Cited by 391Developmental Biology and Gene RegulationWnt/β-catenin signaling in development and cancerPluripotent Stem Cells Research

The DOI matches its Crossref record; 154 of the 156 references it cites were found in a registry or an index.

Conserved Patterns of Cell Movements during Vertebrate Gastrulation

Open access

Solnica-Krezel, Lilianna·2005·Current Biology

DOI 10.1016/j.cub.2005.03.016

Open this paper in CoChat — free account Open PDF

Abstract

Vertebrate embryogenesis entails an exquisitely coordinated combination of cell proliferation, fate specification and movement. After induction of the germ layers, the blastula is transformed by gastrulation movements into a multilayered embryo with head, trunk and tail rudiments. Gastrulation is heralded by formation of a blastopore, an opening in the blastula. The axial side of the blastopore is marked by the organizer, a signaling center that patterns the germ layers and regulates gastrulation movements. During internalization, endoderm and mesoderm cells move via the blastopore beneath the ectoderm. Epiboly movements expand and thin the nascent germ layers. Convergence movements narrow the germ layers from lateral to medial while extension movements elongate them from head to tail. Despite different morphology, parallels emerge with respect to the cellular and genetic mechanisms of gastrulation in different vertebrate groups. Patterns of gastrulation cell movements relative to the blastopore and the organizer are similar from fish to mammals, and conserved molecular pathways mediate gastrulation movements.

Integrity signals

Registry

Crossref · 10.1016/j.cub.2005.03.016

Cites

154 of 154 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

Rho GTPases in cell biology
Etienne-Manneville, S., & Hall, A. (2002) · Nature · doi:10.1038/nature01148 · Cited by 4,965
The snail superfamily of zinc-finger transcription factors
Nieto, M. A. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm757 · Cited by 1,719
Embryonic Development and Induction
(1939) · Annals of the Entomological Society of America · doi:10.1093/aesa/32.3.657 · Cited by 1,148
Expression of a dominant negative mutant of the FGF receptor disrupts mesoderm formation in xenopus embryos
Amaya, E., Musci, T. J., & Kirschner, M. W. (1991) · Cell · doi:10.1016/0092-8674(91)90616-7 · Cited by 1,085
A major developmental transition in early xenopus embryos: II. control of the onset of transcription
Newport, J., & Kirschner, M. (1982) · Cell · doi:10.1016/0092-8674(82)90273-2 · Cited by 1,055
Silberblick/Wnt11 mediates convergent extension movements during zebrafish gastrulation
Heisenberg, C.-P., Tada, M., Rauch, G.-J., Saúde, L., Concha, M. L., Geisler, R., Stemple, D. L., Smith, J. C., & Wilson, S. W. (2000) · Nature · doi:10.1038/35011068 · Cited by 1,013
Zebrafish Prickle, a Modulator of Noncanonical Wnt/Fz Signaling, Regulates Gastrulation Movements
Veeman, M. T., Slusarski, D. C., Kaykas, A., Louie, S. H., & Moon, R. T. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00240-9 · Cited by 945
Clonal analysis of epiblast fate during germ layer formation in the mouse embryo
Lawson, K. A., Meneses, J. J., & Pedersen, R. A. (1991) · Development · doi:10.1242/dev.113.3.891 · Cited by 881
Wnt/Frizzled Activation of Rho Regulates Vertebrate Gastrulation and Requires a Novel Formin Homology Protein Daam1
Habas, R., Kato, Y., & He, X. (2001) · Cell · doi:10.1016/s0092-8674(01)00614-6 · Cited by 842
FORMATION AND FUNCTION OF SPEMANN'S ORGANIZER
Harland, R., & Gerhart, J. (1997) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.13.1.611 · Cited by 839

