On the public citation graph
Oscillatory Expression of the bHLH Factor Hes1 Regulated by a Negative Feedback Loop
0 signed · 761 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/dbio.1998.9164openalex-snapshot
Dynamic Expression oflunatic fringeSuggests a Link betweennotchSignaling and an Autonomous Cellular Oscillator Driving Somite Segmentation
inferredcites →https://doi.org/10.1006/dbio.2000.9884openalex-snapshot
Oscillating Expression of c-Hey2 in the Presomitic Mesoderm Suggests That the Segmentation Clock May Use Combinatorial Signaling through Multiple Interacting bHLH Factors
inferredcites →https://doi.org/10.1016/s0021-9258(17)37668-8openalex-snapshot
Structure, chromosomal locus, and promoter analysis of the gene encoding the mouse helix-loop-helix factor HES-1. Negative autoregulation through the multiple N box elements.
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(00)81199-xopenalex-snapshot
A Serum Shock Induces Circadian Gene Expression in Mammalian Tissue Culture Cells
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(01)00054-5openalex-snapshot
Molecular Targets of Vertebrate Segmentation
inferredcites →https://doi.org/10.1016/s1534-5807(02)00211-3openalex-snapshot
Periodic Lunatic fringe Expression Is Controlled during Segmentation by a Cyclic Transcriptional Enhancer Responsive to Notch Signaling
inferredcites →https://doi.org/10.1016/s1534-5807(02)00212-5openalex-snapshot
Clock Regulatory Elements Control Cyclic Expression of Lunatic fringe during Somitogenesis
inferredcites →https://doi.org/10.1038/35002125openalex-snapshot
A synthetic oscillatory network of transcriptional regulators
inferredcites →https://doi.org/10.1038/35044091openalex-snapshot
Notch signalling and the synchronization of the somite segmentation clock
inferredcites →https://doi.org/10.1038/35098552openalex-snapshot
The making of the somite: molecular events in vertebrate segmentation
inferredcites →https://doi.org/10.1038/377355a0openalex-snapshot
Signalling downstream of activated mammalian Notch
inferredcites →https://doi.org/10.1093/emboj/18.8.2196openalex-snapshot
Hes1 and Hes5 as Notch effectors in mammalian neuronal differentiation
inferredcites →https://doi.org/10.1101/gad.11.23.3168openalex-snapshot
Mediation of NGF signaling by post-translational inhibition of HES-1, a basic helix–loop–helix repressor of neuronal differentiation
inferredcites →https://doi.org/10.1101/gad.14.13.1678openalex-snapshot
Control of her1 expression during zebrafish somitogenesis by a Delta -dependent oscillator and an independent wave-front activity
inferredcites →https://doi.org/10.1101/gad.6.12b.2620openalex-snapshot
Two mammalian helix-loop-helix factors structurally related to Drosophila hairy and Enhancer of split.
inferredcites →https://doi.org/10.1101/gad.930601openalex-snapshot
Dynamic expression and essential functions of Hes7 in somite segmentation
inferredcites →https://doi.org/10.1146/annurev.biochem.67.1.425openalex-snapshot
THE UBIQUITIN SYSTEM
inferredcites →https://doi.org/10.1146/annurev.cellbio.17.1.311openalex-snapshot
Vertebrate Somitogenesis
inferredcites →https://doi.org/10.1146/annurev.ne.14.030191.002225openalex-snapshot
Stimulus-Transcription Coupling In The Nervous System: Involvement Of The Inducible Proto-oncogenes fos And jun
inferredcites →https://doi.org/10.1146/annurev.physiol.63.1.647openalex-snapshot
Molecular Analysis of Mammalian Circadian Rhythms
inferredcites →https://doi.org/10.1242/dev.127.7.1421openalex-snapshot
Notch signalling is required for cyclic expression of the hairy-like geneHES1in the presomitic mesoderm
inferredcites →https://doi.org/10.1242/dev.127.8.1691openalex-snapshot
Zebrafish Mesp family genes, mesp-a and mesp-b are segmentally expressed in the presomitic mesoderm, and Mesp-b confers the anterior identity to the developing somites
inferredcites →https://doi.org/10.1242/dev.129.5.1175openalex-snapshot
her1 and the notch pathway function within the oscillator mechanism that regulates zebrafish somitogenesis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.5281/zenodo.1057336openalex-extracted
Stability And Bifurcation Analysis In A Model Of Hes1 Selfregulation With Time Delay
inferred← citeshttps://doi.org/10.1002/1878-0261.13626openalex-snapshot
RIP140 regulates transcription factor HES1 oscillatory expression and mitogenic activity in colon cancer cells
inferred← citeshttps://doi.org/10.1002/9780470121917.ch8openalex-snapshot
