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Regulation of Epithelial Morphogenesis by the G Protein–Coupled Receptor Mist and Its Ligand Fog

https://doi.org/10.1126/scisignal.2004427
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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/arch.1054openalex-snapshot
Insect G protein‐coupled receptors and signal transduction
inferredcites →https://doi.org/10.1002/dvdy.20334openalex-snapshot
Compartmentalized morphogenesis in epithelia: From cell to tissue shape
inferredcites →https://doi.org/10.1006/dbio.1997.8707openalex-snapshot
GFP-Moesin Illuminates Actin Cytoskeleton Dynamics in Living Tissue and Demonstrates Cell Shape Changes during Morphogenesis inDrosophila
inferredcites →https://doi.org/10.1016/0012-1606(85)90490-7openalex-snapshot
Requirements for zygotic gene activity during gastrulation in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/0092-8674(90)90413-9openalex-snapshot
The segment polarity gene armadillo encodes a functionally modular protein that is the Drosophila homolog of human plakoglobin
inferredcites →https://doi.org/10.1016/0092-8674(91)90652-fopenalex-snapshot
The drosophila gastrulation gene concertina encodes a Gα-like protein
inferredcites →https://doi.org/10.1016/0092-8674(94)90384-0openalex-snapshot
A putative cell signal encoded by the folded gastrulation gene coordinates cell shape changes during Drosophila gastrulation
inferredcites →https://doi.org/10.1016/j.ceb.2010.10.014openalex-snapshot
Dynamics and regulation of contractile actin–myosin networks in morphogenesis
inferredcites →https://doi.org/10.1016/j.cub.2004.09.078openalex-snapshot
Drosophila RhoGEF2 Associates with Microtubule Plus Ends in an EB1-Dependent Manner
inferredcites →https://doi.org/10.1016/j.cub.2004.09.080openalex-snapshot
A Rho GTPase Signaling Pathway Is Used Reiteratively in Epithelial Folding and Potentially Selects the Outcome of Rho Activation
inferredcites →https://doi.org/10.1016/j.cub.2005.10.008openalex-snapshot
New Roles for Gα and RGS Proteins: Communication Continues despite Pulling Sisters Apart
inferredcites →https://doi.org/10.1016/j.mod.2006.12.004openalex-snapshot
Analysis and reconstitution of the genetic cascade controlling early mesoderm morphogenesis in the Drosophila embryo
inferredcites →https://doi.org/10.1016/j.ydbio.2004.08.047openalex-snapshot
Gene expression profiling of the developing Drosophila CNS midline cells
inferredcites →https://doi.org/10.1016/j.ydbio.2009.09.009openalex-snapshot
Apical constriction: A cell shape change that can drive morphogenesis
inferredcites →https://doi.org/10.1016/s0092-8674(00)80482-1openalex-snapshot
The Rho GTPase and a Putative RhoGEF Mediate a Signaling Pathway for the Cell Shape Changes in Drosophila Gastrulation
inferredcites →https://doi.org/10.1016/s0092-8674(01)00298-7openalex-snapshot
Drosophila Rho-Associated Kinase (Drok) Links Frizzled-Mediated Planar Cell Polarity Signaling to the Actin Cytoskeleton
inferredcites →https://doi.org/10.1038/330395a0openalex-snapshot
The Drosophila developmental gene snail encodes a protein with nucleic acid binding fingers
inferredcites →https://doi.org/10.1038/nprot.2008.18openalex-snapshot
Culture of Drosophila S2 cells and their use for RNAi-mediated loss-of-function studies and immunofluorescence microscopy
inferredcites →https://doi.org/10.1083/jcb.150.2.f83openalex-snapshot
Drosophila melanogaster G Protein–Coupled Receptors
inferredcites →https://doi.org/10.1083/jcb.200309162openalex-snapshot
Differential functions of G protein and Baz–aPKC signaling pathways in Drosophila neuroblast asymmetric division
inferredcites →https://doi.org/10.1093/genetics/105.3.615openalex-snapshot
MATERNAL-ZYGOTIC GENE INTERACTIONS DURING FORMATION OF THE DORSOVENTRAL PATTERN IN DROSOPHILA EMBRYOS
inferredcites →https://doi.org/10.1093/genetics/155.3.1253openalex-snapshot
Genetic Analysis Demonstrates a Direct Link Between Rho Signaling and Nonmuscle Myosin Function During Drosophila Morphogenesis
inferredcites →https://doi.org/10.1101/gad.12.2.274openalex-snapshot
DRhoGEF2 encodes a member of the Dbl family of oncogenes and controls cell shape changes during gastrulation in Drosophila
inferredcites →https://doi.org/10.1101/gad.5.9.1568openalex-snapshot
twist and snail as positive and negative regulators during Drosophila mesoderm development.
