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Cell dynamics underlying oriented growth of the Drosophila wing imaginal disc

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/3-540-45465-9_88openalex-snapshot
Optimal Net Surface Problems with Applications
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Segmentation and Quantitative Analysis of Epithelial Tissues
inferredcites →https://doi.org/10.1007/bf02982977openalex-snapshot
The genetic control of wing development inDrosophila
inferredcites →https://doi.org/10.1007/s00412-016-0595-4openalex-snapshot
The legacy of Drosophila imaginal discs
inferredcites →https://doi.org/10.1016/0012-1606(71)90047-9openalex-snapshot
Parameters of the wing imaginal disc development ofDrosophila melanogaster
inferredcites →https://doi.org/10.1016/0012-1606(73)90149-8openalex-snapshot
The synthetic and minimal culture requirements for evagination of imaginal discs of Drosophila melanogaster in vitro
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Intrinsic growth control in the imaginal primordia of Drosophila, and the autonomous action of a lethal mutation causing overgrowth
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Mutations at the fat locus interfere with cell proliferation control and epithelial morphogenesis in Drosophila
inferredcites →https://doi.org/10.1016/0925-4773(94)90070-1openalex-snapshot
Cell proliferation patterns in the wing imaginal disc of Drosophila
inferredcites →https://doi.org/10.1016/j.ceb.2016.08.002openalex-snapshot
Planar cell polarity: global inputs establishing cellular asymmetry
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Anaplastic Lymphoma Kinase Spares Organ Growth during Nutrient Restriction in Drosophila
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Nutritional Control of Protein Biosynthetic Capacity by Insulin via Myc in Drosophila
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Drosophila ALS Regulates Growth and Metabolism through Functional Interaction with Insulin-Like Peptides
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Remote Control of Insulin Secretion by Fat Cells in Drosophila
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The Orientation of Cell Divisions Determines the Shape of Drosophila Organs
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Functional Genomics Identifies TOR-Regulated Genes that Control Growth and Division
inferredcites →https://doi.org/10.1016/j.cub.2012.03.053openalex-snapshot
Planar Polarity Specification through Asymmetric Subcellular Localization of Fat and Dachsous
inferredcites →https://doi.org/10.1016/j.cub.2012.04.066openalex-snapshot
Establishment of Global Patterns of Planar Polarity during Growth of the Drosophila Wing Epithelium
inferredcites →https://doi.org/10.1016/j.cub.2012.05.049openalex-snapshot
Propagation of Dachsous-Fat Planar Cell Polarity
inferredcites →https://doi.org/10.1016/j.cub.2014.08.005openalex-snapshot
The Balance of Prickle/Spiny-Legs Isoforms Controls the Amount of Coupling between Core and Fat PCP Systems
inferredcites →https://doi.org/10.1016/j.devcel.2007.04.019openalex-snapshot
Lipoprotein-Heparan Sulfate Interactions in the Hh Pathway
inferredcites →https://doi.org/10.1016/j.devcel.2008.06.003openalex-snapshot
Morphogen Control of Wing Growth through the Fat Signaling Pathway
inferredcites →https://doi.org/10.1016/j.devcel.2010.02.015openalex-snapshot
The Long-Range Activity of Hedgehog Is Regulated in the Apical Extracellular Space by the Glypican Dally and the Hydrolase Notum
inferredcites →https://doi.org/10.1016/j.devcel.2010.05.007openalex-snapshot
The Steroid Hormone Ecdysone Controls Systemic Growth by Repressing dMyc Function in Drosophila Fat Cells
inferredcites →https://doi.org/10.1016/j.devcel.2010.11.007openalex-snapshot
Antagonistic Growth Regulation by Dpp and Fat Drives Uniform Cell Proliferation
inferredcites →https://doi.org/10.1016/j.devcel.2011.06.026openalex-snapshot
Shaping Cells and Organs in Drosophila by Opposing Roles of Fat Body-Secreted Collagen IV and Perlecan
inferredcites →https://doi.org/10.1016/j.devcel.2015.12.012openalex-snapshot
EpiTools: An Open-Source Image Analysis Toolkit for Quantifying Epithelial Growth Dynamics
