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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.
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“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]
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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
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Wang, Y.-M., Khederzadeh, S., Li, S., Otecko, N. O., Irwin, D. M., Thakur, M. K., Ren, X.-D., Wang, M., Wu, D., & Zhang, Y. (2021) · Genomics Proteomics & Bioinformatics · doi:10.1016/j.gpb.2020.06.019 · Cited by 17
The polarising role of cell adhesion molecules in early development
Wedlich, D. (2002) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(02)00374-5 · Cited by 17
Noda, N., & Kamimura, S. (2008) · Review of Scientific Instruments · doi:10.1063/1.2839914 · Cited by 17
Sato, Y., & Takahashi, Y. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.03.007 · Cited by 17
Pitx2c orchestrates embryonic axis extension via mesendodermal cell migration
Collins, M. M., Maischein, H., Dufourcq, P., Charpentier, M., Blader, P., & Stainier, D. Y. R. (2018) · eLife · doi:10.7554/elife.34880 · Cited by 16
Menon, T., Borbora, A. S., Kumar, R., & Nair, S. (2020) · Developmental Biology · doi:10.1016/j.ydbio.2020.09.002 · Cited by 16
Jussila, M., Boswell, C. W., Griffiths, N. W., Pumputis, P. G., & Ciruna, B. G. (2022) · Nature Communications · doi:10.1038/s41467-022-33322-9 · Cited by 18
Gittin, D. I., & Petersen, C. P. (2022) · Current Biology · doi:10.1016/j.cub.2022.10.071 · Cited by 16
Mathewson, A. W., Berman, D., & Moens, C. B. (2019) · Developmental Biology · doi:10.1016/j.ydbio.2019.04.007 · Cited by 17
Sumanas, S., Zhang, B., Dai, R., & Lin, S. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.04.007 · Cited by 16
Protein Phosphatase 1 β Paralogs Encode the Zebrafish Myosin Phosphatase Catalytic Subunit
Jayashankar, V., Nguyen, M. J., Carr, B. W., Zheng, D. C., Rosales, J. B., Rosales, J. B., & Weiser, D. C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0075766 · Cited by 16
López‐Escobar, B., Cano, D. A., Rojas, A., de Felipe, B., Palma, F., Sánchez-Alcázar, J. A., Henderson, D. J., & Ybot‐González, P. (2014) · Disease Models & Mechanisms · doi:10.1242/dmm.017723 · Cited by 16
Kidney development conserved over species: essential roles of Sall1
Nishinakamura, R. (2003) · Seminars in Cell and Developmental Biology · doi:10.1016/s1084-9521(03)00027-2 · Cited by 16
Axelrod, J. D. (2002) · Nature Cell Biology · doi:10.1038/ncb0102-e6 · Cited by 17
Structural Characterization and Statistical-Mechanical Model of Epidermal Patterns
Chen, D., Aw, W. Y., Devenport, D., & Salvatore Torquato, A. (2016) · Biophysical Journal · doi:10.1016/j.bpj.2016.10.036 · Cited by 15
A corset function of exoskeletal ECM promotes body elongation in Drosophila
Tajiri, R., Fujiwara, H., & Kojima, T. (2021) · Communications Biology · doi:10.1038/s42003-020-01630-9 · Cited by 15
Wijesena, N. M., Sun, H., Kumburegama, S., & Wikramanayake, A. H. (2021) · Developmental Biology · doi:10.1016/j.ydbio.2021.11.002 · Cited by 13
Dranow, D. B., Pabic, P. L., & Schilling, T. F. (2023) · Development · doi:10.1242/dev.201273 · Cited by 15
A Yap-dependent mechanoregulatory program sustains cell migration for embryo axis assembly
Sousa‐Ortega, A., Vázquez-Marín, J., Sanabria‐Reinoso, E., Corbacho, J., Polvillo, R., Campoy-López, A., Buono, L., Loosli, F., Almuedo‐Castillo, M., & Martínez‐Morales, J. R. (2023) · Nature Communications · doi:10.1038/s41467-023-38482-w · Cited by 15
Bhattacharya, D., Zhong, J., Tavakoli, S., Kabla, A., & Matsudaira, P. T. (2021) · Scientific Reports · doi:10.1038/s41598-021-98233-z · Cited by 15
Zhang, H., Liu, C., Zhu, D., Zhang, Q., & Li, J. (2022) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.2c01016 · Cited by 15
Combover/CG10732, a Novel PCP Effector for Drosophila Wing Hair Formation
Fagan, J. K., Dollar, G., Lu, Q., Barnett, A. A., Jorge, J. P., Schlösser, A., Pfleger, C. M., Adler, P. N., & Jenny, A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0107311 · Cited by 12
