, C., Schroeder, J., Davies, A., Geisler, R., Lewis, J. H., Jiang, Y., & Holley, S. A. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.06.040 · Cited by 146
Self-citationCha, S., Tadjuidje, E., Tao, Q., Wylie, C. C., & Heasman, J. (2008) · Development · doi:10.1242/dev.029025 · Cited by 153
Wnt'er in liver: Expression of Wnt and frizzled genes in mouse
Zeng, G., Awan, F. T., Otruba, W., Stock, P., Apte, U. M., Tan, X., Gandhi, C. R., Demetris, A. J., & Monga, S. P. (2006) · Hepatology · doi:10.1002/hep.21473 · Cited by 146
Multiple Mechanisms for Wnt11-mediated Repression of the Canonical Wnt Signaling Pathway
Maye, P. F., Zheng, J., Li, L., & Wu, D. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m311724200 · Cited by 144
PTK7 is essential for polarized cell motility and convergent extension during mouse gastrulation
Yen, W., Williams, M. K., Periasamy, A., Conaway, M. R., Burdsal, C. A., Keller, R. E., Lu, X., & Sutherland, A. E. (2009) · Development · doi:10.1242/dev.030601 · Cited by 140
A quest for the mechanism regulating global planar cell polarity of tissues
Wu, J., & Mlodzik, M. (2009) · Trends in Cell Biology · doi:10.1016/j.tcb.2009.04.003 · Cited by 147
Satoh, W., Gotoh, T., Tsunematsu, Y., Aizawa, S., & Shimono, A. (2006) · Development · doi:10.1242/dev.02274 · Cited by 143
DWnt4 Regulates Cell Movement and Focal Adhesion Kinase during Drosophila Ovarian Morphogenesis
Cohen, E. D., Mariol, M., Wallace, R. M. H., Weyers, J., Kamberov, Y. G., Pradel, J., & Wilder, E. L. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00142-9 · Cited by 140
Scholz, C. B., & Technau, U. (2003) · Development Genes and Evolution · doi:10.1007/s00427-002-0272-x · Cited by 142
Wnt/PCP signaling contribution to carcinoma collective cell migration and metastasis
Vandervorst, K., Dreyer, C., Konopelski, S. E., Lee, H., Ho, H.-Y. H., & Carraway, K. (2019) · Cancer Research · doi:10.1158/0008-5472.can-18-2757 · Cited by 105
Wnt11 patterns a myocardial electrical gradient through regulation of the L-type Ca2+ channel
Panáková, D., Werdich, A. A., & MacRae, C. A. (2010) · Nature · doi:10.1038/nature09249 · Cited by 139
Wnt signaling in axon guidance
Zou, Y. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.06.015 · Cited by 138
Wang, X.-N., Li, Z., Ren, Y., Jiang, T., Wang, Y.-Q., Chen, M., Zhang, J., Hao, J., Wang, Y.-B., Sha, R., et al. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003645 · Cited by 128
England, S. J., Blanchard, G. B., Mahadevan, L., & Adams, R. J. (2006) · Development · doi:10.1242/dev.02678 · Cited by 138
Wnt signaling in development and disease
Yang, Y. (2012) · Cell & Bioscience · doi:10.1186/2045-3701-2-14 · Cited by 147
Wharton, K. A., Zimmermann, G., Rousset, R., & Scott, M. P. (2001) · Developmental Biology · doi:10.1006/dbio.2001.0238 · Cited by 140
Bakkers, J., Kramer, C., Pothof, J., Quaedvlieg, N. E. M., Spaink, H. P., & Hammerschmidt, M. (2004) · Development · doi:10.1242/dev.00954 · Cited by 140
Ferrante, M. I., Romio, L., Castro, S., Collins, J. E., Goulding, D., Stemple, D. L., Woolf, A. S., & Wilson, S. W. (2008) · Human Molecular Genetics · doi:10.1093/hmg/ddn356 · Cited by 140
Self-citationPTK7/Otk interacts with Wnts and inhibits canonical Wnt signalling
Peradziryi, H., Kaplan, N., Podleschny, M., Liu, X., Wehner, P., Borchers, A., & Tolwinski, N. S. (2011) · The EMBO Journal · doi:10.1038/emboj.2011.236 · Cited by 135
A systematic genome-wide screen for mutations affecting organogenesis in Medaka, Oryzias latipes
Furutani‐Seiki, M., Sasado, T., Morinaga, C., Suwa, H., Niwa, K., Yoda, H., Deguchi, T., Hirose, Y., Yasuoka, A., Henrich, T., et al. (2004) · Mechanisms of Development · doi:10.1016/j.mod.2004.04.016 · Cited by 135