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Spook and Spookier code for stage-specific components of the ecdysone biosynthetic pathway in Diptera
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Wing tips: The wing disc as a platform for studying Hedgehog signaling
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Chapter 29 Methods for Quantitative Analysis of Transcription in Larvae and Prepupae
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Steroid Regulation of Postembryonic Development and Reproduction in Drosophila
inferredcites →https://doi.org/10.1038/384072a0openalex-snapshot
wingless refines its own expression domain on the Drosophila wing margin
inferredcites →https://doi.org/10.1038/46779openalex-snapshot
Dorsoventral lineage restriction in wing imaginal discs requires Notch
inferredcites →https://doi.org/10.1038/emboj.2013.197openalex-snapshot
Differential proliferation rates generate patterns of mechanical tension that orient tissue growth
inferredcites →https://doi.org/10.1038/msb.2011.36openalex-snapshot
Genome‐wide dFOXO targets and topology of the transcriptomic response to stress and insulin signalling
inferredcites →https://doi.org/10.1038/nature05014openalex-snapshot
The emergence of geometric order in proliferating metazoan epithelia
inferredcites →https://doi.org/10.1038/ncomms12972openalex-snapshot
Insulin and TOR signal in parallel through FOXO and S6K to promote epithelial wound healing
inferredcites →https://doi.org/10.1038/nmeth.2019openalex-snapshot
Fiji: an open-source platform for biological-image analysis
inferredcites →https://doi.org/10.1038/nprot.2012.016openalex-snapshot
Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks
inferredcites →https://doi.org/10.1038/nrg2166openalex-snapshot
The Decapentaplegic morphogen gradient: from pattern formation to growth regulation
inferredcites →https://doi.org/10.1038/srep12383openalex-snapshot
Ecdysone promotes growth of imaginal discs through the regulation of Thor in D. melanogaster
inferredcites →https://doi.org/10.1038/srep42786openalex-snapshot
Calcium spikes, waves and oscillations in a large, patterned epithelial tissue
inferredcites →https://doi.org/10.1073/pnas.072208199openalex-snapshot
Determining the role of patterned cell proliferation in the shape and size of the Drosophila wing
inferredcites →https://doi.org/10.1073/pnas.0900641106openalex-snapshot
Directed, efficient, and versatile modifications of the Drosophila genome by genomic engineering
inferredcites →https://doi.org/10.1073/pnas.1008623107openalex-snapshot
Live imaging of Drosophila imaginal disc development
inferredcites →https://doi.org/10.1073/pnas.93.21.11687openalex-snapshot
Cell cycling and patterned cell proliferation in the Drosophila wing during metamorphosis.
inferredcites →https://doi.org/10.1080/00107518408210979openalex-snapshot
Soap, cells and statistics—random patterns in two dimensions
inferredcites →https://doi.org/10.1089/omi.2011.0118openalex-snapshot
clusterProfiler: an R Package for Comparing Biological Themes Among Gene Clusters
inferredcites →https://doi.org/10.1093/bioinformatics/btp184openalex-snapshot
Globally optimal stitching of tiled 3D microscopic image acquisitions
inferredcites →https://doi.org/10.1093/bioinformatics/btx180openalex-snapshot
Trainable Weka Segmentation: a machine learning tool for microscopy pixel classification
inferredcites →https://doi.org/10.1101/cshperspect.a002493openalex-snapshot
Shaping Morphogen Gradients by Proteoglycans
inferredcites →https://doi.org/10.1101/gad.1098703openalex-snapshot
Control of cell number by Drosophila FOXO: downstream and feedback regulation of the insulin receptor pathway
inferredcites →https://doi.org/10.1101/gad.204479.112openalex-snapshot
A secreted decoy of InR antagonizes insulin/IGF signaling to restrict body growth in Drosophila
inferredcites →https://doi.org/10.1101/gad.610511openalex-snapshot
Planar polarization of the atypical myosin Dachs orients cell divisions in Drosophila
inferredcites →https://doi.org/10.1101/gad.9.12.1530openalex-snapshot
Dachsous encodes a member of the cadherin superfamily that controls imaginal disc morphogenesis in Drosophila.
