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Chase-and-run between adjacent cell populations promotes directional collective migration
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/aja.1001660406openalex-snapshot
Contributions of placodal and neural crest cells to avian cranial peripheral ganglia
inferredcites →https://doi.org/10.1002/dvdy.21758openalex-snapshot
Wnt11r is required for cranial neural crest migration
inferredcites →https://doi.org/10.1006/dbio.2002.0739openalex-snapshot
Extensive Cell Movements Accompany Formation of the Otic Placode
inferredcites →https://doi.org/10.1007/978-0-387-09846-3openalex-snapshot
The Neural Crest and Neural Crest Cells in Vertebrate Development and Evolution
inferredcites →https://doi.org/10.1016/0014-4827(53)90098-6openalex-snapshot
Observations on the social behaviour of cells in tissue culture
inferredcites →https://doi.org/10.1016/0014-4827(75)90636-9openalex-snapshot
Adhesions of fibroblasts to substratum during contact inhibition observed by interference reflection microscopy
inferredcites →https://doi.org/10.1016/j.devcel.2005.08.011openalex-snapshot
Wnt11 Functions in Gastrulation by Controlling Cell Cohesion through Rab5c and E-Cadherin
inferredcites →https://doi.org/10.1016/j.devcel.2010.06.012openalex-snapshot
Collective Chemotaxis Requires Contact-Dependent Cell Polarity
inferredcites →https://doi.org/10.1016/j.diff.2008.10.015openalex-snapshot
The chemokine SDF-1/CXCL12 regulates the migration of melanocyte progenitors in mouse hair follicles
inferredcites →https://doi.org/10.1016/j.ejor.2006.03.070openalex-snapshot
Few statistical tests for proportions comparison
inferredcites →https://doi.org/10.1016/j.ydbio.2008.05.523openalex-snapshot
Eya1 and Six1 promote neurogenesis in the cranial placodes in a SoxB1-dependent fashion
inferredcites →https://doi.org/10.1016/j.ydbio.2009.06.031openalex-snapshot
A role for chemokine signaling in neural crest cell migration and craniofacial development
inferredcites →https://doi.org/10.1016/j.ydbio.2009.11.014openalex-snapshot
Cell migration during morphogenesis
inferredcites →https://doi.org/10.1016/j.ydbio.2011.09.024openalex-snapshot
Origin and segregation of cranial placodes in Xenopus laevis
inferredcites →https://doi.org/10.1016/j.ydbio.2011.12.041openalex-snapshot
Neural crest delamination and migration: From epithelium-to-mesenchyme transition to collective cell migration
inferredcites →https://doi.org/10.1016/s0006-3495(99)77386-8openalex-snapshot
Stresses at the Cell-to-Substrate Interface during Locomotion of Fibroblasts
inferredcites →https://doi.org/10.1016/s0091-679x(08)60307-6openalex-snapshot
Appendix G: In Situ Hybridization: An Improved Whole-Mount Method for Xenopus Embryos
inferredcites →https://doi.org/10.1016/s0925-4773(00)00294-xopenalex-snapshot
Xenopus frizzled 4 is a maternal mRNA and its zygotic expression is localized to the neuroectoderm and trunk lateral plate mesoderm
inferredcites →https://doi.org/10.1016/s0925-4773(01)00393-8openalex-snapshot
Command and control: regulatory pathways controlling invasive behavior of the border cells
inferredcites →https://doi.org/10.1038/nature07441openalex-snapshot
Contact inhibition of locomotion in vivo controls neural crest directional migration
inferredcites →https://doi.org/10.1038/nature09970openalex-snapshot
Neural crest regulates myogenesis through the transient activation of NOTCH
inferredcites →https://doi.org/10.1038/ncb1658openalex-snapshot
Fibroblast-led collective invasion of carcinoma cells with differing roles for RhoGTPases in leading and following cells
inferredcites →https://doi.org/10.1038/nmat3025openalex-snapshot
Collective cell guidance by cooperative intercellular forces
inferredcites →https://doi.org/10.1038/nphys1269openalex-snapshot
Physical forces during collective cell migration
inferredcites →https://doi.org/10.1038/nrm2720openalex-snapshot
Collective cell migration in morphogenesis, regeneration and cancer
inferredcites →https://doi.org/10.1073/pnas.0910213107openalex-snapshot
Epibranchial ganglia orchestrate the development of the cranial neurogenic crest
inferredcites →https://doi.org/10.1073/pnas.1117810109openalex-snapshot
Evidence of a large-scale mechanosensing mechanism for cellular adaptation to substrate stiffness
inferredcites →https://doi.org/10.1073/pnas.252339399openalex-snapshot
Molecular basis of cell migration in the fish lateral line: Role of the chemokine receptor CXCR4 and of its ligand, SDF1
inferredcites →https://doi.org/10.1083/jcb.200606017openalex-snapshot
