Pages that link to "Item:Q4583629"

The following pages link to Global classical solution and boundedness to a chemotaxis-haptotaxis model with re-establishment mechanisms (Q4583629):

Displaying 42 items.

• Global solvability and large time behavior to a chemotaxis-haptotaxis model with nonlinear diffusion (Q1729227) (← links)
• Global solvability and boundedness to a coupled chemotaxis-fluid model with arbitrary porous medium diffusion (Q1743812) (← links)
• Boundedness and global solvability to a chemotaxis model with nonlinear diffusion (Q1785937) (← links)
• Global boundedness of classical solutions to a two species cancer invasion haptotaxis model with tissue remodeling (Q2009311) (← links)
• Global bounded weak solutions and asymptotic behavior to a chemotaxis-Stokes model with non-Newtonian filtration slow diffusion (Q2020209) (← links)
• Modeling multiple taxis: tumor invasion with phenotypic heterogeneity, haptotaxis, and unilateral interspecies repellence (Q2026618) (← 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)
• Global classical solutions to a higher-dimensional doubly haptotactic cross-diffusion system modeling oncolytic virotherapy (Q2087609) (← links)
• Global dynamics of a three-species spatial food chain model (Q2152754) (← links)
• Global classical solutions and convergence to a mathematical model for cancer cells invasion and metastatic spread (Q2180603) (← links)
• Global solvability and optimal control to a haptotaxis cancer invasion model with two cancer cell species (Q2234289) (← links)
• Global classical solutions to a doubly haptotactic cross-diffusion system modeling oncolytic virotherapy (Q2297246) (← links)
• Global existence for a chemotaxis-haptotaxis model with \(p\)-Laplacian (Q2300983) (← 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)
• Global existence and boundedness in a two-species chemotaxis system with nonlinear diffusion (Q2669033) (← links)
• Stabilization to a cancer invasion model with remodeling mechanism and slow diffusion (Q2675220) (← links)
• Global boundedness of solutions to a chemotaxis–haptotaxis model with tissue remodeling (Q4630535) (← links)
• A New Result for Global Solvability of a Two Species Cancer Invasion Haptotaxis Model with Tissue Remodeling (Q5020856) (← links)
• (Q5096487) (← 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)
• Global weak solutions in a three-dimensional two-species cancer invasion haptotaxis model without cell proliferation (Q5884846) (← links)
• Global solvability, pattern formation and stability to a chemotaxis-haptotaxis model with porous medium diffusion (Q6079310) (← links)
• Uniform boundedness and eventual Hölder continuity to a cancer invasion model with remodeling of ECM and nonlinear diffusion (Q6089580) (← links)
• Qualitative properties for a three-species food chain model with cross-diffusion and intra-specific competition (Q6097005) (← links)
• Boundedness in a two-dimensional two-species cancer invasion haptotaxis model without cell proliferation (Q6102488) (← links)
• Global weak solutions for an attraction-repulsion chemotaxis system with \(p\)-Laplacian diffusion and logistic source (Q6152122) (← links)
• Boundedness of solutions to a chemotaxis-haptotaxis model with nonlocal terms (Q6154863) (← links)
• Global boundedness of weak solutions for an attraction-repulsion chemotaxis system with p-Laplacian diffusion and nonlinear production (Q6155163) (← links)
• Global boundedness of a three-species predator-prey model with prey-taxis and competition (Q6165942) (← links)
• A chemotaxis‐Stokes system with nonhomogeneous boundary condition: Global large‐datum solution and asymptotic behavior (Q6202680) (← links)
• Boundedness and stabilization in a haptotaxis model of oncolytic virotherapy with nonlinear sensitivity (Q6569354) (← links)
• Global well-posedness and long-time behavior in a tumor invasion model with cross-diffusion (Q6575462) (← links)
• Global boundedness and stability of a predator-prey model with alarm-taxis (Q6577361) (← links)
• A quasilinear chemotaxis-haptotaxis system: existence and blow-up results (Q6584922) (← links)
• Global strong solution and periodic dynamic behavior to Chaplain-Lolas model (Q6612565) (← links)
• Negligibility of haptotaxis on global dynamics in a chemotaxis-haptotaxis system with indirect signal production (Q6615809) (← links)
• Global solutions to a density-suppressed motility system modeling oncolytic virotherapy (Q6622146) (← links)
• Critical exponent to a cancer invasion model with nonlinear diffusion (Q6632821) (← links)
• Global boundedness and asymptotic stability for a food chain model with nonlinear diffusion (Q6632826) (← links)
• Global boundedness of solutions to a food chain model with nonlinear taxis sensitivity (Q6657502) (← links)