Show all 156 references

Sorted by citations

Reconstruction of Zebrafish Early Embryonic Development by Scanned Light Sheet Microscopy
Keller, P., Schmidt, A. D., Wittbrodt, J., & Stelzer, E. H. K. (2008) · Science · doi:10.1126/science.1162493 · Cited by 1,569
Wnt signal transduction pathways
Komiya, Y., & Habas, R. (2008) · Organogenesis · doi:10.4161/org.4.2.5851 · Cited by 1,528
Forces in Tissue Morphogenesis and Patterning
Heisenberg, C., & Bellaı̈che, Y. (2013) · Cell · doi:10.1016/j.cell.2013.05.008 · Cited by 1,246
Epithelial-Mesenchymal Transition in Cancer: Parallels Between Normal Development and Tumor Progression
Micalizzi, D. S., Farabaugh, S. M., & Ford, H. L. (2010) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1007/s10911-010-9178-9 · Cited by 979
Multicellular Rosette Formation Links Planar Cell Polarity to Tissue Morphogenesis
Blankenship, J. T., Backovic, S. T., Sanny, J., Weitz, O., & Zallen, J. A. (2006) · Developmental Cell · doi:10.1016/j.devcel.2006.09.007 · Cited by 693
Collective Cell Migration
Rørth, P. (2009) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.042308.113231 · Cited by 625
The developmental biology of Dishevelled: an enigmatic protein governing cell fate and cell polarity
Wallingford, J. B., & Habas, R. (2005) · Development · doi:10.1242/dev.02068 · Cited by 509
Molecular Genetics of Axis Formation in Zebrafish
Schier, A. F., & Talbot, W. S. (2005) · Annual Review of Genetics · doi:10.1146/annurev.genet.37.110801.143752 · Cited by 499
Tissue Organization by Cadherin Adhesion Molecules: Dynamic Molecular and Cellular Mechanisms of Morphogenetic Regulation
Niessen, C. M., Leckband, D., & Yap, A. S. (2011) · Physiological Reviews · doi:10.1152/physrev.00004.2010 · Cited by 427
Gastrulation: Making and Shaping Germ Layers
Solnica‐Krezel, L., & Sepich, D. S. (2011) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-092910-154043 · Cited by 373
Self-citation
Tissue Deformation Modulates Twist Expression to Determine Anterior Midgut Differentiation in Drosophila Embryos
Desprat, N., Supatto, W., Pouille, P., Beaurepaire, E., & Farge, E. (2008) · Developmental Cell · doi:10.1016/j.devcel.2008.07.009 · Cited by 331
Comparative transcriptome analysis reveals vertebrate phylotypic period during organogenesis
Irie, N., & Kuratani, S. (2011) · Nature Communications · doi:10.1038/ncomms1248 · Cited by 325
Collective cell migration in development
Weijer, C. J. (2009) · Journal of Cell Science · doi:10.1242/jcs.036517 · Cited by 323
Epithelial–mesenchymal transition in lung development and disease: does it exist and is it important?
Bartis, D., Miše, N., Mahida, R. Y., Eickelberg, O., & THICKETT, D. R. (2013) · Thorax · doi:10.1136/thoraxjnl-2013-204608 · Cited by 317
Cell migration during morphogenesis
Aman, A. J., & Piotrowski, T. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.11.014 · Cited by 298
Cell shape changes indicate a role for extrinsic tensile forces in Drosophila germ-band extension
Butler, L., Blanchard, G. B., Kabla, A., Lawrence, N. J., Welchman, D. P., Mahadevan, L., Adams, R. J., & Sanson, B. (2009) · Nature Cell Biology · doi:10.1038/ncb1894 · Cited by 276
Rho-Kinase Directs Bazooka/Par-3 Planar Polarity during Drosophila Axis Elongation
Simões, S. D. M., Blankenship, J. T., Weitz, O., Farrell, D. L., Tamada, M., Fernández‐González, R., & Zallen, J. A. (2010) · Developmental Cell · doi:10.1016/j.devcel.2010.08.011 · Cited by 274
PKB/Akt-Dependent Regulation of Cell Motility
Xue, G., & Hemmings, B. A. (2013) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djs648 · Cited by 274
The amniote primitive streak is defined by epithelial cell intercalation before gastrulation
Voiculescu, O., Bertocchini, F., Wolpert, L., Keller, R. E., & Stern, C. D. (2007) · Nature · doi:10.1038/nature06211 · Cited by 262
Nodal MorphogensPreprint
Schier, A. F. (2009) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a003459 · Cited by 251
Epithelial-to-mesenchymal transition: What is the impact on breast cancer stem cells and drug resistance
Mallini, P., Lennard, T. W. J., Kirby, J. A., & Meeson, A. P. (2013) · Cancer Treatment Reviews · doi:10.1016/j.ctrv.2013.09.008 · Cited by 247
