DOI10.1016/j.jde.2014.04.014zbMath1295.35144OpenAlexW2009746295MaRDI QIDQ2451888
Michael Winkler, Youshan Tao
Publication date: 26 May 2014
Published in: Journal of Differential Equations (Search for Journal in Brave)
Full work available at URL: https://doi.org/10.1016/j.jde.2014.04.014
Global existence of classical solutions and numerical simulations of a cancer invasion model,
Global existence of solutions to the chemotaxis system with logistic source under nonlinear Neumann boundary conditions,
Uniform boundedness and eventual Hölder continuity to a cancer invasion model with remodeling of ECM and nonlinear diffusion,
Some further progress for boundedness of solutions to a quasilinear higher-dimensional chemotaxis-haptotaxis model with nonlinear diffusion,
Boundedness and asymptotic stabilization in a two-dimensional Keller–Segel–Navier–Stokes system with sub-logistic source,
Boundedness in a logistic chemotaxis system with weakly singular sensitivity in dimension two,
Global existence of a diffusive predator-prey model with prey-stage structure and prey-taxis,
Boundedness in a two-dimensional two-species cancer invasion haptotaxis model without cell proliferation,
A critical exponent for blow-up in a two-dimensional chemotaxis-consumption system,
Asymptotic behaviour in a doubly haptotactic cross-diffusion model for oncolytic virotherapy,
Blow-up prevention by sub-logistic sources in Keller-Segel cross diffusion type system,
The vanishing viscosity limit on a model of Kareiva-Odell type in 2D,
Boundedness of solutions to a chemotaxis-haptotaxis model with nonlocal terms,
Global solvability and large time behavior in a two-species chemotaxis-consumption model,
Convergence analysis from the indirect signal production to the direct one,
Boundedness and large time behavior of solutions of a higher-dimensional haptotactic system modeling oncolytic virotherapy,
Combined effects of nonlinear diffusion and gradient-dependent flux limitation on a chemotaxis-haptotaxis model,
An interpolation inequality involving LlogL$L\log L$ spaces and application to the characterization of blow‐up behavior in a two‐dimensional Keller–Segel–Navier–Stokes system,
Global weak solutions in a three-dimensional two-species cancer invasion haptotaxis model without cell proliferation,
Global existence and uniform boundedness of smooth solutions to a parabolic-parabolic chemotaxis system with nonlinear diffusion,
On a macrophage and tumor cell chemotaxis system with both paracrine and autocrine loops,
Boundedness in a three-dimensional chemotaxis-haptotaxis model,
Global boundedness in a fully parabolic attraction–repulsion chemotaxis model,
Large Time Behavior in a Multidimensional Chemotaxis-Haptotaxis Model with Slow Signal Diffusion,
A critical virus production rate for efficiency of oncolytic virotherapy,
Does indirectness of signal production reduce the explosion-supporting potential in chemotaxis–haptotaxis systems? Global classical solvability in a class of models for cancer invasion (and more),
Global solutions to a haptotaxis system with a potentially degenerate diffusion tensor in two and three dimensions,
Finite-time blow-up and boundedness in a 2D Keller–Segel system with rotation,
Global dynamics in a fully parabolic chemotaxis system with logistic source,
Boundedness in a Keller-Segel system with external signal production,
The small-convection limit in a two-dimensional chemotaxis-Navier-Stokes system,
Global existence and uniqueness of classical solutions for a generalized quasilinear parabolic equation with application to a glioblastoma growth model,
Global weak solution and boundedness in a three-dimensional competing chemotaxis,
Finite time blow-up in the higher dimensional parabolic-elliptic-ODE minimal chemotaxis-haptotaxis system,
Dampening effect of logistic source in a two-dimensional haptotaxis system with nonlinear zero-order interaction,
Boundedness and large time behavior in a quasilinear chemotaxis model for tumor invasion,
Boundedness in a two species attraction-repulsion chemotaxis system with two chemicals,
Global existence and boundedness in a 2D Keller-Segel-Stokes system,
Global well-posedness to a chemotaxis-Stokes system,
Global classical solutions and convergence to a mathematical model for cancer cells invasion and metastatic spread,
A note for global existence of a two-dimensional chemotaxis–haptotaxis model with remodeling of non-diffusible attractant,
A chemotaxis-haptotaxis system with haptoattractant remodeling: boundedness enforced by mild saturation of signal production,
Sub-logistic source can prevent blow-up in the 2D minimal Keller-Segel chemotaxis system,
Blow-up prevention by logistic sources in a parabolic-elliptic Keller-Segel system with singular sensitivity,
Tumor evolution models of phase-field type with nonlocal effects and angiogenesis,
Boundedness in a two-species chemotaxis system with nonlinear resource consumption,
Boundedness in a two-dimensional chemotaxis system with signal-dependent motility and logistic source,
Global boundedness of weak solutions to a chemotaxis-haptotaxis model with \(p\)-Laplacian diffusion,
Global classical solvability and stabilization in a two-dimensional chemotaxis–fluid system with sub-logarithmic sensitivity,
Asymptotic behavior of a three-dimensional haptotactic cross-diffusion system modeling oncolytic virotherapy,
A critical virus production rate for blow-up suppression in a haptotaxis model for oncolytic virotherapy,
Global existence and boundedness of solutions to a two-species chemotaxis-competition system with singular sensitivity and indirect signal production,
On the global existence of solutions to chemotaxis system for two populations in dimension two,
On boundedness, blow-up and convergence in a two-species and two-stimuli chemotaxis system with/without loop,
Global boundedness in an oncolytic virotherapy model with generalized logistic source,