Ray, R. P., Matamoro‐Vidal, A., Ribeiro, P. S., Tapon, N., Houle, D., Salazar‐Ciudad, I., & Thompson, B. J. (2015) · Developmental Cell · doi:10.1016/j.devcel.2015.06.019 · Cited by 124
Andre, P., Wang, Q., Wang, N., Gao, B., Schilit, A., Halford, M. M., Stacker, S. A., Zhang, X., & Yang, Y. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.414441 · Cited by 130
Wnt/Frizzled Signaling Controls C. elegans Gastrulation by Activating Actomyosin Contractility
Lee, J.-Y., Marston, D. J., Walston, T., Hardin, J. D., Halberstadt, A. I., & Goldstein, B. (2006) · Current Biology · doi:10.1016/j.cub.2006.08.090 · Cited by 137
Identification and mechanism of regulation of the zebrafish dorsal determinant
Lu, F., Thisse, C., & Thisse, B. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1106801108 · Cited by 132
microRNA regulation of Wnt signaling pathways in development and disease
Song, J. L., Nigam, P., Tektas, S. S., & Selva, E. M. (2015) · Cellular Signalling · doi:10.1016/j.cellsig.2015.03.018 · Cited by 133
The Role of Brachyury (T) during Gastrulation Movements in the Sea Urchin Lytechinus variegatus
Gross, J. M., & McClay, D. R. (2001) · Developmental Biology · doi:10.1006/dbio.2001.0426 · Cited by 129
Wnt11 controls cell contact persistence by local accumulation of Frizzled 7 at the plasma membrane
Witzel, S., Zimyanin, V. L., Carreira-Barbosa, F., Tada, M., & Heisenberg, C. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200606017 · Cited by 130
Self-citationPlanar cell polarization requires Widerborst, a B′ regulatory subunit of protein phosphatase 2A
Hannus, M., Feiguin, F. M., Heisenberg, C., & Eaton, S. (2002) · Development · doi:10.1242/dev.129.14.3493 · Cited by 133
Self-citationSatoh, W., Matsuyama, M., Takemura, H., Aizawa, S., & Shimono, A. (2008) · genesis · doi:10.1002/dvg.20369 · Cited by 133
Wnt-3a and Dvl Induce Neurite Retraction by Activating Rho-Associated Kinase
Kishida, S., Yamamoto, H., & Kikuchi, A. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.10.4487-4501.2004 · Cited by 128
Shaping the nervous system: role of the core planar cell polarity genes
Tissir, F., & Goffinet, A. M. (2013) · Nature reviews. Neuroscience · doi:10.1038/nrn3525 · Cited by 134
Planar cell polarity, ciliogenesis and neural tube defects
Wallingford, J. B. (2006) · Human Molecular Genetics · doi:10.1093/hmg/ddl216 · Cited by 127
Wnt signaling during development of the gastrointestinal tract
Theodosiou, N. A., & Tabin, C. J. (2003) · Developmental Biology · doi:10.1016/s0012-1606(03)00185-4 · Cited by 127
Inhibition of the Wnt Signaling Pathway by Idax, a Novel Dvl-Binding Protein
Hino, S.-I., Kishida, S., Michiue, T., Fukui, A., Sakamoto, I., Takada, S., Asashima, M., & Kikuchi, A. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.1.330-342.2001 · Cited by 127
Coming to Consensus: A Unifying Model Emerges for Convergent Extension
Huebner, R. J., & Wallingford, J. B. (2018) · Developmental Cell · doi:10.1016/j.devcel.2018.08.003 · Cited by 123
Wnt Signaling in Mammalian Development: Lessons from Mouse GeneticsPreprint
Wang, J., Sinha, T., & Wynshaw-Boris, A. J. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a007963 · Cited by 126
Wada, H., Iwasaki, M., Sato, T., Masai, I., Nishiwaki, Y., Tanaka, H., Sato, A., Nojima, Y., & Okamoto, H. (2005) · Development · doi:10.1242/dev.01810 · Cited by 129
Das, G., Reynolds-Kenneally, J., & Mlodzik, M. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00147-8 · Cited by 125
Wnt11 facilitates embryonic stem cell differentiation to Nkx2.5-positive cardiomyocytes
