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

Items 301–391 of 391

Sizzled (Frzb3) physically interacts with noncanonical Wnt ligands to inhibit gastrulation cell movement
Yoon, J., Kumar, S., Lee, H., Rehman, Z. U., Park, S., Lee, U., & Kim, J. (2024) · Molecules and Cells · doi:10.1016/j.mocell.2024.100068 · Cited by 2
In silico identification of endo16 regulators in the sea urchin endomesoderm gene regulatory network
Chua, H.-E., Bhowmick, S. S., Tucker‐Kellogg, L., Zhao, Q., Dewey, C. F., & Yu, H. (2012) · International Health Informatics Symposium · doi:10.1145/2110363.2110381 · Cited by 2
Early Ontogeny of Semionotiformes and Amiiformes (Neopterygii
Jaroszewska, M., & Dabrowski, K. R. (2009) · Science Publishers eBooks · doi:10.1201/b10184-5 · Cited by 2
Taking the Middle Road
Feldman, B. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-405945-0.00012-0 · Cited by 3
Embryonic development of the fire-eye-tetra Moenkhausia oligolepis (Characiformes: Characidae)
dos Santos, R. S., Rodrigues, J., Cordeiro, J. G., Tercya, H., Leite, M. M., Costa, B. P. D., Costa, R. D. S., Maximino, C., & de Siqueira‐Silva, D. H. (2021) · Zygote · doi:10.1017/s0967199420000647 · Cited by 2
The Adaptor Protein Lurap1 Is Required for Cell Cohesion during Epiboly Movement in Zebrafish
Li, J., Cheng, X.-N., Zhang, C., Shi, D., & Shao, M. (2021) · Biology · doi:10.3390/biology10121337 · Cited by 2
The multicellular relatives of Chlamydomonas
Miller, S. M., & Nozaki, H. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-822457-1.00012-1 · Cited by 2
Developmental Biology: Cell Intercalation One Step beyond
Bénazéraf, B., & Pourquié, O. (2008) · Current Biology · doi:10.1016/j.cub.2007.11.065 · Cited by 2
May the force be with you
Weng, S., & Wallingford, J. B. (2018) · eLife · doi:10.7554/elife.36662 · Cited by 2
Genetic and bioinformatic approaches to characterize ethanol teratogenesisPreprint
Sidik, A., Dixon, G., Kirby, H. G., & Eberhart, J. (2019) · bioRxiv · doi:10.1101/805556 · Cited by 1
Coupling and uncoupling of midline morphogenesis and cell flow in amniote gastrulationPreprint
Asai, R., Prakash, V. N., Sinha, S. C., Prakash, M., & Mikawa, T. (2024) · eLife · doi:10.7554/elife.89948.2 · Cited by 2
On growth and form of animal behavior
Golani, I., & Kafkafi, N. (2025) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2024.1476233 · Cited by 2
Identification and embryonic expression of a highly conserved Meis-linked gene
Cochrane, A. C., Carpenter, B. S., Graham, B., & Zerucha, T. (2011) · Developmental Biology · doi:10.1016/j.ydbio.2011.05.300 · Cited by 1
The Pediatric Femur: Development, Growth, and Surgical Anatomy
May, C. J., & Spencer, S. A. (2016) · Springer eBooks · doi:10.1007/978-1-4899-7986-5_1 · Cited by 1
Fisiología reproductiva del pez Betta splendens en condiciones de laboratorio, Piedemonte Andino Amazónico (Colombia)
Murcia-Ordoñez, B., Chaves, L., España, W. F., Castañeda, D., & Andrade, J. (2016) · Revista Veterinaria · doi:10.30972/vet.2721087 · Cited by 1
Cell Polarity in Morphogenesis—Planar Cell Polarity
Mandrekar, N., Su, B., & Habas, R. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-802438-6.00004-8 · Cited by 1
载脂蛋白C1调控斑马鱼原肠胚形成中的外包运动
周, 莉., 汪, 洋., 桂, 建., 李, 文., & 李, 志. (2014) · Scientia Sinica Vitae · doi:10.1360/zc2014-44-1-29
From network analysis to experimental validation: identification of regulators of non-muscle myosin II contractility using the folded-gastrulation signaling pathway
