Global classical solution and boundedness to a chemotaxis-haptotaxis model with re-establishment mechanisms

DOI10.1112/BLMS.12160zbMATH Open1396.92007OpenAlexW2803944126MaRDI QIDQ4583629FDOQ4583629

Authors: Chunhua Jin 

Publication date: 31 August 2018

Published in: Bulletin of the London Mathematical Society (Search for Journal in Brave)

Full work available at URL: https://doi.org/10.1112/blms.12160

Recommendations

• Global boundedness in a three-dimensional chemotaxis-haptotaxis model
• Global boundedness of solutions to a chemotaxis-haptotaxis model with tissue remodeling
• Boundedness of solutions to a quasilinear chemotaxis-haptotaxis model
• Global boundedness to a chemotaxis-haptotaxis model with nonlinear diffusion
• Boundedness in a three-dimensional chemotaxis-haptotaxis model

zbMATH Keywords

boundednessglobal classical solutionchemotaxis-haptotaxis modelre-establishment mechanisms

Mathematics Subject Classification ID

PDEs in connection with biology, chemistry and other natural sciences (35Q92) Cell movement (chemotaxis, etc.) (92C17)

Cited In (44)

• Global boundedness of weak solutions for an attraction-repulsion chemotaxis system with p-Laplacian diffusion and nonlinear production
• Boundedness and stabilization in a haptotaxis model of oncolytic virotherapy with nonlinear sensitivity
• Global well-posedness and long-time behavior in a tumor invasion model with cross-diffusion
• Global boundedness and stability of a predator-prey model with alarm-taxis
• Global weak solutions for an attraction-repulsion chemotaxis system with \(p\)-Laplacian diffusion and logistic source
• Global solvability and stabilization to a cancer invasion model with remodelling of ECM
• A new result for global solvability of a two species cancer invasion haptotaxis model with tissue remodeling
• Global boundedness of classical solutions to a two species cancer invasion haptotaxis model with tissue remodeling
• Global boundedness of solutions to a chemotaxis-haptotaxis model with tissue remodeling
• Global boundedness for a \(N\)-dimensional two species cancer invasion haptotaxis model with tissue remodeling
• A quasilinear chemotaxis-haptotaxis system: existence and blow-up results
• Global classical solutions and convergence to a mathematical model for cancer cells invasion and metastatic spread
• Global solvability and boundedness to a coupled chemotaxis-fluid model with arbitrary porous medium diffusion
• Boundedness of solutions to a chemotaxis-haptotaxis model with nonlocal terms
• Global existence and boundedness in a two-species chemotaxis system with nonlinear diffusion
• Global solvability and large time behavior to a chemotaxis-haptotaxis model with nonlinear diffusion
• Global classical solutions to a doubly haptotactic cross-diffusion system modeling oncolytic virotherapy
• Global solvability and optimal control to a haptotaxis cancer invasion model with two cancer cell species
• 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
• Global bounded weak solutions and asymptotic behavior to a chemotaxis-Stokes model with non-Newtonian filtration slow diffusion
• Negligibility of haptotaxis effect in a chemotaxis-haptotaxis model
• Global existence for a chemotaxis-haptotaxis model with \(p\)-Laplacian
• Modeling multiple taxis: tumor invasion with phenotypic heterogeneity, haptotaxis, and unilateral interspecies repellence
• Global strong solution and periodic dynamic behavior to Chaplain-Lolas model
• Analysis of a two-dimensional triply haptotactic model with a fusogenic oncolytic virus and syncytia
• Negligibility of haptotaxis on global dynamics in a chemotaxis-haptotaxis system with indirect signal production
• Global classical solvability and stabilization in a reaction-diffusion intraguild predation model with chemotaxis
• Global solutions to a density-suppressed motility system modeling oncolytic virotherapy
• Global boundedness of a three-species predator-prey model with prey-taxis and competition
• Boundedness and global solvability to a chemotaxis model with nonlinear diffusion
• Critical exponent to a cancer invasion model with nonlinear diffusion
• Global boundedness and asymptotic stability for a food chain model with nonlinear diffusion
• A chemotaxis‐Stokes system with nonhomogeneous boundary condition: Global large‐datum solution and asymptotic behavior
• Uniform boundedness and eventual Hölder continuity to a cancer invasion model with remodeling of ECM and nonlinear diffusion
• Qualitative properties for a three-species food chain model with cross-diffusion and intra-specific competition
• Global boundedness of solutions to a food chain model with nonlinear taxis sensitivity
• Stabilization to a cancer invasion model with remodeling mechanism and slow diffusion
• Global solvability, pattern formation and stability to a chemotaxis-haptotaxis model with porous medium diffusion
• Global boundedness for a food chain model with general logistic source
• Global classical solutions to a higher-dimensional doubly haptotactic cross-diffusion system modeling oncolytic virotherapy
• Global dynamics of a three-species spatial food chain model
• Global weak solutions in a three-dimensional two-species cancer invasion haptotaxis model without cell proliferation
• Global boundedness in a chemotaxis-haptotaxis model with nonlinear diffusion and signal production
• Boundedness in a two-dimensional two-species cancer invasion haptotaxis model without cell proliferation

This page was built for publication: Global classical solution and boundedness to a chemotaxis-haptotaxis model with re-establishment mechanisms

Report a bug (only for logged in users!)Click here to report a bug for this page (MaRDI item Q4583629)