Absence of collapse in a parabolic chemotaxis system with signal-dependent sensitivity
From MaRDI portal
Publication:3058200
DOI10.1002/mana.200810838zbMath1205.35037OpenAlexW2061996325MaRDI QIDQ3058200
Publication date: 18 November 2010
Published in: Mathematische Nachrichten (Search for Journal in Brave)
Full work available at URL: https://doi.org/10.1002/mana.200810838
A priori estimates in context of PDEs (35B45) Cell movement (chemotaxis, etc.) (92C17) Semilinear parabolic equations (35K58) Initial-boundary value problems for second-order parabolic systems (35K51)
Related Items
Boundedness of solutions in a fully parabolic quasilinear chemotaxis model with two species and two chemicals, Global boundedness in a quasilinear chemotaxis system with general density-signal governed sensitivity, A quasilinear attraction-repulsion chemotaxis system of parabolic-elliptic type with logistic source, Asymptotic behavior of a quasilinear parabolic-elliptic-elliptic chemotaxis system with logistic source, Global boundedness in a quasilinear attraction-repulsion chemotaxis model with nonlinear sensitivity, Global existence and asymptotic stability of solutions to a two-species chemotaxis system with any chemical diffusion, On a parabolic-elliptic system with chemotaxis and logistic type growth, Global boundedness to a parabolic-parabolic chemotaxis model with nonlinear diffusion and singular sensitivity, Dynamics and pattern formations in a three-species predator-prey model with two prey-taxis, Global existence of solutions and uniform persistence of a diffusive predator-prey model with prey-taxis, Boundedness in a quasilinear 2D parabolic-parabolic attraction-repulsion chemotaxis system, A reaction diffusion system modeling virus dynamics and CTLs response with chemotaxis, Global classical solutions in chemotaxis(-Navier)-Stokes system with rotational flux term, Global existence and boundedness in a Keller-Segel-(Navier-)Stokes system with signal-dependent sensitivity, Global solutions in the species competitive chemotaxis system with inequal diffusion rates, Boundedness in prey-taxis system with rotational flux terms, Convergence rate estimates of a two-species chemotaxis system with two indirect signal production and logistic source in three dimensions, A new result for global solvability in a singular chemotaxis-growth system with indirect signal production, On the multi-dimensional advective Lotka-Volterra competition systems, Global existence and aggregation in a Keller-Segel model with Fokker-Planck diffusion, Boundedness in a parabolic-parabolic quasilinear chemotaxis system with logistic source, Analysis and numerical simulations of a chemotaxis model of aggregation of microglia in Alzheimer's disease, Global existence and boundedness of classical solutions for a chemotaxis model with logistic source, Stabilization and convergence rate in a chemotaxis system with consumption of chemoattractant, Global classical solutions of Keller-Segel-(Navier)-Stokes system with nonlinear motility functions, An optimal result for global existence and boundedness in a three-dimensional Keller-Segel-Stokes system with nonlinear diffusion, Finite-time blow-up in higher dimensional fully-parabolic chemotaxis system for two species, Boundedness and asymptotic behavior in a fully parabolic chemotaxis-growth system with signal-dependent sensitivity, Boundedness and asymptotic stability of solutions to a two-species chemotaxis system with consumption of chemoattractant, Boundedness in chemotaxis systems with rotational flux terms, Boundedness and asymptotic behavior of solutions to a chemotaxis-haptotaxis model in high dimensions, Global existence and boundedness in a parabolic-elliptic Keller-Segel system with general sensitivity, Finite-time blow-up in a quasilinear chemotaxis system with an external signal consumption, Dynamics in two-predator and one-prey models with signal-dependent motility, Boundedness and stabilization in a two-species chemotaxis system with signal absorption, Global boundedness in a three-dimensional chemotaxis-haptotaxis model, Global boundedness in a fully parabolic quasilinear chemotaxis system with singular sensitivity, Blow up criterion for a hyperbolic-parabolic system arising from chemotaxis, On a quasilinear parabolic-elliptic chemotaxis system with logistic source, Global existence and boundedness in a reaction-diffusion-taxis system with three species, Boundedness and stabilization enforced by mild saturation of taxis in a producer-scrounger model, A new result for the global existence (and boundedness) and regularity of a three-dimensional Keller-Segel-Navier-Stokes system modeling coral fertilization, Eventual smoothness and stabilization of large-data solutions in a three-dimensional chemotaxis system with consumption of chemoattractant, A further study on a 3D chemotaxis-Stokes system with tensor-valued sensitivity, Global weak solutions for the three-dimensional chemotaxis-Navier-Stokes system with slow \(p\)-Laplacian diffusion, Boundedness in chemotaxis-Stokes system with rotational flux term, Global weak solutions in a chemotaxis system with large singular sensitivity, Boundedness of solutions in a chemotaxis system with nonlinear sensitivity and logistic source, Boundedness in a fully parabolic chemotaxis system with singular sensitivity, Global well-posedness and asymptotic stabilization for chemotaxis system with signal-dependent sensitivity, Uniform boundedness and pattern formation for Keller-Segel systems with two competing species, Global asymptotic stability of steady states in a chemotaxis-growth system with singular sensitivity, Boundedness and blow-up for a chemotaxis system with generalized volume-filling effect and logistic source, Global existence to a higher-dimensional quasilinear chemotaxis system with consumption of chemoattractant, Boundedness in a full parabolic two-species chemotaxis system, Existence of weak solutions to the Keller-Segel chemotaxis system with additional cross-diffusion, Global existence and asymptotic dynamics in a 3D fractional chemotaxis system with singular sensitivity, Global existence and asymptotic behavior in a two-species chemotaxis system with logistic source, Global weak solutions in a three-dimensional Keller-Segel-Navier-Stokes system involving a tensor-valued sensitivity with saturation, Global existence of solutions to an attraction-repulsion chemotaxis model with growth, Global solutions to a chemotaxis model with consumption of chemoattractant, Boundedness and asymptotic stability in a two-species chemotaxis-competition model with signal-dependent sensitivity, Global boundedness in a two-competing-species chemotaxis system with two chemicals, Boundedness in a three-dimensional Keller-Segel-Stokes system involving tensor-valued sensitivity with saturation, Boundedness in a parabolic-parabolic chemotaxis system with nonlinear diffusion, Global well-posedness and zero diffusion limit of classical solutions to 3D conservation laws arising in chemotaxis, Boundedness in a chemotaxis model with oxygen consumption by bacteria, Boundedness in the higher dimensional attraction-repulsion chemotaxis-growth system, Global solutions of a Keller-Segel system with saturated logarithmic sensitivity function, Global existence and boundedness to a two-species chemotaxis-competition model with singular sensitivity, Boundedness and stability in a chemotaxis-growth model with indirect attractant production and signal-dependent sensitivity, Keller-Segel chemotaxis models: a review, Boundedness and global stability of the two-predator and one-prey models with nonlinear prey-taxis, Global existence and blow up of solutions of quasilinear chemotaxis system, Global existence and boundedness in a chemorepulsion system with superlinear diffusion, Global generalized solutions to a Keller-Segel system with nonlinear diffusion and singular sensitivity, Large time behavior of solution to an attraction-repulsion chemotaxis system with logistic source in three dimensions, A user's guide to PDE models for chemotaxis, Global solvability and large-time behavior to a three-dimensional chemotaxis-Stokes system modeling coral fertilization, A model of space-fractional-order diffusion in the glial scar, The Keller-Segel system of parabolic-parabolic type in homogeneous Besov spaces framework, Finite-time blow-up in a higher-dimensional quasilinear parabolic-elliptic chemotaxis system with space dependent logistic source, Global existence in a chemotaxis system with singular sensitivity and signal production, Boundedness in a quasilinear chemotaxis model with logistic growth and indirect signal production, Analysis of a chemotaxis model with indirect signal absorption, Stabilization in three-dimensional chemotaxis-growth model with indirect attractant production, Global well-posedness in a chemotaxis system with oxygen consumption, Global classical solutions in a Keller-Segel(-Navier)-Stokes system modeling coral fertilization, Dynamics and pattern formation in a cross-diffusion model with stage structure for predators, Global boundedness of solutions to