inferredcites →https://doi.org/10.1101/gr.081349.108openalex-snapshot
Genomic mapping of binding regions for the Ecdysone receptor protein complex
inferredcites →https://doi.org/10.1103/physreve.95.032401openalex-snapshot
Triangles bridge the scales: Quantifying cellular contributions to tissue deformation
inferredcites →https://doi.org/10.1126/science.1070058openalex-snapshot
Ablation of Insulin-Producing Neurons in Flies: Growth and Diabetic Phenotypes
inferredcites →https://doi.org/10.1126/science.1182228openalex-snapshot
Sestrin as a Feedback Inhibitor of TOR That Prevents Age-Related Pathologies
inferredcites →https://doi.org/10.1152/physiolgenomics.00061.2006openalex-snapshot
High-resolution dynamics of the transcriptional response to nutrition in Drosophila: a key role for dFOXO
inferredcites →https://doi.org/10.1186/1471-2105-12-35openalex-snapshot
VennDiagram: a package for the generation of highly-customizable Venn and Euler diagrams in R
inferredcites →https://doi.org/10.1186/1471-2121-11-7openalex-snapshot
Nutritional control of gene expression in Drosophila larvae via TOR, Myc and a novel cis-regulatory element
inferredcites →https://doi.org/10.1186/1471-213x-13-28openalex-snapshot
The Ecdysone receptor constrains wingless expression to pattern cell cycle across the Drosophilawing margin in a cyclin B-dependent manner
inferredcites →https://doi.org/10.1186/gb-2005-6-12-r99openalex-snapshot
The genomic response to 20-hydroxyecdysone at the onset of Drosophila metamorphosis
inferredcites →https://doi.org/10.1186/gb-2013-14-4-r36openalex-snapshot
TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions
inferredcites →https://doi.org/10.1186/jbiol72openalex-snapshot
Imp-L2, a putative homolog of vertebrate IGF-binding protein 7, counteracts insulin signaling in Drosophila and is essential for starvation resistance
inferredcites →https://doi.org/10.1242/dev.00205openalex-snapshot
EcR isoforms in Drosophila : testing tissue-specific requirements by targeted blockade and rescue
inferredcites →https://doi.org/10.1242/dev.01061openalex-snapshot
Abrogation of heparan sulfate synthesis inDrosophiladisrupts the Wingless, Hedgehog and Decapentaplegic signaling pathways
inferredcites →https://doi.org/10.1242/dev.014779openalex-snapshot
The role of Polycomb-group response elements in regulation of engrailed transcription in Drosophila
inferredcites →https://doi.org/10.1242/dev.02197openalex-snapshot
The endocytic pathway and formation of the Wingless morphogen gradient
inferredcites →https://doi.org/10.1242/dev.02243openalex-snapshot
Fat and Wingless signaling oppositely regulate epithelial cell-cell adhesion and distal wing development inDrosophila
inferredcites →https://doi.org/10.1242/dev.02427openalex-snapshot
Dachs: an unconventional myosin that functions downstream of Fat to regulate growth, affinity and gene expression inDrosophila
inferredcites →https://doi.org/10.1242/dev.02428openalex-snapshot
Neverland is an evolutionally conserved Rieske-domain protein that is essential for ecdysone synthesis and insect growth
inferredcites →https://doi.org/10.1242/dev.032672openalex-snapshot
The Ecdysone receptor controls the post-critical weight switch to nutrition-independent differentiation inDrosophilawing imaginal discs
inferredcites →https://doi.org/10.1242/dev.078402openalex-snapshot
Dally and Notum regulate the switch between low and high level Hedgehog pathway signalling
inferredcites →https://doi.org/10.1242/dev.082800openalex-snapshot
Integrating force-sensing and signaling pathways in a model for the regulation of wing imaginal disc size
inferredcites →https://doi.org/10.1242/dev.088872openalex-snapshot
A high-throughput template for optimizingDrosophilaorgan culture with response-surface methods
inferredcites →https://doi.org/10.1242/dev.090878openalex-snapshot
A global pattern of mechanical stress polarizes cell divisions and cell shape in the growing Drosophila wing disc
inferredcites →https://doi.org/10.1242/dev.096057openalex-snapshot
TIE-DYE: a combinatorial marking system to visualize and genetically manipulate clones during development in Drosophila melanogaster