Polarized trafficking provides spatial cues for planar cell polarization within a tissue
Galic, M., & Matis, M. (2015) · BioEssays · doi:10.1002/bies.201400196 · Cited by 15
LZIC regulates neuronal survival during zebrafish development
Clements, W. K., & Kimelman, D. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.04.026 · Cited by 16
Lou, Q., He, J., Hu, L., & Yin, Z. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2012.02.013 · Cited by 15
Basal bodies exhibit polarized positioning in zebrafish cone photoreceptors
Ramsey, M., & Perkins, B. D. (2012) · The Journal of Comparative Neurology · doi:10.1002/cne.23260 · Cited by 13
Tbx16 cooperates with Wnt11 in assembling the zebrafish organizer
Muyskens, J. B., & Kimmel, C. B. (2006) · Mechanisms of Development · doi:10.1016/j.mod.2006.09.003 · Cited by 14
Axis Formation— β-Catenin Catches a Wnt
Jessen, J. R., & Solnica‐Krezel, L. (2005) · Cell · doi:10.1016/j.cell.2005.03.005 · Cited by 14
Wnt Signaling Mediates Diverse Developmental Processes in Zebrafish
Verkade, H. M., & Heath, J. K. (2008) · Methods in molecular biology · doi:10.1007/978-1-60327-469-2_17 · Cited by 14
Castanon, I., Hannich, J. T., Abrami, L., Huber, F., Dubois, M., Müller, M., van der Goot, F. G., & González‐Gaitán, M. (2020) · Nature Communications · doi:10.1038/s41467-020-17196-3 · Cited by 14
Putting in the Erk: Growth factor signaling and mesoderm morphogenesis
McFann, S. E., Shvartsman, S. Y., & Toettcher, J. E. (2022) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2022.02.007 · Cited by 14
Morphogenetic cell movements shaping the zebrafish gastrula
Jessen, J. R., & Solnica‐Krezel, L. (2005) · Advances in developmental biology · doi:10.1016/s1574-3349(05)14007-1 · Cited by 14
Pair-Wise Regulation of Convergence and Extension Cell Movements by Four Phosphatases via RhoA
van Eekelen, M., Runtuwene, V., Masselink, W., & den Hertog, J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0035913 · Cited by 14
Expression of planar cell polarity genes during mouse tooth development
Obara, N., Suzuki, Y., Irie, K., & Shibata, S. (2017) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2017.07.008 · Cited by 14
Planar Cell Polarity Signaling: Coordinated Crosstalk for Cell Orientation
Kacker, S., Parsad, V., Singh, N. K., Hordiichuk, D., Alvarez, S., Gohar, M., Kacker, A., & Rai, S. K. (2024) · Journal of Developmental Biology · doi:10.3390/jdb12020012 · Cited by 13
Essential role for Csk upstream of Fyn and Yes in zebrafish gastrulation
Jopling, C., & den Hertog, J. (2006) · Mechanisms of Development · doi:10.1016/j.mod.2006.10.003 · Cited by 13
Feng, K., & Guo, H. (2017) · Molecular Medicine Reports · doi:10.3892/mmr.2017.8246 · Cited by 13
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Zohn, I. E. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-981-15-2389-2_2 · Cited by 15
Expression and function ofWnt5ain the development of the glandular stomach in the chicken embryo
Listyorini, D. I., & Yasugi, S. (2006) · Development Growth & Differentiation · doi:10.1111/j.1440-169x.2006.00861.x · Cited by 13
Origin and function of fluctuations in cell behaviour and the emergence of patterns
Mateus, A. M., Gorfinkiel, N., & Arias, A. M. (2009) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2009.07.009 · Cited by 13
Frazzetto, G., Klingbeil, P., & Bouwmeester, T. (2002) · Mechanisms of Development · doi:10.1016/s0925-4773(01)00664-5 · Cited by 13
RNA Localization in Xenopus Oocytes
Rand, K., & Yisraeli, J. K. (2001) · Results and problems in cell differentiation · doi:10.1007/978-3-540-40025-7_10 · Cited by 13
Wnt Signaling Pathway: Biological Function, Diseases, and Therapeutic Interventions
Jin, X., Wang, J., Cao, R., & Jiang, D. (2026) · MedComm · doi:10.1002/mco2.70580 · Cited by 14
Structural basis of human VANGL-PRICKLE interaction
Song, Y., Jian, S., Teng, J., Zheng, P., & Zhang, Z. (2025) · Nature Communications · doi:10.1038/s41467-024-55396-3 · Cited by 13
Evolutionary Origin and Nomenclature of Vertebrate Wnt11 -Family Genes
