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A cell-based computational model of early embryogenesis coupling mechanical behaviour and gene regulation

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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.1002030302openalex-snapshot
Stages of embryonic development of the zebrafish
inferredcites →https://doi.org/10.1002/jez.10187openalex-snapshot
Ingeneue: A versatile tool for reconstituting genetic networks, with examples from the segment polarity network
inferredcites →https://doi.org/10.1006/dbio.1994.1326openalex-snapshot
Delta-Notch Signaling and Drosophila Cell Fate Choice
inferredcites →https://doi.org/10.1007/978-3-7643-8123-3_5openalex-snapshot
The Cellular Potts Model and Biophysical Properties of Cells, Tissues and Morphogenesis
inferredcites →https://doi.org/10.1016/b978-0-12-388403-9.00013-8openalex-snapshot
Multi-Scale Modeling of Tissues Using CompuCell3D
inferredcites →https://doi.org/10.1016/j.bpj.2013.11.4498openalex-snapshot
Vertex Models of Epithelial Morphogenesis
inferredcites →https://doi.org/10.1016/j.febslet.2009.11.060openalex-snapshot
Modularity and design principles in the sea urchin embryo gene regulatory network
inferredcites →https://doi.org/10.1016/j.gde.2005.02.007openalex-snapshot
Transcriptional regulation by the numbers: models
inferredcites →https://doi.org/10.1016/j.gde.2007.05.002openalex-snapshot
Differential adhesion in morphogenesis: a modern view
inferredcites →https://doi.org/10.1016/j.molcel.2011.12.032openalex-snapshot
XIAP Monoubiquitylates Groucho/TLE to Promote Canonical Wnt Signaling
inferredcites →https://doi.org/10.1016/j.physrep.2012.03.004openalex-snapshot
Collective motion
inferredcites →https://doi.org/10.1016/j.semcdb.2014.08.015openalex-snapshot
Computational and mathematical methods for morphogenetic gradient analysis, boundary formation and axonal targeting
inferredcites →https://doi.org/10.1016/s0070-2153(07)81013-1openalex-snapshot
Delaunay-Object-Dynamics: Cell Mechanics with a 3D Kinetic and Dynamic Weighted Delaunay-Triangulation
inferredcites →https://doi.org/10.1016/s0167-739x(00)00062-5openalex-snapshot
A three-dimensional model of cell movement in multicellular systems
inferredcites →https://doi.org/10.1038/ncomms9674openalex-snapshot
A workflow to process 3D+time microscopy images of developing organisms and reconstruct their cell lineage
inferredcites →https://doi.org/10.1038/nmeth.1327openalex-snapshot
Tissue tectonics: morphogenetic strain rates, cell shape change and intercalation
inferredcites →https://doi.org/10.1038/nmeth.3036openalex-snapshot
Fast, accurate reconstruction of cell lineages from large-scale fluorescence microscopy data
inferredcites →https://doi.org/10.1038/nrm2503openalex-snapshot
Modelling and analysis of gene regulatory networks
inferredcites →https://doi.org/10.1073/pnas.0704235104openalex-snapshot
Cell adhesion and cortex contractility determine cell patterning in the Drosophila retina
inferredcites →https://doi.org/10.1073/pnas.0806007105openalex-snapshot
Properties of developmental gene regulatory networks
inferredcites →https://doi.org/10.1073/pnas.0902859106openalex-snapshot
EphrinB2 coordinates the formation of a morphological boundary and cell epithelialization during somite segmentation
inferredcites →https://doi.org/10.1073/pnas.1003743107openalex-snapshot
Coaction of intercellular adhesion and cortical tension specifies tissue surface tension
inferredcites →https://doi.org/10.1073/pnas.1207852109openalex-snapshot
Predictive computation of genomic logic processing functions in embryonic development
inferredcites →https://doi.org/10.1073/pnas.1507100112openalex-snapshot
Dynamic cross-links tune the solid–fluid behavior of living cells
inferredcites →https://doi.org/10.1073/pnas.1533293100openalex-snapshot
Transcriptional regulatory cascades in development: Initial rates, not steady state, determine network kinetics
inferredcites →https://doi.org/10.1093/bioinformatics/btq437openalex-snapshot
A cell-based simulation software for multi-cellular systems
inferredcites →https://doi.org/10.1093/bioinformatics/btv147openalex-snapshot
LBIBCell: a cell-based simulation environment for morphogenetic problems
inferredcites →https://doi.org/10.1098/rsfs.2011.0097openalex-snapshot
Turing's theory of morphogenesis of 1952 and the subsequent discovery of the crucial role of local self-enhancement and long-range inhibition
inferredcites →https://doi.org/10.1101/gad.987402openalex-snapshot
Default repression and Notch signaling: Hairless acts as an adaptor to recruit the corepressors Groucho and dCtBP to Suppressor of Hairless
inferredcites →https://doi.org/10.1103/physreve.47.2128openalex-snapshot
Simulation of the differential adhesion driven rearrangement of biological cells
inferredcites →https://doi.org/10.1103/physrevlett.69.2013openalex-snapshot
Simulation of biological cell sorting using a two-dimensional extended Potts model
inferredcites →https://doi.org/10.1104/pp.110.167619openalex-snapshot
VirtualLeaf: An Open-Source Framework for Cell-Based Modeling of Plant Tissue Growth and Development
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.04009.xopenalex-snapshot
Computational models of plant development and form
inferredcites →https://doi.org/10.1115/1.1288205openalex-snapshot
The Mechanics of Heterotypic Cell Aggregates: Insights From Computer Simulations
inferredcites →https://doi.org/10.1126/science.1189428openalex-snapshot
Cell Lineage Reconstruction of Early Zebrafish Embryos Using Label-Free Nonlinear Microscopy
inferredcites →https://doi.org/10.1126/science.1230718openalex-snapshot
Physical Biology Returns to Morphogenesis
inferredcites →https://doi.org/10.1126/science.1235249openalex-snapshot
Mechanics of Epithelial Tissue Homeostasis and Morphogenesis
inferredcites →https://doi.org/10.1146/annurev.cellbio.17.1.189openalex-snapshot
Boundaries in Development: Formation and Function
inferredcites →https://doi.org/10.1242/bio.20134614openalex-snapshot
Non-directional radial intercalation dominates deep cell behavior during zebrafish epiboly
inferredcites →https://doi.org/10.1242/dev.108.4.569openalex-snapshot