inferredcites →https://doi.org/10.1242/dev.109264openalex-snapshot
Dynamic clonal analysis based on chronic in vivo imaging allows multiscale quantification of growth in the Drosophila wing disc
inferredcites →https://doi.org/10.1242/dev.124.17.3241openalex-snapshot
Feed-back mechanisms affecting Notch activation at the dorsoventral boundary in the Drosophila wing
inferredcites →https://doi.org/10.1242/dev.124.18.3565openalex-snapshot
The Drosophila sugarless gene modulates Wingless signaling and encodes an enzyme involved in polysaccharide biosynthesis
inferredcites →https://doi.org/10.1242/dev.124.8.1485openalex-snapshot
The function and regulation of cut expression on the wing margin of Drosophila: Notch, Wingless and a dominant negative role for Delta and Serrate
inferredcites →https://doi.org/10.1242/dev.124982openalex-snapshot
The Ecdysteroidome of Drosophila: influence of diet and development
inferredcites →https://doi.org/10.1242/dev.125.11.2149openalex-snapshot
Environmental control of the cell cycle in Drosophila: nutrition activates mitotic and endoreplicative cells by distinct mechanisms
inferredcites →https://doi.org/10.1242/dev.125.14.2653openalex-snapshot
Ecdysone pathway is required for furrow progression in the developing Drosophila eye
inferredcites →https://doi.org/10.1242/dev.128.1.1openalex-snapshot
Broad-complex, but not Ecdysone receptor, is required for progression of the morphogenetic furrow in the Drosophila eye
inferredcites →https://doi.org/10.1242/dev.147538openalex-snapshot
Oxygenation and adenosine deaminase support growth and proliferation of ex vivo cultured Drosophila wing imaginal discs
inferredcites →https://doi.org/10.1371/journal.pone.0107333openalex-snapshot
Towards Long Term Cultivation of Drosophila Wing Imaginal Discs In Vitro
inferredcites →https://doi.org/10.1371/journal.pone.0163744openalex-snapshot
Long Term Ex Vivo Culture and Live Imaging of Drosophila Larval Imaginal Discs
inferredcites →https://doi.org/10.14806/ej.17.1.200openalex-snapshot
Cutadapt removes adapter sequences from high-throughput sequencing reads
inferredcites →https://doi.org/10.2307/1538049openalex-snapshot
HORMONES AND TISSUE COMPETENCE IN THE DEVELOPMENT OF DROSOPHILA
inferredcites →https://doi.org/10.7554/elife.00542openalex-snapshot
The insulin receptor cellular IRES confers resistance to eIF4A inhibition
inferredcites →https://doi.org/10.7554/elife.07090openalex-snapshot
Interplay of cell dynamics and epithelial tension during morphogenesis of the Drosophila pupal wing
inferredcites →https://doi.org/10.7554/elife.08519openalex-snapshot
Unified quantitative characterization of epithelial tissue development
inferredcites →https://doi.org/10.7554/elife.14334openalex-snapshot
TissueMiner: A multiscale analysis toolkit to quantify how cellular processes create tissue dynamics

What points at this work

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

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Resilin in Insect Flight Systems
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Competitive and Coordinative Interactions between Body Parts Produce Adaptive Developmental Outcomes
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The development of shape. Modular control of growth in the lepidopteran forewing
inferred← citeshttps://doi.org/10.1007/978-1-0716-2541-5_16openalex-snapshot
Cultivation and Live Imaging of Drosophila Imaginal Discs
inferred← citeshttps://doi.org/10.1007/978-1-0716-4164-4_19openalex-snapshot
Calcium Imaging in Drosophila
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A Benchmark for Epithelial Cell Tracking
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Regulation of phenotypic plasticity from the perspective of evolutionary developmental biology
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Ecdysteroid signalling in insects—From biosynthesis to gene expression regulation
inferred← citeshttps://doi.org/10.1016/j.bpj.2019.01.007openalex-snapshot
Decoding Calcium Signaling Dynamics during Drosophila Wing Disc Development