inferredcites →https://doi.org/10.1101/pdb.prot4515openalex-snapshot
Synthesis of siRNA for RNAi in Drosophila
inferredcites →https://doi.org/10.1111/j.1749-6632.1990.tb21683.xopenalex-snapshot
Contractile Proteins in Drosophila Developmenta
inferredcites →https://doi.org/10.1126/science.1134833openalex-snapshot
Control of Drosophila Gastrulation by Apical Localization of Adherens Junctions and RhoGEF2
inferredcites →https://doi.org/10.1146/annurev.cb.11.110195.001201openalex-snapshot
Drosophila Gastrulation: From Pattern Formation to Morphogenesis
inferredcites →https://doi.org/10.1186/gb-2007-8-10-r216openalex-snapshot
The ribosomal protein genes and Minute loci of Drosophila melanogaster
inferredcites →https://doi.org/10.1242/dev.01938openalex-snapshot
folded gastrulation , cell shape change and the control of myosin localization
inferredcites →https://doi.org/10.1242/dev.110.1.73openalex-snapshot
Cell shape changes during gastrulation in Drosophila
inferredcites →https://doi.org/10.1242/dev.112.3.775openalex-snapshot
Gastrulation in Drosophila: the formation of the ventral furrow and posterior midgut invaginations
inferredcites →https://doi.org/10.1242/dev.125.4.589openalex-snapshot
Hyperactivation of the folded gastrulation pathway induces specific cell shape changes
inferredcites →https://doi.org/10.1371/journal.pone.0007437openalex-snapshot
A Small Genomic Region Containing Several Loci Required for Gastrulation in Drosophila
inferredcites →https://doi.org/10.1371/journal.pone.0007574openalex-snapshot
A Second-Site Noncomplementation Screen for Modifiers of Rho1 Signaling during Imaginal Disc Morphogenesis in Drosophila
inferredcites →https://doi.org/10.1371/journal.pone.0015397openalex-snapshot
An Essential Role of the Cytoplasmic Tail of CXCR4 in G-Protein Signaling and Organogenesis
inferredcites →https://doi.org/10.1534/genetics.104.026427openalex-snapshot
The BDGP Gene Disruption Project

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.3363748openalex-extracted
Distinct RhoGEFs Activate Apical and Junctional 1 Actomyosin Contractility Under Control of G Proteins During Epithelial Morphogenesis
inferred← citeshttps://doi.org/10.1002/bies.70107openalex-snapshot
Linking Planar Cell Polarity to Mechanotransduction During Morphogenesis
inferred← citeshttps://doi.org/10.1002/bies.70154openalex-snapshot
Opposing Activity at the Apical Surface: An Antagonistic Collaboration Between Crumbs and Myosin II Determines Organ Shape
inferred← citeshttps://doi.org/10.1002/wdev.140openalex-snapshot
Building and specializing epithelial tubular organs: the Drosophila salivary gland as a model system for revealing how epithelial organs are specified, form and specialize
inferred← citeshttps://doi.org/10.1007/978-1-0716-0779-4_8openalex-snapshot
Live Imaging of Epithelial-Mesenchymal Transition in Mesoderm Cells of Gastrulating Drosophila Embryos
inferred← citeshttps://doi.org/10.1007/978-981-13-1571-8_1openalex-snapshot
Overview of G-Protein Coupled Receptor
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2019.08.003openalex-snapshot
The cellular and molecular mechanisms that establish the mechanics of Drosophila gastrulation
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2019.11.004openalex-snapshot
Setting up for gastrulation: D. melanogaster
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2019.11.008openalex-snapshot
The design and logic of terminal patterning in Drosophila
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2019.11.014openalex-snapshot
Cellular, molecular, and biophysical control of epithelial cell intercalation
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2023.02.005openalex-snapshot
Contractile and expansive actin networks in Drosophila: Developmental cell biology controlled by network polarization and higher-order interactions