Wnt11 controls cell contact persistence by local accumulation of Frizzled 7 at the plasma membrane
inferredcites →https://doi.org/10.1083/jcb.200909003openalex-snapshot
Plasticity of cell migration: a multiscale tuning model
inferredcites →https://doi.org/10.1093/biomet/67.1.175openalex-snapshot
A Modification of the Rayleigh Test for Vector Data
inferredcites →https://doi.org/10.1126/science.1062028openalex-snapshot
Integration Between the Epibranchial Placodes and the Hindbrain
inferredcites →https://doi.org/10.1126/science.1092053openalex-snapshot
Cell Migration: Integrating Signals from Front to Back
inferredcites →https://doi.org/10.1126/science.220.4594.268openalex-snapshot
Neural Crest and the Origin of Vertebrates: A New Head
inferredcites →https://doi.org/10.1146/annurev.cellbio.042308.113231openalex-snapshot
Collective Cell Migration
inferredcites →https://doi.org/10.1152/ajpcell.00269.2001openalex-snapshot
Cell prestress. I. Stiffness and prestress are closely associated in adherent contractile cells
inferredcites →https://doi.org/10.1158/0008-5472.can-09-1618openalex-snapshot
Epithelial-Mesenchymal Transition and Cell Cooperativity in Metastasis
inferredcites →https://doi.org/10.1242/dev.017350openalex-snapshot
Directional migration of neural crest cells in vivo is regulated by Syndecan-4/Rac1 and non-canonical Wnt signaling/RhoA
inferredcites →https://doi.org/10.1242/dev.01857openalex-snapshot
Essential role of non-canonical Wnt signalling in neural crest migration
inferredcites →https://doi.org/10.1242/dev.031203openalex-snapshot
N- and E-cadherins in Xenopus are specifically required in the neural and non-neural ectoderm, respectively, for F-actin assembly and morphogenetic movements
inferredcites →https://doi.org/10.1242/dev.067306openalex-snapshot
A novel role for MuSK and non-canonical Wnt signaling during segmental neural crest cell migration
inferredcites →https://doi.org/10.1371/journal.pone.0001142openalex-snapshot
Ets-1 Confers Cranial Features on Neural Crest Delamination
inferredcites →https://doi.org/10.1371/journal.pone.0024443openalex-snapshot
Chondrogenic and Gliogenic Subpopulations of Neural Crest Play Distinct Roles during the Assembly of Epibranchial Ganglia
inferredcites →https://doi.org/10.1371/journal.pone.0027778openalex-snapshot
Integrin-α5 Coordinates Assembly of Posterior Cranial Placodes in Zebrafish and Enhances Fgf-Dependent Regulation of Otic/Epibranchial Cells
inferredcites →https://doi.org/10.1387/ijdb.072327asopenalex-snapshot
The preplacodal region: an ectodermal domain with multipotential progenitors that contribute to sense organs and cranial sensory ganglia
inferredcites →https://doi.org/10.1523/jneurosci.0892-10.2010openalex-snapshot
CXCR4 Controls Ventral Migration of Sympathetic Precursor Cells
inferredcites →https://doi.org/10.1523/jneurosci.4631-04.2005openalex-snapshot
The Chemokine Stromal Cell-Derived Factor-1 Regulates the Migration of Sensory Neuron Progenitors
inferredcites →https://doi.org/10.1523/jneurosci.5137-09.2010openalex-snapshot
Origin and Early Development of the Posterior Lateral Line System of Zebrafish
inferredcites →https://doi.org/10.2144/000112462openalex-snapshot
Cellular Resolution Expression Profiling Using Confocal Detection of NBT/BCIP Precipitate by Reflection Microscopy
inferredcites →https://doi.org/10.2144/000112476openalex-snapshot
Fluorescent in Situ Hybridization Employing the Conventional NBT/BCIP Chromogenic Stain
inferredcites →https://doi.org/10.3824/stembook.1.31.1openalex-snapshot
The cranial sensory nervous system: specification of sensory progenitors and placodes
inferredcites →https://doi.org/10.4161/cam.2.4.6747openalex-snapshot
Directional cell migration in vivo
inferredcites →https://doi.org/10.4161/cam.5.6.18623openalex-snapshot
Can mesenchymal cells undergo collective cell migration? The case of the neural crest
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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A Mathematical Model for Collective Cell Migration in the Presence of Multiple Distinct Stimuli
inferred← citeshttps://doi.org/10.1002/2211-5463.12313openalex-snapshot
Fibroblasts promote the collective invasion of ameloblastoma tumor cells in a 3D coculture model
inferred← citeshttps://doi.org/10.1002/9780470015902.a0020864.pub2openalex-snapshot
Cell Migration during Development
inferred← citeshttps://doi.org/10.1002/9780470015902.a0025976openalex-snapshot
Collective Cell Migration in Neural Crest Development
