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):
Displaying 50 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)
- 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)
- Global boundedness of classical solutions to a two species cancer invasion haptotaxis model with tissue remodeling (Q2009311) (← links)
- Global existence of classical solutions to a chemotaxis-haptotaxis model (Q2022953) (← links)
- Global weak solutions to an oncolytic viral therapy model with doubly haptotactic terms (Q2025878) (← links)
- Global classical solutions to an oncolytic viral therapy model with triply haptotactic terms (Q2026546) (← links)
- Analysis of a two-dimensional triply haptotactic model with a fusogenic oncolytic virus and syncytia (Q2035753) (← links)
- Global boundedness for a \(N\)-dimensional two species cancer invasion haptotaxis model with tissue remodeling (Q2064499) (← links)
- Boundedness in a quasilinear chemotaxis-haptotaxis model of parabolic-parabolic-ODE type (Q2108363) (← links)
- Finite time blow-up in the higher dimensional parabolic-elliptic-ODE minimal chemotaxis-haptotaxis system (Q2168015) (← links)
- Solving a chemotaxis-haptotaxis system in 2D using generalized finite difference method (Q2194796) (← links)
- A new (and optimal) result for the boundedness of a solution of a quasilinear chemotaxis-haptotaxis model (with a logistic source) (Q2195158) (← links)
- Global boundedness in a three-dimensional chemotaxis-haptotaxis model (Q2203941) (← links)
- Critical mass for infinite-time blow-up in a haptotaxis system with nonlinear zero-order interaction (Q2229257) (← links)
- Global solvability and optimal control to a haptotaxis cancer invasion model with two cancer cell species (Q2234289) (← links)
- Boundedness in a chemotaxis-haptotaxis model with gradient-dependent flux limitation (Q2236712) (← links)
- Global classical solutions to a doubly haptotactic cross-diffusion system modeling oncolytic virotherapy (Q2297246) (← links)
- Facing low regularity in chemotaxis systems (Q2304971) (← 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)
- Global boundedness in an oncolytic virotherapy model with generalized logistic source (Q2679221) (← 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 Global Solvability of a Two Species Cancer Invasion Haptotaxis Model with Tissue Remodeling (Q5020856) (← 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)
- A Glioblastoma PDE-ODE model including chemotaxis and vasculature (Q5061529) (← links)
- Global solvability and stabilization to a cancer invasion model with remodelling of ECM (Q5130935) (← links)
- Negligibility of haptotaxis effect in a chemotaxis–haptotaxis model (Q5164239) (← links)
