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Pigment cell movement is not required for generation of Turing patterns in zebrafish skin
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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/dvdy.10334openalex-snapshot
Pigment cell organization in the hypodermis of zebrafish
inferredcites →https://doi.org/10.1002/jemt.10162openalex-snapshot
Pigment pattern formation in zebrafish: A model for developmental genetics and the evolution of form
inferredcites →https://doi.org/10.1016/j.crme.2012.10.030openalex-snapshot
A quantitative theory of vegetation patterns based on plant structure and the non-local F–KPP equation
inferredcites →https://doi.org/10.1016/j.gde.2012.10.004openalex-snapshot
Towards a statistical mechanics of cell fate decisions
inferredcites →https://doi.org/10.1016/j.semcdb.2008.10.001openalex-snapshot
Stripes and belly-spots—A review of pigment cell morphogenesis in vertebrates
inferredcites →https://doi.org/10.1016/s0925-4773(99)00211-7openalex-snapshot
Zebrafish Leopard gene as a component of the putative reaction-diffusion system
inferredcites →https://doi.org/10.1038/376765a0openalex-snapshot
A reaction–diffusion wave on the skin of the marine angelfish Pomacanthus
inferredcites →https://doi.org/10.1038/ncb2955openalex-snapshot
Proliferation, dispersal and patterned aggregation of iridophores in the skin prefigure striped colouration of zebrafish
inferredcites →https://doi.org/10.1063/1.1668896openalex-snapshot
Symmetry Breaking Instabilities in Dissipative Systems. II
inferredcites →https://doi.org/10.1073/pnas.0607790104openalex-snapshot
Pattern regulation in the stripe of zebrafish suggests an underlying dynamic and autonomous mechanism
inferredcites →https://doi.org/10.1073/pnas.0808622106openalex-snapshot
Interactions between zebrafish pigment cells responsible for the generation of Turing patterns
inferredcites →https://doi.org/10.1073/pnas.1315416111openalex-snapshot
In vitro analysis suggests that difference in cell movement during direct interaction can generate various pigment patterns in vivo
inferredcites →https://doi.org/10.1098/rstb.1952.0012openalex-snapshot
The chemical basis of morphogenesis
inferredcites →https://doi.org/10.1101/cshperspect.a001255openalex-snapshot
Morphogen Gradient Formation
inferredcites →https://doi.org/10.1103/physreve.69.036203openalex-snapshot
Propagating waves in one-dimensional discrete networks of coupled units
inferredcites →https://doi.org/10.1103/physrevlett.64.2953openalex-snapshot
Experimental evidence of a sustained standing Turing-type nonequilibrium chemical pattern
inferredcites →https://doi.org/10.1111/j.1755-148x.2008.00504.xopenalex-snapshot
Melanophores in the stripes of adult zebrafish do not have the nature to gather, but disperse when they have the space to move
inferredcites →https://doi.org/10.1119/1.1987158openalex-snapshot
Thermodynamic Theory of Structure, Stability and Fluctuations
inferredcites →https://doi.org/10.1126/science.1169973openalex-snapshot
An Experimental Design Method Leading to Chemical Turing Patterns
inferredcites →https://doi.org/10.1126/science.1212821openalex-snapshot
Pigment Pattern Formation by Contact-Dependent Depolarization
inferredcites →https://doi.org/10.1126/science.1230718openalex-snapshot
Physical Biology Returns to Morphogenesis
inferredcites →https://doi.org/10.1126/science.1254837openalex-snapshot
Local reorganization of xanthophores fine-tunes and colors the striped pattern of zebrafish
inferredcites →https://doi.org/10.1242/dev.096719openalex-snapshot
Iridophores and their interactions with other chromatophores are required for stripe formation in zebrafish
inferredcites →https://doi.org/10.1242/dev.099804openalex-snapshot
Involvement of Delta/Notch signaling in zebrafish adult pigment stripe patterning
inferredcites →https://doi.org/10.1371/journal.pgen.1003561openalex-snapshot
Interactions with Iridophores and the Tissue Environment Required for Patterning Melanophores and Xanthophores during Zebrafish Adult Pigment Stripe Formation
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.4767229openalex-extracted
Transcriptome and Metabolome Provide Insight into the Formation Mechanism of Skin Pigmentation Diversity in Chinese Soft-Shelled Turtle (Pelodiscus Sinensis)
inferred← citeshttps://doi.org/10.1002/dneu.22405openalex-snapshot
Gap junctional signaling in pattern regulation: Physiological network connectivity instructs growth and form
inferred← citeshttps://doi.org/10.1002/syst.202400028openalex-snapshot
Life in Lab: Chemically Fueled Systems Chemistry for Emergent Properties
inferred← citeshttps://doi.org/10.1007/978-981-16-1490-3_10openalex-snapshot
Evolution of Pigment Pattern Formation in Teleosts
inferred← citeshttps://doi.org/10.1007/978-981-16-1490-3_9openalex-snapshot
Theoretical Studies of Pigment Pattern Formation
inferred← citeshttps://doi.org/10.1007/s11538-020-00731-0openalex-snapshot
Modeling Stripe Formation on Growing Zebrafish Tailfins
inferred← citeshttps://doi.org/10.1016/j.cbd.2024.101237openalex-snapshot
Insights into the mechanism of color formation of the freshwater prawn (Macrobrachium rosenbergii) revealed by de novo assembly transcriptome analysis
inferred← citeshttps://doi.org/10.1016/j.chaos.2020.109707openalex-snapshot
Generalized patterns from local and non local reactions
inferred← citeshttps://doi.org/10.1016/j.chaos.2022.112638openalex-snapshot
Non-reciprocal interactions enhance heterogeneity
inferred← citeshttps://doi.org/10.1016/j.gde.2020.05.010openalex-snapshot
Linking genotype, cell behavior, and phenotype: multidisciplinary perspectives with a basis in zebrafish patterns
inferred← citeshttps://doi.org/10.1016/j.jtbi.2016.08.005openalex-snapshot
Identifying network topologies that can generate turing pattern
inferred← citeshttps://doi.org/10.1016/j.jtbi.2017.11.014openalex-snapshot
Understanding interactions between populations: Individual based modelling and quantification using pair correlation functions
inferred← citeshttps://doi.org/10.1016/j.mbs.2025.109463openalex-snapshot
The mean-field survival model for stripe formation in zebrafish exhibits Turing instability
inferred← citeshttps://doi.org/10.1016/j.physd.2016.05.005openalex-snapshot
Emergence of chaos in a spatially confined reactive system
inferred← citeshttps://doi.org/10.1016/j.ydbio.2018.12.019openalex-snapshot
Method for disarranging the pigment pattern of zebrafish by optogenetics
inferred← citeshttps://doi.org/10.1021/acs.jpclett.0c00072openalex-snapshot
Membrane Structure Drives Synchronization Patterns in Arrays of Diffusively Coupled Self-Oscillating Droplets
inferred← citeshttps://doi.org/10.1038/ncomms11729openalex-snapshot
Cox process representation and inference for stochastic reaction–diffusion processes
inferred← citeshttps://doi.org/10.1038/s41467-018-05629-zopenalex-snapshot
Iridophores as a source of robustness in zebrafish stripes and variability in Danio patterns
inferred← citeshttps://doi.org/10.1038/s41598-021-89116-4openalex-snapshot
Influence of survival, promotion, and growth on pattern formation in zebrafish skin
inferred← citeshttps://doi.org/10.1038/srep19274openalex-snapshot
Analysis of spatial-temporal gene expression patterns reveals dynamics and regionalization in developing mouse brain
inferred← citeshttps://doi.org/10.1039/d4sm01309copenalex-snapshot
Turing patterns on polymerized membranes: coarse-grained lattice modelling with an internal degree of freedom for polymer direction
inferred← citeshttps://doi.org/10.1063/1.4990783openalex-snapshot
Dissipative structures and biological rhythms
inferred← citeshttps://doi.org/10.1063/1.5140520openalex-snapshot
Widening the criteria for emergence of Turing patterns
inferred← citeshttps://doi.org/10.1063/5.0099753openalex-snapshot
Effect of obstructions on growing Turing patterns
inferred← citeshttps://doi.org/10.1073/pnas.1917763117openalex-snapshot
Topological data analysis of zebrafish patterns
inferred← citeshttps://doi.org/10.1098/rsif.2015.0812openalex-snapshot
Modelling stripe formation in zebrafish: an agent-based approach
inferred← citeshttps://doi.org/10.1098/rsif.2025.0536openalex-snapshot
Inference and prediction for stochastic models of biological populations undergoing migration and proliferation
inferred← citeshttps://doi.org/10.1098/rsos.232002openalex-snapshot
Linking discrete and continuous models of cell birth and migration
inferred← citeshttps://doi.org/10.1098/rsta.2017.0376openalex-snapshot
Dissipative structures in biological systems: bistability, oscillations, spatial patterns and waves
inferred← citeshttps://doi.org/10.1098/rsta.2020.0269openalex-snapshot
Insights from chemical systems into Turing-type morphogenesis
inferred← citeshttps://doi.org/10.1098/rsta.2020.0274openalex-snapshot
Studies of Turing pattern formation in zebrafish skin
inferred← citeshttps://doi.org/10.1103/physreve.101.022203openalex-snapshot
Turing patterns in a network-reduced FitzHugh-Nagumo model
inferred← citeshttps://doi.org/10.1103/physreve.109.014213openalex-snapshot
Numerical study of anisotropic diffusion in Turing patterns based on Finsler geometry modeling
inferred← citeshttps://doi.org/10.1103/physreve.98.040201openalex-snapshot
Turing-Hopf front invasion: Rings and shells
inferred← citeshttps://doi.org/10.1103/physrevlett.117.056001openalex-snapshot
Multifold Increases in Turing Pattern Wavelength in the Chlorine Dioxide-Iodine-Malonic Acid Reaction-Diffusion System
inferred← citeshttps://doi.org/10.1103/physrevlett.132.023801openalex-snapshot
Threshold and Laser Conversion in Nanostructured-Resonator Parametric Oscillators
inferred← citeshttps://doi.org/10.1109/tnse.2017.2730261openalex-snapshot
Pattern Formation over Multigraphs
inferred← citeshttps://doi.org/10.1137/22m1543082openalex-snapshot
Quantifying Different Modeling Frameworks Using Topological Data Analysis: A Case Study with Zebrafish Patterns
inferred← citeshttps://doi.org/10.1137/24m165644xopenalex-snapshot
Data-Driven Continuation of Patterns and Their Bifurcations
inferred← citeshttps://doi.org/10.1186/s12898-018-0170-3openalex-snapshot
Judging a salmon by its spots: environmental variation is the primary determinant of spot patterns in Salmo salar
inferred← citeshttps://doi.org/10.1242/dev.200974openalex-snapshot
The present and future of Turing models in developmental biology
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1006943openalex-snapshot
Isolating and quantifying the role of developmental noise in generating phenotypic variation
inferred← citeshttps://doi.org/10.2139/ssrn.6251796openalex-snapshot
Turing patterns on non-fluctuating surfaces under mechanical stresses
inferred← citeshttps://doi.org/10.3389/fmars.2023.1234940openalex-snapshot
Transcriptome analysis provides insights into the mechanism of carapace stripe formation in two closely related Marsupenaeus species
inferred← citeshttps://doi.org/10.3389/fphy.2021.805659openalex-snapshot
Correspondences Between Parameters in a Reaction-Diffusion Model and Connexin Functions During Zebrafish Stripe Formation
inferred← citeshttps://doi.org/10.3389/frym.2022.834049openalex-snapshot
What Does Math Have to Do With Patterns in Fish?
inferred← citeshttps://doi.org/10.3390/biophysica4020020openalex-snapshot
Emergence of Diverse Epidermal Patterns via the Integration of the Turing Pattern Model with the Majority Voting Model
inferred← citeshttps://doi.org/10.3410/f.733813954.793560054openalex-snapshot
Faculty Opinions recommendation of Iridophores as a source of robustness in zebrafish stripes and variability in Danio patterns.
inferred← citeshttps://doi.org/10.7554/elife.12401openalex-snapshot
Long-distance communication by specialized cellular projections during pigment pattern development and evolution
inferred← citeshttps://doi.org/10.7554/elife.52998openalex-snapshot
A quantitative modelling approach to zebrafish pigment pattern formation
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