inferred← citeshttps://doi.org/10.1002/9780470015902.a0026602openalex-snapshot
Vertebrate Embryo: Craniofacial Development
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Neural Crest: Origin, Migration and Differentiation
inferred← citeshttps://doi.org/10.1002/dvdy.122openalex-snapshot
Neural crest development: insights from the zebrafish
inferred← citeshttps://doi.org/10.1002/dvdy.24172openalex-snapshot
Pard3 regulates contact between neural crest cells and the timing of Schwann cell differentiation but is not essential for neural crest migration or myelination
inferred← citeshttps://doi.org/10.1002/dvdy.24661openalex-snapshot
MMP14 Regulates Cranial Neural Crest Epithelial‐to‐Mesenchymal Transition and Migration
inferred← citeshttps://doi.org/10.1002/dvdy.569openalex-snapshot
Colec12 and Trail signaling confine cranial neural crest cell trajectories and promote collective cell migration
inferred← citeshttps://doi.org/10.1002/dvg.22736openalex-snapshot
Protocadherin PAPC is expressed in the CNC and can compensate for the loss of PCNS
inferred← citeshttps://doi.org/10.1002/dvg.23008openalex-snapshot
Xenopus as a model organism to study heterotrimeric G‐protein pathway during collective cell migration of neural crest
inferred← citeshttps://doi.org/10.1002/dvg.23028openalex-snapshot
Should I stay or should I go? Cadherin function and regulation in the neural crest
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Neural crest delamination and migration: Looking forward to the next 150 years
inferred← citeshttps://doi.org/10.1002/dvg.23264openalex-snapshot
Cadherin‐7 mediates proper neural crest cell–placodal neuron interactions during trigeminal ganglion assembly
inferred← citeshttps://doi.org/10.1002/dvg.23271openalex-snapshot
Cellular organization and boundary formation in craniofacial development
inferred← citeshttps://doi.org/10.1002/dvg.23282openalex-snapshot
The emerging role of cranial nerves in shaping craniofacial development
inferred← citeshttps://doi.org/10.1002/dvg.23356openalex-snapshot
Neural crest and placode roles in formation and patterning of cranial sensory ganglia in lamprey
inferred← citeshttps://doi.org/10.1002/dvg.23404openalex-snapshot
Using Xenopus to analyze neurocristopathies like Kabuki syndrome
inferred← citeshttps://doi.org/10.1002/jcp.30931openalex-snapshot
Neural crest cells development and neuroblastoma progression: Role of Wnt signaling
inferred← citeshttps://doi.org/10.1002/lpor.202200177openalex-snapshot
Breaking the Action‐Reaction Principle of Light Interactions Under a Stroboscopic Nonlinearity
inferred← citeshttps://doi.org/10.1002/wdev.142openalex-snapshot
Early embryonic specification of vertebrate cranial placodes
inferred← citeshttps://doi.org/10.1002/wdev.322openalex-snapshot
Specifying neural crest cells: From chromatin to morphogens and factors in between
inferred← citeshttps://doi.org/10.1007/978-1-0716-2035-9_30openalex-snapshot
Quantitative Analysis of Directional Neural Crest Cell Migration
inferred← citeshttps://doi.org/10.1007/978-1-4939-9412-0_11openalex-snapshot
In Vivo and In Vitro Quantitative Analysis of Neural Crest Cell Migration
inferred← citeshttps://doi.org/10.1007/978-3-031-22802-5_1openalex-snapshot
Mechanobiology of Collective Cell Migration in 3D Microenvironments
inferred← citeshttps://doi.org/10.1007/978-3-031-64532-7_2openalex-snapshot
Cell Migration in Development
inferred← citeshttps://doi.org/10.1007/978-3-319-42767-6_8openalex-snapshot
Morphogenetic Mechanisms of Inner Ear Development
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Molecular basis of contact inhibition of locomotion
inferred← citeshttps://doi.org/10.1007/s00285-019-01421-9openalex-snapshot
Modelling chase-and-run migration in heterogeneous populations
inferred← citeshttps://doi.org/10.1007/s10555-020-09900-yopenalex-snapshot
Tumor-stroma biomechanical crosstalk: a perspective on the role of caveolin-1 in tumor progression
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Mechanical transmission enables EMT cancer cells to drive epithelial cancer cell migration to guide tumor spheroid disaggregation
inferred← citeshttps://doi.org/10.1007/s11538-019-00626-9openalex-snapshot
Spatial Memory and Taxis-Driven Pattern Formation in Model Ecosystems
inferred← citeshttps://doi.org/10.1007/s11538-021-00859-7openalex-snapshot
Modelling Cell Invasion: A Review of What JD Murray and the Embryo Can Teach Us
inferred← citeshttps://doi.org/10.1007/s11538-021-00901-8openalex-snapshot
Leadership Through Influence: What Mechanisms Allow Leaders to Steer a Swarm?
