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

Flagged first, then by citations

Show all 156 references

2 of the 156 references couldn’t be matched to a known paper.

Sorted by citations

Items 101–200 of 391

Cystic diseases of the kidney: ciliary dysfunction and cystogenic mechanisms
Gascue, C., Katsanis, N., & Badano, J. L. (2010) · Pediatric Nephrology · doi:10.1007/s00467-010-1697-5 · Cited by 59
Comparative Phosphoproteomics of Zebrafish Fyn/Yes Morpholino Knockdown Embryos
Lemeer, S., Jopling, C., Gouw, J. W., Mohammed, S., Heck, A. J. R., Slijper, M., & den Hertog, J. (2008) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m800081-mcp200 · Cited by 59
A Novel Role for MAPKAPK2 in Morphogenesis during Zebrafish Development
Holloway, B. A., Canny, S. G. D. L. T., Ye, Y., Slusarski, D. C., Freisinger, C. M., Dosch, R., Chou, M. M., Wagner, D. S., & Mullins, M. C. (2009) · PLoS Genetics · doi:10.1371/journal.pgen.1000413 · Cited by 58
Exploring the Link Between Human Embryonic Stem Cell Organization and Fate Using Tension-Calibrated Extracellular Matrix Functionalized Polyacrylamide Gels
Lakins, J. N., Chin, A. R., & Weaver, V. M. (2012) · Methods in molecular biology · doi:10.1007/978-1-61779-980-8_24 · Cited by 58
Ror2 Receptor Mediates Wnt11 Ligand Signaling and Affects Convergence and Extension Movements in Zebrafish
Bai, Y., Tan, X., Zhang, H., Liu, C., Zhao, B., Li, Y., Lu, L., Liu, Y., & Zhou, J. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.586099 · Cited by 57
Epithelial type, ingression, blastopore architecture and the evolution of chordate mesoderm morphogenesis
Shook, D. R., & Keller, R. E. (2007) · Journal of Experimental Zoology Part B Molecular and Developmental Evolution · doi:10.1002/jez.b.21198 · Cited by 57
Tension and Epithelial Morphogenesis in Drosophila Early Embryos
Lye, C. M., & Sanson, B. (2011) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-385065-2.00005-0 · Cited by 56
RhoA regulates initiation of invagination, but not convergent extension, during sea urchin gastrulation
Beane, W. S., Gross, J. M., & McClay, D. R. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2005.12.031 · Cited by 58
Unexpected mosaicism of R201H-GNAS1 mutant-bearing cells in the testes underlie macro-orchidism without sexual precocity in McCune–Albright syndrome
Rey, R. A., Venara, M. C., Coutant, R., Trabut, J., Rouleau, S., Lahlou, N., Sultan, C., Limal, J. M., Picard, J., & Lumbroso, S. (2006) · Human Molecular Genetics · doi:10.1093/hmg/ddl430 · Cited by 56
Primary body axes of vertebrates: Generation of a near‐Cartesian coordinate system and the role of Spemann‐type organizer
Meinhardt, H. (2006) · Developmental Dynamics · doi:10.1002/dvdy.20952 · Cited by 54
Planar cell polarity proteins differentially regulate extracellular matrix organization and assembly during zebrafish gastrulation
Dohn, M. R., Mundell, N. A., Sawyer, L. M., Dunlap, J. A., & Jessen, J. R. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.08.027 · Cited by 52
Biomechanics of Collective Cell Migration in Cancer Progression: Experimental and Computational Methods
Spatarelu, C.-P., Zhang, H., Nguyen, D., Han, X., Liu, R., Guo, Q., Notbohm, J., Fan, J., Liu, L., & Chen, Z. (2019) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.8b01428 · Cited by 52
Budding behaviors: Growth of the limb as a model of morphogenesis
