Pages that link to "Item:Q2878989"

The following pages link to Global Weak Solutions in a PDE-ODE System Modeling Multiscale Cancer Cell Invasion (Q2878989):

Displaying 50 items.

• Chemotaxis can prevent thresholds on population density (Q256845) (← links)
• Boundedness in a three-dimensional chemotaxis-haptotaxis model (Q286427) (← links)
• On a parabolic-elliptic system with chemotaxis and logistic type growth (Q306242) (← links)
• A stochastic multiscale model for acid mediated cancer invasion (Q475006) (← links)
• Glioma follow white matter tracts: a multiscale DTI-based model (Q493077) (← links)
• Persistence of mass in a chemotaxis system with logistic source (Q496738) (← links)
• Boundedness of solutions to a quasilinear higher-dimensional chemotaxis-haptotaxis model with nonlinear diffusion (Q501454) (← links)
• Global existence for a degenerate haptotaxis model of cancer invasion (Q506394) (← links)
• Blow-up prevention by quadratic degradation in a two-dimensional Keller-Segel-Navier-Stokes system (Q506406) (← links)
• Convergence of global and bounded solutions of a two-species chemotaxis model with a logistic source (Q521493) (← links)
• Asymptotic behavior in a chemotaxis-growth system with nonlinear production of signals (Q524005) (← links)
• Global existence and asymptotic stability in a competitive two-species chemotaxis system with two signals (Q524080) (← links)
• Global existence and boundedness of a chemotaxis model with indirect production and general kinetic function (Q777341) (← links)
• Global bounded weak solutions for a chemotaxis-Stokes system with nonlinear diffusion and rotation (Q831100) (← links)
• Boundedness and decay enforced by quadratic degradation in a three-dimensional chemotaxis-fluid system (Q894905) (← links)
• A multiscale model for glioma spread including cell-tissue interactions and proliferation (Q907299) (← links)
• On a coupled SDE-PDE system modeling acid-mediated tumor invasion (Q1634879) (← links)
• Chemotaxis effect vs. logistic damping on boundedness in the 2-D minimal Keller-Segel model (Q1657937) (← links)
• Global classical solution and stability to a coupled chemotaxis-fluid model with logistic source (Q1661123) (← links)
• Global weak solution and boundedness in a three-dimensional competing chemotaxis (Q1661144) (← links)
• Boundedness and global solvability to a chemotaxis-haptotaxis model with slow and fast diffusion (Q1671109) (← links)
• Boundedness in a chemotaxis system with indirect signal production and generalized logistic source (Q1691040) (← links)
• Global existence and stabilization in a degenerate chemotaxis-Stokes system with mildly strong diffusion enhancement (Q1704539) (← links)
• Singular structure formation in a degenerate haptotaxis model involving myopic diffusion (Q1707304) (← links)
• Global dynamics for an attraction-repulsion chemotaxis-(Navier)-Stokes system with logistic source (Q1729182) (← 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)
• Global classical solvability and generic infinite-time blow-up in quasilinear Keller-Segel systems with bounded sensitivities (Q1733221) (← links)
• Global solvability and boundedness to a coupled chemotaxis-fluid model with arbitrary porous medium diffusion (Q1743812) (← links)
• Blow-up profiles and refined extensibility criteria in quasilinear Keller-Segel systems (Q1747080) (← links)
• Existence and uniqueness of global classical solutions to a two dimensional two species cancer invasion haptotaxis model (Q1756887) (← links)
• Boundedness and global solvability to a chemotaxis model with nonlinear diffusion (Q1785937) (← links)
• Global existence and boundedness in a chemorepulsion system with superlinear diffusion (Q1791660) (← links)
• Global existence and asymptotic stability in a predator-prey chemotaxis model (Q1987381) (← links)
• Global bounded solution to a chemotaxis-convection model of capillary-sprout growth during tumor angiogenesis (Q1995734) (← links)
• Nonlocal adhesion models for two cancer cell phenotypes in a multidimensional bounded domain (Q2021517) (← links)
• Blow-up phenomena of a cancer invasion model with nonlinear diffusion and haptotaxis term (Q2021582) (← links)
• Global existence of classical solutions to a chemotaxis-haptotaxis model (Q2022953) (← links)
• Boundedness and stability in a chemotaxis-growth model with indirect attractant production and signal-dependent sensitivity (Q2023048) (← links)
• Global weak solutions to an oncolytic viral therapy model with doubly haptotactic terms (Q2025878) (← links)
• On a fully parabolic singular chemotaxis-(growth) system with indirect signal production or consumption (Q2026413) (← links)
• Global classical solutions to an oncolytic viral therapy model with triply haptotactic terms (Q2026546) (← links)
• A new result for boundedness and stabilization in a two-species chemotaxis system with two chemicals (Q2026568) (← links)
• Modeling multiple taxis: tumor invasion with phenotypic heterogeneity, haptotaxis, and unilateral interspecies repellence (Q2026618) (← links)
• Global generalized solutions to a chemotaxis model of capillary-sprout growth during tumor angiogenesis (Q2031214) (← links)
• Global classical solutions in a chemotaxis(-Navier)-Stokes system with indirect signal production (Q2038190) (← links)
• Solvability of solid tumor invasion model (Q2038372) (← links)
• The phenomenon of large population densities in a chemotaxis competition system with loop (Q2044650) (← links)
• Asymptotic behavior of a quasilinear Keller-Segel system with signal-suppressed motility (Q2048901) (← links)
• Global boundedness for a chemotaxis-competition system with signal dependent sensitivity and loop (Q2055164) (← links)