inferred← citeshttps://doi.org/10.1016/j.ceb.2021.05.002openalex-snapshot
Growth across scales: Dynamic signaling impacts tissue size and shape
inferred← citeshttps://doi.org/10.1016/j.celrep.2019.03.094openalex-snapshot
Upregulation of E93 Gene Expression Acts as the Trigger for Metamorphosis Independently of the Threshold Size in the Beetle Tribolium castaneum
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114398openalex-snapshot
Piezo regulates epithelial topology and promotes precision in organ size control
inferred← citeshttps://doi.org/10.1016/j.cois.2020.08.008openalex-snapshot
From genes to shape during metamorphosis: a history
inferred← citeshttps://doi.org/10.1016/j.cub.2019.01.044openalex-snapshot
Oriented Cell Divisions Are Not Required for Drosophila Wing Shape
inferred← citeshttps://doi.org/10.1016/j.cub.2019.05.020openalex-snapshot
Evolution of Ovipositor Length in Drosophila suzukii Is Driven by Enhanced Cell Size Expansion and Anisotropic Tissue Reorganization
inferred← citeshttps://doi.org/10.1016/j.cub.2021.07.078openalex-snapshot
Dynamic changes in epithelial cell packing during tissue morphogenesis
inferred← citeshttps://doi.org/10.1016/j.devcel.2019.03.016openalex-snapshot
Inter-Organ Growth Coordination Is Mediated by the Xrp1-Dilp8 Axis in Drosophila
inferred← citeshttps://doi.org/10.1016/j.devcel.2021.03.030openalex-snapshot
Formation of polarized contractile interfaces by self-organized Toll-8/Cirl GPCR asymmetry
inferred← citeshttps://doi.org/10.1016/j.devcel.2023.08.032openalex-snapshot
The Drosophila ecdysone receptor promotes or suppresses proliferation according to ligand level
inferred← citeshttps://doi.org/10.1016/j.pbiomolbio.2018.04.008openalex-snapshot
Wing morphogenesis in Lepidoptera
inferred← citeshttps://doi.org/10.1016/j.semcdb.2021.05.026openalex-snapshot
Forced into shape: Mechanical forces in Drosophila development and homeostasis
inferred← citeshttps://doi.org/10.1016/j.xpro.2022.101138openalex-snapshot
Protocol for ex vivo time lapse imaging of Drosophila melanogaster cytonemes
inferred← citeshttps://doi.org/10.1038/s41467-018-06497-3openalex-snapshot
Differential lateral and basal tension drive folding of Drosophila wing discs through two distinct mechanisms
inferred← citeshttps://doi.org/10.1038/s41467-021-22010-9openalex-snapshot
Apico-basal cell compression regulates Lamin A/C levels in epithelial tissues
inferred← citeshttps://doi.org/10.1038/s41467-021-26780-0openalex-snapshot
Ecdysone regulates Drosophila wing disc size via a TORC1 dependent mechanism
inferred← citeshttps://doi.org/10.1038/s41467-022-30492-4openalex-snapshot
Metabolic control of progenitor cell propagation during Drosophila tracheal remodeling
inferred← citeshttps://doi.org/10.1038/s41467-023-36739-yopenalex-snapshot
Growth anisotropy of the extracellular matrix shapes a developing organ
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Microfluidics on the fly: Inexpensive rapid fabrication of thermally laminated microfluidic devices for live imaging and multimodal perturbations of multicellular systems
inferred← citeshttps://doi.org/10.1073/pnas.1816100116openalex-snapshot
Statistics of noisy growth with mechanical feedback in elastic tissues
inferred← citeshttps://doi.org/10.1073/pnas.2410430122openalex-snapshot
Phased ERK responsiveness and developmental robustness regulate teleost skin morphogenesis
inferred← citeshttps://doi.org/10.1080/19336934.2022.2142460openalex-snapshot
HaloTag-based reporters for sparse labeling and cell tracking
inferred← citeshttps://doi.org/10.1088/1367-2630/abcbc7openalex-snapshot
Inferring the flow properties of epithelial tissues from their geometry
inferred← citeshttps://doi.org/10.1093/genetics/iyac020openalex-snapshot
The wing imaginal disc
inferred← citeshttps://doi.org/10.1093/icb/icz080openalex-snapshot
Exploring the Role of Insulin Signaling in Relative Growth: A Case Study on Wing-Body Scaling in Lepidoptera
inferred← citeshttps://doi.org/10.1098/rsob.200373openalex-snapshot
Regulation of ecdysone production in Drosophila by neuropeptides and peptide hormones
inferred← citeshttps://doi.org/10.1098/rstb.2023.0051openalex-snapshot