Biological Rhythms as Temporal Dissipative Structures
inferred← citeshttps://doi.org/10.1002/9781118016435.ch3openalex-snapshot
Methods inIn SilicoBiology: Modeling Feedback Dynamics in Pathways
inferred← citeshttps://doi.org/10.1002/9781119860914.ch30openalex-snapshot
Signal Transduction during Cortical Neurogenesis
inferred← citeshttps://doi.org/10.1002/9781119860914.ch6openalex-snapshot
Dynamic Transcriptional Control of Neural Stem Cells
inferred← citeshttps://doi.org/10.1002/9783527631209.ch75openalex-snapshot
Synthetic Biology: Dynamic Modeling and Construction of Cell Systems
inferred← citeshttps://doi.org/10.1002/9783527631339.ch15openalex-snapshot
Synthetic Biology: Dynamic Modeling and Construction of Cell Systems
inferred← citeshttps://doi.org/10.1002/9783527696130.ch10openalex-snapshot
Modeling the Dynamics of the Immune Response
inferred← citeshttps://doi.org/10.1002/bdrc.20090openalex-snapshot
The vertebrate segmentation clock and its role in skeletal birth defects
inferred← citeshttps://doi.org/10.1002/bdrc.20091openalex-snapshot
Genetic analysis of molecular oscillators in mammalian somitogenesis: Clues for studies of human vertebral disorders
inferred← citeshttps://doi.org/10.1002/bdrc.20093openalex-snapshot
Disruption of the somitic molecular clock causes abnormal vertebral segmentation
inferred← citeshttps://doi.org/10.1002/bdrc.20094openalex-snapshot
Molecular clocks underlying vertebrate embryo segmentation: A 10‐year‐old hairy‐go‐round
inferred← citeshttps://doi.org/10.1002/bdrc.21008openalex-snapshot
Experiments, measurements, and mathematical modeling to decipher time signals in development
inferred← citeshttps://doi.org/10.1002/bies.10253openalex-snapshot
A Hes1‐based oscillator in cultured cells and its potential implications for the segmentation clock
inferred← citeshttps://doi.org/10.1002/bies.10383openalex-snapshot
The next step in systems biology: simulating the temporospatial dynamics of molecular network
inferred← citeshttps://doi.org/10.1002/bies.200800212openalex-snapshot
The interplay between transcription factors and microRNAs in genome‐scale regulatory networks
inferred← citeshttps://doi.org/10.1002/cne.25648openalex-snapshot
Emergence of the ZNF675 Gene During Primate Evolution–Influenced Human Neurodevelopment Through Changing HES1 Autoregulation
inferred← citeshttps://doi.org/10.1002/dneu.20826openalex-snapshot
The dorsal neural tube: A dynamic setting for cell fate decisions
inferred← citeshttps://doi.org/10.1002/dneu.22243openalex-snapshot
Differential regulation of Hes/Hey genes during inner ear development
inferred← citeshttps://doi.org/10.1002/dvdy.10460openalex-snapshot
Gene regulatory factors in pancreatic development
inferred← citeshttps://doi.org/10.1002/dvdy.20249openalex-snapshot
The somite segmentation clock: It takes a licking and keeps on ticking
inferred← citeshttps://doi.org/10.1002/dvdy.21114openalex-snapshot
Oscillator mechanism of notch pathway in the segmentation clock
inferred← citeshttps://doi.org/10.1002/dvdy.21139openalex-snapshot
Coupling cellular oscillators: A mechanism that maintains synchrony against developmental noise in the segmentation clock
inferred← citeshttps://doi.org/10.1002/dvdy.22680openalex-snapshot
Aberrant expression of genes necessary for neuronal development and notch signaling in an epileptic mind bomb zebrafish
inferred← citeshttps://doi.org/10.1002/dvdy.70151openalex-snapshot
An accessible microfluidic perfusion platform for time‐restricted control of zebrafish embryonic patterning
inferred← citeshttps://doi.org/10.1002/dvg.22771openalex-snapshot
The role of targeted protein degradation in early neural development
inferred← citeshttps://doi.org/10.1002/dvg.23051openalex-snapshot
Basic helix‐loop‐helix transcription factors in evolution: Roles in development of mesoderm and neural tissues
inferred← citeshttps://doi.org/10.1002/eji.201545821openalex-snapshot
Transcriptional regulation of early T‐cell development in the thymus
inferred← citeshttps://doi.org/10.1002/gene.20171openalex-snapshot
Negative feedback loop formed by Lunatic fringe and Hes7 controls their oscillatory expression during somitogenesis
inferred← citeshttps://doi.org/10.1002/glia.20553openalex-snapshot
Notch signaling modulates the activation of microglial cells
inferred← citeshttps://doi.org/10.1002/glia.70234openalex-snapshot
Molecular Control of Neural Stem Cell Quiescence in the Adult Zebrafish Telencephalon: Established Mechanisms and an Integrative Hypothesis