inferred← citeshttps://doi.org/10.1007/s11538-025-01539-6openalex-snapshot
Chase-and-Run and Chirality in Nonlocal Models of Pattern Formation
inferred← citeshttps://doi.org/10.1007/s11626-020-00528-4openalex-snapshot
Tracking the movement of individual avian neural crest cells in vitro
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Substance P modulates properties of bone marrow-derived mesenchymal stem cells
inferred← citeshttps://doi.org/10.1016/b978-0-12-401730-6.00004-1openalex-snapshot
Neural Crest Cell Migration
inferred← citeshttps://doi.org/10.1016/b978-0-12-401730-6.00009-0openalex-snapshot
Neural Crest Cell and Placode Interactions in Cranial PNS Development
inferred← citeshttps://doi.org/10.1016/b978-0-12-405945-0.00015-6openalex-snapshot
Lessons from the Zebrafish Lateral Line System
inferred← citeshttps://doi.org/10.1016/b978-0-12-405945-0.00019-3openalex-snapshot
Development of the Pre-Placodal Ectoderm and Cranial Sensory Placodes
inferred← citeshttps://doi.org/10.1016/b978-0-12-809633-8.90752-0openalex-snapshot
Sensory Placode Formation in Vertebrates
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How can Inflammation Affect Surrounding Stem Cells? From the Viewpoint of Cardiovascular Medicine and Biology
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Embryonic Cell–Cell Adhesion
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Collective migration in complex environments: The case of the trunk neural crest
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2025.02.003openalex-snapshot
From neural crest migration to the onset of gangliogenesis
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Patterning, morphogenesis, and neurogenesis of zebrafish cranial sensory placodes
inferred← citeshttps://doi.org/10.1016/j.aanat.2024.152323openalex-snapshot
Fibroblast growth factor 8 promotes in vitro neurite outgrowth of placode-derived petrosal and nodose ganglia to varying degrees
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Cell jamming: Collective invasion of mesenchymal tumor cells imposed by tissue confinement
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2015.04.021openalex-snapshot
Controlled surface topography regulates collective 3D migration by epithelial–mesenchymal composite embryonic tissues
inferred← citeshttps://doi.org/10.1016/j.biosystems.2024.105155openalex-snapshot
Collective durotaxis along a self-generated mobile stiffness gradient in vivo
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Cell Division Induces and Switches Coherent Angular Motion within Bounded Cellular Collectives
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Disentangling cadherin-mediated cell-cell interactions in collective cancer cell migration
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Neighborly relations during collective migration
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Diverse and dynamic sources and sinks in gradient formation and directed migration
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Epithelial-to-mesenchymal transition and different migration strategies as viewed from the neural crest
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Identification of CCL3 as a Schwann cell chemotactic factor essential for nerve regeneration
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Nonreciprocal alignment as a minimal mechanism for tunable collective chirality
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Cadherin Switch during EMT in Neural Crest Cells Leads to Contact Inhibition of Locomotion via Repolarization of Forces
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Difference in Dachsous Levels between Migrating Cells Coordinates the Direction of Collective Cell Migration
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BMP-gated cell-cycle progression drives anoikis during mesenchymal collective migration
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Cellular plasticity in the neural crest and cancer
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P-cadherin-dependent adhesions are required for single lumen formation and HGF-mediated cell protrusions during epithelial morphogenesis
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The eIF2 kinase GCN2 directs keratinocyte collective cell migration during wound healing via coordination of reactive oxygen species and amino acids
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IMPETUS – Interactive MultiPhysics Environment for Unified Simulations
