Pages that link to "Item:Q4910885"
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The following pages link to CONVERGENCE OF A CANCER INVASION MODEL TO A LOGISTIC CHEMOTAXIS MODEL (Q4910885):
Displayed 50 items.
- On the boundedness and decay of solutions for a chemotaxis-haptotaxis system with nonlinear diffusion (Q256196) (← links)
- Global boundedness and decay for a multi-dimensional chemotaxis-haptotaxis system with nonlinear diffusion (Q321731) (← links)
- Blow-up prevention by logistic sources in a parabolic-elliptic Keller-Segel system with singular sensitivity (Q399091) (← links)
- Boundedness in a fully parabolic chemotaxis system with singular sensitivity (Q482001) (← links)
- Persistence of mass in a chemotaxis system with logistic source (Q496738) (← links)
- Boundedness of solutions to a quasilinear higher-dimensional chemotaxis-haptotaxis model with nonlinear diffusion (Q501454) (← links)
- Global existence of a two-dimensional chemotaxis-haptotaxis model with remodeling of non-diffusible attractant (Q526015) (← links)
- A study on time discretization and adaptive mesh refinement methods for the simulation of cancer invasion: the urokinase model (Q668491) (← links)
- On the fractional Fisher information with applications to a hyperbolic-parabolic system of chemotaxis (Q729889) (← links)
- Singular structure formation in a degenerate haptotaxis model involving myopic diffusion (Q1707304) (← links)
- Global solvability and large time behavior to a chemotaxis-haptotaxis model with nonlinear diffusion (Q1729227) (← links)
- Global existence for an attraction-repulsion chemotaxis fluid model with logistic source (Q1755920) (← links)
- Existence and uniqueness of global classical solutions to a two dimensional two species cancer invasion haptotaxis model (Q1756887) (← links)
- A quasilinear predator-prey model with indirect prey-taxis (Q1981909) (← 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)
- A multiscale mathematical model of tumour invasive growth (Q2012304) (← links)
- Convergence and positivity of finite element methods for a haptotaxis model of tumoral invasion (Q2019563) (← links)
- Global weak solutions to an oncolytic viral therapy model with doubly haptotactic terms (Q2025878) (← links)
- On a fully parabolic singular chemotaxis-(growth) system with indirect signal production or consumption (Q2026413) (← links)
- Modeling multiple taxis: tumor invasion with phenotypic heterogeneity, haptotaxis, and unilateral interspecies repellence (Q2026618) (← links)
- Asymptotic behavior of a quasilinear Keller-Segel system with signal-suppressed motility (Q2048901) (← links)
- Global dynamics of a chemotaxis model with signal-dependent diffusion and sensitivity (Q2056186) (← links)
- Global existence in a chemotaxis system with singular sensitivity and signal production (Q2064500) (← links)
- Analysis of a new multispecies tumor growth model coupling 3D phase-fields with a 1D vascular network (Q2066556) (← links)
- Mathematical modeling of gastro-intestinal metastasis resistance to tyrosine kinase inhibitors (Q2088494) (← links)
- Boundedness in a quasilinear chemotaxis-haptotaxis model of parabolic-parabolic-ODE type (Q2108363) (← links)
- Global solvability and stabilization in a three-dimensional cross-diffusion system modeling urban crime propagation (Q2125058) (← links)
- Numerical analysis of a chemotaxis model for tumor invasion (Q2135623) (← links)
- Convergence rate estimates of a higher-dimension reaction-diffusion system with density-dependent motility (Q2155964) (← links)
- Finite time blow-up in the higher dimensional parabolic-elliptic-ODE minimal chemotaxis-haptotaxis system (Q2168015) (← links)
- A new result for global solvability in a singular chemotaxis-growth system with indirect signal production (Q2172472) (← links)
- Boundedness and homogeneous asymptotics for a fractional logistic Keller-Segel equations (Q2178723) (← links)
- Global classical solutions and convergence to a mathematical model for cancer cells invasion and metastatic spread (Q2180603) (← links)
- Boundedness and asymptotics of a reaction-diffusion system with density-dependent motility (Q2189784) (← links)
- Finite-time blow-up of solutions to a cancer invasion mathematical model with haptotaxis effects (Q2203925) (← 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)
- Modeling and simulation of vascular tumors embedded in evolving capillary networks (Q2237476) (← links)
- Boundedness and asymptotic behavior to a chemotaxis system with indirect signal generation and singular sensitivity (Q2244272) (← links)
- Boundedness and asymptotic behavior to a chemotaxis-fluid system with singular sensitivity and logistic source (Q2287343) (← links)
- Global solvability and stabilization in a two-dimensional cross-diffusion system modeling urban crime propagation (Q2323962) (← links)
- Global boundedness in a quasilinear chemotaxis system with signal-dependent sensitivity (Q2347152) (← links)
- Boundedness in a fully parabolic chemotaxis system with strongly singular sensitivity (Q2349468) (← links)
- Galerkin finite element method for cancer invasion mathematical model (Q2403861) (← links)
- A chemotaxis-haptotaxis system with haptoattractant remodeling: boundedness enforced by mild saturation of signal production (Q2415191) (← links)
- Large time behavior of solutions to a fully parabolic chemotaxis-haptotaxis model in \(N\) dimensions (Q2423238) (← 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)
- Stabilization to a cancer invasion model with remodeling mechanism and slow diffusion (Q2675220) (← links)