Pages that link to "Item:Q3560028"
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The following pages link to BOUNDEDNESS OF SOLUTIONS OF A HAPTOTAXIS MODEL (Q3560028):
Displayed 50 items.
- Boundedness in a quasilinear chemotaxis-haptotaxis system with logistic source (Q294043) (← links)
- Existence of solutions and optimal control for a model of tissue invasion by solid tumours (Q401410) (← 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)
- A study on time discretization and adaptive mesh refinement methods for the simulation of cancer invasion: the urokinase model (Q668491) (← links)
- Blow-up in a higher-dimensional chemotaxis system despite logistic growth restriction (Q719554) (← 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)
- 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)
- 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)
- Convergence and positivity of finite element methods for a haptotaxis model of tumoral invasion (Q2019563) (← links)
- Global weak solutions to an oncolytic viral therapy model with doubly haptotactic terms (Q2025878) (← links)
- Global boundedness for a \(N\)-dimensional two species cancer invasion haptotaxis model with tissue remodeling (Q2064499) (← links)
- Optimal control for a chemotaxis-haptotaxis model in two space dimensions (Q2098274) (← 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)
- 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 new (and optimal) result for the boundedness of a solution of a quasilinear chemotaxis-haptotaxis model (with a logistic source) (Q2195158) (← 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)
- 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)
- 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)
- Chemotactic cross-diffusion in complex frameworks (Q2830974) (← 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)
- 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)
- On the derivation of angiogenesis tissue models: From the micro-scale to the macro-scale (Q2950693) (← links)
- Global existence and uniqueness of positive solutions and optimal control for a novel model of pest control (Q2978084) (← links)
- A quasilinear chemotaxis-haptotaxis model: The roles of nonlinear diffusion and logistic source (Q2978111) (← links)
- Boundedness and large time behavior in a quasilinear chemotaxis model for tumor invasion (Q4569328) (← links)
- Existence of Solutions and Local Null Controllability for a Model of Tissue Invasion by Solid Tumors (Q4570978) (← 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)
- CONVERGENCE OF A CANCER INVASION MODEL TO A LOGISTIC CHEMOTAXIS MODEL (Q4910885) (← 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 Glioblastoma PDE-ODE model including chemotaxis and vasculature (Q5061529) (← links)
- (Q5096487) (← links)
- Mathematical Research for Models Which is Related to Chemotaxis System (Q5110837) (← links)
- A Hybrid Multiscale Model for Cancer Invasion of the Extracellular Matrix (Q5112048) (← links)