Terami, H., Hidaka, K., Katsumata, T., Iio, A., & Morisaki, T. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.10.103 · Cited by 124
TGF-β signaling-mediated morphogenesis: modulation of cell adhesion via cadherin endocytosisPreprint
Ogata, S., Morokuma, J., Hayata, T., Kolle, G., Niehrs, C., Ueno, N., & Cho, K. W. Y. (2007) · Genes & Development · doi:10.1101/gad.1541807 · Cited by 124
Mechanical regulation of early vertebrate embryogenesis
Valet, M., Siggia, E. D., & Brivanlou, A. H. (2021) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-021-00424-z · Cited by 123
Takahashi, M., & Osumi, N. (2002) · Development · doi:10.1242/dev.129.6.1327 · Cited by 123
Progress and challenges in understanding planar cell polarity signaling
Axelrod, J. D. (2009) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2009.08.001 · Cited by 122
Taki, M., Kamata, N., Yokoyama, K., Fujimoto, R., Tsutsumi, S., & Nagayama, M. (2003) · Cancer Science · doi:10.1111/j.1349-7006.2003.tb01488.x · Cited by 122
Dvl2-Dependent Activation of Daam1 and RhoA Regulates Wnt5a-Induced Breast Cancer Cell Migration
Zhu, Y., Tian, Y., Du, J., Hu, Z., Yang, L., Liu, J., & Gu, L. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037823 · Cited by 124
Xenopus paraxial protocadherin has signaling functions and is involved in tissue separation
Medina, A., Swain, R. K., Kuerner, K., & Steinbeißer, H. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600329 · Cited by 122
Molecular genetic cascades for external genitalia formation: An emerging organogenesis program
Yamada, G., Suzuki, K., Haraguchi, R., Miyagawa, S., Satoh, Y., Kamimura, M., Nakagata, N., Kataoka, H., Kuroiwa, A., & Chen, Y. (2006) · Developmental Dynamics · doi:10.1002/dvdy.20807 · Cited by 122
Dishevelled-1 Regulates Microtubule Stability
Krylova, O. Y., Messenger, M. J., & Salinas, P. C. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.151.1.83 · Cited by 124
Molecular specification of germ layers in vertebrate embryos
Kiecker, C. M., Bates, T. J. D., & Bell, E. J. D. H. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-2092-y · Cited by 119
Sørhus, E., Incardona, J. P., Karlsen, Ø., Linbo, T. L., Sørensen, L., Nordtug, T., van der Meeren, T., Thorsen, A., Thorbjørnsen, M., Jentoft, S., et al. (2016) · Scientific Reports · doi:10.1038/srep31058 · Cited by 119
T‐targets: Clues to understanding the functions of T‐box proteins
Tada, M., & Smith, J. C. (2001) · Development Growth & Differentiation · doi:10.1046/j.1440-169x.2001.00556.x · Cited by 118
Self-citationPera, E. M., & Robertis, E. M. D. (2000) · Mechanisms of Development · doi:10.1016/s0925-4773(00)00394-4 · Cited by 117
Mammary Development and Breast Cancer: A Wnt Perspective
Yu, Q. C., Verheyen, E. M., & Zeng, Y. A. (2016) · Cancers · doi:10.3390/cancers8070065 · Cited by 122
Wnt Regulation of Planar Cell Polarity (PCP)
Gao, B. (2012) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-394592-1.00008-9 · Cited by 119
Planar polarity and actin dynamics in the epidermis of Drosophila
Kaltschmidt, J. A., Lawrence, N. J., Morel, V., Balayo, T., Fernández, B. G., Pélissier-Monier, A., Jacinto, A., & Arias, A. M. (2002) · Nature Cell Biology · doi:10.1038/ncb882 · Cited by 115
Analysis of Wnt Gene Expression in Prostate Cancer
Zhu, H., Mazor, M., Kawano, Y., Walker, M. M., Leung, H. Y., Armstrong, K., Waxman, J., & Kypta, R. M. (2004) · Cancer Research · doi:10.1158/0008-5472.can-04-2704 · Cited by 115
Tumor formation due to abnormalities in the β‐catenin‐independent pathway of Wnt signaling
Kikuchi, A., & Yamamoto, H. (2008) · Cancer Science · doi:10.1111/j.1349-7006.2007.00675.x · Cited by 117
Zhu, S., Liu, L., Korzh, V. P., Gong, Z., & Low, B. C. (2005) · Cellular Signalling · doi:10.1016/j.cellsig.2005.05.019 · Cited by 115