Hopyan, S., Sharpe, J. A., & Yang, Y. (2011) · Developmental Dynamics · doi:10.1002/dvdy.22601 · Cited by 49
Syntenin, a syndecan adaptor and an Arf6 phosphatidylinositol 4,5-bisphosphate effector, is essential for epiboly and gastrulation cell movements in zebrafish
Lambaerts, K., Dyck, S. V., Mortier, E., Ivarsson, Y., Degeest, G., Luyten, A., Vermeiren, E., Peers, B., David, G., & Zimmermann, P. (2012) · Journal of Cell Science · doi:10.1242/jcs.089987 · Cited by 50
An early requirement for maternal FoxH1 during zebrafish gastrulation
Pei, W., Noushmehr, H., Costa, J. A., Ouspenskaia, M. V., Elkahloun, A. G., & Feldman, B. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.07.011 · Cited by 50
A novel RIPK4–IRF6 connection is required to prevent epithelial fusions characteristic for popliteal pterygium syndromes
Groote, P. D., Tran, H. T., Fransen, M., Tanghe, G., Urwyler-Rösselet, C., Craene, B. D., Leurs, K., Gilbert, B., Imschoot, G. V., Rycke, R. M. D., et al. (2014) · Cell Death and Differentiation · doi:10.1038/cdd.2014.191 · Cited by 49
Diaphanous-Related Formin 2 and Profilin I Are Required for Gastrulation Cell Movements
Lai, S.-L., Chan, T., Lin, M., Huang, W., Lou, S.-W., & Lee, S. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003439 · Cited by 49
Nodal signaling promotes the speed and directional movement of cardiomyocytes in zebrafish
de Campos-Baptista, M.-I. M., Holtzman, N. G., Yelon, D. L., & Schier, A. F. (2008) · Developmental Dynamics · doi:10.1002/dvdy.21777 · Cited by 49
The developmental stage determines the distribution and duration of gene expression after early intra-amniotic gene transfer using lentiviral vectors
Endo, M., Henriques‐Coelho, T., Zoltick, P. W., Stitelman, D. H., Peranteau, W. H., Radu, A. P., & Flake, A. W. (2009) · Gene Therapy · doi:10.1038/gt.2009.115 · Cited by 47
Polychaete trunk neuroectoderm converges and extends by mediolateral cell intercalation
Steinmetz, P. R. H., González, F. Z., Burgtorf, C., Wittbrodt, J., & Arendt, D. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0606589104 · Cited by 47
Requirement of Npc1 and availability of cholesterol for early embryonic cell movements in zebrafish
Schwend, T., Loucks, E. J., Snyder, D., & Ahlgren, S. C. (2011) · Journal of Lipid Research · doi:10.1194/jlr.m012377 · Cited by 46
Zebrafish gastrulation: Putting fate in motion
Pinheiro, D., & Heisenberg, C. (2019) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2019.10.009 · Cited by 45
Zebrafish Nkd1 promotes Dvl degradation and is required for left–right patterning
Schneider, I., Schneider, P. N., Derry, S. W., Lin, S., Barton, L. J., Westfall, T. A., & Slusarski, D. C. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2010.08.040 · Cited by 44
Repulsive cues combined with physical barriers and cell–cell adhesion determine progenitor cell positioning during organogenesis
Paksa, A., Bandemer, J., Höckendorf, B., Razin, N., Tarbashevich, K., Minina, S., Meyen, D., Biundo, A., Leidel, S. A., Peyriéras, N., et al. (2016) · Nature Communications · doi:10.1038/ncomms11288 · Cited by 45
FAK transduces extracellular forces that orient the mitotic spindle and control tissue morphogenesis
Petridou, N. I., & Skourides, P. A. (2014) · Nature Communications · doi:10.1038/ncomms6240 · Cited by 47
Using Zebrafish to Study Collective Cell Migration in Development and Disease