inferred← citeshttps://doi.org/10.1002/jcb.22065openalex-snapshot
The autonomous notch signal pathway is activated by baicalin and baicalein but is suppressed by niclosamide in K562 cells
inferred← citeshttps://doi.org/10.1002/jcb.26306openalex-snapshot
Induction of transient cell cycle arrest by H2O2 via modulation of ultradian oscillations of Hes1, Socs3, and p‐Stat3 in fibroblast cells
inferred← citeshttps://doi.org/10.1002/mc.20865openalex-snapshot
Notch2‐induced COX‐2 expression enhancing gastric cancer progression
inferred← citeshttps://doi.org/10.1002/mma.8961openalex-snapshot
Hopf bifurcation in time‐delayed gene expression model with dimers
inferred← citeshttps://doi.org/10.1002/stem.1231openalex-snapshot
Hes4 Controls Proliferative Properties of Neural Stem Cells During Retinal Ontogenesis
inferred← citeshttps://doi.org/10.1002/wdev.34openalex-snapshot
Scoliosis and segmentation defects of the vertebrae
inferred← citeshttps://doi.org/10.1002/wdev.46openalex-snapshot
Oscillatory gene expression and somitogenesis
inferred← citeshttps://doi.org/10.1002/wsbm.108openalex-snapshot
Live cell imaging and systems biology
inferred← citeshttps://doi.org/10.1007/1-4020-2340-5_11openalex-snapshot
Oscillating Gene Expressions in Regulatory Networks
inferred← citeshttps://doi.org/10.1007/82_2012_230openalex-snapshot
Notch Signaling During Human T cell Development
inferred← citeshttps://doi.org/10.1007/978-0-387-09606-3_4openalex-snapshot
Old Wares and New: Five Decades of Investigation of Somitogenesis in Xenopus laevis
inferred← citeshttps://doi.org/10.1007/978-0-387-09606-3_7openalex-snapshot
bHLH Proteins and Their Role in Somitogenesis
inferred← citeshttps://doi.org/10.1007/978-0-387-09794-7_6openalex-snapshot
Oscillatory Expression of Hes Family Transcription Factors: Insights from Mathematical Modelling
inferred← citeshttps://doi.org/10.1007/978-0-8176-4751-3_5openalex-snapshot
Signaling and Feedback in Biological Networks
inferred← citeshttps://doi.org/10.1007/978-1-0716-3036-5_19openalex-snapshot
Visualizing MyoD Oscillations in Muscle Stem Cells
inferred← citeshttps://doi.org/10.1007/978-1-4020-8352-5openalex-snapshot
Ultradian Rhythms from Molecules to Mind
inferred← citeshttps://doi.org/10.1007/978-1-4020-8352-5_12openalex-snapshot
The Mammalian Circadian Timekeeping System
inferred← citeshttps://doi.org/10.1007/978-1-4020-8761-5_5openalex-snapshot
Dynamical Genetic Regulation
inferred← citeshttps://doi.org/10.1007/978-1-4419-1406-4openalex-snapshot
The Genetics and Development of Scoliosis
inferred← citeshttps://doi.org/10.1007/978-1-4419-1406-4_1openalex-snapshot
Genetic Regulation of Somite and Early Spinal Patterning
inferred← citeshttps://doi.org/10.1007/978-1-4419-5797-9_2openalex-snapshot
Current Progress in Static and Dynamic Modeling of Biological Networks
inferred← citeshttps://doi.org/10.1007/978-1-4939-1139-4_13openalex-snapshot
Visualization of Notch Signaling Oscillation in Cells and Tissues
inferred← citeshttps://doi.org/10.1007/978-1-4939-7290-6_34openalex-snapshot
On the Potential for Multiscale Oscillatory Behavior in HIV
inferred← citeshttps://doi.org/10.1007/978-1-59745-531-2_15openalex-snapshot
Mechanisms Generating Ultrasensitivity, Bistability, and Oscillations in Signal Transduction
inferred← citeshttps://doi.org/10.1007/978-3-030-32857-3_7openalex-snapshot
Multiscale Modelling of Cancer: Micro-, Meso- and Macro-scales of Growth and Spread
inferred← citeshttps://doi.org/10.1007/978-3-030-34436-8_2openalex-snapshot
Notch Signaling and Embryonic Development: An Ancient Friend, Revisited
inferred← citeshttps://doi.org/10.1007/978-3-319-89512-3_13openalex-snapshot
Oscillatory Control of Notch Signaling in Development
inferred← citeshttps://doi.org/10.1007/978-3-540-72584-8_103openalex-snapshot
Stochastic Modelling and Simulation of Coupled Autoregulated Oscillators in a Multicellular Environment: The her1/her7 Genes
inferred← citeshttps://doi.org/10.1007/978-3-642-02469-6_50openalex-snapshot
Frequency Domain Analysis of a Stochastic Biological Network Motif with Delay
inferred← citeshttps://doi.org/10.1007/978-3-642-14859-0_20openalex-snapshot
Numerical and Experimental Analysis of the p53-mdm2 Regulatory Pathway
inferred← citeshttps://doi.org/10.1007/978-3-642-20164-6_9openalex-snapshot
Modelling Oscillator Synchronisation During Vertebrate Axis Segmentation
inferred← citeshttps://doi.org/10.1007/978-3-642-25950-0_14openalex-snapshot
