Pages that link to "Item:Q4630535"

The following pages link to Global boundedness of solutions to a chemotaxis–haptotaxis model with tissue remodeling (Q4630535):

Displaying 41 items.

• Global boundedness of classical solutions to a two species cancer invasion haptotaxis model with tissue remodeling (Q2009311) (← links)
• Theoretical analysis for a PDE-ODE system related to a glioblastoma tumor with vasculature (Q2026401) (← links)
• Modeling multiple taxis: tumor invasion with phenotypic heterogeneity, haptotaxis, and unilateral interspecies repellence (Q2026618) (← links)
• Theoretical and numerical analysis for a hybrid tumor model with diffusion depending on vasculature (Q2041715) (← 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 for a chemotaxis consumption system with signal-dependent motility and logistic source (Q2111980) (← links)
• Global classical solutions and convergence to a mathematical model for cancer cells invasion and metastatic spread (Q2180603) (← links)
• A critical virus production rate for blow-up suppression in a haptotaxis model for oncolytic virotherapy (Q2188508) (← links)
• Boundedness in a haptotactic cross-diffusion system modeling oncolytic virotherapy (Q2208440) (← 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)
• Global classical solutions to a doubly haptotactic cross-diffusion system modeling oncolytic virotherapy (Q2297246) (← 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)
• Dampening effect of logistic source in a two-dimensional haptotaxis system with nonlinear zero-order interaction (Q2657693) (← links)
• Global generalized solutions of a haptotaxis model describing cancer cells invasion and metastatic spread (Q2669230) (← links)
• Stabilization to a cancer invasion model with remodeling mechanism and slow diffusion (Q2675220) (← links)
• Global boundedness in an oncolytic virotherapy model with generalized logistic source (Q2679221) (← links)
• Cross-diffusion models: Analytic and multiscale problems (Q4630530) (← links)
• A multiscale view of nonlinear diffusion in biology: From cells to tissues (Q4972954) (← links)
• Asymptotic behavior of solutions to a tumor angiogenesis model with chemotaxis–haptotaxis (Q4973287) (← links)
• A New Result for Global Solvability of a Two Species Cancer Invasion Haptotaxis Model with Tissue Remodeling (Q5020856) (← links)
• A critical virus production rate for efficiency of oncolytic virotherapy (Q5056748) (← 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)
• Chemotaxis and cross-diffusion models in complex environments: Models and analytic problems toward a multiscale vision (Q5083464) (← links)
• Contraction for large perturbations of traveling waves in a hyperbolic–parabolic system arising from a chemotaxis model (Q5112028) (← 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)
• A new result for 2D boundedness of solutions to a chemotaxis–haptotaxis model with/without sub-logistic source (Q5243473) (← links)
• Asymptotic stability of spatial homogeneity in a haptotaxis model for oncolytic virotherapy (Q5861961) (← links)
• Global weak solutions in a three-dimensional two-species cancer invasion haptotaxis model without cell proliferation (Q5884846) (← links)
• Global boundedness of weak solutions to a chemotaxis-haptotaxis model with \(p\)-Laplacian diffusion (Q6054930) (← links)
• Asymptotic behavior of a three-dimensional haptotactic cross-diffusion system modeling oncolytic virotherapy (Q6057512) (← links)
• Uniform boundedness and eventual Hölder continuity to a cancer invasion model with remodeling of ECM and nonlinear diffusion (Q6089580) (← links)
• Boundedness of solutions in a predator-prey system with density-dependent motilities and indirect pursuit-evasion interaction (Q6099560) (← links)
• Boundedness in a two-dimensional two-species cancer invasion haptotaxis model without cell proliferation (Q6102488) (← links)
• Asymptotic behaviour in a doubly haptotactic cross-diffusion model for oncolytic virotherapy (Q6111246) (← links)
• Boundedness of solutions to a fully parabolic indirect pursuit-evasion predator-prey system with density-dependent diffusion in \(\mathbb{R}^2\) (Q6127149) (← links)
• Boundedness and large time behavior of solutions of a higher-dimensional haptotactic system modeling oncolytic virotherapy (Q6166572) (← links)
• Cross-diffusion models in complex frameworks from microscopic to macroscopic (Q6166573) (← links)