Olson, H. M., & Nechiporuk, A. V. (2018) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2018.00083 · Cited by 44
αE-catenin regulates cell-cell adhesion and membrane blebbing during zebrafish epiboly
Schepis, A., Sepich, D. S., & Nelson, W. J. (2011) · Development · doi:10.1242/dev.073932 · Cited by 43
Dachsous1b cadherin regulates actin and microtubule cytoskeleton during early zebrafish embryogenesis
Li-Villarreal, N., Forbes, M. M., Loza, A. J., Chen, J., Ma, T. P., Helde, K. A., Moens, C. B., Shin, J., Sawada, A., Hindes, A. E., et al. (2015) · Development · doi:10.1242/dev.119800 · Cited by 43
Self-citation
Estimation of cell lineage trees by maximum-likelihood phylogenetics
Feng, J., DeWitt, W. S., McKenna, A., Simon, N., Willis, A. D., & Matsen, F. A., IV (2021) · The Annals of Applied Statistics · doi:10.1214/20-aoas1400 · Cited by 42
Cellular mechanisms of posterior neural tube morphogenesis in the zebrafish
Harrington, M., Chalasani, K., & Brewster, R. M. (2010) · Developmental Dynamics · doi:10.1002/dvdy.22184 · Cited by 43
Using Single-Cell and Spatial Transcriptomes to Understand Stem Cell Lineage Specification During Early Embryo Development
Peng, G., Cui, G., Ke, J., & Jing, N. (2020) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-120219-083220 · Cited by 42
Completion of the epithelial to mesenchymal transition in zebrafish mesoderm requires Spadetail
Row, R. H., Maître, J., Martin, B. L., Stockinger, P., Heisenberg, C., & Kimelman, D. (2011) · Developmental Biology · doi:10.1016/j.ydbio.2011.03.025 · Cited by 42
On the origins of morphological disparity and its diverse developmental bases
Salazar‐Ciudad, I. (2006) · BioEssays · doi:10.1002/bies.20482 · Cited by 42
Role of PKA as a negative regulator of PCP signaling pathway during Xenopus gastrulation movements
Park, E., Kim, G.-H., Choi, S.-C., & Han, J.-K. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.01.011 · Cited by 41
The involvement of Eph–Ephrin signaling in tissue separation and convergence during Xenopus gastrulation movements
Park, E. C., Cho, G.-S., Kim, G., Choi, S., & Han, J. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2010.12.012 · Cited by 41
Studying evolution of the primary body axis in vivo and in vitro
Anlaş, K., & Trivedi, V. (2021) · eLife · doi:10.7554/elife.69066 · Cited by 41
Monitoring developmental force distributions in reconstituted embryonic epithelia
Przybyla, L., Lakins, J. N., Sunyer, R., Trepat, X., & Weaver, V. M. (2015) · Methods · doi:10.1016/j.ymeth.2015.09.003 · Cited by 40
Prostaglandin Gβγ signaling stimulates gastrulation movements by limiting cell adhesion through Snai1a stabilization
Speirs, C. K., Jernigan, K. K., Kim, S. H., Cha, Y. I., Lin, F. H., Sepich, D. S., DuBois, R. N., Lee, E. N., & Solnica‐Krezel, L. (2010) · Development · doi:10.1242/dev.045971 · Cited by 40
Self-citation
Formins in development: Orchestrating body plan origami
Liu, R., Linardopoulou, E. V., Osborn, G. E., & Parkhurst, S. M. (2008) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2008.09.016 · Cited by 42
Calcium dynamics integrated into signalling pathways that influence vertebrate axial patterning
Freisinger, C. M., Schneider, I., Westfall, T. A., & Slusarski, D. C. (2008) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2007.2255 · Cited by 39
Nemo kinase phosphorylates β-catenin to promote ommatidial rotation and connects core PCP factors to E-cadherin–β-catenin