Mathematical Modeling in Chronobiology
inferred← citeshttps://doi.org/10.1007/978-3-642-31346-2_35openalex-snapshot
Mean Square Stability of Stochastic Impulsive Genetic Regulatory Networks with Mixed Time-Delays
inferred← citeshttps://doi.org/10.1007/978-4-431-54496-8_1openalex-snapshot
Dynamic Notch Signaling in Neural Progenitor Cells
inferred← citeshttps://doi.org/10.1007/978-4-431-87704-2_10openalex-snapshot
A Posttranslational Chemical Circadian Oscillator in Cyanobacteria
inferred← citeshttps://doi.org/10.1007/978-4-431-87704-2_21openalex-snapshot
Ultradian Oscillation Networks in Somite Segmentation and Other Biological Events
inferred← citeshttps://doi.org/10.1007/978-4-431-88981-6_10openalex-snapshot
Self-organized Spatio-temporal Oscillation Observed in a Chain of Non-oscillatory Cells
inferred← citeshttps://doi.org/10.1007/978-88-470-2571-4_4openalex-snapshot
Spatio-Temporal Modelling of Intracellular Signalling Pathways: Transcription Factors, Negative Feedback Systems and Oscillations
inferred← citeshttps://doi.org/10.1007/978-90-481-3375-8_10openalex-snapshot
Rhythmic Expression of Notch Signaling in Neural Progenitor Cells
inferred← citeshttps://doi.org/10.1007/978-94-007-2828-8_3openalex-snapshot
Maintenance of Neural Stem Cells in the Brain: Role of Notch Signaling
inferred← citeshttps://doi.org/10.1007/978-981-97-6695-6_2openalex-snapshot
Mechanisms of Circadian Oscillations
inferred← citeshttps://doi.org/10.1007/s00018-012-1151-xopenalex-snapshot
Genetic visualization of notch signaling in mammalian neurogenesis
inferred← citeshttps://doi.org/10.1007/s00018-016-2277-zopenalex-snapshot
Hes1: the maestro in neurogenesis
inferred← citeshttps://doi.org/10.1007/s00285-003-0247-1openalex-snapshot
Oscillations and patterns in spatially discrete models for developmental intercellular signalling
inferred← citeshttps://doi.org/10.1007/s00285-009-0296-1openalex-snapshot
Synchronized oscillation of the segmentation clock gene in vertebrate development
inferred← citeshttps://doi.org/10.1007/s00285-014-0837-0openalex-snapshot
Mean field analysis of a spatial stochastic model of a gene regulatory network
inferred← citeshttps://doi.org/10.1007/s00427-004-0427-zopenalex-snapshot
her11 is involved in the somitogenesis clock in zebrafish
inferred← citeshttps://doi.org/10.1007/s00429-023-02639-6openalex-snapshot
The Notch pathway regulates autophagy after hypoxic–ischemic injury and affects synaptic plasticity
inferred← citeshttps://doi.org/10.1007/s00441-014-1888-7openalex-snapshot
Dynamic expression and roles of Hes factors in neural development
inferred← citeshttps://doi.org/10.1007/s00774-011-0295-3openalex-snapshot
A fluorescence spotlight on the clockwork development and metabolism of bone
inferred← citeshttps://doi.org/10.1007/s10059-009-0068-1openalex-snapshot
Rhythmic Gene Expression in Somite Formation and Neural Development
inferred← citeshttps://doi.org/10.1007/s10549-009-0381-6openalex-snapshot
SOX9 mediates the retinoic acid-induced HES-1 gene expression in human breast cancer cells
inferred← citeshttps://doi.org/10.1007/s10867-015-9391-2openalex-snapshot
Neural fate decisions mediated by combinatorial regulation of Hes1 and miR-9
inferred← citeshttps://doi.org/10.1007/s11033-020-05884-8openalex-snapshot
Distinct roles for Notch1 and Notch3 in human adipose-derived stem/stromal cell adipogenesis
inferred← citeshttps://doi.org/10.1007/s11432-016-0526-8openalex-snapshot
Stability of gene regulatory networks with Lévy noise
inferred← citeshttps://doi.org/10.1007/s11467-010-0152-1openalex-snapshot
Oscillation sources and wave propagation paths in complex networks consisting of excitable nodes
inferred← citeshttps://doi.org/10.1007/s11515-011-1178-7openalex-snapshot
BMP signaling pathway and spinal cord development
inferred← citeshttps://doi.org/10.1007/s11538-008-9391-5openalex-snapshot
Hybrid Modeling of Noise Reduction by a Negatively Autoregulated System
inferred← citeshttps://doi.org/10.1007/s11538-012-9725-1openalex-snapshot
Influence of the Nuclear Membrane, Active Transport, and Cell Shape on the Hes1 and p53–Mdm2 Pathways: Insights from Spatio-temporal Modelling
inferred← citeshttps://doi.org/10.1007/s11538-013-9842-5openalex-snapshot
The Role of Dimerisation and Nuclear Transport in the Hes1 Gene Regulatory Network
inferred← citeshttps://doi.org/10.1007/s11538-014-9959-1openalex-snapshot
Cyclic Negative Feedback Systems: What is the Chance of Oscillation?
