Pages that link to "Item:Q3531236"

The following pages link to Global solution for a chemotactic–haptotactic model of cancer invasion (Q3531236):

Displaying 50 items.

• On the boundedness and decay of solutions for a chemotaxis-haptotaxis system with nonlinear diffusion (Q256196) (← links)
• Boundedness in a three-dimensional chemotaxis-haptotaxis model (Q286427) (← links)
• Boundedness in a quasilinear chemotaxis-haptotaxis system with logistic source (Q294043) (← links)
• On a parabolic-elliptic system with chemotaxis and logistic type growth (Q306242) (← links)
• Global boundedness and decay for a multi-dimensional chemotaxis-haptotaxis system with nonlinear diffusion (Q321731) (← links)
• Mini-workshop: Mathematical models for cancer cell migration. Abstracts from the mini-workshop held April 13--19, 2014. (Q347199) (← links)
• Global existence of classical solutions to a three-species predator-prey model with two prey-taxes (Q411076) (← links)
• Global existence of classical solutions to an acid-mediated invasion model for tumor-stromal interactions (Q470836) (← links)
• The global existence of solutions for two classes of chemotaxis models (Q477463) (← links)
• Boundedness of solutions to a quasilinear higher-dimensional chemotaxis-haptotaxis model with nonlinear diffusion (Q501454) (← links)
• Boundedness in a three-dimensional chemotaxis-haptotaxis model with nonlinear diffusion (Q514389) (← links)
• Existence and uniqueness of solutions of degenerate chemotaxis system (Q514782) (← links)
• Global existence of classical solutions to the cross-diffusion three-species model with prey-taxis (Q516693) (← links)
• Global existence of a two-dimensional chemotaxis-haptotaxis model with remodeling of non-diffusible attractant (Q526015) (← links)
• Global existence for a haptotaxis model of cancer invasion with tissue remodeling (Q611260) (← links)
• Existence and uniqueness of solutions of predator-prey type model with mixed boundary conditions (Q645009) (← links)
• Global existence and boundedness of a chemotaxis model with indirect production and general kinetic function (Q777341) (← 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)
• Global existence of classical solutions to a predator-prey model with nonlinear prey-taxis (Q974624) (← links)
• Global existence of classical solutions to a combined chemotaxis-haptotaxis model with logistic source (Q1018160) (← links)
• Global solvability and large time behavior to a chemotaxis-haptotaxis model with nonlinear diffusion (Q1729227) (← links)
• Mini-workshop: PDE models of motility and invasion in active biosystems. Abstracts from the mini-workshop held October 22--28, 2017 (Q1731958) (← links)
• Boundedness in the higher-dimensional quasilinear chemotaxis-growth system with indirect attractant production (Q1732534) (← links)
• Boundedness of solutions for a quasilinear chemotaxis-haptotaxis model (Q1982567) (← links)
• Asymptotic stability in a quasilinear chemotaxis-haptotaxis model with general logistic source and nonlinear signal production (Q2003944) (← links)
• Boundedness of solutions to a quasilinear chemotaxis-haptotaxis model (Q2007228) (← links)
• Nonlocal adhesion models for two cancer cell phenotypes in a multidimensional bounded domain (Q2021517) (← links)
• Global existence of classical solutions to a chemotaxis-haptotaxis model (Q2022953) (← links)
• Modeling multiple taxis: tumor invasion with phenotypic heterogeneity, haptotaxis, and unilateral interspecies repellence (Q2026618) (← links)
• Analysis of a two-dimensional triply haptotactic model with a fusogenic oncolytic virus and syncytia (Q2035753) (← links)
• Solvability of solid tumor invasion model (Q2038372) (← links)
• Propagation of chaos in the nonlocal adhesion models for two cancer cell phenotypes (Q2083231) (← links)
• Boundedness and asymptotic stability in a two-species predator-prey chemotaxis model (Q2090344) (← links)
• Boundedness in a quasilinear chemotaxis-haptotaxis model of parabolic-parabolic-ODE type (Q2108363) (← links)
• Boundedness of the higher-dimensional quasilinear chemotaxis system with generalized logistic source (Q2153375) (← links)
• Boundedness and asymptotic stability in a predator-prey chemotaxis system with indirect pursuit-evasion dynamics (Q2157869) (← links)
• Finite time blow-up in the higher dimensional parabolic-elliptic-ODE minimal chemotaxis-haptotaxis system (Q2168015) (← links)
• Global classical solutions and convergence to a mathematical model for cancer cells invasion and metastatic spread (Q2180603) (← links)
• What mathematical models can or cannot do in glioma description and understanding (Q2206309) (← links)
• Global solution for a general cross-diffusion two-competitive-predator and one-prey system with predator-taxis (Q2208133) (← links)
• Existence of solutions of cancer invasion parabolic system with integrable data (Q2211840) (← links)
• Global dynamics of a two-species chemotaxis-consumption system with signal-dependent motilities (Q2215480) (← links)
• Mathematical and numerical analysis of an acid-mediated cancer invasion model with nonlinear diffusion (Q2218926) (← links)
• On the existence of weak solutions of nonlinear degenerate parabolic system with variable exponents (Q2314288) (← links)
• Global generalized solutions of a haptotaxis model describing cancer cells invasion and metastatic spread (Q2669230) (← links)
• Boundedness in a two-dimensional attraction-repulsion system with nonlinear diffusion (Q2786696) (← links)
• A quasilinear chemotaxis-haptotaxis model: The roles of nonlinear diffusion and logistic source (Q2978111) (← links)
• ASYMPTOTIC BEHAVIOR OF GLOBAL SOLUTIONS TO A MODEL OF CELL INVASION (Q3056451) (← links)
• A note for global existence of a two-dimensional chemotaxis–haptotaxis model with remodeling of non-diffusible attractant (Q4585726) (← links)