Models of Biological Pattern Formation: From Elementary Steps to the Organization of Embryonic Axes
Meinhardt, H. (2007) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(07)81001-5 · Cited by 219
Mechanisms of endothelial cell migration
Michaelis, U. R. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1678-0 · Cited by 202
Apelin and Its Receptor Control Heart Field Formation during Zebrafish Gastrulation
Zeng, X.-X. I., Wilm, T. P., Sepich, D. S., & Solnica‐Krezel, L. (2007) · Developmental Cell · doi:10.1016/j.devcel.2007.01.011 · Cited by 190
Self-citation
Epithelial to mesenchymal transition during gastrulation: An embryological view
Nakaya, Y., & Sheng, G. (2008) · Development Growth & Differentiation · doi:10.1111/j.1440-169x.2008.01070.x · Cited by 188
Integrin α5β1 and Fibronectin Regulate Polarized Cell Protrusions Required for Xenopus Convergence and Extension
Davidson, L. A., Marsden, M., Keller, R. E., & DeSimone, D. W. (2006) · Current Biology · doi:10.1016/j.cub.2006.03.038 · Cited by 187
Sdf1/Cxcr4 signaling controls the dorsal migration of endodermal cells during zebrafish gastrulation
Mizoguchi, T., Verkade, H. M., Heath, J. K., Kuroiwa, A., & Kikuchi, Y. (2008) · Development · doi:10.1242/dev.020107 · Cited by 185
Evolution of the Wnt Pathways
Croce, J. C., & McClay, D. R. (2008) · Methods in molecular biology · doi:10.1007/978-1-60327-469-2_1 · Cited by 186
Calcium signaling in vertebrate embryonic patterning and morphogenesis
Slusarski, D. C., & Pelegri, F. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.04.043 · Cited by 178
Epithelial–Mesenchymal Transitions
Savagner, P. (2015) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2014.11.021 · Cited by 174
Developmental toxicity screening in zebrafish
McCollum, C. W., Ducharme, N. A., Bondesson, M., & Gustafsson, J.-Α. (2011) · Birth Defects Research Part C Embryo Today Reviews · doi:10.1002/bdrc.20210 · Cited by 161
In vivo cell biology: following the zebrafish trend
Beis, D., & Stainier, D. Y. R. (2006) · Trends in Cell Biology · doi:10.1016/j.tcb.2005.12.001 · Cited by 162
A stepwise model of Reaction-Diffusion and Positional-Information governs self-organized human peri-gastrulation-like patterning
Tewary, M., Östblom, J., Prochazka, L., Zulueta-Coarasa, T., Shakiba, N., Fernández‐González, R., & Zandstra, P. W. (2017) · Development · doi:10.1242/dev.149658 · Cited by 152
Wnt5a is essential for intestinal elongation in mice
Cervantes, S., Yamaguchi, T. P., & Hebrok, M. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2008.11.020 · Cited by 155
Quantitative differences in tissue surface tension influence zebrafish germ layer positioning
Schötz, E., Burdine, R. D., Jülicher, F., Steinberg, M. S., Heisenberg, C., & Foty, R. A. (2008) · HFSP journal · doi:10.2976/1.2834817 · Cited by 161
Head-tail patterning of the vertebrate embryo: one, two or many unresolved problems?
Stern, C. D., Charité, J., Deschamps, J., Duboule, D., Durston, A. J., Kmita, M., Nicolas, J.-F., Palmeirim, I., Smith, J. C., & Wolpert, L. (2005) · The International Journal of Developmental Biology · doi:10.1387/ijdb.052095cs · Cited by 150
The yolk syncytial layer in early zebrafish development
Carvalho, L., & Heisenberg, C. (2010) · Trends in Cell Biology · doi:10.1016/j.tcb.2010.06.009 · Cited by 143
Epithelial–Mesenchymal Transition in Development and Cancer
Micalizzi, D. S., & Ford, H. L. (2009) · Future Oncology · doi:10.2217/fon.09.94 · Cited by 145
Syndecan-4 regulates non-canonical Wnt signalling and is essential for convergent and extension movements in Xenopus embryos
Muñoz, R., Moreno, M., Oliva, C., Orbenes, C., & Larraín, J. (2006) · Nature Cell Biology · doi:10.1038/ncb1399 · Cited by 150
Fetal alcohol exposure impairs hedgehog cholesterol modification and signaling
Li, Y., Yang, H., Zdanowicz, M., Sicklick, J. K., Qi, Y. P., Camp, T., & Diehl, A. M. (2007) · Laboratory Investigation · doi:10.1038/labinvest.3700516 · Cited by 141
Chemokine Signaling Controls Endodermal Migration During Zebrafish Gastrulation
Nair, S., & Schilling, T. F. (2008) · Science · doi:10.1126/science.1160038 · Cited by 127
Chemokine signaling in embryonic cell migration: a fisheye view
Raz, E., & Mahabaleshwar, H. (2009) · Development · doi:10.1242/dev.022418 · Cited by 129