inferred← citeshttps://doi.org/10.1016/j.bpj.2014.07.013openalex-snapshot
Passive Mechanical Forces Control Cell-Shape Change during Drosophila Ventral Furrow Formation
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112707openalex-snapshot
Single-cell transcriptome atlas of Drosophila gastrula 2.0
inferred← citeshttps://doi.org/10.1016/j.cub.2016.11.047openalex-snapshot
Transcriptional Pre-patterning of Drosophila Gastrulation
inferred← citeshttps://doi.org/10.1016/j.cub.2018.03.068openalex-snapshot
Quantitative Control of GPCR Organization and Signaling by Endocytosis in Epithelial Morphogenesis
inferred← citeshttps://doi.org/10.1016/j.cub.2019.08.017openalex-snapshot
Distinct RhoGEFs Activate Apical and Junctional Contractility under Control of G Proteins during Epithelial Morphogenesis
inferred← citeshttps://doi.org/10.1016/j.cub.2023.07.050openalex-snapshot
Maintaining symmetry during body axis elongation
inferred← citeshttps://doi.org/10.1016/j.devcel.2019.01.009openalex-snapshot
Signaling Dynamics Control Cell Fate in the Early Drosophila Embryo
inferred← citeshttps://doi.org/10.1016/j.devcel.2023.11.003openalex-snapshot
The dynamics and biophysics of shape formation: Common themes in plant and animal morphogenesis
inferred← citeshttps://doi.org/10.1016/j.devcel.2023.11.022openalex-snapshot
Mechanical regulation of substrate adhesion and de-adhesion drives a cell-contractile wave during Drosophila tissue morphogenesis
inferred← citeshttps://doi.org/10.1016/j.jsbmb.2017.05.005openalex-snapshot
A role for G-protein coupled estrogen receptor (GPER) in estrogen-induced carcinogenesis: Dysregulated glandular homeostasis, survival and metastasis
inferred← citeshttps://doi.org/10.1016/j.mod.2020.103624openalex-snapshot
Cellular processes driving gastrulation in the avian embryo
inferred← citeshttps://doi.org/10.1016/j.mod.2020.103629openalex-snapshot
Gastrulation in Drosophila melanogaster: Genetic control, cellular basis and biomechanics
inferred← citeshttps://doi.org/10.1016/j.mod.2020.103648openalex-snapshot
Comparing gastrulation in flies: Links between cell biology and the evolution of embryonic morphogenesis
inferred← citeshttps://doi.org/10.1016/j.semcdb.2021.05.027openalex-snapshot
The origin and the mechanism of mechanical polarity during epithelial folding
inferred← citeshttps://doi.org/10.1016/j.tcb.2018.09.006openalex-snapshot
Principles of Actomyosin Regulation In Vivo
inferred← citeshttps://doi.org/10.1016/j.ydbio.2014.08.003openalex-snapshot
The Fog signaling pathway: Insights into signaling in morphogenesis
inferred← citeshttps://doi.org/10.1016/j.ydbio.2019.07.013openalex-snapshot
Structure-function analysis of β-arrestin Kurtz reveals a critical role of receptor interactions in downregulation of GPCR signaling in vivo
inferred← citeshttps://doi.org/10.1016/j.ydbio.2022.06.014openalex-snapshot
Independent pathways control muscle tissue size and sarcomere remodeling
inferred← citeshttps://doi.org/10.1016/j.ydbio.2026.04.002openalex-snapshot
Fog signaling is dispensable for Drosophila tracheal invagination
inferred← citeshttps://doi.org/10.1016/j.ymeth.2014.01.006openalex-snapshot
Cell lines
inferred← citeshttps://doi.org/10.1038/nature14198openalex-snapshot
Death drags down the neighbourhood
inferred← citeshttps://doi.org/10.1038/nature21348openalex-snapshot
From morphogen to morphogenesis and back
inferred← citeshttps://doi.org/10.1038/ncb3138openalex-snapshot
Myosin-II-mediated cell shape changes and cell intercalation contribute to primitive streak formation
inferred← citeshttps://doi.org/10.1038/ncb3302openalex-snapshot
Modular activation of Rho1 by GPCR signalling imparts polarized myosin II activation during morphogenesis
