Pages that link to "Item:Q3056451"
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The following pages link to ASYMPTOTIC BEHAVIOR OF GLOBAL SOLUTIONS TO A MODEL OF CELL INVASION (Q3056451):
Displayed 50 items.
- Boundedness in a quasilinear chemotaxis-haptotaxis system with logistic source (Q294043) (← links)
- Boundedness of solutions to a quasilinear higher-dimensional chemotaxis-haptotaxis model with nonlinear diffusion (Q501454) (← links)
- Global existence of a two-dimensional chemotaxis-haptotaxis model with remodeling of non-diffusible attractant (Q526015) (← links)
- Boundedness in the higher-dimensional chemotaxis-haptotaxis model with nonlinear diffusion (Q890222) (← links)
- A density-dependent chemotaxis-haptotaxis system modeling cancer invasion (Q968855) (← links)
- Critical mass for infinite-time aggregation in a chemotaxis model with indirect signal production (Q1687383) (← links)
- Singular structure formation in a degenerate haptotaxis model involving myopic diffusion (Q1707304) (← links)
- Asymptotic stability in a quasilinear chemotaxis-haptotaxis model with general logistic source and nonlinear signal production (Q2003944) (← links)
- A new result for boundedness in the quasilinear parabolic-parabolic Keller-Segel model (with logistic source) (Q2004591) (← links)
- Boundedness of solutions to a quasilinear chemotaxis-haptotaxis model (Q2007228) (← links)
- Global boundedness of classical solutions to a two species cancer invasion haptotaxis model with tissue remodeling (Q2009311) (← links)
- Nonlocal adhesion models for two cancer cell phenotypes in a multidimensional bounded domain (Q2021517) (← 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)
- Propagation of chaos in the nonlocal adhesion models for two cancer cell phenotypes (Q2083231) (← links)
- Finite time blow-up in the higher dimensional parabolic-elliptic-ODE minimal chemotaxis-haptotaxis system (Q2168015) (← links)
- Cellular transport through nonlinear mechanical waves in fibrous and absorbing biological tissues (Q2169595) (← links)
- Global asymptotic stability in a chemotaxis-growth model for tumor invasion (Q2178726) (← links)
- A critical virus production rate for blow-up suppression in a haptotaxis model for oncolytic virotherapy (Q2188508) (← links)
- Solving a chemotaxis-haptotaxis system in 2D using generalized finite difference method (Q2194796) (← links)
- Global boundedness in a three-dimensional chemotaxis-haptotaxis model (Q2203941) (← 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)
- Global existence for a chemotaxis-haptotaxis model with \(p\)-Laplacian (Q2300983) (← links)
- Large time behavior of solutions to a fully parabolic chemotaxis-haptotaxis model in \(N\) dimensions (Q2423238) (← 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)
- 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)
- Global boundedness in an oncolytic virotherapy model with generalized logistic source (Q2679221) (← links)
- Chemotactic cross-diffusion in complex frameworks (Q2830974) (← links)
- Global existence for a go-or-grow multiscale model for tumor invasion with therapy (Q2830979) (← links)
- Boundedness and stabilization in a multi-dimensional chemotaxis—haptotaxis model (Q2935511) (← links)
- A quasilinear chemotaxis-haptotaxis model: The roles of nonlinear diffusion and logistic source (Q2978111) (← links)
- Large Time Behavior in a Multidimensional Chemotaxis-Haptotaxis Model with Slow Signal Diffusion (Q3451747) (← links)
- Boundedness and large time behavior in a quasilinear chemotaxis model for tumor invasion (Q4569328) (← links)
- Global boundedness of solutions to a chemotaxis–haptotaxis model with tissue remodeling (Q4630535) (← links)
- CONVERGENCE OF A CANCER INVASION MODEL TO A LOGISTIC CHEMOTAXIS MODEL (Q4910885) (← 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)
- Global solutions to a haptotaxis system with a potentially degenerate diffusion tensor in two and three dimensions (Q5060031) (← links)
- A Glioblastoma PDE-ODE model including chemotaxis and vasculature (Q5061529) (← links)
- Chemotaxis and cross-diffusion models in complex environments: Models and analytic problems toward a multiscale vision (Q5083464) (← links)
- (Q5096487) (← links)