Cell movements during epiboly and gastrulation in zebrafish
inferredcites →https://doi.org/10.1242/dev.123.1.461openalex-snapshot
A flipbook of zebrafish embryogenesis
inferredcites →https://doi.org/10.1242/dev.129.15.3633openalex-snapshot
Morphological boundary forms by a novel inductive event mediated by Lunatic fringe and Notch during somitic segmentation
inferredcites →https://doi.org/10.1371/journal.pcbi.1003670openalex-snapshot
A Digital Framework to Build, Visualize and Analyze a Gene Expression Atlas with Cellular Resolution in Zebrafish Early Embryogenesis
inferredcites →https://doi.org/10.3389/fpls.2013.00408openalex-snapshot
Using cellzilla for plant growth simulations at the cellular level

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.3188399openalex-extracted
inferred← citeshttps://doi.org/10.1002/dvdy.182openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/smll.202103466openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/wsbm.1527openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-1-0716-1831-8_14openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-1-0716-2281-0_20openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-030-18202-1_12openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-030-71737-7_10openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-031-07802-6_17openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-031-35180-8_2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-031-64532-7_10openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-16-5180-9_8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-981-32-9084-6_21openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00285-021-01697-wopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10237-019-01204-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11538-020-00810-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s13721-024-00455-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-817931-4.00010-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-817931-4.00011-xopenalex-snapshot
Computational Morphogenesis of Embryonic Bone Development: Past, Present, and Future
inferred← citeshttps://doi.org/10.1016/b978-0-12-824349-7.00030-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.mcb.2019.01.008openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.actbio.2022.07.024openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.actbio.2025.12.013openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.addr.2020.11.012openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.amc.2024.129069openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.biosystems.2018.05.006openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.biosystems.2018.07.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.brain.2022.100062openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cdev.2025.204028openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cell.2018.07.028openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cels.2019.02.007openalex-snapshot
ya||a: GPU-Powered Spheroid Models for Mesenchyme and Epithelium
inferred← citeshttps://doi.org/10.1016/j.coisb.2017.03.005openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.coisb.2017.07.011openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.coisb.2018.09.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.compbiomed.2022.106499openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.csbj.2019.08.007openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.csbj.2020.11.017openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.csbj.2021.07.005openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cub.2017.07.010openalex-snapshot
Coordination of Morphogenesis and Cell-Fate Specification in Development
inferred← citeshttps://doi.org/10.1016/j.enganabound.2019.03.025openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.exer.2022.109003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.gde.2018.05.006openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.isci.2021.102505openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.isci.2025.111753openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jbiosc.2023.10.003openalex-snapshot
Agent-based approach for elucidating the release from collective arrest of cell motion in corneal epithelial cell sheet
inferred← citeshttps://doi.org/10.1016/j.jtbi.2020.110205openalex-snapshot
Structure encoding in DNA
inferred← citeshttps://doi.org/10.1016/j.jtbi.2024.111922openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jtbi.2025.112070openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jtbi.2025.112354openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.matt.2020.02.016openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.physrep.2022.12.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.semcdb.2023.02.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.semcdb.2023.03.010openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.xcrp.2025.102865openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ydbio.2018.01.013openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41540-024-00477-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41540-025-00529-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41598-019-50921-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41598-022-13281-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41598-025-04495-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41598-025-31696-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41598-025-92541-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s42003-025-08411-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s43588-021-00154-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/srep37438openalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d2sm00063fopenalex-snapshot
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inferred← citeshttps://doi.org/10.1063/1.5038337openalex-snapshot
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inferred← citeshttps://doi.org/10.1088/1478-3975/aaf92dopenalex-snapshot