Postlethwait, J. H., Acedo, J. N., & Piotrowski, T. (2019) · Zebrafish · doi:10.1089/zeb.2019.1760 · Cited by 12
The distribution of Dishevelled in convergently extending mesoderm
Panousopoulou, E., Tyson, R. A., Bretschneider, T., & Green, J. B. A. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.07.012 · Cited by 12
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Ma, Y., Sun, Y., Jiang, L., Zuo, K., Chen, H., Guo, J., Chen, F., Lai, Y., & Shi, J. (2016) · Cytoskeleton · doi:10.1002/cm.21351 · Cited by 12
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Jarsch, I. K., Gadsby, J. R., Nuccitelli, A., Mason, J., Shimo, H., Pilloux, L., Marzook, N. B., Mulvey, C. M., Dobramysl, U., Bradshaw, C. R., et al. (2020) · The Journal of Cell Biology · doi:10.1083/jcb.201909178 · Cited by 12
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Bösze, B., Mattes, B., Sinner, C., Stricker, K., Gourain, V., Thumberger, T., Tlili, S., Weber, S., Wittbrodt, J., Saunders, T. E., et al. (2020) · Histochemistry and Cell Biology · doi:10.1007/s00418-020-01887-5 · Cited by 12
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Huang, Y., & Winklbauer, R. (2022) · The Journal of Cell Biology · doi:10.1083/jcb.202008116 · Cited by 12
Chauvigné, F., Rallière, C., Cauty, C., & Rescan, P. (2006) · Journal of Experimental Biology · doi:10.1242/jeb.02006 · Cited by 12
Lawrence, N. J., & Morel, V. (2003) · Mechanisms of Development · doi:10.1016/j.mod.2003.07.004 · Cited by 11
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Paramore, S. V., Goodwin, K., Fowler, E. W., Devenport, D., & Nelson, C. M. (2024) · Development · doi:10.1242/dev.202692 · Cited by 10
Huljev, K., Shamipour, S., Pinheiro, D., Preußer, F., Steccari, I., Sommer, C. M., Naik, S., & Heisenberg, C. (2022) · Developmental Cell · doi:10.1016/j.devcel.2023.02.016 · Cited by 11
Self-citationFarrera‐Hernández, A., Marín‐Llera, J. C., & Chimal‐Monroy, J. (2020) · Developmental Biology · doi:10.1016/j.ydbio.2020.10.003 · Cited by 11
nlz1 is required for cilia formation in zebrafish embryogenesis
Dutta, S., Sriskanda, S., Boobalan, E., Alur, R. P., Elkahloun, A. G., & Brooks, B. P. (2015) · Developmental Biology · doi:10.1016/j.ydbio.2015.08.019 · Cited by 13
Kong, W., Yang, Y., Zhang, T., Shi, D., & Zhang, Y. (2012) · Evolution & Development · doi:10.1111/j.1525-142x.2012.00533.x · Cited by 11
Hingwing, K., Lee, S., Nykilchuk, L., Walston, T., Hardin, J. D., & Hawkins, N. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.01.025 · Cited by 11
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Heisenberg, C. (2002) · Current Biology · doi:10.1016/s0960-9822(02)01160-0 · Cited by 11
Self-citationSchmidt, C., Otto, A., Luke, G. N., Valášek, P., Otto, W. R., & Patel, K. (2006) · Anatomy and Embryology · doi:10.1007/s00429-006-0102-4 · Cited by 11
Somorjai, I., Ehebauer, M. T., Escrivá, H., & García‐Fernàndez, J. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.749806 · Cited by 10
Thompson, E., Hensley, J., & Taylor, R. S. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25179443 · Cited by 10
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Wang, J., Feng, D., & Gao, B. (2021) · Handbook of experimental pharmacology · doi:10.1007/164_2021_533 · Cited by 10
Kimura-Yoshida, C., Mochida, K., Kanno, S.-I., & Matsuo, I. (2022) · Communications Biology · doi:10.1038/s42003-022-03254-7 · Cited by 10
Cyclic stretching combined with cell-cell adhesion is sufficient for inducing cell intercalation
Lien, J.-C., & Wang, Y. (2023) · Biophysical Journal · doi:10.1016/j.bpj.2023.06.019 · Cited by 10
Katanaev, V. L., & Kryuchkov, M. (2011) · Biochemistry (Moscow) · doi:10.1134/s0006297911130116 · Cited by 11
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Ulrich, F., & Heisenberg, C. (2008) · Methods in molecular biology · doi:10.1007/978-1-59745-178-9_27 · Cited by 10
Self-citationCellular Processes of Notochord Formation
Smith, W. C. (2018) · Advances in experimental medicine and biology · doi:10.1007/978-981-10-7545-2_15 · Cited by 10
Yang, X., Li, X., Gu, Q., Li, Q., & Cui, Z. (2019) · Cells · doi:10.3390/cells8091038 · Cited by 10