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A cell model about symmetric and asymmetric stem cell division
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An integro-differential non-local model for cell migration and its efficient numerical solution
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A non local model for cell migration in response to mechanical stimuli
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Cadherins function during the collective cell migration of Xenopus Cranial Neural Crest cells: revisiting the role of E-cadherin
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Neural crest and cancer: Divergent travelers on similar paths
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Chemotaxis during neural crest migration
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Sculpting the labyrinth: Morphogenesis of the developing inner ear
inferred← citeshttps://doi.org/10.1016/j.semcdb.2022.03.037openalex-snapshot
Directing with restraint: Mechanisms of protrusion restriction in collective cell migrations
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Collective cell migration across scales: A systems perspective
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Joint representation: Modeling a phenomenon with multiple biological systems
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Cranial placode differentiation defect in individuals born without a nose
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Collective cell migration: guidance principles and hierarchies
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Front–Rear Polarization by Mechanical Cues: From Single Cells to Tissues
inferred← citeshttps://doi.org/10.1016/j.tcb.2020.08.002openalex-snapshot
All Roads Lead to Directional Cell Migration
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Setting appropriate boundaries: Fate, patterning and competence at the neural plate border
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The evolutionary history of vertebrate cranial placodes – I: Cell type evolution
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Neural crest and placode interaction during the development of the cranial sensory system
inferred← citeshttps://doi.org/10.1016/j.ydbio.2014.02.011openalex-snapshot
Establishing the pre-placodal region and breaking it into placodes with distinct identities
inferred← citeshttps://doi.org/10.1016/j.ydbio.2014.05.016openalex-snapshot
Migratory neural crest cell αN-catenin impacts chick trigeminal ganglia formation
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Cranial placodes: Models for exploring the multi-facets of cell adhesion in epithelial rearrangement, collective migration and neuronal movements
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Pentimento: Neural Crest and the origin of mesectoderm
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Cdon promotes neural crest migration by regulating N-cadherin localization
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VEGF signals induce trailblazer cell identity that drives neural crest migration
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E-cadherin is required for cranial neural crest migration in Xenopus laevis
inferred← citeshttps://doi.org/10.1016/j.ydbio.2017.01.008openalex-snapshot
Knockdown of CXCL14 disrupts neurovascular patterning during ocular development
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Prickle1 is required for EMT and migration of zebrafish cranial neural crest
inferred← citeshttps://doi.org/10.1016/j.ydbio.2024.07.005openalex-snapshot
Tlx3 mediates neuronal differentiation and proper condensation of the developing trigeminal ganglion
inferred← citeshttps://doi.org/10.1016/j.ydbio.2025.05.025openalex-snapshot
Development of the zebrafish anterior lateral line system is influenced by underlying cranial neural crest
inferred← citeshttps://doi.org/10.1016/j.ydbio.2025.06.001openalex-snapshot
Measuring cell movement: Concepts and quantification
inferred← citeshttps://doi.org/10.1016/j.ydbio.2026.06.001openalex-snapshot
Placode-derived orphan chemokine CXCL14 is critical for proper chick trigeminal ganglion formation
inferred← citeshttps://doi.org/10.1016/j.ydbio.2026.08.001openalex-snapshot
Lifetime imaging reveals long-distance non-neural bioelectric patterns on timescales from seconds to hours
inferred← citeshttps://doi.org/10.1016/j.yexcr.2014.03.015openalex-snapshot