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inferred← citeshttps://doi.org/10.1093/bioinformatics/btab201openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/bioinformatics/bty766openalex-snapshot
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inferred← citeshttps://doi.org/10.1098/rsif.2018.0454openalex-snapshot
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inferred← citeshttps://doi.org/10.1101/054353openalex-snapshot
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inferred← citeshttps://doi.org/10.1101/2021.02.10.430170openalex-snapshot
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inferred← citeshttps://doi.org/10.1101/2023.09.29.560237openalex-snapshot
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inferred← citeshttps://doi.org/10.1101/2024.01.06.574290openalex-snapshot
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inferred← citeshttps://doi.org/10.1101/2025.05.06.652477openalex-snapshot
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inferred← citeshttps://doi.org/10.1101/2025.09.27.678924openalex-snapshot
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inferred← citeshttps://doi.org/10.1101/273847openalex-snapshot
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inferred← citeshttps://doi.org/10.1101/296400openalex-snapshot
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inferred← citeshttps://doi.org/10.1101/470559openalex-snapshot
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inferred← citeshttps://doi.org/10.1101/785337openalex-snapshot
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inferred← citeshttps://doi.org/10.1101/812198openalex-snapshot
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inferred← citeshttps://doi.org/10.1103/physrevresearch.6.l012036openalex-snapshot
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inferred← citeshttps://doi.org/10.1109/access.2019.2915575openalex-snapshot
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inferred← citeshttps://doi.org/10.1109/escience.2018.00032openalex-snapshot
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inferred← citeshttps://doi.org/10.1109/searis44442.2018.9180233openalex-snapshot
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inferred← citeshttps://doi.org/10.1162/posc_a_00408openalex-snapshot
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inferred← citeshttps://doi.org/10.1186/s12859-022-04575-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1242/dev.151274openalex-snapshot
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inferred← citeshttps://doi.org/10.1242/dev.175596openalex-snapshot
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inferred← citeshttps://doi.org/10.1242/dev.202870openalex-snapshot
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inferred← citeshttps://doi.org/10.1371/journal.pcbi.1009653openalex-snapshot
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inferred← citeshttps://doi.org/10.1371/journal.pcbi.1011306openalex-snapshot
Effective mechanical potential of cell–cell interaction explains three-dimensional morphologies during early embryogenesis
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1011658openalex-snapshot
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inferred← citeshttps://doi.org/10.1371/journal.pcbi.1012352openalex-snapshot
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inferred← citeshttps://doi.org/10.1371/journal.pone.0254763openalex-snapshot
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inferred← citeshttps://doi.org/10.17513/msnv.18100openalex-snapshot
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inferred← citeshttps://doi.org/10.20944/preprints202007.0022.v1openalex-snapshot
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inferred← citeshttps://doi.org/10.21105/joss.07723openalex-snapshot
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inferred← citeshttps://doi.org/10.21203/rs.3.rs-3240050/v1openalex-snapshot
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inferred← citeshttps://doi.org/10.33063/diva-442412openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fncom.2020.588224openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fphy.2020.00031openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fphy.2021.649821openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fphy.2021.666709openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fphy.2021.666916openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fphy.2022.968409openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fpls.2021.746183openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/bioengineering9100543openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/biophysica4040040openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/genes14010154openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms25020870openalex-snapshot
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inferred← citeshttps://doi.org/10.53846/goediss-8893openalex-snapshot
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inferred← citeshttps://doi.org/10.70675/27258badz60cez4eb3zba1bz82f165c2aa33openalex-snapshot
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inferred← citeshttps://doi.org/10.70675/74f92d6dz74eaz46bdzbcf9ze92dd56249a2openalex-snapshot
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inferred← citeshttps://doi.org/10.70675/a4542914z1070z4bb1z87cfzaaa97f8ab733openalex-snapshot
Deep Learning for Advanced Microscopy
inferred← citeshttps://doi.org/10.70675/f277de8azd645z4977z911fzf805797824d4openalex-snapshot
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inferred← citeshttps://doi.org/10.7554/elife.107563openalex-snapshot
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inferred← citeshttps://doi.org/10.7554/elife.107563.1openalex-snapshot
The zoo of the gene networks capable of pattern formation by extracellular signaling
inferred← citeshttps://doi.org/10.7554/elife.107563.3openalex-snapshot
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inferred← citeshttps://doi.org/10.7554/elife.72132openalex-snapshot
A coupled mechano-biochemical model for cell polarity guided anisotropic root growth
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