inferred← citeshttps://doi.org/10.1038/ncomms13883openalex-snapshot
Mechanotransductive cascade of Myo-II-dependent mesoderm and endoderm invaginations in embryo gastrulation
inferred← citeshttps://doi.org/10.1038/ncomms14708openalex-snapshot
Cell-matrix adhesion and cell-cell adhesion differentially control basal myosin oscillation and Drosophila egg chamber elongation
inferred← citeshttps://doi.org/10.1038/ncomms15014openalex-snapshot
Actomyosin meshwork mechanosensing enables tissue shape to orient cell force
inferred← citeshttps://doi.org/10.1038/s41467-017-01482-8openalex-snapshot
Spatial regulation of contractility by Neuralized and Bearded during furrow invagination in Drosophila
inferred← citeshttps://doi.org/10.1038/s41467-023-41178-wopenalex-snapshot
Serotonin signaling regulates actomyosin contractility during morphogenesis in evolutionarily divergent lineages
inferred← citeshttps://doi.org/10.1038/s41467-024-55100-5openalex-snapshot
Mechanical induction in metazoan development and evolution: from earliest multi-cellular organisms to modern animal embryos
inferred← citeshttps://doi.org/10.1038/s41467-025-56880-0openalex-snapshot
Nuclear position controls the activity of cortical actomyosin networks powering simultaneous morphogenetic events
inferred← citeshttps://doi.org/10.1038/s41467-026-68418-zopenalex-snapshot
Spatial patterning of contractility by a self-organized mechanogen activity gradient underlies Drosophila gastrulation
inferred← citeshttps://doi.org/10.1038/s41580-020-00318-6openalex-snapshot
Programmed and self-organized flow of information during morphogenesis
inferred← citeshttps://doi.org/10.1038/s41586-019-1492-9openalex-snapshot
Genetic induction and mechanochemical propagation of a morphogenetic wave
inferred← citeshttps://doi.org/10.1073/pnas.2102691118openalex-snapshot
Temporal integration of inductive cues on the way to gastrulation
inferred← citeshttps://doi.org/10.1073/pnas.2407083121openalex-snapshot
Actomyosin contraction in the follicular epithelium provides the major mechanical force for follicle rupture during Drosophila ovulation
inferred← citeshttps://doi.org/10.1080/21541248.2021.1926879openalex-snapshot
Small GTPases modulate intrinsic and extrinsic forces that control epithelial folding inDrosophilaembryos
inferred← citeshttps://doi.org/10.1083/jcb.201508056openalex-snapshot
Myosin-dependent remodeling of adherens junctions protects junctions from Snail-dependent disassembly
inferred← citeshttps://doi.org/10.1083/jcb.201603077openalex-snapshot
RhoA GTPase inhibition organizes contraction during epithelial morphogenesis
inferred← citeshttps://doi.org/10.1083/jcb.201811174openalex-snapshot
GPCR-independent activation of G proteins promotes apical cell constriction in vivo
inferred← citeshttps://doi.org/10.1083/jcb.202103069openalex-snapshot
Actomyosin activity-dependent apical targeting of Rab11 vesicles reinforces apical constriction
inferred← citeshttps://doi.org/10.1083/jcb.202111002openalex-snapshot
DAPLE orchestrates apical actomyosin assembly from junctional polarity complexes
inferred← citeshttps://doi.org/10.1091/mbc.e16-05-0305openalex-snapshot
Loss of Gα12/13exacerbates apical area dependence of actomyosin contractility
inferred← citeshttps://doi.org/10.1091/mbc.e19-12-0673openalex-snapshot
Apical Constriction Reversal upon Mitotic Entry Underlies Different Morphogenetic Outcomes of Cell Division
inferred← citeshttps://doi.org/10.1091/mbc.e20-03-0181openalex-snapshot
TheDrosophila melanogasterRab GAP RN-tre cross-talks with the Rho1 signaling pathway to regulate nonmuscle myosin II localization and function
inferred← citeshttps://doi.org/10.1091/mbc.e21-01-0021openalex-snapshot
Regulation of apical constriction via microtubule- and Rab11-dependent apical transport during tissue invagination
