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Positional information encoded in the dynamic differences between neighbouring oscillators during vertebrate segmentation
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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/10.1002/jez.b.21305openalex-snapshot
Developmental control of segment numbers in vertebrates
inferredcites →https://doi.org/10.1016/j.cell.2016.01.028openalex-snapshot
Self-Organization of Embryonic Genetic Oscillators into Spatiotemporal Wave Patterns
inferredcites →https://doi.org/10.1016/j.cell.2018.01.026openalex-snapshot
Modulation of Phase Shift between Wnt and Notch Signaling Oscillations Controls Mesoderm Segmentation
inferredcites →https://doi.org/10.1016/j.celrep.2016.11.069openalex-snapshot
Cdx and T Brachyury Co-activate Growth Signaling in the Embryonic Axial Progenitor Niche
inferredcites →https://doi.org/10.1016/j.celrep.2018.06.023openalex-snapshot
Spatial Fold Change of FGF Signaling Encodes Positional Information for Segmental Determination in Zebrafish
inferredcites →https://doi.org/10.1016/j.devcel.2007.07.013openalex-snapshot
The Initiation and Propagation of Hes7 Oscillation Are Cooperatively Regulated by Fgf and Notch Signaling in the Somite Segmentation Clock
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.pbiomolbio.2018.04.004openalex-snapshot
Travelling waves in somitogenesis: Collective cellular properties emerge from time-delayed juxtacrine oscillation coupling
inferredcites →https://doi.org/10.1016/j.ydbio.2009.02.035openalex-snapshot
Interfering with Wnt signalling alters the periodicity of the segmentation clock
inferredcites →https://doi.org/10.1016/s0022-5193(69)80016-0openalex-snapshot
Positional information and the spatial pattern of cellular differentiation
inferredcites →https://doi.org/10.1016/s0022-5193(69)80017-2openalex-snapshot
A phase-shift model for the spatial and temporal organization of developing systems
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/s0092-8674(01)00437-8openalex-snapshot
FGF Signaling Controls Somite Boundary Position and Regulates Segmentation Clock Control of Spatiotemporal Hox Gene Activation
inferredcites →https://doi.org/10.1016/s0925-4773(99)00039-8openalex-snapshot
Heat shock produces periodic somitic disturbances in the zebrafish embryo
inferredcites →https://doi.org/10.1016/s0960-9822(03)00534-7openalex-snapshot
Autoinhibition with Transcriptional Delay
inferredcites →https://doi.org/10.1016/s0960-9822(07)00424-1openalex-snapshot
Waves of mouse Lunatic fringe expression, in four-hour cycles at two-hour intervals, precede somite boundary formation
inferredcites →https://doi.org/10.1016/s0960-9822(98)70401-4openalex-snapshot
The lunatic Fringe gene is a target of the molecular clock linked to somite segmentation in avian embryos
inferredcites →https://doi.org/10.1016/s1534-5807(03)00055-8openalex-snapshot
Wnt3a Plays a Major Role in the Segmentation Clock Controlling Somitogenesis
inferredcites →https://doi.org/10.1038/254196a0openalex-snapshot
Control of somite number during morphogenesis of a vertebrate, Xenopus laevis
inferredcites →https://doi.org/10.1038/35044091openalex-snapshot
Notch signalling and the synchronization of the somite segmentation clock
inferredcites →https://doi.org/10.1038/78062openalex-snapshot
Mesp2 initiates somite segmentation through the Notch signalling pathway
inferredcites →https://doi.org/10.1038/nature02216openalex-snapshot
fgf8 mRNA decay establishes a gradient that couples axial elongation to patterning in the vertebrate embryo
inferredcites →https://doi.org/10.1038/nature03591openalex-snapshot
The Mesp2 transcription factor establishes segmental borders by suppressing Notch activity
inferredcites →https://doi.org/10.1038/nature07020openalex-snapshot
Control of segment number in vertebrate embryos
inferredcites →https://doi.org/10.1038/nature11804openalex-snapshot
Scaling of embryonic patterning based on phase-gradient encoding