Choice of friction coefficient deeply affects tissue behaviour in stochastic epithelial vertex models
inferred← citeshttps://doi.org/10.1101/2021.02.23.432493openalex-snapshot
GPI-anchored FGF directs cytoneme-mediated bidirectional signaling to self-regulate tissue-specific dispersion
inferred← citeshttps://doi.org/10.1101/2021.04.11.439313openalex-snapshot
Adhesion dynamics regulate cell intercalation behaviour in an active tissue
inferred← citeshttps://doi.org/10.1101/2022.04.07.487542openalex-snapshot
An EcR probe reveals mechanisms of the ecdysone-mediated switch from repression-to-activation on target genes in the larval wing disc
inferred← citeshttps://doi.org/10.1101/2022.09.18.508456openalex-snapshot
Vestigial-dependent recruitment contributes to robust patterning but is not required for wing-fate induction in Drosophila
inferred← citeshttps://doi.org/10.1101/2022.11.07.515433openalex-snapshot
Choice of Friction Coefficient Deeply Affects Tissue Behaviour in Epithelial Vertex Models
inferred← citeshttps://doi.org/10.1101/2023.02.10.527985openalex-snapshot
The ecdysone receptor promotes or suppresses proliferation according to ligand level
inferred← citeshttps://doi.org/10.1101/2023.03.06.531386openalex-snapshot
Orthogonal coupling of a 3D cytoskeletal scaffold coordinates cell morphogenesis and maintains tissue organization in the Drosophila pupal retina
inferred← citeshttps://doi.org/10.1101/2024.07.11.603179openalex-snapshot
Pulsatile dynamics propagate crystalline order in the developing Drosophil a eye
inferred← citeshttps://doi.org/10.1101/2024.09.21.614249openalex-snapshot
Mechanical regulation of cuboidal-to-squamous epithelial transition in the Drosophila developing wing
inferred← citeshttps://doi.org/10.1101/2024.12.21.629882openalex-snapshot
Developmental delay ensures global tissue size robustness upon local induction of apoptosis
inferred← citeshttps://doi.org/10.1101/2025.01.09.632245openalex-snapshot
A switch in the mode of tissue growth extends the growth phase of Drosophila wing primordia during early pupal development
inferred← citeshttps://doi.org/10.1101/536342openalex-snapshot
Neuronal differentiation affects tissue mechanics and progenitor arrangement in the vertebrate neuroepithelium
inferred← citeshttps://doi.org/10.1103/jgll-wsvtopenalex-snapshot
Proliferation symmetry breaking in growing tissues
inferred← citeshttps://doi.org/10.1103/lh3v-v2c9openalex-snapshot
Cell Divisions Imprint Long Lasting Elastic Strain Fields in Epithelial Tissues
inferred← citeshttps://doi.org/10.1103/physrevx.15.021068openalex-snapshot
“Morphogenetic Action” Principle for 3D Shape Formation by the Growth of Thin Sheets
inferred← citeshttps://doi.org/10.1140/epje/s10189-025-00495-2openalex-snapshot
In vivo assessment of kinematic relationships for epithelial morphogenesis
inferred← citeshttps://doi.org/10.1242/bio.059908openalex-snapshot
Vestigial-dependent induction contributes to robust patterning but is not essential for wing-fate recruitment in Drosophila
inferred← citeshttps://doi.org/10.1242/dev.160101openalex-snapshot
Hormonal control of growth in the wing imaginal disks of Junonia coenia: the relative contributions of insulin and ecdysone
inferred← citeshttps://doi.org/10.1242/dev.161125openalex-snapshot
Morphogenesis one century after On Growth and Form
inferred← citeshttps://doi.org/10.1242/dev.176297openalex-snapshot
Neuronal differentiation influences progenitor arrangement in the vertebrate neuroepithelium
inferred← citeshttps://doi.org/10.1242/dev.186403openalex-snapshot
Charting the unknown currents of cellular flows and forces
inferred← citeshttps://doi.org/10.1242/dev.201757openalex-snapshot
Inter-plane feedback coordinates cell morphogenesis and maintains 3D tissue organization in the Drosophila pupal retina
inferred← citeshttps://doi.org/10.1242/dev.202828openalex-snapshot
Local Ecdysone synthesis in a wounded epithelium sustains developmental delay and promotes regeneration in Drosophila
inferred← citeshttps://doi.org/10.1242/dev.204951openalex-snapshot
Transitions in development – an interview with Natalie Dye
