Pages that link to "Item:Q3584125"
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The following pages link to A Combined Chemotaxis-haptotaxis System: The Role of Logistic Source (Q3584125):
Displayed 30 items.
- On the boundedness and decay of solutions for a chemotaxis-haptotaxis system with nonlinear diffusion (Q256196) (← links)
- Boundedness and blow up in the higher-dimensional attraction-repulsion chemotaxis system with nonlinear diffusion (Q306238) (← links)
- Global boundedness and decay for a multi-dimensional chemotaxis-haptotaxis system with nonlinear diffusion (Q321731) (← 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)
- On a parabolic-elliptic chemotactic model with coupled boundary conditions (Q708551) (← links)
- Boundedness in the higher-dimensional chemotaxis-haptotaxis model with nonlinear diffusion (Q890222) (← links)
- Boundedness and asymptotic behavior of solutions to a chemotaxis-haptotaxis model in high dimensions (Q894410) (← links)
- A density-dependent chemotaxis-haptotaxis system modeling cancer invasion (Q968855) (← links)
- Singular structure formation in a degenerate haptotaxis model involving myopic diffusion (Q1707304) (← links)
- Global boundedness of classical solutions to a two species cancer invasion haptotaxis model with tissue remodeling (Q2009311) (← links)
- Optimal control and pattern formation for a haptotaxis model of solid tumor invasion (Q2334162) (← 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)
- Energy-type estimates and global solvability in a two-dimensional chemotaxis-haptotaxis model with remodeling of non-diffusible attractant (Q2451888) (← links)
- Global asymptotic stability of constant equilibria in a fully parabolic chemotaxis system with strong logistic dampening (Q2451921) (← links)
- Stabilization in a chemotaxis model for tumor invasion (Q2515675) (← 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)
- Global boundedness of solutions to a chemotaxis–haptotaxis model with tissue remodeling (Q4630535) (← links)
- COMPETING EFFECTS OF ATTRACTION VS. REPULSION IN CHEMOTAXIS (Q4910881) (← links)
- CONVERGENCE OF A CANCER INVASION MODEL TO A LOGISTIC CHEMOTAXIS MODEL (Q4910885) (← 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)
- GLOBAL EXISTENCE AND ASYMPTOTIC BEHAVIOR OF A TUMOR ANGIOGENESIS MODEL WITH CHEMOTAXIS AND HAPTOTAXIS (Q5411762) (← links)
- Large time behavior of solution to a fully parabolic chemotaxis-haptotaxis model in higher dimensions (Q5964043) (← links)