Pages that link to "Item:Q5168067"

The following pages link to Dominance of chemotaxis in a chemotaxis–haptotaxis model (Q5168067):

Displaying 50 items.

• On the boundedness and decay of solutions for a chemotaxis-haptotaxis system with nonlinear diffusion (Q256196) (← links)
• Boundedness in a multi-dimensional chemotaxis-haptotaxis model with nonlinear diffusion (Q285105) (← links)
• Boundedness in a three-dimensional chemotaxis-haptotaxis model (Q286427) (← links)
• Boundedness in a quasilinear chemotaxis-haptotaxis system with logistic source (Q294043) (← 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)
• Persistence of mass in a chemotaxis system with logistic source (Q496738) (← links)
• Boundedness vs. blow-up in a two-species chemotaxis system with two chemicals (Q500160) (← 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 existence of a two-dimensional chemotaxis-haptotaxis model with remodeling of non-diffusible attractant (Q526015) (← links)
• Blow up and bounded solutions in a two-species chemotaxis system in two dimensional domains (Q683664) (← links)
• Boundedness in the higher-dimensional chemotaxis-haptotaxis model with nonlinear diffusion (Q890222) (← links)
• Boundedness and asymptotic behavior of solutions to a chemotaxis-haptotaxis model in high dimensions (Q894410) (← links)
• Dynamics in a parabolic-elliptic chemotaxis system with growth source and nonlinear secretion (Q1615702) (← 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)
• Early and late stage profiles for a chemotaxis model with density-dependent jump probability (Q2000768) (← 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)
• Global existence of classical solutions to a chemotaxis-haptotaxis model (Q2022953) (← 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)
• Global boundedness for a \(N\)-dimensional two species cancer invasion haptotaxis model with tissue remodeling (Q2064499) (← links)
• Boundedness in a quasilinear chemotaxis-haptotaxis model of parabolic-parabolic-ODE type (Q2108363) (← links)
• Combined effects of nonlinear proliferation and logistic damping in a three-component chemotaxis system for alopecia areata (Q2113906) (← links)
• Finite time blow-up in the higher dimensional parabolic-elliptic-ODE minimal chemotaxis-haptotaxis system (Q2168015) (← links)
• A critical virus production rate for blow-up suppression in a haptotaxis model for oncolytic virotherapy (Q2188508) (← links)
• A new (and optimal) result for the boundedness of a solution of a quasilinear chemotaxis-haptotaxis model (with a logistic source) (Q2195158) (← links)
• Global boundedness in a three-dimensional chemotaxis-haptotaxis model (Q2203941) (← links)
• Critical mass for infinite-time blow-up in a haptotaxis system with nonlinear zero-order interaction (Q2229257) (← links)
• Boundedness in a chemotaxis-haptotaxis model with gradient-dependent flux limitation (Q2236712) (← links)
• Global classical solutions to a doubly haptotactic cross-diffusion system modeling oncolytic virotherapy (Q2297246) (← links)
• Finite-time blow-up and global boundedness for chemotaxis system with strong logistic dampening (Q2304875) (← links)
• The fast signal diffusion limit in Keller-Segel(-fluid) systems (Q2334535) (← 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)
• 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)
• Stabilization in a chemotaxis model for tumor invasion (Q2515675) (← links)
• Boundedness in a two-species chemotaxis system (Q2795272) (← links)
• A quasilinear chemotaxis-haptotaxis model: The roles of nonlinear diffusion and logistic source (Q2978111) (← links)
• Global boundedness and asymptotic behavior in a quasilinear attraction–repulsion chemotaxis model with nonlinear signal production and logistic-type source (Q3388776) (← links)
• Large Time Behavior in a Multidimensional Chemotaxis-Haptotaxis Model with Slow Signal Diffusion (Q3451747) (← links)
• A Combined Chemotaxis-haptotaxis System: The Role of Logistic Source (Q3584125) (← links)
• (Q4392932) (← links)
• Coexistence with Chemotaxis (Q4509964) (← links)
• Boundedness and large time behavior in a quasilinear chemotaxis model for tumor invasion (Q4569328) (← links)
• A note for global existence of a two-dimensional chemotaxis–haptotaxis model with remodeling of non-diffusible attractant (Q4585726) (← links)
• Critical mass for an attraction–repulsion chemotaxis system (Q4685484) (← links)