Garriock, R. J., D'Agostino, S. L., Pilcher, K. C., & Krieg, P. A. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2004.12.013 · Cited by 114
Genetic analysis of the exed region in mouse
Kendall, S. K., Strong, S. J., Litman, R. T., Litman, G. W., & Magnuson, T. (2000) · genesis · doi:10.1002/1526-968x(200008)27:4
Friction forces position the neural anlage
Smutny, M., Ákos, Z., Grigolon, S., Shamipour, S., Ruprecht, V., Čapek, D., Behrndt, M., Papusheva, E., Tada, M., Hof, B., et al. (2017) · Nature Cell Biology · doi:10.1038/ncb3492 · Cited by 112
Self-citationTorban, E., Kor, C., & Gros, P. (2004) · Trends in Genetics · doi:10.1016/j.tig.2004.09.003 · Cited by 115
A gene regulatory network directed by zebrafish No tail accounts for its roles in mesoderm formation
Morley, R. H., Lachani, K., Keefe, D., Gilchrist, M. J., Flicek, P., Smith, J. C., & Wardle, F. C. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0808382106 · Cited by 111
Self-citationPhysical control of tissue morphogenesis across scales
Stooke‐Vaughan, G. A., & Campàs, O. (2018) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2018.09.002 · Cited by 111
Wang, B., Sinha, T., Jiao, K., Serra, R. A., & Wang, J. (2010) · Human Molecular Genetics · doi:10.1093/hmg/ddq462 · Cited by 111
Sculpting tissues by phase transitions
Lenne, P.-F., & Trivedi, V. (2022) · Nature Communications · doi:10.1038/s41467-022-28151-9 · Cited by 110
Zebrafish Gastrulation: Cell Movements, Signals, and Mechanisms
Rohde, L. A., & Heisenberg, C. (2007) · International review of cytology · doi:10.1016/s0074-7696(07)61004-3 · Cited by 115
Self-citationLele, Z., Bakkers, J., & Hammerschmidt, M. (2001) · genesis · doi:10.1002/gene.1063 · Cited by 110
Wnts and wing: Wnt signaling in vertebrate limb development and musculoskeletal morphogenesis
Yang, Y. (2003) · Birth Defects Research Part C Embryo Today Reviews · doi:10.1002/bdrc.10026 · Cited by 113
Ogon/Secreted Frizzled functions as a negative feedback regulator of Bmp signaling
Yabe, T., Shimizu, T., Muraoka, O., Bae, Y., Hirata, T., Nojima, H., Kawakami, A., Hirano, T., & Hibi, M. (2003) · Development · doi:10.1242/dev.00506 · Cited by 110
Ouko, L., Ziegler, T. R., Gu, L. H., Eisenberg, L. M., & Yang, V. W. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m402877200 · Cited by 109
Non-canonical Wnt signaling in Xenopus: regulation of axis formation and gastrulation
Kühl, M. (2002) · Seminars in Cell and Developmental Biology · doi:10.1016/s1084-9521(02)00050-2 · Cited by 105
Association of Dishevelled with Eph tyrosine kinase receptor and ephrin mediates cell repulsion
Tanaka, M., Kamo, T., Ota, S., & Sugimura, H. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg088 · Cited by 108
Lin, F. H., Sepich, D. S., Chen, S., Topczewski, J., Yin, C., Solnica‐Krezel, L., & Hamm, H. E. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200501104 · Cited by 107
Minegishi, K., Hashimoto, M., Ajima, R., Takaoka, K., Shinohara, K., Ikawa, Y., Nishimura, H., McMahon, A. P., Willert, K., Okada, Y., et al. (2017) · Developmental Cell · doi:10.1016/j.devcel.2017.02.010 · Cited by 107
Ascidian notochord morphogenesis
Jiang, D., & Smith, W. C. (2007) · Developmental Dynamics · doi:10.1002/dvdy.21184 · Cited by 106
Endo, Y., Wolf, V., Muraiso, K., Kamijo, K., Soon, L., Üren, A., Barshishat-Küpper, M., & Rubin, J. S. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m406391200 · Cited by 110
Kim, G., & Han, J. (2005) · Developmental Dynamics · doi:10.1002/dvdy.20262 · Cited by 105
Wnt signal transduction and the formation of the myocardium