Mirkovic, I., Gault, W. J., Rahnama, M., Jenny, A., Gaengel, K., Bessette, D. C., Gottardi, C. J., Verheyen, E. M., & Mlodzik, M. (2011) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.2049 · Cited by 40
Beyond “Second Animals”: Making Sense of Plant Ethics
Pouteau, S. (2013) · Journal of Agricultural and Environmental Ethics · doi:10.1007/s10806-013-9439-x · Cited by 39
The actin nucleator Cordon-bleu is required for development of motile cilia in zebrafish
Ravanelli, A. M., & Klingensmith, J. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2010.11.023 · Cited by 39
VANGL2 interacts with integrin αv to regulate matrix metalloproteinase activity and cell adhesion to the extracellular matrix
Jessen, T. N., & Jessen, J. R. (2017) · Experimental Cell Research · doi:10.1016/j.yexcr.2017.10.026 · Cited by 36
The evolution of gastrulation morphologies
Nájera, G. S., & Weijer, C. J. (2023) · Development · doi:10.1242/dev.200885 · Cited by 32
Decoupling of amniote gastrulation and streak formation reveals a morphogenetic unity in vertebrate mesoderm induction
Alev, C., Wu, Y., Nakaya, Y., & Sheng, G. (2013) · Development · doi:10.1242/dev.094318 · Cited by 39
Sphingosine-1-phosphate receptors regulate individual cell behaviours underlying the directed migration of prechordal plate progenitor cells during zebrafish gastrulation
Kai, M., Heisenberg, C., & Tada, M. (2008) · Development · doi:10.1242/dev.020396 · Cited by 39
Zebrafish as a Model for Developmental Biology and Toxicology
Roper, C., & Tanguay, R. L. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-809405-1.00012-2 · Cited by 42
Oriented cell division in vertebrate embryogenesis
Castanon, I., & González‐Gaitán, M. (2011) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2011.09.009 · Cited by 37
Neural commitment of embryonic stem cells: molecules, pathways and potential for cell therapy
Suter, D. M., & Krause, K. (2008) · The Journal of Pathology · doi:10.1002/path.2380 · Cited by 39
Toddler signaling regulates mesodermal cell migration downstream of Nodal signaling
Norris, M. L., Pauli, A., Gagnon, J. A., Lord, N. D., Rogers, K. W., Mosimann, C., Zon, L. I., & Schier, A. F. (2017) · eLife · doi:10.7554/elife.22626 · Cited by 37
Purines as potential morphogens during embryonic development
Massé, K. L., & Dale, N. (2012) · Purinergic Signalling · doi:10.1007/s11302-012-9290-y · Cited by 38
Nutritional endoderm: a way to breach the holoblastic–meroblastic barrier in tetrapods
Elinson, R. P. (2008) · Journal of Experimental Zoology Part B Molecular and Developmental Evolution · doi:10.1002/jez.b.21218 · Cited by 37
Differentiation of Definitive Endoderm from Mouse Embryonic Stem Cells
Kim, P. T. W., & Ong, C. J. (2012) · Results and problems in cell differentiation · doi:10.1007/978-3-642-30406-4_17 · Cited by 36
Molecular signaling in zebrafish development and the vertebrate phylotypic period
Comte, A., Roux, J., & Robinson‐Rechavi, M. (2010) · Evolution & Development · doi:10.1111/j.1525-142x.2010.00400.x · Cited by 36
Vertebrate Axial Patterning: From Egg to Asymmetry
Houston, D. W. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-46095-6_6 · Cited by 36
Inhibition of Six1 affects tumour invasion and the expression of cancer stem cell markers in pancreatic cancer
Lerbs, T., Bisht, S., Schölch, S., Pecqueux, M., Kristiansen, G., Schneider, M., Hofmann, B. T., Welsch, T., Reißfelder, C., Rahbari, N. N., et al. (2017) · BMC Cancer · doi:10.1186/s12885-017-3225-5 · Cited by 35
