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Morphomechanics: An Updated View
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/adma.201802579openalex-extracted
Biological Tissues as Active Nematic Liquid Crystals
inferredcites →https://doi.org/10.1002/dvdy.401openalex-extracted
Emerging role of Piezo ion channels in cardiovascular development
inferredcites →https://doi.org/10.1002/jcb.22545openalex-extracted
Tissue geometry patterns epithelial–mesenchymal transition via intercellular mechanotransduction
inferredcites →https://doi.org/10.1007/978-3-642-33902-8_1openalex-extracted
Morphogenetic Engineering: Reconciling Self-Organization and Architecture
inferredcites →https://doi.org/10.1007/s10237-007-0106-xopenalex-extracted
Theoretical study of Beloussov’s hyper-restoration hypothesis for mechanical regulation of morphogenesis
inferredcites →https://doi.org/10.1007/s12064-020-00317-3openalex-extracted
On the problem of biological form
inferredcites →https://doi.org/10.1016/j.biosystems.2006.09.015openalex-extracted
Information about a form (on the dynamic laws of morphogenesis)
inferredcites →https://doi.org/10.1016/j.biosystems.2012.05.003openalex-extracted
Morphogenesis as a macroscopic self-organizing process
inferredcites →https://doi.org/10.1016/j.biosystems.2017.08.009openalex-extracted
The bioelectric code: An ancient computational medium for dynamic control of growth and form
inferredcites →https://doi.org/10.1016/j.cell.2021.02.034openalex-extracted
Bioelectric signaling: Reprogrammable circuits underlying embryogenesis, regeneration, and cancer
inferredcites →https://doi.org/10.1016/j.celrep.2019.08.075openalex-extracted
Biophysical Principles of Ion-Channel-Mediated Mechanosensory Transduction
inferredcites →https://doi.org/10.1016/j.devcel.2021.08.012openalex-extracted
Establishment of the vertebrate body plan: Rethinking gastrulation through stem cell models of early embryogenesis
inferredcites →https://doi.org/10.1016/j.gde.2021.101897openalex-extracted
Active nematics across scales from cytoskeleton organization to tissue morphogenesis
inferredcites →https://doi.org/10.1016/j.ijengsci.2014.05.003openalex-extracted
A mechanical perspective on vertebral segmentation
inferredcites →https://doi.org/10.1016/j.physrep.2014.10.001openalex-extracted
Tuned, driven, and active soft matter
inferredcites →https://doi.org/10.1016/j.tcb.2021.06.007openalex-extracted
3D gastruloids: a novel frontier in stem cell-based in vitro modeling of mammalian gastrulation
inferredcites →https://doi.org/10.1016/s0074-7696(08)61535-1openalex-extracted
Mechanical Stresses in Embryonic Tissues: Patterns, Morphogenetic Role, and Involvement in Regulatory Feedback
inferredcites →https://doi.org/10.1021/acs.nanolett.7b00177openalex-extracted
Mechanical Stimulation of Piezo1 Receptors Depends on Extracellular Matrix Proteins and Directionality of Force
inferredcites →https://doi.org/10.1038/natrevmats.2017.48openalex-extracted
Active matter at the interface between materials science and cell biology
inferredcites →https://doi.org/10.1038/nature09312openalex-extracted
Polar patterns of driven filaments
inferredcites →https://doi.org/10.1038/nature10277openalex-extracted
On the growth and form of the gut
inferredcites →https://doi.org/10.1038/nature21718openalex-extracted
Topological defects in epithelia govern cell death and extrusion
inferredcites →https://doi.org/10.1038/s41563-020-00901-4openalex-extracted
Spatiotemporal control of liquid crystal structure and dynamics through activity patterning
inferredcites →https://doi.org/10.1038/s41563-021-00919-2openalex-extracted
Investigating the nature of active forces in tissues reveals how contractile cells can form extensile monolayers
inferredcites →https://doi.org/10.1038/s41563-022-01194-5openalex-extracted
Integer topological defects organize stresses driving tissue morphogenesis
inferredcites →https://doi.org/10.1038/s41567-020-01083-1openalex-extracted
Topological defects in the nematic order of actin fibres as organization centres of Hydra morphogenesis
inferredcites →https://doi.org/10.1038/s41578-020-00272-xopenalex-extracted
Autonomous materials systems from active liquid crystals
inferredcites →https://doi.org/10.1038/s41586-018-0479-2openalex-extracted
A fluid-to-solid jamming transition underlies vertebrate body axis elongation
inferredcites →https://doi.org/10.1038/s41586-018-0578-0openalex-extracted
Multi-axial self-organization properties of mouse embryonic stem cells into gastruloids
inferredcites →https://doi.org/10.1038/s41586-019-1447-1openalex-extracted