Cranial neural crest: Migratory cell behavior and regulatory networks
inferred← citeshttps://doi.org/10.1016/j.yexcr.2019.01.006openalex-snapshot
Cadherin mechanotransduction in leader-follower cell specification during collective migration
inferred← citeshttps://doi.org/10.1021/acsbiomaterials.8b01359openalex-snapshot
Directed Collective Cell Migration Using Three-Dimensional Bioprinted Micropatterns on Thermoresponsive Surfaces for Myotube Formation
inferred← citeshttps://doi.org/10.1021/jacs.5c10021openalex-snapshot
Chemically Induced Ferroic-like Phase and Collective Chemotaxis in an Active Swarm
inferred← citeshttps://doi.org/10.1021/nn507467yopenalex-snapshot
Harvesting Low Molecular Weight Biomarkers Using Gold Nanoparticles
inferred← citeshttps://doi.org/10.1038/ncb3115openalex-snapshot
A molecular mechanotransduction pathway regulates collective migration of epithelial cells
inferred← citeshttps://doi.org/10.1038/ncb3135openalex-snapshot
Control of cell–cell forces and collective cell dynamics by the intercellular adhesome
inferred← citeshttps://doi.org/10.1038/ncb3438openalex-snapshot
Engulfed cadherin fingers are polarized junctional structures between collectively migrating endothelial cells
inferred← citeshttps://doi.org/10.1038/ncb3447openalex-snapshot
Getting a grip on collective cell migration
inferred← citeshttps://doi.org/10.1038/ncb3478openalex-snapshot
A mechanically active heterotypic E-cadherin/N-cadherin adhesion enables fibroblasts to drive cancer cell invasion
inferred← citeshttps://doi.org/10.1038/ncomms11373openalex-snapshot
Mechanical cell competition kills cells via induction of lethal p53 levels
inferred← citeshttps://doi.org/10.1038/ncomms15831openalex-snapshot
Optogenetic activation of Plexin-B1 reveals contact repulsion between osteoclasts and osteoblasts
inferred← citeshttps://doi.org/10.1038/ncomms7556openalex-snapshot
Notch1–Dll4 signalling and mechanical force regulate leader cell formation during collective cell migration
inferred← citeshttps://doi.org/10.1038/nrm.2015.14openalex-snapshot
The front and rear of collective cell migration
inferred← citeshttps://doi.org/10.1038/nrm.2016.118openalex-snapshot
Mechanisms and in vivo functions of contact inhibition of locomotion
inferred← citeshttps://doi.org/10.1038/nrm.2017.98openalex-snapshot
Mechanobiology of collective cell behaviours
inferred← citeshttps://doi.org/10.1038/s41377-025-02139-8openalex-snapshot
Unusual impulse-momentum relationship in non-reciprocal light interactions
inferred← citeshttps://doi.org/10.1038/s41467-017-00283-3openalex-snapshot
Extrinsic mechanical forces mediate retrograde axon extension in a developing neuronal circuit
inferred← citeshttps://doi.org/10.1038/s41467-018-05924-9openalex-snapshot
TBC1d24-ephrinB2 interaction regulates contact inhibition of locomotion in neural crest cell migration
inferred← citeshttps://doi.org/10.1038/s41467-019-09548-5openalex-snapshot
In vivo topology converts competition for cell-matrix adhesion into directional migration
inferred← citeshttps://doi.org/10.1038/s41467-020-20362-2openalex-snapshot
Filopodia-based contact stimulation of cell migration drives tissue morphogenesis
inferred← citeshttps://doi.org/10.1038/s41467-023-38526-1openalex-snapshot
Neural crest E-cadherin loss drives cleft lip/palate by epigenetic modulation via pro-inflammatory gene–environment interaction
inferred← citeshttps://doi.org/10.1038/s41467-024-51372-zopenalex-snapshot
Modelling variability and heterogeneity of EMT scenarios highlights nuclear positioning and protrusions as main drivers of extrusion
inferred← citeshttps://doi.org/10.1038/s41467-025-63071-4openalex-snapshot
Nonreciprocal field theory for decision-making in multi-agent control systems
inferred← citeshttps://doi.org/10.1038/s41556-021-00699-6openalex-snapshot
Mechanical compartmentalization of the intestinal organoid enables crypt folding and collective cell migration
inferred← citeshttps://doi.org/10.1038/s41563-019-0504-3openalex-snapshot
Extracellular matrix anisotropy is determined by TFAP2C-dependent regulation of cell collisions
inferred← citeshttps://doi.org/10.1038/s41567-020-0964-zopenalex-snapshot
Cooperative pattern formation in multi-component bacterial systems through reciprocal motility regulation
inferred← citeshttps://doi.org/10.1038/s41580-019-0172-9openalex-snapshot
Mechanisms of 3D cell migration
inferred← citeshttps://doi.org/10.1038/s41580-025-00858-9openalex-snapshot
