Pages that link to "Item:Q286427"

The following pages link to Boundedness in a three-dimensional chemotaxis-haptotaxis model (Q286427):

Displaying 50 items.

• Boundedness in a multi-dimensional chemotaxis-haptotaxis model with nonlinear diffusion (Q285105) (← links)
• Global dynamics in a fully parabolic chemotaxis system with logistic source (Q321614) (← links)
• Global boundedness and decay for a multi-dimensional chemotaxis-haptotaxis system with nonlinear diffusion (Q321731) (← 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)
• Global boundedness in a two-competing-species chemotaxis system with two chemicals (Q522543) (← links)
• Global existence of a two-dimensional chemotaxis-haptotaxis model with remodeling of non-diffusible attractant (Q526015) (← links)
• Boundedness and asymptotic behavior of solutions to a chemotaxis-haptotaxis model in high dimensions (Q894410) (← links)
• Global boundedness of solutions to a quasilinear parabolic-parabolic Keller-Segel system with logistic source (Q900992) (← links)
• Finite-time blow-up in low-dimensional Keller-Segel systems with logistic-type superlinear degradation (Q1635943) (← links)
• Boundedness and global solvability to a chemotaxis-haptotaxis model with slow and fast diffusion (Q1671109) (← links)
• Global solvability and large time behavior to a chemotaxis-haptotaxis model with nonlinear diffusion (Q1729227) (← links)
• Global existence and boundedness in a chemotaxis-haptotaxis system with signal-dependent sensitivity (Q1748313) (← 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 in the higher dimensional attraction-repulsion chemotaxis-growth system (Q2012694) (← links)
• Global classical solutions to an oncolytic viral therapy model with triply haptotactic terms (Q2026546) (← 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)
• Global attractors in a two-species chemotaxis system with two chemicals and logistic sources (Q2062599) (← links)
• Global boundedness for a \(N\)-dimensional two species cancer invasion haptotaxis model with tissue remodeling (Q2064499) (← links)
• Boundedness of solutions to a quasilinear parabolic-parabolic chemotaxis model with variable logistic source (Q2082154) (← links)
• Optimal control for a chemotaxis-haptotaxis model in two space dimensions (Q2098274) (← links)
• Boundedness in a quasilinear chemotaxis-haptotaxis model of parabolic-parabolic-ODE type (Q2108363) (← links)
• Global dynamics of a three-species spatial food chain model (Q2152754) (← links)
• Finite time blow-up in the higher dimensional parabolic-elliptic-ODE minimal chemotaxis-haptotaxis system (Q2168015) (← links)
• Boundedness in a quasilinear fully parabolic Keller-Segel system via maximal Sobolev regularity (Q2178727) (← links)
• Solving a chemotaxis-haptotaxis system in 2D using generalized finite difference method (Q2194796) (← links)
• A new (and optimal) result for the boundedness of a solution of a quasilinear chemotaxis-haptotaxis model (with a logistic source) (Q2195158) (← links)
• Boundedness in a high-dimensional forager-exploiter model with nonlinear resource consumption by two species (Q2198145) (← links)
• Global boundedness in a three-dimensional chemotaxis-haptotaxis model (Q2203941) (← links)
• Boundedness and stabilization enforced by mild saturation of taxis in a producer-scrounger model (Q2215479) (← links)
• Critical mass for infinite-time blow-up in a haptotaxis system with nonlinear zero-order interaction (Q2229257) (← 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)
• Finite-time blow-up and global boundedness for chemotaxis system with strong logistic dampening (Q2304875) (← links)
• Fluid interaction does not affect the critical exponent in a three-dimensional Keller-Segel-Stokes model (Q2306973) (← 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)
• Large time behavior in the logistic Keller-Segel model via maximal Sobolev regularity (Q2364739) (← links)
• A chemotaxis-haptotaxis system with haptoattractant remodeling: boundedness enforced by mild saturation of signal production (Q2415191) (← links)
• Large time behavior of solutions to a fully parabolic chemotaxis-haptotaxis model in \(N\) dimensions (Q2423238) (← links)
• A new result for global solvability and boundedness in the \(N\)-dimensional quasilinear chemotaxis model with logistic source and consumption of chemoattractant (Q2633772) (← links)
• On a chemotaxis-type Solow-Swan model for economic growth with capital-induced labor migration (Q2668936) (← 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)
• Global boundedness in a parabolic-parabolic-elliptic attraction-repulsion chemotaxis system with nonlinear productions (Q2697269) (← links)
• A quasilinear chemotaxis-haptotaxis model: The roles of nonlinear diffusion and logistic source (Q2978111) (← 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)
• A New Result for Global Solvability of a Two Species Cancer Invasion Haptotaxis Model with Tissue Remodeling (Q5020856) (← links)