inferred← citeshttps://doi.org/10.1007/s11538-017-0292-3openalex-snapshot
Computational Modelling of Cancer Development and Growth: Modelling at Multiple Scales and Multiscale Modelling
inferred← citeshttps://doi.org/10.1007/s11538-023-01143-6openalex-snapshot
Autoregulation of Transcription and Translation: A Qualitative Analysis
inferred← citeshttps://doi.org/10.1007/s11538-025-01447-9openalex-snapshot
Modelling Population-Level Hes1 Dynamics: Insights from a Multi-framework Approach
inferred← citeshttps://doi.org/10.1007/s11557-017-1342-9openalex-snapshot
Multistep phosphorelay in fungi: the enigma of multiple signals and a limited number of signaling pathways
inferred← citeshttps://doi.org/10.1007/s11571-010-9105-1openalex-snapshot
Mean square exponential and robust stability of stochastic discrete-time genetic regulatory networks with uncertainties
inferred← citeshttps://doi.org/10.1007/s11704-007-0011-9openalex-snapshot
Integrative biological systems modeling: challenges and opportunities
inferred← citeshttps://doi.org/10.1007/s12039-023-02177-yopenalex-snapshot
Deciphering the impact of pulsatile input in the population-level synchrony of the Hes1 oscillators
inferred← citeshttps://doi.org/10.1007/s12250-017-3956-0openalex-snapshot
Human cytomegalovirus infection dysregulates neural progenitor cell fate by disrupting Hes1 rhythm and down-regulating its expression
inferred← citeshttps://doi.org/10.1016/b978-0-12-374729-7.00018-4openalex-snapshot
Neurogenesis in the Vertebrate Embryo
inferred← citeshttps://doi.org/10.1016/b978-0-12-385942-6.00058-5openalex-snapshot
Neurogenesis in the Vertebrate Embryo
inferred← citeshttps://doi.org/10.1016/b978-0-12-397265-1.00065-4openalex-snapshot
bHLH Factors in Neurogenesis and Neuronal Subtype Specification
inferred← citeshttps://doi.org/10.1016/b978-0-12-397265-1.00070-8openalex-snapshot
Notch and Neural Development
inferred← citeshttps://doi.org/10.1016/b978-0-12-397265-1.00079-4openalex-snapshot
Neural Stem Cells Among Glia
inferred← citeshttps://doi.org/10.1016/b978-0-12-405943-6.00007-5openalex-snapshot
Expression Dynamics and Functions of Hes Factors in Development and Diseases
inferred← citeshttps://doi.org/10.1016/b978-0-12-800174-5.00015-6openalex-snapshot
The NOTCH Pathway in β-Cell Growth and Differentiation
inferred← citeshttps://doi.org/10.1016/b978-0-12-814405-3.00013-8openalex-snapshot
Notch and neural development
inferred← citeshttps://doi.org/10.1016/b978-0-12-814405-3.00014-xopenalex-snapshot
bHLH factors in neurogenesis and neuronal subtype specification
inferred← citeshttps://doi.org/10.1016/b978-0-12-814405-3.00031-xopenalex-snapshot
Neural stem cells among glia
inferred← citeshttps://doi.org/10.1016/b978-008045046-9.01028-7openalex-snapshot
Helix–Loop–Helix (bHLH) Proteins: Hes Family
inferred← citeshttps://doi.org/10.1016/b978-012436643-5/50027-4openalex-snapshot
Neurogenesis in the Vertebrate Embryo
inferred← citeshttps://doi.org/10.1016/b978-012436643-5/50108-5openalex-snapshot
Neurogenesis in the Vertebrate Embryo
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2022.02.011openalex-snapshot
Signaling oscillations in embryonic development
inferred← citeshttps://doi.org/10.1016/j.ajpath.2012.06.003openalex-snapshot
The Alarmin IL-33 Is a Notch Target in Quiescent Endothelial Cells
inferred← citeshttps://doi.org/10.1016/j.amc.2014.05.122openalex-snapshot
Stability and Hopf bifurcation in a model of gene expression with distributed time delays
inferred← citeshttps://doi.org/10.1016/j.asd.2016.11.007openalex-snapshot
Delta-Notch signalling in segmentation
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2012.03.004openalex-snapshot
Complex dynamics of transcription regulation
inferred← citeshttps://doi.org/10.1016/j.bbapap.2010.08.010openalex-snapshot
Different degrees of structural order in distinct regions of the transcriptional repressor HES-1