inferred← citeshttps://doi.org/10.1091/mbc.e24-02-0050openalex-snapshot
Drosophila Fog/Cta and T48 pathways have overlapping and distinct contributions to mesoderm invagination
inferred← citeshttps://doi.org/10.1091/mbc.e24-04-0177openalex-snapshot
A novel protein Moat prevents ectopic epithelial folding by limiting Bazooka/Par3-dependent adherens junctions
inferred← citeshttps://doi.org/10.1093/g3journal/jkaa029openalex-snapshot
FGFR/Heartless and Smog interact synergistically to negatively regulate Fog mediated G-protein coupled receptor signaling in the Drosophila nervous system
inferred← citeshttps://doi.org/10.1093/g3journal/jkae032openalex-snapshot
Embryonic spatiotemporal expression pattern of Folded gastrulation suggests roles in multiple morphogenetic events and regulation by AbdA
inferred← citeshttps://doi.org/10.1101/2021.10.29.466358openalex-snapshot
A phosphoregulated RhoGEF feedback loop tunes cortical flow driven amoeboid migration in vivo
inferred← citeshttps://doi.org/10.1101/2022.09.09.506847openalex-snapshot
G protein-coupled Receptor Contributions to Wing Growth and Morphogenesis in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1101/2023.04.12.535044openalex-snapshot
Evolutionarily conserved role of serotonin signaling in regulating actomyosin contractility during morphogenesis
inferred← citeshttps://doi.org/10.1101/2023.05.02.539070openalex-snapshot
Mechanical regulation of substrate adhesion and de-adhesion drives a cell contractile wave during tissue morphogenesis
inferred← citeshttps://doi.org/10.1101/2025.04.11.648359openalex-snapshot
Spatial patterning of contractility by a mechanogen gradient underlies Drosophila gastrulation
inferred← citeshttps://doi.org/10.1126/sciadv.abo0323openalex-snapshot
An AMPK phosphoregulated RhoGEF feedback loop tunes cortical flow–driven amoeboid migration in vivo
inferred← citeshttps://doi.org/10.1126/sciadv.adl4694openalex-snapshot
Astrocytes control quiescent NSC reactivation via GPCR signaling–mediated F-actin remodeling
inferred← citeshttps://doi.org/10.1126/scisignal.2004837openalex-snapshot
Science Signaling Podcast: 12 November 2013
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-102314-112441openalex-snapshot
Mechanotransduction's Impact on Animal Development, Evolution, and Tumorigenesis
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-111315-125218openalex-snapshot
Transcriptional Control of Developmental Cell Behaviors
inferred← citeshttps://doi.org/10.1186/s12860-023-00492-3openalex-snapshot
From network analysis to experimental validation: identification of regulators of non-muscle myosin II contractility using the folded-gastrulation signaling pathway
inferred← citeshttps://doi.org/10.1242/dev.091645openalex-snapshot
Actomyosin networks and tissue morphogenesis
inferred← citeshttps://doi.org/10.1242/dev.102228openalex-snapshot
Apical constriction: themes and variations on a cellular mechanism driving morphogenesis
inferred← citeshttps://doi.org/10.1242/dev.146761openalex-snapshot
Actomyosin-based tissue folding requires a multicellular myosin gradient
inferred← citeshttps://doi.org/10.1242/dev.186502openalex-snapshot
The pulse of morphogenesis: actomyosin dynamics and regulation in epithelia
inferred← citeshttps://doi.org/10.1242/dev.191049openalex-snapshot
Orchestrating morphogenesis: building the body plan by cell shape changes and movements
inferred← citeshttps://doi.org/10.1242/dev.199232openalex-snapshot
Combinatorial patterns of graded RhoA activation and uniform F-actin depletion promote tissue curvature
inferred← citeshttps://doi.org/10.1242/dev.199991openalex-snapshot
Generation and timing of graded responses to morphogen gradients
inferred← citeshttps://doi.org/10.1242/dev.200468openalex-snapshot