Automatic cell counting for phase‐contrast microscopic images based on a combination of Otsu and watershed segmentation method
Lin, Y., Diao, Y., Du, Y., Zhang, J., Li, L., & Liu, P. (2021) · Microscopy Research and Technique · doi:10.1002/jemt.23893 · Cited by 35
Temporal control over the initiation of cell motility by a regulator of G-protein signaling
Hartwig, J., Tarbashevich, K., Seggewiß, J., Stehling, M., Bandemer, J., Grimaldi, C., Paksa, A., Groß-Thebing, T., Meyen, D., & Raz, E. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1400043111 · Cited by 34
There is more than one way to turn a spherical cellular monolayer inside out: type B embryo inversion in Volvox globator
Höhn, S. S. M. H., & Hallmann, A. (2011) · BMC Biology · doi:10.1186/1741-7007-9-89 · Cited by 34
Molecular basis of morphogenesis during vertebrate gastrulation
Wang, Y., & Steinbeißer, H. (2009) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-009-0018-2 · Cited by 34
Tumor suppressor Lzap regulates cell cycle progression, doming, and zebrafish epiboly
Liu, D., Wang, W., Melville, D. B., Cha, Y. I., Yin, Z., Issaeva, N., Knapik, E. W., & Yarbrough, W. G. (2011) · Developmental Dynamics · doi:10.1002/dvdy.22644 · Cited by 34
Ankrd6 is a mammalian functional homolog of Drosophila planar cell polarity gene diego and regulates coordinated cellular orientation in the mouse inner ear
Jones, C., Qian, D., Kim, S. M., Li, S., Ren, D., Knapp, L., Sprinzak, D., Avraham, K. B., Matsuzaki, F., Chi, F., et al. (2014) · Developmental Biology · doi:10.1016/j.ydbio.2014.08.029 · Cited by 33
Human Embryonic Stem Cell Differentiation on Tissue Engineering Scaffolds: Effects of NGF and Retinoic Acid Induction
İnanç, B., Elçin, A. E., & Elçin, Y. M. (2008) · Tissue Engineering Part A · doi:10.1089/tea.2007.0213 · Cited by 33
Maternally regulated gastrulation as a source of variation contributing to cavefish forebrain evolution
Torres‐Paz, J., Leclercq, J., & Rétaux, S. (2019) · eLife · doi:10.7554/elife.50160 · Cited by 31
Control of convergent yolk syncytial layer nuclear movement in zebrafish
Carvalho, L., Stühmer, J., Bois, J. S., Kalaidzidis, Y. L., Lecaudey, V., & Heisenberg, C. (2009) · Development · doi:10.1242/dev.026922 · Cited by 35
Mechanical Control of Cell Differentiation: Insights from the Early Embryo
Nelson, C. M. (2022) · Annual Review of Biomedical Engineering · doi:10.1146/annurev-bioeng-060418-052527 · Cited by 33
Human Embryonic Stem Cell Differentiation on Tissue Engineering Scaffolds: Effects of NGF and Retinoic Acid Induction
İnanç, B., Elçin, A. E., & Elçin, Y. M. (2008) · Tissue Engineering Part A · doi:10.1089/ten.tea.2007.0213 · Cited by 31
Gene Expression Profiling of Atlantic Cod (Gadus morhua) Embryogenesis Using Microarray
Drivenes, Ø., Taranger, G. L., & Edvardsen, R. B. (2011) · Marine Biotechnology · doi:10.1007/s10126-011-9399-y · Cited by 29
Non-directional radial intercalation dominates deep cell behavior during zebrafish epiboly
Bensch, R., Song, S., Ronneberger, O., & Driever, W. (2013) · Biology Open · doi:10.1242/bio.20134614 · Cited by 29
A two-tier junctional mechanism drives simultaneous tissue folding and extension
John, A., & Rauzi, M. (2021) · Developmental Cell · doi:10.1016/j.devcel.2021.04.003 · Cited by 29
