Pages that link to "Item:Q526015"

The following pages link to Global existence of a two-dimensional chemotaxis-haptotaxis model with remodeling of non-diffusible attractant (Q526015):

Displaying 28 items.

• Boundedness of solutions for a quasilinear chemotaxis-haptotaxis model (Q1982567) (← links)
• Global boundedness of classical solutions to a two species cancer invasion haptotaxis model with tissue remodeling (Q2009311) (← links)
• The dampening role of large repulsive convection in a chemotaxis system modeling tumor angiogenesis (Q2019404) (← links)
• Modeling multiple taxis: tumor invasion with phenotypic heterogeneity, haptotaxis, and unilateral interspecies repellence (Q2026618) (← 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)
• Asymptotic behavior for solutions to an oncolytic virotherapy model involving triply haptotactic terms (Q2116231) (← 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 solvability and optimal control to a haptotaxis cancer invasion model with two cancer cell species (Q2234289) (← 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)
• Stabilization to a cancer invasion model with remodeling mechanism and slow diffusion (Q2675220) (← 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)
• 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)
• 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)
• Global solutions to a haptotaxis system with a potentially degenerate diffusion tensor in two and three dimensions (Q5060031) (← links)
• Global solvability and stabilization to a cancer invasion model with remodelling of ECM (Q5130935) (← links)
• A new result for 2D boundedness of solutions to a chemotaxis–haptotaxis model with/without sub-logistic source (Q5243473) (← links)
• Global weak solutions in a three-dimensional two-species cancer invasion haptotaxis model without cell proliferation (Q5884846) (← links)
• Uniform boundedness and eventual Hölder continuity to a cancer invasion model with remodeling of ECM and nonlinear diffusion (Q6089580) (← links)
• Boundedness in a two-dimensional two-species cancer invasion haptotaxis model without cell proliferation (Q6102488) (← links)
• Boundedness of solutions to a chemotaxis-haptotaxis model with nonlocal terms (Q6154863) (← links)
• Boundedness and stabilization in a haptotaxis model of oncolytic virotherapy with nonlinear sensitivity (Q6569354) (← links)
• Exact traveling wave solutions of one-dimensional models of cancer invasion (Q6586471) (← links)
• Global strong solution and periodic dynamic behavior to Chaplain-Lolas model (Q6612565) (← links)
• Critical exponent to a cancer invasion model with nonlinear diffusion (Q6632821) (← links)