Pages that link to "Item:Q1018160"
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The following pages link to Global existence of classical solutions to a combined chemotaxis-haptotaxis model with logistic source (Q1018160):
Displayed 50 items.
- On the boundedness and decay of solutions for a chemotaxis-haptotaxis system with nonlinear diffusion (Q256196) (← links)
- Boundedness in a quasilinear chemotaxis-haptotaxis system with logistic source (Q294043) (← links)
- Global boundedness and decay for a multi-dimensional chemotaxis-haptotaxis system with nonlinear diffusion (Q321731) (← links)
- Boundedness of solutions to a quasilinear higher-dimensional chemotaxis-haptotaxis model with nonlinear diffusion (Q501454) (← links)
- Global existence for a degenerate haptotaxis model of cancer invasion (Q506394) (← links)
- Boundedness in a three-dimensional chemotaxis-haptotaxis model with nonlinear diffusion (Q514389) (← links)
- Global existence of a two-dimensional chemotaxis-haptotaxis model with remodeling of non-diffusible attractant (Q526015) (← links)
- Global existence for a haptotaxis model of cancer invasion with tissue remodeling (Q611260) (← links)
- Existence and uniqueness of solutions of predator-prey type model with mixed boundary conditions (Q645009) (← links)
- Asymptotic-preserving and well-balanced schemes for the 1D Cattaneo model of chemotaxis movement in both hyperbolic and diffusive regimes (Q663648) (← links)
- A study on time discretization and adaptive mesh refinement methods for the simulation of cancer invasion: the urokinase model (Q668491) (← links)
- Boundedness in the higher-dimensional chemotaxis-haptotaxis model with nonlinear diffusion (Q890222) (← links)
- A density-dependent chemotaxis-haptotaxis system modeling cancer invasion (Q968855) (← links)
- Global existence of classical solutions to a predator-prey model with nonlinear prey-taxis (Q974624) (← links)
- Existence and uniqueness of global classical solutions to a two dimensional two species cancer invasion haptotaxis model (Q1756887) (← links)
- Boundedness of solutions for a quasilinear chemotaxis-haptotaxis model (Q1982567) (← links)
- Asymptotic stability in a quasilinear chemotaxis-haptotaxis model with general logistic source and nonlinear signal production (Q2003944) (← links)
- Boundedness of solutions to a quasilinear chemotaxis-haptotaxis model (Q2007228) (← links)
- Blow-up phenomena of a cancer invasion model with nonlinear diffusion and haptotaxis term (Q2021582) (← links)
- Global existence of classical solutions to a chemotaxis-haptotaxis model (Q2022953) (← links)
- Modeling multiple taxis: tumor invasion with phenotypic heterogeneity, haptotaxis, and unilateral interspecies repellence (Q2026618) (← links)
- Boundedness in a quasilinear chemotaxis-haptotaxis model of parabolic-parabolic-ODE type (Q2108363) (← links)
- Solving a chemotaxis-haptotaxis system in 2D using generalized finite difference method (Q2194796) (← links)
- Global boundedness in a three-dimensional chemotaxis-haptotaxis model (Q2203941) (← links)
- Mathematical and numerical analysis of an acid-mediated cancer invasion model with nonlinear diffusion (Q2218926) (← links)
- Critical mass for infinite-time blow-up in a haptotaxis system with nonlinear zero-order interaction (Q2229257) (← links)
- On the existence of weak solutions of nonlinear degenerate parabolic system with variable exponents (Q2314288) (← links)
- 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 (Q2334747) (← links)
- A chemotaxis-haptotaxis system with haptoattractant remodeling: boundedness enforced by mild saturation of signal production (Q2415191) (← links)
- Stabilization in a chemotaxis model for tumor invasion (Q2515675) (← links)
- Stabilization to a cancer invasion model with remodeling mechanism and slow diffusion (Q2675220) (← links)
- Qualitative analysis of a parabolic–elliptic attraction–repulsion chemotaxis model with logistic source (Q2809293) (← links)
- Analysis of a chemotaxis system modeling ant foraging (Q2816545) (← links)
- Boundedness and stabilization in a multi-dimensional chemotaxis—haptotaxis model (Q2935511) (← links)
- A quasilinear chemotaxis-haptotaxis model: The roles of nonlinear diffusion and logistic source (Q2978111) (← links)
- ASYMPTOTIC BEHAVIOR OF GLOBAL SOLUTIONS TO A MODEL OF CELL INVASION (Q3056451) (← links)
- Large Time Behavior in a Multidimensional Chemotaxis-Haptotaxis Model with Slow Signal Diffusion (Q3451747) (← links)
- Boundedness and large time behavior in a quasilinear chemotaxis model for tumor invasion (Q4569328) (← links)
- A note for global existence of a two-dimensional chemotaxis–haptotaxis model with remodeling of non-diffusible attractant (Q4585726) (← links)
- A Stokes Two-Fluid Model for Cell Migration that Can Account for Physical Cues in the Microenvironment (Q4602443) (← links)
- Global boundedness of solutions to a chemotaxis–haptotaxis model with tissue remodeling (Q4630535) (← links)
- CONVERGENCE OF A CANCER INVASION MODEL TO A LOGISTIC CHEMOTAXIS MODEL (Q4910885) (← links)
- 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) (Q5056753) (← links)
- (Q5096487) (← links)
- Mathematical Research for Models Which is Related to Chemotaxis System (Q5110837) (← links)
- Global solvability and stabilization to a cancer invasion model with remodelling of ECM (Q5130935) (← links)
- Solvability of reaction–diffusion model with variable exponents (Q5170223) (← links)
- A new result for 2D boundedness of solutions to a chemotaxis–haptotaxis model with/without sub-logistic source (Q5243473) (← links)
- Toward a mathematical theory of Keller–Segel models of pattern formation in biological tissues (Q5265465) (← links)
- Large time behavior of solution to a fully parabolic chemotaxis-haptotaxis model in higher dimensions (Q5964043) (← links)