inferred← citeshttps://doi.org/10.1016/j.bbrc.2005.04.089openalex-snapshot
The conserved WRPW motif of Hes6 mediates proteasomal degradation
inferred← citeshttps://doi.org/10.1016/j.bbrc.2007.01.153openalex-snapshot
HES6 reverses nuclear reprogramming of insulin-producing cells following cell fusion
inferred← citeshttps://doi.org/10.1016/j.bbrc.2007.04.207openalex-snapshot
The role of microRNA in the delayed negative feedback regulation of gene expression
inferred← citeshttps://doi.org/10.1016/j.bbrc.2008.05.015openalex-snapshot
Requirement of multiple lysine residues for the transcriptional activity and the instability of Hes7
inferred← citeshttps://doi.org/10.1016/j.bbrc.2015.08.039openalex-snapshot
Neuronal differentiation of human iPS cells induced by baicalin via regulation of bHLH gene expression
inferred← citeshttps://doi.org/10.1016/j.bbrc.2016.09.124openalex-snapshot
Light-induced Notch activity controls neurogenic and gliogenic potential of neural progenitors
inferred← citeshttps://doi.org/10.1016/j.biocel.2003.10.010openalex-snapshot
Serum concentration modifies amplitude and kinetics of voltage-gated Na+ current in the Mat-LyLu cell line of rat prostate cancer
inferred← citeshttps://doi.org/10.1016/j.biosystems.2022.104717openalex-snapshot
Degradation-driven protein level oscillation in the yeast Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1016/j.bpj.2009.11.039openalex-snapshot
A Wnt Oscillator Model for Somitogenesis
inferred← citeshttps://doi.org/10.1016/j.bpj.2013.03.031openalex-snapshot
Mechanistically Consistent Reduced Models of Synthetic Gene Networks
inferred← citeshttps://doi.org/10.1016/j.bpj.2014.06.011openalex-snapshot
Collective Cell Movement Promotes Synchronization of Coupled Genetic Oscillators
inferred← citeshttps://doi.org/10.1016/j.bpj.2014.09.042openalex-snapshot
Stochastic Oscillations Induced by Intrinsic Fluctuations in a Self-Repressing Gene
inferred← citeshttps://doi.org/10.1016/j.cam.2006.02.063openalex-snapshot
Stochastic delay differential equations for genetic regulatory networks
inferred← citeshttps://doi.org/10.1016/j.cbpb.2016.03.004openalex-snapshot
Effect of anthocyanidins on myogenic differentiation in induced and non-induced primary myoblasts from rainbow trout ( Oncorhynchus mykiss )
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.ceb.2008.09.002openalex-snapshot
Oscillating signaling pathways during embryonic development
inferred← citeshttps://doi.org/10.1016/j.ceb.2009.08.009openalex-snapshot
Dynamic regulation of Notch signaling in neural progenitor cells
inferred← citeshttps://doi.org/10.1016/j.ceb.2022.102130openalex-snapshot
Signaling oscillations: Molecular mechanisms and functional roles
inferred← citeshttps://doi.org/10.1016/j.cell.2011.06.030openalex-snapshot
Development and Evolution of the Human Neocortex
inferred← citeshttps://doi.org/10.1016/j.cell.2012.02.018openalex-snapshot
Coding Region Polyadenylation Generates a Truncated tRNA Synthetase that Counters Translation Repression
inferred← citeshttps://doi.org/10.1016/j.cell.2016.01.028openalex-snapshot
Self-Organization of Embryonic Genetic Oscillators into Spatiotemporal Wave Patterns
inferred← citeshttps://doi.org/10.1016/j.cell.2017.08.043openalex-snapshot
Excitable Dynamics and Yap-Dependent Mechanical Cues Drive the Segmentation Clock
inferred← citeshttps://doi.org/10.1016/j.cell.2018.01.002openalex-snapshot
Dynamic Ligand Discrimination in the Notch Signaling Pathway
inferred← citeshttps://doi.org/10.1016/j.cell.2018.05.035openalex-snapshot
Dynamics and Spatial Genomics of the Nascent Transcriptome by Intron seqFISH
inferred← citeshttps://doi.org/10.1016/j.cell.2024.04.050openalex-snapshot
Massively parallel in vivo Perturb-seq reveals cell-type-specific transcriptional networks in cortical development
inferred← citeshttps://doi.org/10.1016/j.cellsig.2012.09.014openalex-snapshot
Feedforward and feedback regulation of the MAPK and PI3K oscillatory circuit in breast cancer
