Pages that link to "Item:Q2451888"
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The following pages link to Energy-type estimates and global solvability in a two-dimensional chemotaxis-haptotaxis model with remodeling of non-diffusible attractant (Q2451888):
Displayed 50 items.
- Global existence and uniform boundedness of smooth solutions to a parabolic-parabolic chemotaxis system with nonlinear diffusion (Q283421) (← links)
- Boundedness in a three-dimensional chemotaxis-haptotaxis model (Q286427) (← links)
- Global dynamics in a fully parabolic chemotaxis system with logistic source (Q321614) (← links)
- Boundedness in a Keller-Segel system with external signal production (Q321792) (← links)
- Global existence and uniqueness of classical solutions for a generalized quasilinear parabolic equation with application to a glioblastoma growth model (Q335287) (← links)
- Blow-up prevention by logistic sources in a parabolic-elliptic Keller-Segel system with singular sensitivity (Q399091) (← links)
- Boundedness of solutions to a quasilinear higher-dimensional chemotaxis-haptotaxis model with nonlinear diffusion (Q501454) (← links)
- Global boundedness in a two-competing-species chemotaxis system with two chemicals (Q522543) (← links)
- Global existence and asymptotic stability in a competitive two-species chemotaxis system with two signals (Q524080) (← 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)
- Boundedness and asymptotic behavior of solutions to a chemotaxis-haptotaxis model in high dimensions (Q894410) (← links)
- The small-convection limit in a two-dimensional chemotaxis-Navier-Stokes system (Q1650169) (← links)
- Global weak solution and boundedness in a three-dimensional competing chemotaxis (Q1661144) (← links)
- Singular structure formation in a degenerate haptotaxis model involving myopic diffusion (Q1707304) (← links)
- Global solvability and large time behavior to a chemotaxis-haptotaxis model with nonlinear diffusion (Q1729227) (← links)
- Global solvability and boundedness to a coupled chemotaxis-fluid model with arbitrary porous medium diffusion (Q1743812) (← links)
- Existence and uniqueness of global classical solutions to a two dimensional two species cancer invasion haptotaxis model (Q1756887) (← links)
- Boundedness of solutions for a quasilinear chemotaxis-haptotaxis model (Q1982567) (← links)
- Global stability in a multi-dimensional predator-prey system with prey-taxis (Q1995564) (← 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)
- Can fluid interaction influence the critical mass for taxis-driven blow-up in bounded planar domains? (Q2023062) (← links)
- Global classical solutions to an oncolytic viral therapy model with triply haptotactic terms (Q2026546) (← links)
- The Keller-Segel system with logistic growth and signal-dependent motility (Q2033546) (← 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)
- Boundedness and stabilization in a two-species and two-stimuli chemotaxis system with signaling loop (Q2051410) (← links)
- Boundedness of classical solutions to a degenerate Keller-Segel type model with signal-dependent motilities (Q2051415) (← links)
- Dampening effects on global boundedness and asymptotic behavior in an oncolytic virotherapy model (Q2054010) (← links)
- Global boundedness for a chemotaxis-competition system with signal dependent sensitivity and loop (Q2055164) (← links)
- Boundedness and stabilization in a two-species chemotaxis-competition system with indirect signal production (Q2059978) (← links)
- Global boundedness for a \(N\)-dimensional two species cancer invasion haptotaxis model with tissue remodeling (Q2064499) (← links)
- Mathematical analysis of a tumor invasion model -- global existence and stability (Q2066540) (← links)
- Analysis of a new multispecies tumor growth model coupling 3D phase-fields with a 1D vascular network (Q2066556) (← links)
- Global well-posedness in a chemotaxis system with oxygen consumption (Q2075877) (← links)
- Global classical solutions to a higher-dimensional doubly haptotactic cross-diffusion system modeling oncolytic virotherapy (Q2087609) (← links)
- Dampening effects on global boundedness in a quartic haptotactic model with fusogenic oncolytic virus and syncytia (Q2096964) (← 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)
- On a macrophage and tumor cell chemotaxis system with both paracrine and autocrine loops (Q2128884) (← links)
- Finite time blow-up in the higher dimensional parabolic-elliptic-ODE minimal chemotaxis-haptotaxis system (Q2168015) (← links)
- Boundedness in a two species attraction-repulsion chemotaxis system with two chemicals (Q2169040) (← links)
- Global classical solutions and convergence to a mathematical model for cancer cells invasion and metastatic spread (Q2180603) (← links)
- A critical virus production rate for blow-up suppression in a haptotaxis model for oncolytic virotherapy (Q2188508) (← links)
- On boundedness, blow-up and convergence in a two-species and two-stimuli chemotaxis system with/without loop (Q2189554) (← 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)
- 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)