The following pages link to (Q5453781):
Displaying 14 items.
- Global boundedness of classical solutions to a two species cancer invasion haptotaxis model with tissue remodeling (Q2009311) (← links)
- Global boundedness for a \(N\)-dimensional two species cancer invasion haptotaxis model with tissue remodeling (Q2064499) (← links)
- Finite time blow-up in the higher dimensional parabolic-elliptic-ODE minimal chemotaxis-haptotaxis system (Q2168015) (← links)
- Global boundedness in a three-dimensional chemotaxis-haptotaxis model (Q2203941) (← links)
- Global dynamics of a tumor invasion model with/without logistic source (Q2230532) (← links)
- Global solvability and optimal control to a haptotaxis cancer invasion model with two cancer cell species (Q2234289) (← links)
- Boundedness and large time behavior in a quasilinear chemotaxis model for tumor invasion (Q4569328) (← links)
- Existence of global solution to a two-species Keller–Segel chemotaxis model (Q4636787) (← links)
- A New Result for Global Solvability of a Two Species Cancer Invasion Haptotaxis Model with Tissue Remodeling (Q5020856) (← 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)
- Global weak solutions in a three-dimensional two-species cancer invasion haptotaxis model without cell proliferation (Q5884846) (← links)
- Global existence of classical solutions and numerical simulations of a cancer invasion model (Q6073731) (← links)
- Boundedness in a two-dimensional two-species cancer invasion haptotaxis model without cell proliferation (Q6102488) (← links)