inferred← citeshttps://doi.org/10.1016/j.celrep.2012.05.017openalex-snapshot
MicroRNA-9 Modulates Hes1 Ultradian Oscillations by Forming a Double-Negative Feedback Loop
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.115077openalex-snapshot
Activation-derepression synergy enables a bHLH network to coordinate a signal-specific fate response
inferred← citeshttps://doi.org/10.1016/j.cels.2019.10.010openalex-snapshot
Inferring Leading Interactions in the p53/Mdm2/Mdmx Circuit through Live-Cell Imaging and Modeling
inferred← citeshttps://doi.org/10.1016/j.cels.2024.10.002openalex-snapshot
Plausible, robust biological oscillations through allelic buffering
inferred← citeshttps://doi.org/10.1016/j.chaos.2008.03.010openalex-snapshot
A simple model of genetic oscillations through regulated degradation
inferred← citeshttps://doi.org/10.1016/j.chaos.2012.03.006openalex-snapshot
Robust filtering of uncertain stochastic genetic regulatory networks with time-varying delays
inferred← citeshttps://doi.org/10.1016/j.chaos.2012.11.011openalex-snapshot
Coupling switches and oscillators as a means to shape cellular signals in biomolecular systems
inferred← citeshttps://doi.org/10.1016/j.chaos.2021.111659openalex-snapshot
Dynamics of fuzzy genetic regulatory networks with leakage and mixed delays in doubly-measure pseudo-almost periodic environment
inferred← citeshttps://doi.org/10.1016/j.chaos.2024.114479openalex-snapshot
Complex role of time delay in dynamical coordination of neural progenitor fate decisions mediated by Notch pathway
inferred← citeshttps://doi.org/10.1016/j.cnsns.2011.12.024openalex-snapshot
Delay-dependent stability criteria for genetic regulatory networks with time-varying delays and nonlinear disturbance
inferred← citeshttps://doi.org/10.1016/j.cnsns.2020.105166openalex-snapshot
Justification of quasi-stationary approximation in models of gene expression of a self-regulating protein
inferred← citeshttps://doi.org/10.1016/j.compbiomed.2011.07.009openalex-snapshot
Measurement of phase synchrony of coupled segmentation clocks
inferred← citeshttps://doi.org/10.1016/j.cub.2008.03.013openalex-snapshot
FGF induces oscillations of Hes1 expression and Ras/ERK activation
inferred← citeshttps://doi.org/10.1016/j.cub.2008.06.044openalex-snapshot
Biological rhythms: Clocks for all times
inferred← citeshttps://doi.org/10.1016/j.devcel.2005.02.019openalex-snapshot
Analysis of Notch Function in Presomitic Mesoderm Suggests a γ-Secretase-Independent Role for Presenilins in Somite Differentiation
inferred← citeshttps://doi.org/10.1016/j.devcel.2007.05.014openalex-snapshot
Id Sustains Hes1 Expression to Inhibit Precocious Neurogenesis by Releasing Negative Autoregulation of Hes1
inferred← citeshttps://doi.org/10.1016/j.devcel.2008.01.017openalex-snapshot
Multiple Roles of Notch Signaling in the Regulation of Epidermal Development
inferred← citeshttps://doi.org/10.1016/j.devcel.2010.11.018openalex-snapshot
MicroRNA-9 Reveals Regional Diversity of Neural Progenitors along the Anterior-Posterior Axis
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.devcel.2024.04.019openalex-snapshot
The Neurog2-Tbr2 axis forms a continuous transition to the neurogenic gene expression state in neural stem cells
inferred← citeshttps://doi.org/10.1016/j.devcel.2026.01.006openalex-snapshot
Bmp9 regulates Notch signaling and the temporal dynamics of angiogenesis via Lunatic Fringe
inferred← citeshttps://doi.org/10.1016/j.dtrs.2026.100025openalex-snapshot
Notch signalling in alveolar bone development and regeneration: A critical regulator for osteoblasts to osteocytes transitioning
inferred← citeshttps://doi.org/10.1016/j.febslet.2012.07.041openalex-snapshot
Systems biology of cellular rhythms
inferred← citeshttps://doi.org/10.1016/j.gde.2004.06.001openalex-snapshot
Noise, delays, robustness, canalization and all that