The cell polarity determinant Dlg1 facilitates epithelial invagination by promoting tissue-scale mechanical coordination
inferred← citeshttps://doi.org/10.1242/dev.200519openalex-snapshot
Multifunctional role of GPCR signaling in epithelial tube formation
inferred← citeshttps://doi.org/10.1242/dev.202892openalex-snapshot
Viscous shear is a key force in Drosophila ventral furrow morphogenesis
inferred← citeshttps://doi.org/10.1242/dev.204896openalex-snapshot
Supracellular actomyosin assemblies: master coordinators of development
inferred← citeshttps://doi.org/10.1242/jcs.175158openalex-snapshot
Outside-in signaling – a brief review of GPCR signaling with a focus on theDrosophilaGPCR family
inferred← citeshttps://doi.org/10.1242/prelights.9773openalex-snapshot
Distinct RhoGEFs activate apical and junctional actomyosin contractility under control of G proteins during epithelial morphogenesis
inferred← citeshttps://doi.org/10.1371/journal.ppat.1006260openalex-snapshot
The genetic basis for variation in resistance to infection in the Drosophila melanogaster genetic reference panel
inferred← citeshttps://doi.org/10.1534/genetics.117.200576openalex-snapshot
Maternal Torso-Like Coordinates Tissue Folding During Drosophila Gastrulation
inferred← citeshttps://doi.org/10.1534/genetics.119.301292openalex-snapshot
The Physical Mechanisms ofDrosophilaGastrulation: Mesoderm and Endoderm Invagination
inferred← citeshttps://doi.org/10.1534/genetics.120.303258openalex-snapshot
Collective Migrations of Drosophila Embryonic Trunk and Caudal Mesoderm-Derived Muscle Precursor Cells
inferred← citeshttps://doi.org/10.3389/fcell.2022.867438openalex-snapshot
Evidence for a Role of the Lateral Ectoderm in Drosophila Mesoderm Invagination
inferred← citeshttps://doi.org/10.3389/fnins.2019.00244openalex-snapshot
Expressional Profiling of Carpet Glia in the Developing Drosophila Eye Reveals Its Molecular Signature of Morphology Regulators
inferred← citeshttps://doi.org/10.3410/f.727233803.793570853openalex-snapshot
Faculty Opinions recommendation of Mechanotransductive cascade of Myo-II-dependent mesoderm and endoderm invaginations in embryo gastrulation.
inferred← citeshttps://doi.org/10.3410/f.727615179.793570831openalex-snapshot
Faculty Opinions recommendation of Actomyosin meshwork mechanosensing enables tissue shape to orient cell force.
inferred← citeshttps://doi.org/10.3791/58325openalex-snapshot
A Cell-based Assay to Investigate Non-muscle Myosin II Contractility via the Folded-gastrulation Signaling Pathway in Drosophila S2R+ Cells
inferred← citeshttps://doi.org/10.3791/58325-vopenalex-snapshot
A Cell-based Assay to Investigate Non-muscle Myosin II Contractility via the Folded-gastrulation Signaling Pathway in Drosophila S2R+ Cells
inferred← citeshttps://doi.org/10.70675/24d2aadez7101z4acfz8a13z5aab9709930copenalex-snapshot
Quantitative control of GPCR organization and signaling by endocytosis in epithelial morphogenesis
inferred← citeshttps://doi.org/10.70675/38599129z7e97z497bz9d63za6fab54b776aopenalex-snapshot
Regulation of apical basal polarity and mesoderm invagination by the E3 ubiquitin ligase Neuralized in Drosophila
inferred← citeshttps://doi.org/10.70675/50b37a00z5589z4d26za7cfz84c1f7d1cfbeopenalex-snapshot
Intercellular coupling and mechanical feedback during tissue morphogenesis
inferred← citeshttps://doi.org/10.70675/627e8e68z0a93z4b41z8e39zed872a42c063openalex-snapshot
Regulation of a bio-mechanical network driving shape changes during tissue morphogenesis
inferred← citeshttps://doi.org/10.70675/8dd97dc3ze393z4727zbd8fzce552df56eafopenalex-snapshot
Spatio-temporal and quantitative control of Rho1 activity by GPCR signaling during tissue morphogenesis
inferred← citeshttps://doi.org/10.70675/b6eb2d91z239fz4d4dz9824z27fdda94d3a9openalex-snapshot