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Aparicio, L. M. A., Espinosa, J., Campelo, R. G., Veiga, F. G., Díaz‐Prado, S., & Gallego, G. A. (2007) · Clinical & Translational Oncology · doi:10.1007/s12094-007-0015-6 · Cited by 10
Tes regulates neural crest migration and axial elongation in Xenopus
Dingwell, K. S., & Smith, J. C. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.02.004 · Cited by 9
Self-citationZebrafish Ext2 is necessary for Fgf and Wnt signaling, but not for Hh signaling
Fischer, S., Filipek‐Górniok, B., & Ledin, J. (2011) · BMC Developmental Biology · doi:10.1186/1471-213x-11-53 · Cited by 10
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Weiser, D. C., & Kimelman, D. (2011) · Methods in molecular biology · doi:10.1007/978-1-61779-510-7_5 · Cited by 9
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Vellutini, B. C., Martín-Durán, J. M., Børve, A., & Hejnol, A. (2024) · BMC Biology · doi:10.1186/s12915-024-01988-w · Cited by 8
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Self-citationHouston, D. W., Elliott, K. L., Coppenrath, K., Wlizla, M., & Horb, M. E. (2022) · Development · doi:10.1242/dev.200552 · Cited by 11
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Tonoyama, Y., Anzai, D., Ikeda, A., Kakuda, S., Kinoshita, M., Kawasaki, T., & Oka, S. (2009) · Mechanisms of Development · doi:10.1016/j.mod.2009.03.004 · Cited by 9
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Lecuit, T. (2003) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(03)00078-9 · Cited by 9
Hayata, T., Tanegashima, K., Takahashi, S., Sogame, A., & Asashima, M. (2002) · Mechanisms of Development · doi:10.1016/s0925-4773(01)00638-4 · Cited by 9
Shiu, W.-L., Huang, K.-R., Hung, J.-C., Wu, J., & Hong, J. (2016) · Journal of Biomedical Science · doi:10.1186/s12929-016-0248-1 · Cited by 8
Nguyen, N. D. S., & Farge, E. (2024) · Nature Communications · doi:10.1038/s41467-024-55100-5 · Cited by 9
Tavano, S., Brückner, D. B., Tasciyan, S., Tong, X., Kardos, R., Schauer, A., Hauschild, R., & Heisenberg, C. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115387 · Cited by 8
Self-citationFold-and-fuse neurulation in zebrafish requires Vangl2
MacGowan, J., Cardenas, M. G., & Williams, M. K. (2023) · Developmental Biology · doi:10.1016/j.ydbio.2025.05.001 · Cited by 10
Xu, X., Shuen, T. W. H., Chen, C., Goudevenou, K., Jones, P., & Sablitzky, F. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.10.020 · Cited by 8
RetractedGuo, S. S., Au, T. Y. K., Wynn, S. L., Aszódi, A., Chan, D. T.-M., Fässler, R., & Cheah, K. S. E. (2020) · Development · doi:10.1242/dev.192724 · Cited by 9
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da Silva, C. C., Ostertag, A., Raman, R., Müller, M., Cohen-Solal, M. E., & Collet, C. (2023) · Zebrafish · doi:10.1089/zeb.2022.0042 · Cited by 8
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Schepis, A., & Nelson, W. J. (2012) · Cell Adhesion & Migration · doi:10.4161/cam.20583 · Cited by 8
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Kiefer, J. C. (2005) · Developmental Dynamics · doi:10.1002/dvdy.20359 · Cited by 8
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Yang, G., & Luo, Z. (2010) · Developmental Neurobiology · doi:10.1002/dneu.20851 · Cited by 8
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Shao, M., Cheng, X.-N., Liu, Y., Li, J., & Shi, D. (2017) · Zebrafish · doi:10.1089/zeb.2017.1495 · Cited by 8
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Itoh, K., Lisovsky, M., Hikasa, H., & Sokol, S. Y. (2005) · Developmental Dynamics · doi:10.1002/dvdy.20526 · Cited by 8
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Rothschild, S. C., & Tombes, R. M. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-12457-1_21 · Cited by 7
Wang, X., Wang, Z., Adeniran, S. O., Huang, F., Ma, M., Zhang, H., Li, X., Zheng, P., & Zhang, G. (2020) · Reproduction Fertility and Development · doi:10.1071/rd19088 · Cited by 7
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 ›
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