Boundedness and asymptotic behavior of solutions to a chemotaxis-haptotaxis model in high dimensions,
Large time behavior of solutions to a fully parabolic chemotaxis-haptotaxis model in \(N\) dimensions,
A new (and optimal) result for the boundedness of a solution of a quasilinear chemotaxis-haptotaxis model (with a logistic source),
Boundedness and stabilization in a predator-prey model with prey-taxis and disease in predator species,
Mathematical Research for Models Which is Related to Chemotaxis System,
A Hybrid Multiscale Model for Cancer Invasion of the Extracellular Matrix,
Mathematical modelling of cancer invasion: The multiple roles of TGF-β pathway on tumour proliferation and cell adhesion,
A Stokes Two-Fluid Model for Cell Migration that Can Account for Physical Cues in the Microenvironment,
Global boundedness in a three-dimensional chemotaxis-haptotaxis model,
Critical mass on the Keller-Segel system with signal-dependent motility,
Singular structure formation in a degenerate haptotaxis model involving myopic diffusion,
Boundedness in a haptotactic cross-diffusion system modeling oncolytic virotherapy,
Global solvability and large time behavior to a chemotaxis-haptotaxis model with nonlinear diffusion,
Global boundedness of solutions to a chemotaxis–haptotaxis model with tissue remodeling,
Critical mass for infinite-time blow-up in a haptotaxis system with nonlinear zero-order interaction,
A study on time discretization and adaptive mesh refinement methods for the simulation of cancer invasion: the urokinase model,
Global solvability and optimal control to a haptotaxis cancer invasion model with two cancer cell species,
Boundedness of solutions for a quasilinear chemotaxis-haptotaxis model,
Boundedness of solutions to a quasilinear higher-dimensional chemotaxis-haptotaxis model with nonlinear diffusion,
Global solvability and boundedness to a coupled chemotaxis-fluid model with arbitrary porous medium diffusion,
Global existence and eventual smoothness in a 2-D parabolic-elliptic system arising from ion transport networks,
Global stability in a multi-dimensional predator-prey system with prey-taxis,
Global boundedness in a two-competing-species chemotaxis system with two chemicals,
Global existence and asymptotic stability in a competitive two-species chemotaxis system with two signals,
Negligibility of haptotaxis effect in a chemotaxis–haptotaxis model,
Global existence of a two-dimensional chemotaxis-haptotaxis model with remodeling of non-diffusible attractant,
Existence and uniqueness of global classical solutions to a two dimensional two species cancer invasion haptotaxis model,
Boundedness of solutions to a quasilinear chemotaxis-haptotaxis model,
Global boundedness of classical solutions to a two species cancer invasion haptotaxis model with tissue remodeling,
Can fluid interaction influence the critical mass for taxis-driven blow-up in bounded planar domains?,
Boundedness in a two-dimensional attraction-repulsion system with nonlinear diffusion,
Global classical solutions to an oncolytic viral therapy model with triply haptotactic terms,
Boundedness in a two-species chemotaxis system,
The Keller-Segel system with logistic growth and signal-dependent motility,
Analysis of a two-dimensional triply haptotactic model with a fusogenic oncolytic virus and syncytia,
Solvability of solid tumor invasion model,
Stabilization in a chemotaxis model for tumor invasion,
Global classical solutions to a doubly haptotactic cross-diffusion system modeling oncolytic virotherapy,
Boundedness and stabilization in a two-species chemotaxis system with two chemicals,
Boundedness and stabilization in a two-species and two-stimuli chemotaxis system with signaling loop,
Boundedness of classical solutions to a degenerate Keller-Segel type model with signal-dependent motilities,
Dampening effects on global boundedness and asymptotic behavior in an oncolytic virotherapy model,
Global boundedness for a chemotaxis-competition system with signal dependent sensitivity and loop,
Asymptotic behavior of solutions to a tumor angiogenesis model with chemotaxis–haptotaxis,
Boundedness and stabilization in a two-species chemotaxis-competition system with indirect signal production,
Effects of signal-dependent motilities in a Keller–Segel-type reaction–diffusion system,
Global boundedness for a \(N\)-dimensional two species cancer invasion haptotaxis model with tissue remodeling,
Mathematical analysis of a tumor invasion model -- global existence and stability,
Analysis of a new multispecies tumor growth model coupling 3D phase-fields with a 1D vascular network,
Global well-posedness in a chemotaxis system with oxygen consumption,
A new result for 2D boundedness of solutions to a chemotaxis–haptotaxis model with/without sub-logistic source,
A simultaneous blow-up problem arising in tumor modeling,
Global classical solutions to a higher-dimensional doubly haptotactic cross-diffusion system modeling oncolytic virotherapy,
Large-data solutions in a three-dimensional chemotaxis-haptotaxis system with remodeling of non-diffusible attractant: the role of sub-linear production of diffusible signal,
Dampening effects on global boundedness in a quartic haptotactic model with fusogenic oncolytic virus and syncytia,
Asymptotic stability of spatial homogeneity in a haptotaxis model for oncolytic virotherapy,
Blow-up vs boundedness in a two-species attraction–repulsion chemotaxis system with two chemicals,
A New Result for Global Solvability of a Two Species Cancer Invasion Haptotaxis Model with Tissue Remodeling,
Toward a mathematical theory of Keller–Segel models of pattern formation in biological tissues,
Boundedness in a quasilinear chemotaxis-haptotaxis model of parabolic-parabolic-ODE type,
Combined effects of nonlinear proliferation and logistic damping in a three-component chemotaxis system for alopecia areata,
Boundedness in a two-species chemotaxis parabolic system with two chemicals