Cooperation between Toll receptors and the GPCR Cirl in the control of planar polarized cell contractility during morphogenesis
inferred← citeshttps://doi.org/10.70675/b9d56902ze634z4a25z987ezb324e4a02c1dopenalex-snapshot
Dynamique cellulaire et mécanismes moléculaires de l’émergence des cellules souches hématopoïétiques chez l’embryon de poisson zèbre
inferred← citeshttps://doi.org/10.70675/bc416db6za1e3z4d2dzaab6z4755b34d4fa5openalex-snapshot
Evolutionarily conserved mechanical function of serotonin signalling during morphogenesis
inferred← citeshttps://doi.org/10.70675/c46f25cazdc6fz49bdzab03z6db400b54845openalex-snapshot
Regulation of Myosin-II activation and planar polarity during epithelial morphogenesis in Drosophila embryo
inferred← citeshttps://doi.org/10.70675/d5cc0105z6556z4924zbb45ze37ac5b21d6aopenalex-snapshot
Generation and impact of mechanical forces during epithelial-mesenchymal transition
inferred← citeshttps://doi.org/10.70675/eb57dd31zed08z40f7zba58z5a78b3671f85openalex-snapshot
Regulation of Rho1 by RhoGAPs during drosophila germ band extension
inferred← citeshttps://doi.org/10.70675/ec238205z853fz458cz88fcz4626c89ad374openalex-snapshot
Controlling mechanism of basal myosin oscillation in epithelial cells during Drosophila tissue elongation
inferred← citeshttps://doi.org/10.70675/eca4359ezb819z494dz9dd8zab38da0b6cdeopenalex-snapshot
Biochemical and mechanical interplay during Drosophila endoderm morphogenesis
inferred← citeshttps://doi.org/10.7554/elife.18318openalex-snapshot
Folded gastrulation and T48 drive the evolution of coordinated mesoderm internalization in flies
inferred← citeshttps://doi.org/10.7554/elife.22235openalex-snapshot
Uncoupling apical constriction from tissue invagination
inferred← citeshttps://doi.org/10.7554/elife.35717openalex-snapshot
Radially patterned cell behaviours during tube budding from an epithelium
inferred← citeshttps://doi.org/10.7554/elife.47346openalex-snapshot
Fog signaling has diverse roles in epithelial morphogenesis in insects
inferred← citeshttps://doi.org/10.7554/elife.56893openalex-snapshot
Rho1 activation recapitulates early gastrulation events in the ventral, but not dorsal, epithelium of Drosophila embryos
inferred← citeshttps://doi.org/10.7554/elife.69082openalex-snapshot
Optogenetic inhibition of actomyosin reveals mechanical bistability of the mesoderm epithelium during Drosophila mesoderm invagination
inferred← citeshttps://doi.org/10.7554/elife.72369openalex-snapshot
Correct regionalization of a tissue primordium is essential for coordinated morphogenesis
inferred← citeshttps://doi.org/10.7554/elife.73656openalex-snapshot
Notch-dependent and -independent transcription are modulated by tissue movements at gastrulation
inferred← citeshttps://doi.org/10.7554/elife.93496openalex-snapshot
Apical constriction requires patterned apical surface remodeling to synchronize cellular deformation
inferred← citeshttps://doi.org/10.7554/elife.93496.1openalex-snapshot
Apical constriction requires patterned apical surface remodeling to synchronize cellular deformation
inferred← citeshttps://doi.org/10.7554/elife.93496.2openalex-snapshot
Apical constriction requires patterned apical surface remodeling to synchronize cellular deformation
inferred← citeshttps://doi.org/10.7554/elife.93496.3openalex-snapshot
Apical constriction requires patterned apical surface remodeling to synchronize cellular deformation
inferred← citeshttps://doi.org/10.7554/elife.93496.4openalex-snapshot
Apical constriction requires patterned apical surface remodeling to synchronize cellular deformation
inferred← citeshttps://doi.org/10.7554/elife.99263openalex-snapshot
Differential regulation of the proteome and phosphoproteome along the dorso-ventral axis of the early Drosophila embryo
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