Collective cell migration modes in development, tissue repair and cancer
inferred← citeshttps://doi.org/10.1038/s41580-026-00949-1openalex-snapshot
Neural crest gene regulatory networks as drivers of development, diversification and disease
inferred← citeshttps://doi.org/10.1038/s41586-021-04210-xopenalex-snapshot
Collective durotaxis along a self-generated stiffness gradient in vivo
inferred← citeshttps://doi.org/10.1038/s41598-020-73862-yopenalex-snapshot
Non-junctional role of Cadherin3 in cell migration and contact inhibition of locomotion via domain-dependent, opposing regulation of Rac1
inferred← citeshttps://doi.org/10.1038/s41598-023-39094-6openalex-snapshot
Droplet duos on water display pairing, autonomous motion, and periodic eruption
inferred← citeshttps://doi.org/10.1038/s42005-025-02098-xopenalex-snapshot
Emergent complex phases in a discrete flocking model with reciprocal and non-reciprocal interactions
inferred← citeshttps://doi.org/10.1038/s42005-025-02220-zopenalex-snapshot
Synchronization and exceptional points in nonreciprocal active polar mixtures
inferred← citeshttps://doi.org/10.1039/c7sm00888kopenalex-snapshot
Tunable emergent structures and traveling waves in mixtures of passive and contact-triggered-active particles
inferred← citeshttps://doi.org/10.1039/c9lc00173eopenalex-snapshot
Traction microscopy with integrated microfluidics: responses of the multi-cellular island to gradients of HGF
inferred← citeshttps://doi.org/10.1042/bj20131182openalex-snapshot
The role of the non-canonical Wnt–planar cell polarity pathway in neural crest migration
inferred← citeshttps://doi.org/10.1042/bst20221202openalex-snapshot
Expect the unexpected: conventional and unconventional roles for cadherins in collective cell migration
inferred← citeshttps://doi.org/10.1042/bst20230211openalex-snapshot
Cell–matrix and cell–cell interaction mechanics in guiding migration
inferred← citeshttps://doi.org/10.1051/medsci/20143008012openalex-snapshot
Migrations cellulaires collectives
inferred← citeshttps://doi.org/10.1063/5.0214730openalex-snapshot
Impact of non-reciprocal interactions on colloidal self-assembly with tunable anisotropy
inferred← citeshttps://doi.org/10.1073/pnas.1612208113openalex-snapshot
Epithelial self-healing is recapitulated by a 3D biomimetic E-cadherin junction
inferred← citeshttps://doi.org/10.1073/pnas.2010318117openalex-snapshot
Nonreciprocity as a generic route to traveling states
inferred← citeshttps://doi.org/10.1080/19336918.2015.1019997openalex-snapshot
Cell traction in collective cell migration and morphogenesis: The chase and run mechanism
inferred← citeshttps://doi.org/10.1080/19336918.2015.1131388openalex-snapshot
In vitro formation of neuroclusters in microfluidic devices and cell migration as a function of stromal-derived growth factor 1 gradients
inferred← citeshttps://doi.org/10.1083/jcb.201402093openalex-snapshot
In vivo collective cell migration requires an LPAR2-dependent increase in tissue fluidity
inferred← citeshttps://doi.org/10.1083/jcb.201408090openalex-snapshot
Redox and Src family kinase signaling control leukocyte wound attraction and neutrophil reverse migration
inferred← citeshttps://doi.org/10.1083/jcb.201503071openalex-snapshot
Histone demethylase KDM4B regulates otic vesicle invagination via epigenetic control ofDlx3expression
inferred← citeshttps://doi.org/10.1083/jcb.201508047openalex-snapshot
Collective cell migration in development
inferred← citeshttps://doi.org/10.1083/jcb.201510019openalex-snapshot
Ca2+/H+ exchange by acidic organelles regulates cell migration in vivo
inferred← citeshttps://doi.org/10.1083/jcb.201602083openalex-snapshot
In vivo confinement promotes collective migration of neural crest cells
inferred← citeshttps://doi.org/10.1083/jcb.202505198openalex-snapshot
Patterning in motion: Cell interfaces guide mesenchymal collective migration and morphogenesis
inferred← citeshttps://doi.org/10.1083/jcb.202507211openalex-snapshot
Force coordination distinguishes epithelial and mesenchymal modes of collective chemotaxis
inferred← citeshttps://doi.org/10.1088/1361-6463/aa56feopenalex-snapshot
Physical models of collective cell motility: from cell to tissue
inferred← citeshttps://doi.org/10.1088/1361-6633/aa65efopenalex-snapshot
Collective cell migration: a physics perspective
inferred← citeshttps://doi.org/10.1088/1367-2630/ac9cc3openalex-snapshot
Clustering and flocking of repulsive chiral active particles with non-reciprocal couplings