Zhao, A., Varady, S., O’Kelley-Bangsberg, M., Deng, V., Platenkamp, A., Wijngaard, P., Bern, M., Gormley, W., Kushkowski, E. E., Thompson, K., et al. (2023) · BMC Molecular and Cell Biology · doi:10.1186/s12860-023-00492-3 · Cited by 1
Spatio-Temporal Dynamics of Embryonic Tissue Deformations during Gastrulation in Xenopus laevis: Morphometric Analysis
Бредов, Д. В., Volodyaev, I., & Luchinskaya, N. N. (2021) · Russian Journal of Developmental Biology · doi:10.1134/s1062360421050027 · Cited by 1
Hox Genes, a Molecular Constraint for the Development and Evolution of the Vertebrate Body Plan
Iimura, T., Himeno, A., Nakane, A., & Yamaguchi, A. (2010) · Journal of Oral Biosciences · doi:10.1016/s1349-0079(10)80045-3 · Cited by 1
FGF signaling in specification of hESC-derived definitive endoderm
Ameri, J. (2010) · Lund University Publications (Lund University) · Cited by 1
Trecento : in silico network-driven identification of target combinations for combination therapy
Chua, H. E. (2015) · DR-NTU (Nanyang Technological University) · doi:10.32657/10356/64995 · Cited by 2
From cells to tissues: physical modelling of the collective behaviour of embryonic cells
Käfer, J. (2008) · HAL · Cited by 1
Modelling of active contraction pulses in epithelial cells using the vertex modelPreprint
Pérez-Verdugo, F., Reig, G., Cerda, M., Concha, M. L., & Soto, R. (2021) · arXiv (Cornell University) · doi:10.48550/arxiv.2106.00824 · Cited by 1
On the growth and form of animal behaviorPreprint
Golani, I. (2022) · doi:10.31219/osf.io/mqeg3 · Cited by 1
hoxb genes determine the timing of cell ingression by regulating cell surface fluctuations during zebrafish gastrulationPreprint
Moriyama, Y., Mitsui, T., & Heisenberg, C. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.02.06.579056 · Cited by 1
Supplemental Dietary Nano Zinc Can Impart Higher Antioxidant Status by Modulating Cu-Zn SOD ExpressionPreprint
Tah, A., Pal, A., De, D., & Chatterjee, P. N. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.21.614296 · Cited by 1
Extracellular Matrix Deposition Controls Early Differentiation Patterns in Human Cardiac GastruloidsPreprint
Marchand, M., Sahni, G., Arora, A., Serhrouchni, S., Dilasser, F., Monet, A., Lucciani, F., Rajendiran, H., Chabot, L., Raffi, S. B. M., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.18.643854 · Cited by 1
Molecular factors influencing epithelial-mesenchymal transition in breast cancer
Nilsson, G. (2014) · Gothenburg University Publications Electronic Archive (Gothenburg University) · Cited by 1
Essential Roles of Stat3 in Zebrafish Development
Liu, Y. (2015) · Open Scholarship Institutional Repository (Washington University in St. Louis) · doi:10.7936/k7qr4v97
The Development of Small Molecules and Growth Supplements to Control the Differentiation of Stem Cells and the Formation of Neural Tissues
Christie, V. B., Maltman, D. J., Whiting, A., Marder, T. B., & Przyborski, S. A. (2010) · Stem cell biology and regenerative medicine · doi:10.1007/978-1-60761-860-7_31
The interplay of JNK and SCG10 during cortical development and in excitotoxic responses in brain
Zdrojewska, J. (2014) · Doria (University of Helsinki)
3D magnetic resonance microscopy of dehydrated biological specimens
Mietchen, D. (2006) · Publikationsdatenbank der Fraunhofer-Gesellschaft (Fraunhofer-Gesellschaft) · doi:10.22028/d291-22613
Investigating the genetic program of germ cell specification in pig
Sun, X. (2010) · Nottingham ePrints (University of Nottingham)
Developmental Mechanisms that Support Genome Stability and Embryonic Survival in Stress-tolerant Embryos of the Annual Killifish Austrofundulus limnaeus
