Global classical solution and boundedness to a chemotaxis-haptotaxis model with re-establishment mechanisms
From MaRDI portal
(Redirected from Publication:4583629)
Recommendations
- Global boundedness in a three-dimensional chemotaxis-haptotaxis model
- Global boundedness of solutions to a chemotaxis-haptotaxis model with tissue remodeling
- Boundedness of solutions to a quasilinear chemotaxis-haptotaxis model
- Global boundedness to a chemotaxis-haptotaxis model with nonlinear diffusion
- Boundedness in a three-dimensional chemotaxis-haptotaxis model
Cited in
(61)- Global solvability and large time behavior to a chemotaxis-haptotaxis model with nonlinear diffusion
- Global solvability and boundedness to a coupled chemotaxis-fluid model with arbitrary porous medium diffusion
- Boundedness and global solvability to a chemotaxis model with nonlinear diffusion
- Global boundedness of classical solutions to a two species cancer invasion haptotaxis model with tissue remodeling
- Global bounded weak solutions and asymptotic behavior to a chemotaxis-Stokes model with non-Newtonian filtration slow diffusion
- Modeling multiple taxis: tumor invasion with phenotypic heterogeneity, haptotaxis, and unilateral interspecies repellence
- Analysis of a two-dimensional triply haptotactic model with a fusogenic oncolytic virus and syncytia
- Global boundedness for a \(N\)-dimensional two species cancer invasion haptotaxis model with tissue remodeling
- Global classical solutions to a higher-dimensional doubly haptotactic cross-diffusion system modeling oncolytic virotherapy
- Global classical solvability and stabilization in a reaction-diffusion intraguild predation model with chemotaxis
- Global dynamics of a three-species spatial food chain model
- Global classical solutions and convergence to a mathematical model for cancer cells invasion and metastatic spread
- Global solvability and optimal control to a haptotaxis cancer invasion model with two cancer cell species
- Global classical solutions to a doubly haptotactic cross-diffusion system modeling oncolytic virotherapy
- Global existence for a chemotaxis-haptotaxis model with \(p\)-Laplacian
- 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
- Global existence and boundedness in a two-species chemotaxis system with nonlinear diffusion
- Stabilization to a cancer invasion model with remodeling mechanism and slow diffusion
- Global boundedness of solutions to a chemotaxis-haptotaxis model with tissue remodeling
- A new result for global solvability of a two species cancer invasion haptotaxis model with tissue remodeling
- Global boundedness in a chemotaxis-haptotaxis model with nonlinear diffusion and signal production
- Global solvability and stabilization to a cancer invasion model with remodelling of ECM
- Negligibility of haptotaxis effect in a chemotaxis-haptotaxis model
- Global weak solutions in a three-dimensional two-species cancer invasion haptotaxis model without cell proliferation
- Global solvability, pattern formation and stability to a chemotaxis-haptotaxis model with porous medium diffusion
- Uniform boundedness and eventual Hölder continuity to a cancer invasion model with remodeling of ECM and nonlinear diffusion
- Qualitative properties for a three-species food chain model with cross-diffusion and intra-specific competition
- Boundedness in a two-dimensional two-species cancer invasion haptotaxis model without cell proliferation
- Global boundedness for a food chain model with general logistic source
- Global weak solutions for an attraction-repulsion chemotaxis system with \(p\)-Laplacian diffusion and logistic source
- Boundedness of solutions to a chemotaxis-haptotaxis model with nonlocal terms
- Global boundedness of weak solutions for an attraction-repulsion chemotaxis system with p-Laplacian diffusion and nonlinear production
- Global boundedness of a three-species predator-prey model with prey-taxis and competition
- A chemotaxis‐Stokes system with nonhomogeneous boundary condition: Global large‐datum solution and asymptotic behavior
- Boundedness and stabilization in a haptotaxis model of oncolytic virotherapy with nonlinear sensitivity
- Global well-posedness and long-time behavior in a tumor invasion model with cross-diffusion
- Global boundedness and stability of a predator-prey model with alarm-taxis
- A quasilinear chemotaxis-haptotaxis system: existence and blow-up results
- Global strong solution and periodic dynamic behavior to Chaplain-Lolas model
- Negligibility of haptotaxis on global dynamics in a chemotaxis-haptotaxis system with indirect signal production
- Global solutions to a density-suppressed motility system modeling oncolytic virotherapy
- Critical exponent to a cancer invasion model with nonlinear diffusion
- Global boundedness and asymptotic stability for a food chain model with nonlinear diffusion
- Global boundedness of solutions to a food chain model with nonlinear taxis sensitivity
- Global well-posedness to a parabolic-degenerate angiogenesis system
- Global existence and boundedness of weak solutions for a three-species predator-prey system with p-Laplacian diffusion
- Global weak solutions in a 3D chemotaxis-Stokes system with doubly degenerate diffusion
- Global boundedness of a forager-exploiter model with nonlinear tactic sensitivity and logistic source
- Boundedness of solutions to an alarm-taxis model with/without growth sources
- Global existence in a three-dimensional chemotaxis-Stokes system with p-Laplacian diffusion and singular sensitivity
- Global existence of solutions to a quasilinear three-species spatial food chain model
- Boundedness and global existence in a higher-dimensional parabolic-elliptic-ODE chemotaxis-haptotaxis model with remodeling of non-diffusible attractant
- Global existence for a three-species predator-prey model with slow p-Laplacian diffusion
- Global boundedness of Lotka-Volterra competition system with cross-diffusion
- Global boundedness and stability to a three-species food chain model with density-dependent motion
- A finite element approach to the Keller-Segel chemotaxis system with impact of nonlocal diffusion
- Boundedness and global solvability for a three-dimensional nonlinear chemotaxis system with indirect signal consumption
- Critical exponents to a chemotaxis-haptotaxis model with slow and fast diffusion
- Existence and boundedness of global weak solutions in three-dimensional predator-prey system including slow p-Laplacian diffusion dynamics
- Global classical solution of chemotaxis-haptotaxis model with re-establishment mechanisms
- Global weak solutions in a doubly degenerate chemotaxis-Stokes system with rotation
This page was built for publication: Global classical solution and boundedness to a chemotaxis-haptotaxis model with re-establishment mechanisms
Report a bug (only for logged in users!)Click here to report a bug for this page (MaRDI item Q4583629)