inferred← citeshttps://doi.org/10.1016/j.gde.2004.06.014openalex-snapshot
The vertebrate segmentation clock
inferred← citeshttps://doi.org/10.1016/j.gde.2010.08.004openalex-snapshot
Oscillatory control of signalling molecules
inferred← citeshttps://doi.org/10.1016/j.gde.2013.02.011openalex-snapshot
A large-scale view of the evolution of amniote development: insights from somitogenesis in reptiles
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.gde.2026.102470openalex-snapshot
Oscillatory gene expression in cell differentiation and tissue patterning
inferred← citeshttps://doi.org/10.1016/j.gene.2012.08.022openalex-snapshot
Identification of a new clock-related element EL-box involved in circadian regulation by BMAL1/CLOCK and HES1
inferred← citeshttps://doi.org/10.1016/j.gene.2014.12.054openalex-snapshot
Control of hair cell development by molecular pathways involving Atoh1, Hes1 and Hes5
inferred← citeshttps://doi.org/10.1016/j.gep.2011.06.004openalex-snapshot
A BAC transgenic Hes1-EGFP reporter reveals novel expression domains in mouse embryos
inferred← citeshttps://doi.org/10.1016/j.gep.2019.119094openalex-snapshot
Dynamic Delta-like1 expression in presomitic mesoderm cells during somite segmentation
inferred← citeshttps://doi.org/10.1016/j.gep.2021.119170openalex-snapshot
Hes1 oscillation frequency correlates with activation of neural stem cells
inferred← citeshttps://doi.org/10.1016/j.gep.2021.119198openalex-snapshot
Oscillatory expression of Ascl1 in oligodendrogenesis
inferred← citeshttps://doi.org/10.1016/j.ifacol.2017.08.2248openalex-snapshot
Modeling & Analysis of Gene Expression as a Nonlinear Feedback Problem With State-Dependent Delay
inferred← citeshttps://doi.org/10.1016/j.immuni.2008.08.016openalex-snapshot
Integrated Regulation of Toll-like Receptor Responses by Notch and Interferon-γ Pathways
inferred← citeshttps://doi.org/10.1016/j.ins.2010.05.032openalex-snapshot
Robust stability for uncertain genetic regulatory networks with interval time-varying delays
inferred← citeshttps://doi.org/10.1016/j.ins.2010.10.007openalex-snapshot
Mean square exponential stability of stochastic genetic regulatory networks with time-varying delays
inferred← citeshttps://doi.org/10.1016/j.jbi.2011.11.016openalex-snapshot
Oscillabolastic model, a new model for oscillatory dynamics, applied to the analysis of Hes1 gene expression and Ehrlich ascites tumor growth
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2016.03.053openalex-snapshot
Transcriptional kinetics of the cross-talk between the ortho -cleavage and TOL pathways of toluene biodegradation in Pseudomonas putida mt-2
inferred← citeshttps://doi.org/10.1016/j.jfranklin.2013.05.016openalex-snapshot
Finite-time H control for discrete-time genetic regulatory networks with random delays and partly unknown transition probabilities
inferred← citeshttps://doi.org/10.1016/j.jmaa.2012.05.032openalex-snapshot
The stability and Hopf bifurcation analysis of a gene expression model
inferred← citeshttps://doi.org/10.1016/j.jmb.2007.01.089openalex-snapshot
A Molecular Clock Operates During Chick Autopod Proximal-distal Outgrowth
inferred← citeshttps://doi.org/10.1016/j.jmb.2015.03.007openalex-snapshot
Metabolic Regulation of the Ultradian Oscillator Hes1 by Reactive Oxygen Species
inferred← citeshttps://doi.org/10.1016/j.jot.2021.09.007openalex-snapshot
Transient activation of notch signaling enhances endogenous stromal cell expansion and subsequent bone defect repair
inferred← citeshttps://doi.org/10.1016/j.jtbi.2006.11.012openalex-snapshot
Superstability of the yeast cell-cycle dynamics: Ensuring causality in the presence of biochemical stochasticity
inferred← citeshttps://doi.org/10.1016/j.jtbi.2007.05.014openalex-snapshot
Cell-based simulation of dynamic expression patterns in the presomitic mesoderm
showing the first 200 of 735 · page through all 735
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.