Wagner, J. T. (2000) · doi:10.15760/etd.2517
Analysis of the arachidonyl-CoA synthetase ACSL4a as a potential regulator of BMP expression and of the role of BMPs in timing of cell commitment along the dorsoventral axis of the gastrulating zebrafish embryo
Renisch, B. (2009) · Kölner Universitäts PublikationsServer (Universität zu Köln)
Mechanisms of Wnt signaling: from embryonic stem cells to dopaminergic neurons
Čajánek, L. (2011) · Figshare
Expression of the avian gene cNOC2 encoding nucleolar complex associated protein 2 during embryonic development
Zhang, X., Dai, F., Weise, C., Faisal, Y., Bonafede, A., Moroşan‐Puopolo, G., Rehimi, R., Wang, J., & Brand‐Saberi, B. (2006) · Anatomy and Embryology · doi:10.1007/s00429-006-0115-z
Linking the embryonic clock with temporal collinearity of Hox gene activation
Fernandes, C. S. R. (2010) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)
The role of Mesogenin1 in the dynamics of movement and differentiation of mesoderm progenitor cells
Figueira, A. M. D. S. (2013) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)
Dietary Supplementation of Omega-3 Fatty Acids Influences the Equine Maternal Uterine Environment and Embryonic Development
Jacobs, R. D. (2015) · VTechWorks (Virginia Tech)
Zebrafishcellmovements during gastrulation
Zhang, T., & Mo, X. (2013) · Hereditas (Beijing) · doi:10.3724/sp.j.1005.2013.00441
Roles of Extrinsic Forces in Early Mouse Limb Bud Ectoderm Rearrangement
Wen, J. (2015) · TSpace (University of Toronto)
Investigating microRNA-target interactions during skeletal muscle development in chicken embryos
Viaut, C. (2017) · UEA Digital Repository (University of East Anglia)
Control of E-cadherin Function in Cell Intercalation by ER Glucosylation Enzymes
Zhang, Y. (2012) · doi:10.53846/goediss-1488
Edge Detection of Cryptic Lamellipodia Assisted by Deep LearningPreprint
Wang, C., Kang, S., Kim, E., Zhang, X., Choi, H. J., Choi, A., & Lee, K. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/181263
The Role of Iroquois 3 and 5 in Limb Bud Pattern Formation and Morphogenesis
Li, D. (2014) · TSpace (University of Toronto)
Article Integrin a 5 b 1 and Fibronectin Regulate Polarized Cell Protrusions Required for Xenopus Convergence and Extension
Davidson, L. A., Marsden, M., Keller, R. E., & DeSimone, D. W. (2006)
Building Relationships: A Role for Innexins in Tissue Formation
Labbaf, Z., & Raz, E. (2020) · Developmental Cell · doi:10.1016/j.devcel.2020.07.004
Az embrionális fejlődés során zajló sejtmozgások szabályozásának vizsgálata zebradánió modellben
Zsigmond, Á. (2018) · Eötvös Loránd Tudományegyetem · doi:10.15476/elte.2017.122
The adaptive value of sex ratio adjustment
Szász, E. (2018) · Eötvös Loránd Tudományegyetem · doi:10.15476/elte.2018.187
The role of yolk syncytial layer and blastoderm movements during gastrulation in zebrafish
Carvalho, L. C. D. J. (2007) · Max Planck Institute for Plasma Physics
Faculty Opinions recommendation of A Wnt-CKIvarepsilon-Rap1 pathway regulates gastrulation by modulating SIPA1L1, a Rap GTPase activating protein.
Kimelman, D. (2007) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1069738.522660
Faculty Opinions recommendation of Galpha12/13 regulate epiboly by inhibiting E-cadherin activity and modulating the actin cytoskeleton.
Labouesse, M. (2009) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1158697.618912
Faculty Opinions recommendation of Mouse prickle1, the homolog of a PCP gene, is essential for epiblast apical-basal polarity.