Gastrulation in zebrafish — all just about adhesion?
Solnica‐Krezel, L. (2006) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2006.06.009 · Cited by 124
Self-citation
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
From Zygote to Implantation: Morphological and Molecular Dynamics during Embryo Development in the Pig
Oestrup, O., Hall, V. J., Petkov, S. G., Wolf, X., Hyldig, S. M. W., & Hyttel, P. (2009) · Reproduction in Domestic Animals · doi:10.1111/j.1439-0531.2009.01482.x · Cited by 123
Rap1, a mercenary among the Ras-like GTPases
Frische, E. W., & Zwartkruis, F. J. T. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2009.12.043 · Cited by 113
Geometric control of tissue morphogenesis
Nelson, C. M. (2009) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2008.12.014 · Cited by 117
Developmental Constraints on Vertebrate Genome Evolution
Roux, J., & Robinson‐Rechavi, M. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.1000311 · Cited by 108
Mouse prickle1 , the homolog of a PCP gene, is essential for epiblast apical-basal polarity
Tao, H., Suzuki, M., Kiyonari, H., Abe, T., Sasaoka, T., & Ueno, N. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0901332106 · Cited by 108
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
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
Zebrafish epiboly: Spreading thin over the yolk
Bruce, A. E. E. (2015) · Developmental Dynamics · doi:10.1002/dvdy.24353 · Cited by 101
Ribosomal Proteins Rpl22 and Rpl22l1 Control Morphogenesis by Regulating Pre-mRNA Splicing
Zhang, Y., O’Leary, M. N., Peri, S., Wang, M., Zha, J., Melov, S., Kappes, D. J., Feng, Q., Rhodes, J., Amieux, P. S., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2016.12.034 · Cited by 98
Imaging of cell migration
Dormann, D., & Weijer, C. J. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601227 · Cited by 100
Epithelial morphogenesis in embryos: asymmetries, motors and brakes
Quintin, S., Gally, C., & Labouesse, M. (2008) · Trends in Genetics · doi:10.1016/j.tig.2008.02.005 · Cited by 99
Temporally coordinated signals progressively pattern the anteroposterior and dorsoventral body axes
Tuazon, F. B., & Mullins, M. C. (2015) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2015.06.003 · Cited by 98
Initiation of convergence and extension movements of lateral mesoderm during zebrafish gastrulation
Sepich, D. S., Calmelet, C., Kiskowski, M. A., & Solnica‐Krezel, L. (2005) · Developmental Dynamics · doi:10.1002/dvdy.20507 · Cited by 98
Self-citation
Chapter 7 Establishment of Hox Vertebral Identities in the Embryonic Spine Precursors
Iimura, T., Denans, N., & Pourquié, O. (2009) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(09)88007-1 · Cited by 98
Kinase-activating and kinase-impaired cardio-facio-cutaneous syndrome alleles have activity during zebrafish development and are sensitive to small molecule inhibitors
Anastasaki, C., Estep, A. L., Marais, R., Rauen, K. A., & Patton, E. E. (2009) · Human Molecular Genetics · doi:10.1093/hmg/ddp186 · Cited by 96
FGF signalling through RAS/MAPK and PI3K pathways regulates cell movement and gene expression in the chicken primitive streak without affecting E-cadherin expression
Hardy, K. M., Yatskievych, T. A., Konieczka, J. H., Bobbs, A. S., & Antin, P. B. (2011) · BMC Developmental Biology · doi:10.1186/1471-213x-11-20 · Cited by 92
Role of the extracellular matrix in cancer‐associated epithelial to mesenchymal transition phenomenon
Tzanakakis, G. N., Kavasi, R., Voudouri, K., Berdiaki, A., Spyridaki, I., Tsatsakis, A. M., & Nikitovic, D. (2017) · Developmental Dynamics · doi:10.1002/dvdy.24557 · Cited by 95
Cell Sorting in Development
Krens, G., & Heisenberg, C. (2011) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-385065-2.00006-2 · Cited by 91
The Physical Basis of Coordinated Tissue Spreading in Zebrafish Gastrulation
Morita, H., Grigolon, S., Bock, M., Krens, G., Salbreux, G., & Heisenberg, C. (2017) · Developmental Cell · doi:10.1016/j.devcel.2017.01.010 · Cited by 91
Secreted inducers in vertebrate eye development: more functions for old morphogens
Esteve, P., & Bovolenta, P. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.01.001 · Cited by 89