Pyriproxyfen exposure induces DNA damage, cell proliferation impairments and apoptosis in the brain vesicles layers of chicken embryos
Luckmann, M. R., de Melo, M. S., Spricigo, M. C., da Silva, N. M., & Nazari, E. M. (2021) · Toxicology · doi:10.1016/j.tox.2021.152998 · Cited by 29
A self-generated Toddler gradient guides mesodermal cell migration
Stock, J., Kazmar, T., Schlumm, F., Hannezo, É., & Pauli, A. (2022) · Science Advances · doi:10.1126/sciadv.add2488 · Cited by 29
Negative regulation of wnt11 expression by Jnk signaling during zebrafish gastrulation
Seo, J., Asaoka, Y., Nagai, Y., Hirayama, J., Yamasaki, T., Namae, M., Ohata, S., Shimizu, N., Negishi, T., Kitagawa, D., et al. (2010) · Journal of Cellular Biochemistry · doi:10.1002/jcb.22616 · Cited by 30
The role of Wnt in cell signaling and cell adhesion during early vertebrate development
Wee, B. (2011) · Frontiers in bioscience · doi:10.2741/3858 · Cited by 27
Apolipoprotein C1 regulates epiboly during gastrulation in zebrafish
Wang, Y., Zhou, L., Li, Z., Li, W., & Gui, J. (2013) · Science China Life Sciences · doi:10.1007/s11427-013-4563-4 · Cited by 27
Morphological evidence of neurotoxic effects in chicken embryos after exposure to perfluorooctanoic acid (PFOA) and inorganic cadmium
Kmecick, M., da Costa, M. C. V., Ribeiro, C. A. D. O., & Ortolani-Machado, C. F. (2019) · Toxicology · doi:10.1016/j.tox.2019.152286 · Cited by 27
Making cardiomyocytes: How mechanical stimulation can influence differentiation of pluripotent stem cells
Geuss, L. R., & Suggs, L. J. (2013) · Biotechnology Progress · doi:10.1002/btpr.1794 · Cited by 28
Cancer metastasis and EGFR signaling is suppressed by amiodarone-induced versican V2
Lee, H., Su, M.-Y., Lo, H.-C., Wu, C., Hu, J.-R., Lo, D.-M., Chao, T.-Y., Tsai, H., & Dai, M. (2015) · Oncotarget · doi:10.18632/oncotarget.5621 · Cited by 27
MicroRNA-127 Promotes Mesendoderm Differentiation of Mouse Embryonic Stem Cells by Targeting Left-Right Determination Factor 2
Ma, H., Lin, Y., Zhao, Z., Lu, X., Yu, Y., Zhang, X., Wang, Q., & Li, L. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.723247 · Cited by 27
Gene expression patterns that support novel developmental stress buffering in embryos of the annual killifish Austrofundulus limnaeus
Wagner, J. T., & Podrabsky, J. E. (2015) · EvoDevo · doi:10.1186/2041-9139-6-2 · Cited by 26
Establishment of the Vertebrate Germ Layers
Tseng, W.-C., Munisha, M., Gutiérrez, J. B., & Dougan, S. T. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-46095-6_7 · Cited by 25
Reassembling gastrulation
Schauer, A., & Heisenberg, C. (2020) · Developmental Biology · doi:10.1016/j.ydbio.2020.12.014 · Cited by 25
Plasma membrane phosphatidylinositol (4,5)-bisphosphate is critical for determination of epithelial characteristics
Kanemaru, K., Shimozawa, M., Kitamata, M., Furuishi, R., Hinako, K., Sukawa, Y., Chiba, Y., Fukuyama, T., Hasegawa, J., Nakanishi, H., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-30061-9 · Cited by 24
Proteoglycans Determine the Dynamic Landscape of EMT and Cancer Cell Stemness
Karagiorgou, Z., Fountas, P. N., Manou, D., Knutsen, E., & Theocharis, A. D. (2022) · Cancers · doi:10.3390/cancers14215328 · Cited by 24
Embryonic Neural Inducing Factor Churchill Is not a DNA-binding Zinc Finger Protein: Solution Structure Reveals a Solvent-exposed β-Sheet and Zinc Binuclear Cluster