inferred← citeshttps://doi.org/10.1371/journal.pbio.2006018openalex-snapshot
A non-cell-autonomous actin redistribution enables isotropic retinal growth
inferred← citeshttps://doi.org/10.15252/embj.2019101767openalex-snapshot
Glycolysis regulates Hedgehog signalling via the plasma membrane potential
inferred← citeshttps://doi.org/10.15252/embr.202154025openalex-snapshot
Hedgehog signaling can enhance glycolytic ATP production in the Drosophila wing disc
inferred← citeshttps://doi.org/10.1534/genetics.120.303095openalex-snapshot
Regulation of Body Size and Growth Control
inferred← citeshttps://doi.org/10.21203/rs.3.pex-2630/v1openalex-snapshot
Calcium Imaging in Drosophila Organs
inferred← citeshttps://doi.org/10.2139/ssrn.4124624openalex-snapshot
Quantitative Analysis of Three-Dimensional Cell Organisation and Concentration Profiles within Curved Epithelial Tissues
inferred← citeshttps://doi.org/10.3389/fcell.2020.590094openalex-snapshot
An Immobilization Technique for Long-Term Time-Lapse Imaging of Explanted Drosophila Tissues
inferred← citeshttps://doi.org/10.3390/ijms21249754openalex-snapshot
Identification and Analysis of MicroRNAs Associated with Wing Polyphenism in the Brown Planthopper, Nilaparvata lugens
inferred← citeshttps://doi.org/10.3410/f.733797121.793550332openalex-snapshot
Faculty Opinions recommendation of A non-cell-autonomous actin redistribution enables isotropic retinal growth.
inferred← citeshttps://doi.org/10.48550/arxiv.2002.11166openalex-snapshot
E2 distribution and statistical regularity in polygonal planar tessellations
inferred← citeshttps://doi.org/10.48550/arxiv.2010.06656openalex-snapshot
Dimensionality-Reduction in the Drosophila Wing as Revealed by Landmark-Free Measure-ments of Phenotype
inferred← citeshttps://doi.org/10.7554/elife.34410openalex-snapshot
Multi-view light-sheet imaging and tracking with the MaMuT software reveals the cell lineage of a direct developing arthropod limb
inferred← citeshttps://doi.org/10.7554/elife.44860openalex-snapshot
Liquid-crystal organization of liver tissue
inferred← citeshttps://doi.org/10.7554/elife.57964openalex-snapshot
Self-organized patterning of cell morphology via mechanosensitive feedback
inferred← citeshttps://doi.org/10.7554/elife.66750openalex-snapshot
Global constraints within the developmental program of the Drosophila wing
inferred← citeshttps://doi.org/10.7554/elife.72666openalex-snapshot
Ecdysone coordinates plastic growth with robust pattern in the developing wing
inferred← citeshttps://doi.org/10.7554/elife.72806openalex-snapshot
Emergence of a geometric pattern of cell fates from tissue-scale mechanics in the Drosophila eye
inferred← citeshttps://doi.org/10.7554/elife.79257openalex-snapshot
Cellular compartmentalisation and receptor promiscuity as a strategy for accurate and robust inference of position during morphogenesis
inferred← citeshttps://doi.org/10.7554/elife.84918openalex-snapshot
Competition between myosin II and βH-spectrin regulates cytoskeletal tension
inferred← citeshttps://doi.org/10.7554/elife.84918.1openalex-snapshot
Competition between myosin II and βH-Spectrin regulates cytoskeletal tension
inferred← citeshttps://doi.org/10.7554/elife.84918.1.sa0openalex-snapshot
Reviewer #2 (Public Review): Competition between myosin II and βH-Spectrin regulates cytoskeletal tension
inferred← citeshttps://doi.org/10.7554/elife.84918.1.sa1openalex-snapshot
Reviewer #1 (Public Review): Competition between myosin II and βH-Spectrin regulates cytoskeletal tension
inferred← citeshttps://doi.org/10.7554/elife.84918.1.sa2openalex-snapshot
eLife Assessment: Competition between myosin II and βH-Spectrin regulates cytoskeletal tension
inferred← citeshttps://doi.org/10.7554/elife.84918.3openalex-snapshot
Competition between myosin II and βH-spectrin regulates cytoskeletal tension
inferred← citeshttps://doi.org/10.7554/elife.95521openalex-snapshot
The geometric basis of epithelial convergent extension
inferred← citeshttps://doi.org/10.7554/elife.95521.3openalex-snapshot
The geometric basis of epithelial convergent extension
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