Alterations of the cytoskeleton in all three embryonic lineages contribute to the epiboly defect of Pou5f1/Oct4 deficient MZspg zebrafish embryos
Lachnit, M., Kur, E., & Driever, W. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.10.008 · Cited by 89
Hand2 Regulates Extracellular Matrix Remodeling Essential for Gut-Looping Morphogenesis in Zebrafish
Yin, C., Kikuchi, K., Hochgreb, T., Poss, K. D., & Stainier, D. Y. R. (2010) · Developmental Cell · doi:10.1016/j.devcel.2010.05.009 · Cited by 87
Wnt5b–Ryk pathway provides directional signals to regulate gastrulation movement
Lin, S., Baye, L. M., Westfall, T. A., & Slusarski, D. C. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.200912128 · Cited by 95
Extracellular matrix assembly and organization during zebrafish gastrulation
Latimer, A., & Jessen, J. R. (2009) · Matrix Biology · doi:10.1016/j.matbio.2009.10.002 · Cited by 85
Back and forth between cell fate specification and movement during vertebrate gastrulation
Heisenberg, C., & Solnica‐Krezel, L. (2008) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2008.07.011 · Cited by 86
Self-citation
Regionalized tissue fluidization is required for epithelial gap closure during insect gastrulation
Jain, A., Ulman, V., Mukherjee, A., Prakash, M., Cuenca, M. B., Pimpale, L. G., Münster, S., Haase, R., Panfilio, K. A., Jug, F., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-19356-x · Cited by 88
Flamingo regulates epiboly and convergence/extension movements through cell cohesive and signalling functions during zebrafish gastrulation
Carreira-Barbosa, F., Kajita, M., Morel, V., Wada, H., Okamoto, H., Arias, A. M., Fujita, Y., Wilson, S. W., & Tada, M. (2008) · Development · doi:10.1242/dev.026542 · Cited by 89
Membrane-type 1 matrix metalloproteinase regulates cell migration during zebrafish gastrulation: Evidence for an interaction with non-canonical Wnt signaling
Coyle, R. C., Latimer, A. J., & Jessen, J. R. (2008) · Experimental Cell Research · doi:10.1016/j.yexcr.2008.03.010 · Cited by 86
Multicellular dynamics during epithelial elongation
Zallen, J. A., & Blankenship, J. T. (2008) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2008.01.005 · Cited by 83
Deeply-supervised density regression for automatic cell counting in microscopy images
He, S., Minn, K. T., Solnica‐Krezel, L., Anastasio, M. A., & Li, H. (2020) · Medical Image Analysis · doi:10.1016/j.media.2020.101892 · Cited by 83
Self-citation
Wnt/PCP signaling controls intracellular position of MTOCs during gastrulation convergence and extension movements
Sepich, D. S., Usmani, M., Pawlicki, S., & Solnica‐Krezel, L. (2011) · Development · doi:10.1242/dev.053959 · Cited by 80
Self-citation
Chemotactic cell movement during Dictyostelium development and gastrulation
Dormann, D., & Weijer, C. J. (2006) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2006.06.003 · Cited by 79
Live Analysis of Endodermal Layer Formation Identifies Random Walk as a Novel Gastrulation Movement
Pézeron, G., Mourrain, P., Courty, S., Ghislain, J. J., Becker, T. S., Rosa, F., & David, N. B. (2008) · Current Biology · doi:10.1016/j.cub.2008.01.028 · Cited by 76
Why does Jack, and not Jill, break his crown? Sex disparity in brain tumors
Sun, T., Warrington, N. M., & Rubin, J. B. (2012) · Biology of Sex Differences · doi:10.1186/2042-6410-3-3 · Cited by 75
Chapter 7 Ciliary Function and Wnt Signal Modulation
Gerdes, J. M., & Katsanis, N. (2008) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(08)00807-7 · Cited by 81
Rack1 is required for Vangl2 membrane localization and planar cell polarity signaling while attenuating canonical Wnt activity
Li, S., Esterberg, R., Lachance, V., Ren, D., Radde‐Gallwitz, K., Chi, F., Parent, J., Fritz, A., & Chen, P. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1013170108 · Cited by 76
Gpr125 modulates Dishevelled distribution and planar cell polarity signaling
Li, X., Roszko, I., Sepich, D. S., Ni, M., Hamm, H. E., Marlow, F. L., & Solnica‐Krezel, L. (2013) · Development · doi:10.1242/dev.094839 · Cited by 76
Self-citation
Context-Dependent Regulation of Wnt Signaling through the Primary Cilium