Tam, P. (2009) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1165316.628267
Introducing a Method for Controllable Deformation of Embryonic Tissues to Study Mechanodependent Cell Movements
Бредов, Д. В., Luchinskaya, N. N., & Volodyaev, I. (2022) · Russian Journal of Developmental Biology · doi:10.1134/s1062360422020047
Faculty Opinions recommendation of Apical and basal matrix remodeling control epithelial morphogenesis.
Chisholm, A. D. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733565022.793580472
Faculty Opinions recommendation of Maternally regulated gastrulation as a source of variation contributing to cavefish forebrain evolution.
Houart, C., & Giger, F. A. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.736836687.793569595
Advanced Techniques
Kinoshita, M., Murata, K., Naruse, K., & Tanaka, M. (2009) · doi:10.1002/9780813818849.ch10
A zebrafish embryo screen utilizing gastrulation for identification of anti-metastasis drugsPreprint
Nakayama, J., Makinoshima, H., & Gong, Z. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.05.07.490997
Generation of functional posterior spinal motor neurons from hPSCs-derived human spinal cord neural progenitor cellsPreprint
Xu, J. H., Yao, Y., Yao, F., Chen, J., Li, M., Yang, X., Li, S., Lu, F., Hu, P., He, S., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.06.26.495599
Celsr1 suppresses WNT5A-mediated chemoattraction to prevent incorrect rostral migration of facial branchiomotor neurons
Hummel, D. (2022) · doi:10.32469/10355/91581
Diferenças sexuais nas redes de regulação gênica durante o período fetal do neurodesenvolvimento
de Toledo, V. H. C. (2022) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.5.2022.tde-01022023-092430
Welcome to the nursery
Marx, V. (2023) · Nature Methods · doi:10.1038/s41592-023-01902-2
Coupling and uncoupling of midline morphogenesis and cell flow in amniote gastrulationPreprint
Asai, R., Prakash, V. N., Sinha, S., Prakash, M., & Mikawa, T. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.26.542486
Coupling and uncoupling of midline morphogenesis and cell flow in amniote gastrulationPreprint
Asai, R., Prakash, V. N., Sinha, S., Prakash, M., & Mikawa, T. (2023) · eLife · doi:10.7554/elife.89948.1
HPSC-Based 2.5D In Vitro Model for Embryonic Morphogenesis Study
Wang, S. (2021) · Journal of Embryology & Stem Cell Research · doi:10.23880/jes-16000151
Suppression of Pcdh8/paraxial protocadherin is required for efficient neighbor exchange in morphogenetic cell movement during zebrafish notochord formation
Kai, M., & Kondō, M. (2024) · Scientific Reports · doi:10.1038/s41598-024-76762-7
A Review on Mechanisms of Single-Cell and Collective Cell Migration: Insights into Tissue Dynamics
Kiran, A., Kumar, N., & Mehandia, V. (2025) · Materials horizons · doi:10.1007/978-981-96-5366-9_8
Resilience in zebrafish embryoidsPreprint
Jovanic, S., Eckert, J., Savy, T., & Peyriéras, N. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.06.18.660370
Developmental system drift and modular gene regulatory networks shape gastrulation in Acropora
Ossa-Gómez, J. P., Rodríguez-Cabal, H. A., & Reyes-Bermúdez, A. (2025) · Life Science Alliance · doi:10.26508/lsa.202503293 · Cited by 4
Planar cell polarity aligns epithelial migration to coordinate tissue architecture and functional zonationPreprint
Lee, R. F., Oluwatade, D., & Sumigray, K. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.30.685585
Exploring Common and Unique Developmental Mechanism in Vertebrate Organogenesis
Penaso, F. G. (2025) · Tropical Environment Biology and Technology · doi:10.53623/tebt.v3i2.773