Controlling organization and forces in active matter through optically defined boundaries
inferredcites →https://doi.org/10.1038/s41586-020-2933-1openalex-extracted
Discoveries in structure and physiology of mechanically activated ion channels
inferredcites →https://doi.org/10.1038/s42254-022-00445-3openalex-extracted
Topological active matter
inferredcites →https://doi.org/10.1073/pnas.1406015111openalex-extracted
Gyrification from constrained cortical expansion
inferredcites →https://doi.org/10.1073/pnas.1410776112openalex-extracted
A strategy for tissue self-organization that is robust to cellular heterogeneity and plasticity
inferredcites →https://doi.org/10.1073/pnas.1817070115openalex-extracted
Mechanically activated ion channel PIEZO1 is required for lymphatic valve formation
inferredcites →https://doi.org/10.1088/1478-3975/5/1/015009openalex-extracted
Mechanically based generative laws of morphogenesis
inferredcites →https://doi.org/10.1091/mbc.e19-12-0719openalex-extracted
Epithelial tissue geometry directs emergence of bioelectric field and pattern of proliferation
inferredcites →https://doi.org/10.1097/brs.0000000000001946openalex-extracted
Restrained Differential Growth
inferredcites →https://doi.org/10.1098/rsta.2003.1198openalex-extracted
The formation of spatial patterns in social insects: from simple behaviours to complex structures
inferredcites →https://doi.org/10.1098/rsta.2009.0100openalex-extracted
Towards a unified theory for morphomechanics
inferredcites →https://doi.org/10.1098/rstb.2015.0443openalex-extracted
‘Biogeneric’ developmental processes: drivers of major transitions in animal evolution
inferredcites →https://doi.org/10.1103/physrevlett.105.208001openalex-extracted
Softening Induced Instability of a Stretched Cohesive Granular Layer
inferredcites →https://doi.org/10.1103/physrevlett.128.048001openalex-extracted
Active Extensile Stress Promotes 3D Director Orientations and Flows
inferredcites →https://doi.org/10.1111/febs.16041openalex-extracted
From stretch to deflection: the importance of context in the activation of mammalian, mechanically activated ion channels
inferredcites →https://doi.org/10.1111/nyas.12874openalex-extracted
How ion channels sense mechanical force: insights from mechanosensitive K2P channels TRAAK, TREK1, and TREK2
inferredcites →https://doi.org/10.1126/sciadv.abk2712openalex-extracted
Theory of defect-mediated morphogenesis
inferredcites →https://doi.org/10.1126/science.1193270openalex-extracted
Piezo1 and Piezo2 Are Essential Components of Distinct Mechanically Activated Cation Channels
inferredcites →https://doi.org/10.1126/science.1226265openalex-extracted
Crocodile Head Scales Are Not Developmental Units But Emerge from Physical Cracking
inferredcites →https://doi.org/10.1126/science.1254784openalex-extracted
Topology and dynamics of active nematic vesicles
inferredcites →https://doi.org/10.1126/science.aba4937openalex-extracted
Mouse embryonic stem cells self-organize into trunk-like structures with neural tube and somites
inferredcites →https://doi.org/10.1134/s1062359012020045openalex-extracted
Mechano-geometric generative rules of morphogenesis
inferredcites →https://doi.org/10.1146/annurev-conmatphys-031119-050611openalex-extracted
Self-Propelled Rods: Insights and Perspectives for Active Matter
inferredcites →https://doi.org/10.1186/2041-9139-2-2openalex-extracted
Strabismus-mediated primary archenteron invagination is uncoupled from Wnt/β-catenin-dependent endoderm cell fate specification in Nematostella vectensis (Anthozoa, Cnidaria): Implications for the evolution of gastrulation
inferredcites →https://doi.org/10.1186/s12976-016-0037-2openalex-extracted
The organelle of differentiation in embryos: the cell state splitter
inferredcites →https://doi.org/10.1242/dev.159525openalex-extracted
On the nature and function of organizers
inferredcites →https://doi.org/10.1387/ijdb.052056lbopenalex-extracted
Morphomechanics: goals, basic experiments and models
inferredcites →https://doi.org/10.3389/fcell.2021.753446openalex-extracted
Molecular and Mechanical Cues for Somite Periodicity
inferredcites →https://doi.org/10.3389/fcell.2022.992371openalex-extracted
Mechano-biochemical marine stimulation of inversion, gastrulation, and endomesoderm specification in multicellular Eukaryota
inferredcites →https://doi.org/10.4161/cib.22595openalex-extracted
Cracking the bioelectric code: Probing endogenous ionic controls of pattern formation
inferredcites →https://doi.org/10.7554/elife.41844openalex-extracted
OSCA/TMEM63 are an evolutionarily conserved family of mechanically activated ion channels
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