Pages that link to "Item:Q611260"

The following pages link to Global existence for a haptotaxis model of cancer invasion with tissue remodeling (Q611260):

Displaying 48 items.

• Boundedness in a three-dimensional chemotaxis-haptotaxis model (Q286427) (← links)
• Mathematical model of growth factor driven haptotaxis and proliferation in a tissue engineering scaffold (Q376427) (← links)
• Periodic solutions of angiogenesis models with time lags (Q420044) (← links)
• Global existence for a degenerate haptotaxis model of cancer invasion (Q506394) (← links)
• Global existence of a two-dimensional chemotaxis-haptotaxis model with remodeling of non-diffusible attractant (Q526015) (← links)
• About a generalized model of lymphoma (Q643586) (← links)
• Nonlinear stability of a heterogeneous state in a PDE-ODE model for acid-mediated tumor invasion (Q746560) (← links)
• Singular structure formation in a degenerate haptotaxis model involving myopic diffusion (Q1707304) (← links)
• Existence and uniqueness of global classical solutions to a two dimensional two species cancer invasion haptotaxis model (Q1756887) (← links)
• The triplex vaccine effects in mammary carcinoma: a nonlinear model in tune with SimTriplex (Q1926169) (← links)
• 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)
• Blow-up phenomena of a cancer invasion model with nonlinear diffusion and haptotaxis term (Q2021582) (← links)
• Global weak solutions to an oncolytic viral therapy model with doubly haptotactic terms (Q2025878) (← links)
• Global classical solutions to an oncolytic viral therapy model with triply haptotactic terms (Q2026546) (← links)
• Solvability of solid tumor invasion model (Q2038372) (← links)
• Dampening effects on global boundedness and asymptotic behavior in an oncolytic virotherapy model (Q2054010) (← links)
• Global boundedness for a \(N\)-dimensional two species cancer invasion haptotaxis model with tissue remodeling (Q2064499) (← links)
• Analysis of a new multispecies tumor growth model coupling 3D phase-fields with a 1D vascular network (Q2066556) (← links)
• Global classical solutions to a higher-dimensional doubly haptotactic cross-diffusion system modeling oncolytic virotherapy (Q2087609) (← links)
• Numerical analysis of a chemotaxis model for tumor invasion (Q2135623) (← links)
• Finite time blow-up in the higher dimensional parabolic-elliptic-ODE minimal chemotaxis-haptotaxis system (Q2168015) (← links)
• Global asymptotic stability in a chemotaxis-growth model for tumor invasion (Q2178726) (← links)
• Global classical solutions and convergence to a mathematical model for cancer cells invasion and metastatic spread (Q2180603) (← links)
• Finite-time blow-up of solutions to a cancer invasion mathematical model with haptotaxis effects (Q2203925) (← links)
• Global boundedness in a three-dimensional chemotaxis-haptotaxis model (Q2203941) (← links)
• Boundedness in a haptotactic cross-diffusion system modeling oncolytic virotherapy (Q2208440) (← links)
• Existence of solutions of cancer invasion parabolic system with integrable data (Q2211840) (← 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)
• Energy-type estimates and global solvability in a two-dimensional chemotaxis-haptotaxis model with remodeling of non-diffusible attractant (Q2451888) (← links)
• Stabilization in a chemotaxis model for tumor invasion (Q2515675) (← links)
• Global generalized solutions of a haptotaxis model describing cancer cells invasion and metastatic spread (Q2669230) (← links)
• Analysis of a chemotaxis system modeling ant foraging (Q2816545) (← links)
• From a multiscale derivation of nonlinear cross-diffusion models to Keller–Segel models in a Navier–Stokes fluid (Q2830975) (← links)
• Global existence for a go-or-grow multiscale model for tumor invasion with therapy (Q2830979) (← links)
• Two positivity preserving flux limited, second-order numerical methods for a haptotaxis model (Q2846176) (← links)
• ON THE ASYMPTOTIC THEORY FROM MICROSCOPIC TO MACROSCOPIC GROWING TISSUE MODELS: AN OVERVIEW WITH PERSPECTIVES (Q2891186) (← links)
• Boundedness and stabilization in a multi-dimensional chemotaxis—haptotaxis model (Q2935511) (← links)
• A note for global existence of a two-dimensional chemotaxis–haptotaxis model with remodeling of non-diffusible attractant (Q4585726) (← 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)
• Some further progress for boundedness of solutions to a quasilinear higher-dimensional chemotaxis-haptotaxis model with nonlinear diffusion (Q6091068) (← links)
• Global existence of a diffusive predator-prey model with prey-stage structure and prey-taxis (Q6102384) (← links)
• Boundedness in a two-dimensional two-species cancer invasion haptotaxis model without cell proliferation (Q6102488) (← links)
• The vanishing viscosity limit on a model of Kareiva-Odell type in 2D (Q6139067) (← links)