Oh, E. C., & Katsanis, N. (2013) · Journal of the American Society of Nephrology · doi:10.1681/asn.2012050526 · Cited by 73
Developmental diversity of amphibians
Elinson, R. P., & del Pino, E. M. (2011) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.23 · Cited by 73
Identification and Regulation of a Molecular Module for Bleb-Based Cell Motility
Goudarzi, M., Banisch, T. U., Mobin, M. B., Maghelli, N., Tarbashevich, K., Strate, I., van den Berg, J., Blaser, H., Bandemer, S., Paluch, E. K., et al. (2012) · Developmental Cell · doi:10.1016/j.devcel.2012.05.007 · Cited by 73
Anteroposterior and dorsoventral patterning are coordinated by an identical patterning clock
Hashiguchi, M., & Mullins, M. C. (2013) · Development · doi:10.1242/dev.088104 · Cited by 70
Identification of regulators of germ layer morphogenesis using proteomics in zebrafish
Link, V., Carvalho, L., Castanon, I., Stockinger, P., Shevchenko, A., & Heisenberg, C. (2006) · Journal of Cell Science · doi:10.1242/jcs.02928 · Cited by 72
Hydrogel-based biomimetic environment for in vitro modulation of branching morphogenesis
Miyajima, H., Matsumoto, T., Sakai, T., Yamaguchi, S., An, S., Abe, M., Wakisaka, S., Lee, K. Y., Egusa, H., & Imazato, S. (2011) · Biomaterials · doi:10.1016/j.biomaterials.2011.05.072 · Cited by 68
Regulated adhesion as a driving force of gastrulation movements
Hammerschmidt, M., & Wedlich, D. (2008) · Development · doi:10.1242/dev.015701 · Cited by 69
Role of G12 proteins in oncogenesis and metastasis
Juneja, J., & Casey, P. J. (2009) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2009.00180.x · Cited by 68
A Wnt-CKIɛ-Rap1 Pathway Regulates Gastrulation by Modulating SIPA1L1, a Rap GTPase Activating Protein
Tsai, I.-C., Amack, J. D., Gao, Z.-H., Band, V., Yost, H. J., & Virshup, D. M. (2007) · Developmental Cell · doi:10.1016/j.devcel.2007.02.009 · Cited by 67
Chapter 7 Convergence and Extension Movements During Vertebrate Gastrulation
Yin, C., Ciruna, B. G., & Solnica‐Krezel, L. (2009) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(09)89007-8 · Cited by 71
Self-citation
Tissue engineering using a combined cell sheet technology and scaffolding approach
Михайловна, З. И., Presniakova, V. S., Butnaru, D. V., Svistunov, A. А., Timashev, P. S., & Rochev, Y. A. (2020) · Acta Biomaterialia · doi:10.1016/j.actbio.2020.06.016 · Cited by 67
Gα12/13 regulate epiboly by inhibiting E-cadherin activity and modulating the actin cytoskeleton
Lin, F. H., Chen, S., Sepich, D. S., Panizzi, J. R., Clendenon, S. G., Marrs, J. A., Hamm, H. E., & Solnica‐Krezel, L. (2009) · The Journal of Cell Biology · doi:10.1083/jcb.200805148 · Cited by 65
Self-citation
Distinct Xenopus Nodal ligands sequentially induce mesendoderm and control gastrulation movements in parallel to the Wnt/PCP pathway
Luxardi, G., Marchal, L., Thomé, V., & Kodjabachian, L. (2010) · Development · doi:10.1242/dev.039735 · Cited by 65
Cell migration that orients the dorsoventral axis is coordinated with anteroposterior patterning mediated by Hedgehog signaling in the early spider embryo
Akiyama‐Oda, Y., & Oda, H. (2010) · Development · doi:10.1242/dev.045625 · Cited by 62
p120‐catenin regulates microtubule dynamics and cell migration in a cadherin‐independent manner
Ichii, T., & Takeichi, M. (2007) · Genes to Cells · doi:10.1111/j.1365-2443.2007.01095.x · Cited by 62
Recent advances in the study of zebrafish extracellular matrix proteins
Jessen, J. R. (2014) · Developmental Biology · doi:10.1016/j.ydbio.2014.12.022 · Cited by 61
Emergent morphogenesis: Elastic mechanics of a self-deforming tissue
Davidson, L. A., Joshi, S. D., Kim, H. Y., von Dassow, M., Zhang, L., & Zhou, J. (2009) · Journal of Biomechanics · doi:10.1016/j.jbiomech.2009.09.010 · Cited by 61
Amotl2 is essential for cell movements in zebrafish embryo and regulates c-Src translocation
Huang, H.-Z., Lu, F.-I., Jia, S.-J., Meng, S., Cao, Y., Wang, Y.-Q., Ma, W., Yin, K., Wen, Z.-L., Peng, J., et al. (2007) · Development · doi:10.1242/dev.02782 · Cited by 69
Selective neuronal requirement for huntingtin in the developing zebrafish
Henshall, T. L., Tucker, B., Lumsden, A. L., Nornes, S., Lardelli, M. T., & Richards, R. I. (2009) · Human Molecular Genetics · doi:10.1093/hmg/ddp455 · Cited by 59