Lee, B. M., Buck‐Koehntop, B. A., Martinez‐Yamout, M. A., Dyson, H. J., & Wright, P. E. (2007) · Journal of Molecular Biology · doi:10.1016/j.jmb.2007.06.021 · Cited by 24
Convergence and extension movements mediate the specification and fate maintenance of zebrafish slow muscle precursors
Yin, C., & Solnica‐Krezel, L. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.12.030 · Cited by 27
Self-citation
Maternal contributions to gastrulation in zebrafish
Solnica‐Krezel, L. (2020) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2020.05.001 · Cited by 25
Self-citation
Learning developmental mode dynamics from single-cell trajectories
Romeo, N., Hastewell, A., Mietke, A., & Dunkel, J. (2021) · eLife · doi:10.7554/elife.68679 · Cited by 23
Regulation of Xenopus gastrulation by ErbB signaling
Nie, S., & Chang, C. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.10.039 · Cited by 24
Optimal cellular mobility for synchronization arising from the gradual recovery of intercellular interactions
Uriu, K., Ares, S., Oates, A. C., & Morelli, L. G. (2012) · Physical Biology · doi:10.1088/1478-3975/9/3/036006 · Cited by 23
Leucine repeat adaptor protein 1 interacts with Dishevelled to regulate gastrulation cell movements in zebrafish
Cheng, X.-N., Shao, M., Li, J., Wang, Y., Qi, J., Xu, Z., & Shi, D. (2017) · Nature Communications · doi:10.1038/s41467-017-01552-x · Cited by 23
Exposure to ethanol leads to midfacial hypoplasia in a zebrafish model of FASD via indirect interactions with the Shh pathway
Sidik, A., Dixon, G., Buckley, D. M., Kirby, H. G., Sun, S.-G., & Eberhart, J. (2021) · BMC Biology · doi:10.1186/s12915-021-01062-9 · Cited by 15
Down syndrome critical region protein 5 regulates membrane localization of Wnt receptors, Dishevelled stability and convergent extension in vertebrate embryos
Shao, M., Liu, Z.-Z., Wang, C., Li, H., Carron, C., Zhang, H.-W., & Shi, D. (2009) · Development · doi:10.1242/dev.032649 · Cited by 22
Maternal-to-zygotic transition as a potential target for niclosamide during early embryogenesis
Vliet, S. M. F., Dasgupta, S., Sparks, N. R. L., Kirkwood, J. S., Vollaro, A., Hur, M., Nieden, N. I. Z., & Volz, D. C. (2019) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2019.114699 · Cited by 22
Ptenb Mediates Gastrulation Cell Movements via Cdc42/AKT1 in Zebrafish
Yeh, C.-M., Liu, Y.-C., Chang, C.-J., Lai, S.-L., Hsiao, C., & Lee, S. (2011) · PLoS ONE · doi:10.1371/journal.pone.0018702 · Cited by 21
Dynamic regulation of the microtubule and actin cytoskeleton in zebrafish epiboly
Lee, S. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.08.005 · Cited by 21
Optimal cellular mobility for synchronization arising from the gradual recovery of intercellular interactions
Uriu, K., Ares, S., Oates, A. C., & Morelli, L. G. (2012) · Max Planck Institute for Plasma Physics · Cited by 21
A zebrafish embryo screen utilizing gastrulation identifies the HTR2C inhibitor pizotifen as a suppressor of EMT-mediated metastasis
Nakayama, J., Tan, L., Li, Y., Goh, B. C., Wang, S., Makinoshima, H., & Gong, Z. (2021) · eLife · doi:10.7554/elife.70151 · Cited by 20
Gastrulation and pre-gastrulation morphogenesis, inductions, and gene expression: Similarities and dissimilarities between urodelean and anuran embryos
Kanéda, T., & Motoki, J.-Y. D. (2012) · Developmental Biology · doi:10.1016/j.ydbio.2012.05.019 · Cited by 21

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