Stationary and germ layer-specific cellular flows shape the zebrafish gastrulaPreprint
Wopat, S., Derksen, P., Jain-Sharma, V., Han, G., Claussen, N. H., & Streichan, S. J. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.10.687746
Elasticity and plasticity of epithelial gap closure
Setoudeh, M., & Haas, P. A. (2026) · Physical review. E · doi:10.1103/qtcv-gk3y
Co-Immunoprecipitation-Coupled Mass Spectrometry Analysis of Zyxin’s Interactome and Phosphosites in Early Xenopus laevis Development
Parshina, E. A., Ziganshin, R. H., Zaraisky, A. G., & Martynova, N. Y. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27020738
Caractérisation de la différenciation de l'endoderme primitif : Coopération entre la voie de signalisation RTK-FGF et le facteur de transcription Gata 6
Hermitte, S. (2017) · theses.fr (ABES) · doi:10.70675/6b207faaze6c2z44d8za445z1d7b4d5bf750
Emerging properties of heterogeneous multicellular systems
Hallou, A. (2017) · doi:10.70675/cbd51c20zf100z4cd9zb5daza9bb0b4a385f
ln vivo and in toto imaging for the reconstruction of multilevel dynamics in embryonic morphogenesis
Jovanic, S. (2022) · theses.fr (ABES) · doi:10.70675/27258badz60cez4eb3zba1bz82f165c2aa33
Bioinformatic and functional analyses of muscle cell diversification in Drosophila melanogaster
Poovathumkadavil, P. (2021) · doi:10.70675/74fca170za64bz46e3zb2bbz13d37d0dfdb5
Régulation épigénétique du développement : approche eco-evo-devo des m6A-épitranscriptomes chez l'huître Crassostrea gigas
Franc, L. L. (2021) · theses.fr (ABES) · doi:10.70675/e23ee282z43a3z4d41zbbe6z4deead48c90a
Evolution of the eye in Astyanax mexicanus : contribution of maternal and early developmental regulations
Leclercq, J. (2022) · theses.fr (ABES) · doi:10.70675/0e2196a4z7dfdz42f6za19fz55c161b9874f
Investigating the role of the centromeric histone variant CENP-A in cancer
Renaud-Pageot, C. (2024) · theses.fr (ABES) · doi:10.70675/eb41b5bfz0c52z4889z9d8czf04f426b8666
Regulation of Rho1 by RhoGAPs during drosophila germ band extension
Sidharthan, S. (2023) · theses.fr (ABES) · doi:10.70675/eb57dd31zed08z40f7zba58z5a78b3671f85
Mechanisms Underlying the Initiation and Termination of Collective Cell Migration: Perspectives for Understanding Development and Cancer Metastasis
Miao, G. (2026) · BioEssays · doi:10.1002/bies.70139
Tetrabromobisphenol S-induced developmental toxicity in zebrafish embryos: impacts on cytoskeletal proteins during gastrulation
Serradimigni, R., Sabatini, H. M., Chouinard, C. D., & Dasgupta, S. (2026) · Toxicological Sciences · doi:10.1093/toxsci/kfag075
Amniote gastrulation in silico
Knudsen, T. E., Utecht, S., Schauser, J. H., & Trusina, A. (2026) · Current Opinion in Systems Biology · doi:10.1016/j.coisb.2026.100603
Embryonic and larval development of the Pacific saury Cololabis saira : Distinctive characteristics of a rapidly growing beloniform fish
Kusakabe, R., Yamauchi, S., & Kuraku, S. (2026) · Developmental Dynamics · doi:10.1002/dvdy.70188
Three-dimensional Cell and Nuclear Geometries Inform Tissue Level Fluid Mechanics During Epithelial Remodeling
Russell, L. (2026) · doi:10.56902/etdcrp.2026.189
Planar cell polarity aligns epithelial migration to coordinate intestinal architecture and functional zonation
Lee, R. F., Oluwatade, D., Wivell, P., Citrin, K. M., Wen, Z., Palikuqi, B., & Sumigray, K. (2026) · Developmental Cell · doi:10.1016/j.devcel.2026.10.001
Role for the Axin-RGS domain during embryonic development
Schneider, P. N. (2010) · doi:10.17077/etd.1lixw2of

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