Eisenberg, L. M., & Eisenberg, C. A. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.02.014 · Cited by 108
Adhesion remodeling underlying tissue morphogenesis
Lecuit, T. (2004) · Trends in Cell Biology · doi:10.1016/j.tcb.2004.11.007 · Cited by 103
Sokol, S. Y. (2015) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2015.05.002 · Cited by 98
McGreevy, E. M., Vijayraghavan, D. S., Davidson, L. A., & Hildebrand, J. D. (2015) · Biology Open · doi:10.1242/bio.20149589 · Cited by 104
Apical and Basal Matrix Remodeling Control Epithelial Morphogenesis
Díaz-de-la-Loza, M.-D.-C., Ray, R. P., Ganguly, P. S., Alt, S., Davis, J. R., Hoppe, A., Tapon, N., Salbreux, G., & Thompson, B. J. (2018) · Developmental Cell · doi:10.1016/j.devcel.2018.06.006 · Cited by 100
Wu, J., Klein, T. J., & Mlodzik, M. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020158 · Cited by 101
Weidinger, G., & Moon, R. T. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200307181 · Cited by 101
The roles of the cadherins Fat and Dachsous in planar polarity specification in Drosophila
Thomas, C., & Strutt, D. I. (2011) · Developmental Dynamics · doi:10.1002/dvdy.22736 · Cited by 100
Planar cell polarity and vertebrate organogenesis
Karner, C. M., WHARTONJR, K., & Carroll, T. J. (2006) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2006.05.003 · Cited by 99
Dabdoub, A., & Kelley, M. W. (2005) · Journal of Neurobiology · doi:10.1002/neu.20171 · Cited by 98
Stereotypical Cell Division Orientation Controls Neural Rod Midline Formation in Zebrafish
Quesada-Hernández, E., Caneparo, L., Kaufmann, S., Winkler, S., Liebling, M., Fraser, S. E., & Heisenberg, C. (2010) · Current Biology · doi:10.1016/j.cub.2010.10.009 · Cited by 97
Self-citationWnt Signaling in Polycystic Kidney Disease
Benzing, T. R., Simons, M., & Walz, G. (2007) · Journal of the American Society of Nephrology · doi:10.1681/asn.2006121355 · Cited by 100
Turner, D. A., Rué, P., Mackenzie, J. P., Davies, E., & Arias, A. M. (2014) · BMC Biology · doi:10.1186/s12915-014-0063-7 · Cited by 96
Forces shaping the Drosophila wing
de la Loza, M. C. D., & Thompson, B. J. (2016) · Mechanisms of Development · doi:10.1016/j.mod.2016.10.003 · Cited by 87
The asymmetric subcellular localisation of components of the planar polarity pathway
Strutt, D. I. (2002) · Seminars in Cell and Developmental Biology · doi:10.1016/s1084-9521(02)00041-1 · Cited by 98
Metadata
- Authors
- Heisenberg, C.-P., Tada, M., Rauch, G.-J., Saúde, L., Concha, M. L., Geisler, R., Stemple, D. L., Smith, J. C., & Wilson, S. W.
- Affiliations
- University College London (GB)
- National Institute for Medical Research (GB)
- Max Planck Institute for Developmental Biology (DE)
- Corresponding author
- Heisenberg, Carl-Philipp
- ORCID
- Venue
- Nature
- Published
- 2000-05
- Volume
- 405
- Issue
- 6782
- Pages
- 76-81
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W1974712344
- Cited by
- 1,013
- References
- 31
- Citations by year
- 2026: 17 · 2025: 23 · 2024: 19 · 2023: 19 · 2022: 25 · 2021: 29 · 2020: 23 · 2019: 23 · 2018: 25 · 2017: 29 · 2016: 29 · 2015: 36 · 2014: 34 · 2013: 34 · 2012: 46
- FWCI
- 20.38
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Wnt/β-catenin signaling in development and cancer
- Health Sciences › Medicine › Oncology › Renal and related cancers
- Keywords
- Wnt11, convergent extension, gastrulation, zebrafish, cyclopia, midline defects, cell intercalation, Dishevelled, non-canonical Wnt signaling, cell motility, germ layer formation
- MeSH terms
- Animals, Cell Movement, Embryo, Nonmammalian, Gastrula, Glycoproteins, Mutation, Zebrafish, Signal Transduction, Zebrafish Proteins, Wnt Proteins
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