Authors: Solnica-Krezel, L.
Venue: Current Biology
Publisher: Elsevier BV
Published: 2005-03
Volume: 15
Issue: 6
Pages: R213-R228
ISSN: 0960-9822 (ISSN-L)
DOI: 10.1016/j.cub.2005.03.016
OpenAlex: W2054132545
Cited by: 391
References: 156
Citations by year: 2026: 9 · 2025: 13 · 2024: 12 · 2023: 12 · 2022: 21 · 2021: 21 · 2020: 18 · 2019: 14 · 2018: 10 · 2017: 16 · 2016: 10 · 2015: 12 · 2014: 19 · 2013: 19 · 2012: 16
FWCI: 2.13
Type: journal article
Language: en
Open access: bronze
doi.org
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
www.elsevier.com/legal/tdmrep-license (tdm)
www.elsevier.com/open-access/userlicense/1.0/ (vor, 3060 d)
doi.org/10.15223/policy-017 (stm-asf)
doi.org/10.15223/policy-037 (stm-asf)
doi.org/10.15223/policy-012 (stm-asf)
doi.org/10.15223/policy-029 (stm-asf)
doi.org/10.15223/policy-004 (stm-asf)
Locations: Current Biology (publishedVersion)
PubMed (publishedVersion)
Funders: National Institutes of Health
March of Dimes Foundation
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
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Pluripotent Stem Cells Research
Keywords: gastrulation, cell motility, blastopore, organizer, epiboly, convergence, extension, germ layer formation, embryonic axis patterning, vertebrate embryonic development
MeSH terms: Animals, Cell Differentiation, Cell Movement, Embryonic Induction, Endoderm, Gastrula, Mesoderm, Models, Biological, Vertebrates, Signal Transduction, Gene Expression Regulation, Developmental, Organizers, Embryonic

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

Conserved Patterns of Cell Movements during Vertebrate Gastrulation

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks