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A Doppler effect in embryonic pattern formation
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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.21458openalex-snapshot
Dynamics of zebrafish somitogenesis
inferredcites →https://doi.org/10.1007/978-1-60327-977-2_8openalex-snapshot
Simple and Efficient Transgenesis with Meganuclease Constructs in Zebrafish
inferredcites →https://doi.org/10.1016/j.devcel.2012.09.009openalex-snapshot
Single-Cell-Resolution Imaging of the Impact of Notch Signaling and Mitosis on Segmentation Clock Dynamics
inferredcites →https://doi.org/10.1016/j.gde.2011.09.006openalex-snapshot
Live transgenic reporters of the vertebrate embryo's Segmentation Clock
inferredcites →https://doi.org/10.1016/j.jtbi.2011.05.004openalex-snapshot
The clock and wavefront model revisited
inferredcites →https://doi.org/10.1016/s0022-5193(76)80131-2openalex-snapshot
A clock and wavefront model for control of the number of repeated structures during animal morphogenesis
inferredcites →https://doi.org/10.1016/s0092-8674(00)80451-1openalex-snapshot
Avian hairy Gene Expression Identifies a Molecular Clock Linked to Vertebrate Segmentation and Somitogenesis
inferredcites →https://doi.org/10.1016/s0925-4773(02)00218-6openalex-snapshot
I-SceI meganuclease mediates highly efficient transgenesis in fish
inferredcites →https://doi.org/10.1038/nature11804openalex-snapshot
Scaling of embryonic patterning based on phase-gradient encoding
inferredcites →https://doi.org/10.1038/ncb1578openalex-snapshot
Priming, initiation and synchronization of the segmentation clock by deltaD and deltaC
inferredcites →https://doi.org/10.1038/ncb1679openalex-snapshot
A β-catenin gradient links the clock and wavefront systems in mouse embryo segmentation
inferredcites →https://doi.org/10.1038/nmeth.1334openalex-snapshot
A toolkit for high-throughput, cross-species gene engineering in Drosophila
inferredcites →https://doi.org/10.1038/nmeth.2019openalex-snapshot
Fiji: an open-source platform for biological-image analysis
inferredcites →https://doi.org/10.1038/nmeth933openalex-snapshot
A recombineering pipeline for functional genomics applied to Caenorhabditis elegans
inferredcites →https://doi.org/10.1073/pnas.0508658103openalex-snapshot
Real-time imaging of the somite segmentation clock: Revelation of unstable oscillators in the individual presomitic mesoderm cells
inferredcites →https://doi.org/10.1103/physreve.65.041903openalex-snapshot
Performance of different synchronization measures in real data: A case study on electroencephalographic signals
inferredcites →https://doi.org/10.1126/science.1142538openalex-snapshot
Synchrony Dynamics During Initiation, Failure, and Rescue of the Segmentation Clock
inferredcites →https://doi.org/10.1126/science.1218256openalex-snapshot
A Segmentation Clock with Two-Segment Periodicity in Insects
inferredcites →https://doi.org/10.1146/annurev-cellbio-101011-155703openalex-snapshot
Formation and Segmentation of the Vertebrate Body Axis
inferredcites →https://doi.org/10.1175/1520-0477(1998)079<0061:apgtwa>2.0.co;2openalex-snapshot
A Practical Guide to Wavelet Analysis
inferredcites →https://doi.org/10.1186/1471-213x-11-43openalex-snapshot
Two-color fluorescent in situ hybridization in the embryonic zebrafish brain using differential detection systems
inferredcites →https://doi.org/10.1242/dev.063735openalex-snapshot
Patterning embryos with oscillations: structure, function and dynamics of the vertebrate segmentation clock
inferredcites →https://doi.org/10.1242/dev.129.12.2929openalex-snapshot
Hairy/E(spl)-related(Her) genes are central components of the segmentation oscillator and display redundancy with the Delta/Notch signaling pathway in the formation of anterior segmental boundaries in the zebrafish
inferredcites →https://doi.org/10.1371/journal.pbio.0050150openalex-snapshot
Setting the Tempo in Development: An Investigation of the Zebrafish Somite Clock Mechanism
inferredcites →https://doi.org/10.1371/journal.pgen.0040015openalex-snapshot
Notch Signalling Synchronizes the Zebrafish Segmentation Clock but Is Not Needed To Create Somite Boundaries
inferredcites →https://doi.org/10.2976/1.3027088openalex-snapshot
Delayed coupling theory of vertebrate segmentation
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9780470015902.a0003820.pub2openalex-snapshot
Somitogenesis in Vertebrate Development
inferred← citeshttps://doi.org/10.1002/chem.201805093openalex-snapshot
Physical Chemistry of Cellular Liquid‐Phase Separation
inferred← citeshttps://doi.org/10.1002/wrna.1751openalex-snapshot
Keeping development on time: Insights into post‐transcriptional mechanisms driving oscillatory gene expression during vertebrate segmentation
inferred← citeshttps://doi.org/10.1007/978-1-0716-3401-1_12openalex-snapshot
Quantitative Live Imaging of Zebrafish Scale Regeneration: From Adult Fish to Signaling Patterns and Tissue Flows
inferred← citeshttps://doi.org/10.1007/978-3-319-33038-9_94-1openalex-snapshot
Mechanisms in Evo-Devo
inferred← citeshttps://doi.org/10.1007/s00018-020-03655-zopenalex-snapshot
Imaging and manipulating the segmentation clock
inferred← citeshttps://doi.org/10.1007/s12038-018-9756-3openalex-snapshot
Spiral waves and vertebrate embryonic handedness
inferred← citeshttps://doi.org/10.1007/s40484-014-0038-2openalex-snapshot
Quantitative biology: from genes, cells to networks
inferred← citeshttps://doi.org/10.1016/b978-0-443-30048-6.00001-2openalex-snapshot
Analysis of the effect of cell movement on gene expression dynamics in development
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2019.10.009openalex-snapshot
Zebrafish gastrulation: Putting fate in motion
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2020.11.001openalex-snapshot
Gene expression oscillations in C. elegans underlie a new developmental clock
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2023.11.001openalex-snapshot
Generation of patterns in the paraxial mesoderm
inferred← citeshttps://doi.org/10.1016/j.asd.2016.11.007openalex-snapshot
Delta-Notch signalling in segmentation
inferred← citeshttps://doi.org/10.1016/j.cdev.2021.203737openalex-snapshot
Positional information encoded in the dynamic differences between neighboring oscillators during vertebrate segmentation
inferred← citeshttps://doi.org/10.1016/j.cdev.2021.203748openalex-snapshot
The zebrafish presomitic mesoderm elongates through compaction-extension
inferred← citeshttps://doi.org/10.1016/j.cell.2018.01.026openalex-snapshot
Modulation of Phase Shift between Wnt and Notch Signaling Oscillations Controls Mesoderm Segmentation
inferred← citeshttps://doi.org/10.1016/j.cell.2021.12.001openalex-snapshot
A segmentation clock patterns cellular differentiation in a bacterial biofilm
inferred← citeshttps://doi.org/10.1016/j.celrep.2018.06.023openalex-snapshot
Spatial Fold Change of FGF Signaling Encodes Positional Information for Segmental Determination in Zebrafish
inferred← citeshttps://doi.org/10.1016/j.cels.2021.03.003openalex-snapshot
A tale of two rhythms: Locked clocks and chaos in biology
inferred← citeshttps://doi.org/10.1016/j.cels.2026.101708openalex-snapshot
Single-cell transcriptional dynamics in a living vertebrate
inferred← citeshttps://doi.org/10.1016/j.coisb.2017.09.007openalex-snapshot
Mechanochemical coupling and developmental pattern formation
inferred← citeshttps://doi.org/10.1016/j.coisb.2024.100520openalex-snapshot
From signalling oscillations to somite formation
inferred← citeshttps://doi.org/10.1016/j.gde.2020.04.008openalex-snapshot
Waiting on the Fringe: cell autonomy and signaling delays in segmentation clocks
inferred← citeshttps://doi.org/10.1016/j.isci.2024.110840openalex-snapshot
Approximated gene expression trajectories for gene regulatory network inference on cell tracks
inferred← citeshttps://doi.org/10.1016/j.isci.2024.111386openalex-snapshot
Intrinsically robust and scalable biofilm segmentation under diverse physical growth conditions
inferred← citeshttps://doi.org/10.1016/j.isci.2025.112942openalex-snapshot
Neuronal synchronization in Drosophila
inferred← citeshttps://doi.org/10.1016/j.jtbi.2019.05.006openalex-snapshot
Cell cycle regulation of oscillations yields coupling of growth and form in a computational model of the presomitic mesoderm
inferred← citeshttps://doi.org/10.1016/j.pbiomolbio.2018.04.004openalex-snapshot
Travelling waves in somitogenesis: Collective cellular properties emerge from time-delayed juxtacrine oscillation coupling
inferred← citeshttps://doi.org/10.1016/j.physrep.2024.05.002openalex-snapshot
Waves, patterns, bifurcations: A tutorial review on the vertebrate segmentation clock
inferred← citeshttps://doi.org/10.1016/j.semcdb.2015.05.005openalex-snapshot
Time, space and the vertebrate body axis
inferred← citeshttps://doi.org/10.1016/j.semcdb.2015.06.001openalex-snapshot
A time space translation hypothesis for vertebrate axial patterning
inferred← citeshttps://doi.org/10.1016/j.semcdb.2015.06.002openalex-snapshot
Multiple roles of timing in somite formation
inferred← citeshttps://doi.org/10.1016/j.semcdb.2015.08.001openalex-snapshot
Mechanics of tissue compaction
inferred← citeshttps://doi.org/10.1016/j.semcdb.2018.09.008openalex-snapshot
Information flow in the presence of cell mixing and signaling delays during embryonic development
inferred← citeshttps://doi.org/10.1016/j.semcdb.2020.04.014openalex-snapshot
Patterning and mechanics of somite boundaries in zebrafish embryos
inferred← citeshttps://doi.org/10.1016/j.semcdb.2022.12.009openalex-snapshot
Orchestration of tissue shape changes and gene expression patterns in development
inferred← citeshttps://doi.org/10.1016/j.semcdb.2025.103630openalex-snapshot
Evolvability in vertebrate segmentation
inferred← citeshttps://doi.org/10.1016/j.shpsc.2018.10.006openalex-snapshot
From seconds to eons: Time scales, hierarchies, and processes in evo-devo
inferred← citeshttps://doi.org/10.1016/j.ydbio.2019.03.008openalex-snapshot
Segmentation clock dynamics is strongly synchronized in the forming somite
inferred← citeshttps://doi.org/10.1016/j.ydbio.2019.06.024openalex-snapshot
What are you synching about? Emerging complexity of Notch signaling in the segmentation clock
inferred← citeshttps://doi.org/10.1021/acs.biochem.8b00001openalex-snapshot
Reentrant Phase Transitions and Non-Equilibrium Dynamics in Membraneless Organelles
inferred← citeshttps://doi.org/10.1021/acssynbio.0c00407openalex-snapshot
Genetically Encoded Fluorescent Biosensor for Rapid Detection of Protein Expression
inferred← citeshttps://doi.org/10.1038/ncomms11861openalex-snapshot
Faster embryonic segmentation through elevated Delta-Notch signalling
inferred← citeshttps://doi.org/10.1038/ncomms7635openalex-snapshot
Changing cell behaviours during beetle embryogenesis correlates with slowing of segmentation
inferred← citeshttps://doi.org/10.1038/ncomms7690openalex-snapshot
Shared rules of development predict patterns of evolution in vertebrate segmentation
inferred← citeshttps://doi.org/10.1038/nrm3891openalex-snapshot
Signalling dynamics in vertebrate segmentation
inferred← citeshttps://doi.org/10.1038/s41467-017-00597-2openalex-snapshot
The brain is required for normal muscle and nerve patterning during early Xenopus development
inferred← citeshttps://doi.org/10.1038/s41467-022-35632-4openalex-snapshot
Deconstructing body axis morphogenesis in zebrafish embryos using robot-assisted tissue micromanipulation
inferred← citeshttps://doi.org/10.1038/s41467-023-37745-wopenalex-snapshot
Ripply suppresses Tbx6 to induce dynamic-to-static conversion in somite segmentation
inferred← citeshttps://doi.org/10.1038/s41567-019-0598-1openalex-snapshot
Low-dimensional dynamics of two coupled biological oscillators
inferred← citeshttps://doi.org/10.1038/s41576-021-00355-7openalex-snapshot
Towards a physical understanding of developmental patterning
inferred← citeshttps://doi.org/10.1038/s41580-024-00709-zopenalex-snapshot
Cellular and molecular control of vertebrate somitogenesis
inferred← citeshttps://doi.org/10.1038/s41586-020-03055-0openalex-snapshot
Pairing of segmentation clock genes drives robust pattern formation
inferred← citeshttps://doi.org/10.1038/s41586-022-05527-xopenalex-snapshot
Periodic inhibition of Erk activity drives sequential somite segmentation
inferred← citeshttps://doi.org/10.1038/s42003-022-03053-0openalex-snapshot
Fgf8 dynamics and critical slowing down may account for the temperature independence of somitogenesis
inferred← citeshttps://doi.org/10.1038/s44318-024-00186-2openalex-snapshot
Modular control of vertebrate axis segmentation in time and space
inferred← citeshttps://doi.org/10.1038/s44319-025-00662-8openalex-snapshot
Keeping up with the neighbours: local synchronisation of cell fate decisions during development
inferred← citeshttps://doi.org/10.1073/pnas.1900819116openalex-snapshot
Shaping the zebrafish myotome by intertissue friction and active stress
inferred← citeshttps://doi.org/10.1083/jcb.201701158openalex-snapshot
Chemical waves in cell and developmental biology
inferred← citeshttps://doi.org/10.1088/1367-2630/17/9/093042openalex-snapshot
Continuum theory of gene expression waves during vertebrate segmentation
inferred← citeshttps://doi.org/10.1088/1367-2630/abd80bopenalex-snapshot
Theory of time delayed genetic oscillations with external noisy regulation
inferred← citeshttps://doi.org/10.1088/1478-3975/13/2/026007openalex-snapshot
Requirements for efficient cell-type proportioning: regulatory timescales, stochasticity and lateral inhibition
inferred← citeshttps://doi.org/10.1088/1478-3975/13/5/05lt03openalex-snapshot
Sequential pattern formation governed by signaling gradients
inferred← citeshttps://doi.org/10.1098/rsfs.2020.0049openalex-snapshot
Time and space in segmentation
inferred← citeshttps://doi.org/10.1098/rsif.2018.0304openalex-snapshot
Temporal development of Drosophila embryos is highly robust across a wide temperature range
inferred← citeshttps://doi.org/10.1098/rsif.2019.0451openalex-snapshot
Constraints on somite formation in developing embryos
inferred← citeshttps://doi.org/10.1101/051722openalex-snapshot
Interactions between Nodal and Wnt signalling Drive Robust Symmetry-Breaking and Axial Organisation in Gastruloids (Embryonic Organoids)
inferred← citeshttps://doi.org/10.1101/2020.04.29.067744openalex-snapshot
Optimal time frequency analysis for biological data - pyBOAT
inferred← citeshttps://doi.org/10.1101/2020.06.22.166215openalex-snapshot
From local resynchronization to global pattern recovery in the zebrafish segmentation clock
inferred← citeshttps://doi.org/10.1101/2020.08.07.241042openalex-snapshot
Theory of genetic oscillations with external noisy regulation
inferred← citeshttps://doi.org/10.1101/2023.06.01.543221openalex-snapshot
But, what are the cells doing? Image Analysis pipeline to follow single cells in the zebrafish embryo
inferred← citeshttps://doi.org/10.1101/2023.11.09.566373openalex-snapshot
Clock driven waves of Tbx6 expression prefigure somite boundaries
inferred← citeshttps://doi.org/10.1101/2024.08.06.606905openalex-snapshot
Multiple Notch ligands in the synchronization of the segmentation clock
inferred← citeshttps://doi.org/10.1101/2024.09.19.613913openalex-snapshot
Neuronal synchronization in Drosophila
inferred← citeshttps://doi.org/10.1101/2024.11.03.621757openalex-snapshot
Self-organization of spermatogenic wave coordinates sustained sperm production in the mouse testis
inferred← citeshttps://doi.org/10.1101/2025.01.10.632257openalex-snapshot
Coupling of cell proliferation to the segmentation clock ensures robust somite scaling
inferred← citeshttps://doi.org/10.1101/286328openalex-snapshot
Positional information encoded in the dynamic differences between neighbouring oscillators during vertebrate segmentation
inferred← citeshttps://doi.org/10.1101/419705openalex-snapshot
Quantitative study of the somitogenetic wavefront in zebrafish
inferred← citeshttps://doi.org/10.1101/505123openalex-snapshot
Shaping the zebrafish myotome by differential friction and active stress
inferred← citeshttps://doi.org/10.1101/743724openalex-snapshot
Reconstruction of the phase dynamics of the somitogenesis clock oscillator
inferred← citeshttps://doi.org/10.1101/789446openalex-snapshot
The effect of Rosovitine on mPSM explants: a real time analysis
inferred← citeshttps://doi.org/10.1103/7g6x-b238openalex-snapshot
Multiple Notch ligands in the synchronization of the segmentation clock
inferred← citeshttps://doi.org/10.1103/7ph2-kj8gopenalex-snapshot
Foci, waves, excitability: Self-organization of phase waves in a model of asymmetrically coupled embryonic oscillators
inferred← citeshttps://doi.org/10.1103/physreve.111.024407openalex-snapshot
Statistical description of mobile oscillators in embryonic pattern formation
inferred← citeshttps://doi.org/10.1103/physreve.98.062412openalex-snapshot
Entrainment as a means of controlling phase waves in populations of coupled oscillators
inferred← citeshttps://doi.org/10.1111/dgd.12242openalex-snapshot
Timing by rhythms: Daily clocks and developmental rulers
inferred← citeshttps://doi.org/10.1111/dgd.12366openalex-snapshot
Determining the impact of cell mixing on signaling during development
inferred← citeshttps://doi.org/10.1111/dgd.12655openalex-snapshot
Somite boundary determination in normal and clock‐less vertebrate embryos
inferred← citeshttps://doi.org/10.1111/dgd.12710openalex-snapshot
In vitro systems: A new window to the segmentation clock
inferred← citeshttps://doi.org/10.1146/annurev-biophys-111521-102500openalex-snapshot
Waves in Embryonic Development
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-120319-024414openalex-snapshot
The Unreasonable Effectiveness of Reaction Diffusion in Vertebrate Skin Color Patterning
inferred← citeshttps://doi.org/10.1146/annurev-conmatphys-031016-025210openalex-snapshot
Intracellular Oscillations and Waves
inferred← citeshttps://doi.org/10.1186/s13227-018-0113-2openalex-snapshot
Around the clock: gradient shape and noise impact the evolution of oscillatory segmentation dynamics
inferred← citeshttps://doi.org/10.1242/bio.025148openalex-snapshot
A framework for quantification and physical modeling of cell mixing applied to oscillator synchronization in vertebrate somitogenesis
inferred← citeshttps://doi.org/10.1242/dev.115535openalex-snapshot
Spatiotemporal oscillations of Notch1, Dll1 and NICD are coordinated across the mouse PSM
inferred← citeshttps://doi.org/10.1242/dev.119057openalex-snapshot
Dynamics of the slowing segmentation clock reveal alternating two-segment periodicity
inferred← citeshttps://doi.org/10.1242/dev.150391openalex-snapshot
Anteroposterior polarity and elongation in the absence of extraembryonic tissues and spatially localised signalling in Gastruloids , mammalian embryonic organoids
inferred← citeshttps://doi.org/10.1242/dev.161257openalex-snapshot
Size-reduced embryos reveal a gradient scaling based mechanism for zebrafish somite formation
inferred← citeshttps://doi.org/10.1242/dev.170977openalex-snapshot
Communication codes in developmental signaling pathways
inferred← citeshttps://doi.org/10.1242/dev.200083openalex-snapshot
Imaging the onset of oscillatory signaling dynamics during mouse embryo gastrulation
inferred← citeshttps://doi.org/10.12688/f1000research.12369.1openalex-snapshot
Recent advances in understanding vertebrate segmentation
inferred← citeshttps://doi.org/10.1371/journal.pbio.3000407openalex-snapshot
Coordinated circadian timing through the integration of local inputs in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1003957openalex-snapshot
Live Imaging-Based Model Selection Reveals Periodic Regulation of the Stochastic G1/S Phase Transition in Vertebrate Axial Development
inferred← citeshttps://doi.org/10.1371/journal.pone.0126740openalex-snapshot
R2OBBIE-3D, a Fast Robotic High-Resolution System for Quantitative Phenotyping of Surface Geometry and Colour-Texture
inferred← citeshttps://doi.org/10.15252/msb.20209498openalex-snapshot
Developmental function and state transitions of a gene expression oscillator in Caenorhabditis elegans
inferred← citeshttps://doi.org/10.21769/bioprotoc.3193openalex-snapshot
Detection of mRNA by Whole Mount in situ Hybridization and DNA Extraction for Genotyping of Zebrafish Embryos
inferred← citeshttps://doi.org/10.3389/fcell.2022.944016openalex-snapshot
The vertebrate Embryo Clock: Common players dancing to a different beat
inferred← citeshttps://doi.org/10.3389/fcell.2023.1087650openalex-snapshot
Closing the loop on morphogenesis: a mathematical model of morphogenesis by closed-loop reaction-diffusion
inferred← citeshttps://doi.org/10.3389/fcell.2023.1327227openalex-snapshot
Species-specific roles of the Notch ligands, receptors, and targets orchestrating the signaling landscape of the segmentation clock
inferred← citeshttps://doi.org/10.3389/fphy.2022.933915openalex-snapshot
Reaction wavefront theory of notochord segment patterning
inferred← citeshttps://doi.org/10.3390/e24060819openalex-snapshot
Competency in Navigating Arbitrary Spaces as an Invariant for Analyzing Cognition in Diverse Embodiments
inferred← citeshttps://doi.org/10.3410/f.725780196.793512076openalex-snapshot
Faculty Opinions recommendation of A balance of positive and negative regulators determines the pace of the segmentation clock.
inferred← citeshttps://doi.org/10.3791/50307openalex-snapshot
Generation of Dispersed Presomitic Mesoderm Cell Cultures for Imaging of the Zebrafish Segmentation Clock in Single Cells
inferred← citeshttps://doi.org/10.3791/50307-vopenalex-snapshot
Generation of Dispersed Presomitic Mesoderm Cell Cultures for Imaging of the Zebrafish Segmentation Clock in Single Cells
inferred← citeshttps://doi.org/10.3791/56224openalex-snapshot
AFM and Microrheology in the Zebrafish Embryo Yolk Cell
inferred← citeshttps://doi.org/10.7554/elife.05842openalex-snapshot
A balance of positive and negative regulators determines the pace of the segmentation clock
inferred← citeshttps://doi.org/10.7554/elife.08438openalex-snapshot
Persistence, period and precision of autonomous cellular oscillators from the zebrafish segmentation clock
inferred← citeshttps://doi.org/10.7554/elife.106316openalex-snapshot
Modularity of the segmentation clock and morphogenesis
inferred← citeshttps://doi.org/10.7554/elife.106316.1openalex-snapshot
Modularity of the segmentation clock and morphogenesis
inferred← citeshttps://doi.org/10.7554/elife.106316.2openalex-snapshot
Modularity of the segmentation clock and morphogenesis
inferred← citeshttps://doi.org/10.7554/elife.33843openalex-snapshot
Segmentation of the zebrafish axial skeleton relies on notochord sheath cells and not on the segmentation clock
inferred← citeshttps://doi.org/10.7554/elife.55778openalex-snapshot
Geometric models for robust encoding of dynamical information into embryonic patterns
inferred← citeshttps://doi.org/10.7554/elife.61358openalex-snapshot
From local resynchronization to global pattern recovery in the zebrafish segmentation clock
inferred← citeshttps://doi.org/10.7554/elife.79575openalex-snapshot
Arnold tongue entrainment reveals dynamical principles of the embryonic segmentation clock
inferred← citeshttps://doi.org/10.7554/elife.83299openalex-snapshot
Glycolytic flux-signaling controls mouse embryo mesoderm development
inferred← citeshttps://doi.org/10.7554/elife.84969openalex-snapshot
How enhancers regulate wavelike gene expression patterns
inferred← citeshttps://doi.org/10.7554/elife.93764openalex-snapshot
Cell-autonomous timing drives the vertebrate segmentation clock’s wave pattern
inferred← citeshttps://doi.org/10.7554/elife.93764.1openalex-snapshot
Cell-autonomous timing drives the vertebrate segmentation clock’s wave pattern
inferred← citeshttps://doi.org/10.7554/elife.93764.2openalex-snapshot
Cell-autonomous timing drives the vertebrate segmentation clock’s wave pattern
inferred← citeshttps://doi.org/10.7554/elife.93764.3openalex-snapshot
Cell-autonomous timing drives the vertebrate segmentation clock’s wave pattern
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