a two-species chemotaxis system, The small-convection limit in a two-dimensional chemotaxis-Navier-Stokes system with density-dependent motion, Global existence and asymptotic stability of solutions to a forager-exploiter model with logistic source, Global boundedness in a quasilinear chemotaxis system with signal-dependent sensitivity, Boundedness in a quasilinear attraction-repulsion chemotaxis system with nonlinear sensitivity and logistic source, Boundedness in a fully parabolic chemotaxis system with strongly singular sensitivity, Boundedness and global stability of the predator-prey model with prey-taxis and competition, Boundedness in a fully parabolic attraction-repulsion chemotaxis system with nonlinear diffusion and signal-dependent sensitivity, Global weak solutions for the three-dimensional chemotaxis-Navier-Stokes system with nonlinear diffusion, On a class of Keller-Segel chemotaxis systems with cross-diffusion, An iterative approach to \(L^\infty\)-boundedness in quasilinear Keller-Segel systems, On the global existence and qualitative behaviour of one-dimensional solutions to a model for urban crime, Boundedness and large time behavior in a quasilinear chemotaxis model for tumor invasion, Mathematical analysis of a model of chemotaxis arising from morphogenesis, Boundedness on a fully parabolic singular chemotaxis system with indirect signal production and logistic source, An attraction‐repulsion chemotaxis system with logistic source, Dynamics of a chemotaxis-May-Nowak model with volume filling sensitivity, Global boundedness in a two-dimensional chemotaxis system with nonlinear diffusion and singular sensitivity, A note to the global solvability of a chemotaxis-Navier-Stokes system with density-suppressed motility, Global well‐posedness and uniform boundedness of a higher dimensional crime model with a logistic source term, Boundedness and large-time behavior in a chemotaxis system with signal-dependent motility arising from tumor invasion, Boundedness in a higher-dimensional singular chemotaxis-growth system with indirect signal production, A predator–prey model with taxis mechanisms and stage structure for the predator, Boundedness of classical solutions for a chemotaxis system with general sensitivity function, Global existence and uniqueness of solutions to a chemotaxis system, Dynamics and pattern formation of a diffusive predator–prey model with predator-taxis, The full Keller–Segel model is well-posed on nonsmooth domains, Chemotaxis Effect on Algae by Inorganic Polymer Flocculants: Backward Bifurcations and Traveling Wave Solutions, Boundedness and global stability of a diffusive prey–predator model with prey-taxis, Global solutions in a fully parabolic chemotaxis system with singular sensitivity, Classical solution of a PDE system stemming from auxin transport model for leaf venation, Boundedness and stabilization in a two-species chemotaxis system with two chemicals, Boundedness and stabilization in a two-species chemotaxis system with two chemicals, Stability and Bifurcation in a Predator–Prey System with Prey-Taxis, Boundedness of solutions to parabolic-elliptic Keller-Segel systems with signal-dependent sensitivity, Global existence of solutions for a fully parabolic chemotaxis system with consumption of chemoattractant and logistic source, Toward a mathematical theory of Keller–Segel models of pattern formation in biological tissues
Cites Work
- Unnamed Item
- Unnamed Item
- Unnamed Item
- Unnamed Item
- Unnamed Item
- Initiation of slime mold aggregation viewed as an instability
- Travelling front solutions arising in the chemotaxis-growth model
- From 1970 until present: The Keller-Segel model in chemotaxis and its consequences. I
- Mathematical biology. Vol. 1: An introduction.
- Mathematical biology. Vol. 2: Spatial models and biomedical applications.
- Parabolic system of chemotaxis: Blowup in a finite and the infinite time.
- Global existence and blowup of solutions to a chemotaxis system.
- Boundedness vs. blow-up in a chemotaxis system
- Blow-up in a chemotaxis model without symmetry assumptions
- Stationary Solutions of Chemotaxis Systems
- LPBounds of solutions of reaction-diffusion equations
- Global Behaviour of a Reaction-Diffusion System Modelling Chemotaxis
- A System of Reaction Diffusion Equations Arising in the Theory of Reinforced Random Walks
- Global existence of solutions to a parabolic system for chemotaxis in two space dimensions
- A Chemotaxis System with Logistic Source
- Chemotactic collapse in a parabolic system of mathematical biology