inferredcites →https://doi.org/10.1073/pnas.0508238103openalex-snapshot
Tbx6-mediated Notch signaling controls somite-specific Mesp2 expression
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/10.1073/pnas.1007417108openalex-snapshot
FGF4 and FGF8 comprise the wavefront activity that controls somitogenesis
inferredcites →https://doi.org/10.1088/1367-2630/17/9/093042openalex-snapshot
Continuum theory of gene expression waves during vertebrate segmentation
inferredcites →https://doi.org/10.1088/1478-3975/13/3/036009openalex-snapshot
Positional information from oscillatory phase shifts : insights fromin silicoevolution
inferredcites →https://doi.org/10.1088/1478-3975/13/5/05lt03openalex-snapshot
Sequential pattern formation governed by signaling gradients
inferredcites →https://doi.org/10.1101/gad.1291205openalex-snapshot
Zebrafish Hairy/Enhancer of split protein links FGF signaling to cyclic gene expression in the periodic segmentation of somites
inferredcites →https://doi.org/10.1101/gad.270785.115openalex-snapshot
Oscillatory control of Delta-like1 in cell interactions regulates dynamic gene expression and tissue morphogenesis
inferredcites →https://doi.org/10.1101/gad.930601openalex-snapshot
Dynamic expression and essential functions of Hes7 in somite segmentation
inferredcites →https://doi.org/10.1119/1.1349543openalex-snapshot
Pendulum waves: A lesson in aliasing
inferredcites →https://doi.org/10.1119/1.16608openalex-snapshot
Pendulum waves: A demonstration of wave motion using pendula
inferredcites →https://doi.org/10.1126/science.1074560openalex-snapshot
Oscillatory Expression of the bHLH Factor Hes1 Regulated by a Negative Feedback Loop
inferredcites →https://doi.org/10.1126/science.1133141openalex-snapshot
A Complex Oscillating Network of Signaling Genes Underlies the Mouse Segmentation Clock
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.1253089openalex-snapshot
A Doppler effect in embryonic pattern formation
inferredcites →https://doi.org/10.1242/dev.000786openalex-snapshot
The Hes gene family: repressors and oscillators that orchestrate embryogenesis
inferredcites →https://doi.org/10.1242/dev.063610openalex-snapshot
Notch signaling: simplicity in design, versatility in function
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.063834openalex-snapshot
Evolutionary plasticity of segmentation clock networks
inferredcites →https://doi.org/10.1242/dev.093435openalex-snapshot
Wnt-regulated dynamics of positional information in zebrafish somitogenesis
inferredcites →https://doi.org/10.1242/dev.098905openalex-snapshot
An anterior limit of FGF/Erk signal activity marks the earliest future somite boundary in zebrafish
inferredcites →https://doi.org/10.1242/dev.104.2.331openalex-snapshot
Heat shock causes repeated segmental anomalies in the chick embryo
inferredcites →https://doi.org/10.1242/dev.119057openalex-snapshot
Dynamics of the slowing segmentation clock reveal alternating two-segment periodicity
inferredcites →https://doi.org/10.1242/dev.126.13.3005openalex-snapshot
her1, a zebrafish pair-rule like gene, acts downstream of notch signalling to control somite development
inferredcites →https://doi.org/10.1242/dev.128.23.4873openalex-snapshot
Fgf/MAPK signalling is a crucial positional cue in somite boundary formation
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/10.1242/dev.65.supplement.103openalex-snapshot
The control of somitogenesis in mouse embryos
inferredcites →https://doi.org/10.12688/f1000research.12369.1openalex-snapshot
Recent advances in understanding vertebrate segmentation
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/10.7554/elife.05842openalex-snapshot
A balance of positive and negative regulators determines the pace of the segmentation clock
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.ydbio.2018.10.024openalex-snapshot
Of mice and plants: Comparative developmental systems biology
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
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