inferred← citeshttps://doi.org/10.1088/1742-5468/adc896openalex-snapshot
Phase transitions in single species Ising models with non-reciprocal couplings
inferred← citeshttps://doi.org/10.1089/ten.tec.2018.0327openalex-snapshot
Primary Mucosal Epithelial Cell Cultivation: A Reliable and Accelerated Isolation
inferred← citeshttps://doi.org/10.1091/mbc.e17-03-0134openalex-snapshot
Single and collective cell migration: the mechanics of adhesions
inferred← citeshttps://doi.org/10.1091/mbc.e25-06-0277openalex-snapshot
PERK protein kinase facilitates keratinocyte collective cell migration by engagement with cell adhesion molecules, independent of its kinase activity
inferred← citeshttps://doi.org/10.1093/toxsci/kfad068openalex-snapshot
Exosome-shuttled miR-126 mediates ethanol-induced disruption of neural crest cell-placode cell interaction by targeting SDF1
inferred← citeshttps://doi.org/10.1098/rsfs.2020.0057openalex-snapshot
Tissue tectonics and the multi-scale regulation of developmental timing
inferred← citeshttps://doi.org/10.1098/rsif.2013.0717openalex-snapshot
Contact inhibition of locomotion probabilities drive solitary versus collective cell migration
inferred← citeshttps://doi.org/10.1098/rsif.2024.0409openalex-snapshot
Variations in non-local interaction range lead to emergent chase-and-run in heterogeneous populations
inferred← citeshttps://doi.org/10.1098/rsob.160056openalex-snapshot
Multidisciplinary approaches to understanding collective cell migration in developmental biology
inferred← citeshttps://doi.org/10.1098/rstb.2019.0387openalex-snapshot
Rules of collective migration: from the wildebeest to the neural crest
inferred← citeshttps://doi.org/10.1098/rstb.2019.0559openalex-snapshot
Dynamic expression of MMP28 during cranial morphogenesis
inferred← citeshttps://doi.org/10.1098/rstb.2020.0087openalex-snapshot
Epithelial–mesenchymal plasticity: emerging parallels between tissue morphogenesis and cancer metastasis
inferred← citeshttps://doi.org/10.1101/114371openalex-snapshot
Connexin43 controls N-cadherin transcription during collective cell migration
inferred← citeshttps://doi.org/10.1101/2020.09.20.299552openalex-snapshot
Mechanical compartmentalization of the intestinal organoid enables crypt folding and collective cell migration
inferred← citeshttps://doi.org/10.1101/2021.10.11.463916openalex-snapshot
Stretch-induced endogenous electric fields drive neural crest directed collective cell migration in vivo
inferred← citeshttps://doi.org/10.1101/2023.03.30.534903openalex-snapshot
Role of pioneer neurons and neuroblast behaviors on otic ganglion assembly
inferred← citeshttps://doi.org/10.1101/2023.11.17.567510openalex-snapshot
Modelling variability and heterogeneity of EMT scenarios highlights nuclear positioning and protrusions as main drivers of extrusion
inferred← citeshttps://doi.org/10.1101/2025.07.28.667246openalex-snapshot
A novel function for Prdm12 during neural crest migration reveals a link between Wnt and N-cadherin
inferred← citeshttps://doi.org/10.1101/2025.09.27.676141openalex-snapshot
Maternal–fetal inflammation affects Cdh1 /E-cadherin epigenetic regulation and craniofacial development
inferred← citeshttps://doi.org/10.1101/373696openalex-snapshot
EphB2 and ERK signaling are required for heterotypic contact inhibition of locomotion to drive cell sorting
inferred← citeshttps://doi.org/10.1101/750752openalex-snapshot
Non-junctional Cadherin3 regulates cell migration and contact inhibition of locomotion via domain-dependent opposing regulations of Rac1
inferred← citeshttps://doi.org/10.1101/798827openalex-snapshot
Engineering cooperative patterns in multi-species bacterial colonies
inferred← citeshttps://doi.org/10.1101/cshperspect.a041741openalex-snapshot
Neighboring Cells as Living Substrates for Guiding Collective Cell Migration during Development
inferred← citeshttps://doi.org/10.1103/physreva.111.013713openalex-snapshot
Nonreciprocal entanglement in cavity magnomechanics via the Barnett effect
inferred← citeshttps://doi.org/10.1103/physrevapplied.22.064001openalex-snapshot
Directional quantum-squeezing-enabled nonreciprocal enhancement of entanglement
inferred← citeshttps://doi.org/10.1103/physreve.105.064602openalex-snapshot
Active nonreciprocal attraction between motile particles in an elastic medium
inferred← citeshttps://doi.org/10.1103/physreve.106.024604openalex-snapshot
Pairing-induced motion of source and inert particles driven by surface tension
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