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.

• Facing low regularity in chemotaxis systems (Q2304971) (← links)
• On a fully parabolic chemotaxis system with source term and periodic asymptotic behavior (Q2306978) (← links)
• The role of superlinear damping in the construction of solutions to drift-diffusion problems with initial data in \(L^{1}\) (Q2311849) (← links)
• Analysis of a chemotaxis-convection model of capillary-sprout growth during tumor angiogenesis (Q2326008) (← links)
• On a Keller-Segel-Stokes system with logistic type growth: blow-up prevention enforced by sublinear signal production (Q2327883) (← 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)
• Emergence of large population densities despite logistic growth restrictions in fully parabolic chemotaxis systems (Q2356883) (← links)
• Coupling vs decoupling approaches for PDE/ODE systems modeling intercellular signaling (Q2375147) (← links)
• Existence of global bounded classical solution to a quasilinear attraction-repulsion chemotaxis system with logistic source (Q2399696) (← links)
• Global existence and decay for a chemotaxis-growth system with generalized volume-filling effect and sublinear secretion (Q2410981) (← 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)
• Homogenization and solvability in a chemotaxis-convection angiogenesis model with leakage boundary conditions (Q2660483) (← links)
• Boundedness in a two-species chemotaxis system with nonlinear sensitivity and signal secretion (Q2661250) (← links)
• Global well-posedness to a chemotaxis-Stokes system (Q2665500) (← links)
• Global existence and boundedness in a two-species chemotaxis system with nonlinear diffusion (Q2669033) (← links)
• Global generalized solutions of a haptotaxis model describing cancer cells invasion and metastatic spread (Q2669230) (← links)
• Global existence and boundedness of solutions to a two-species chemotaxis-competition system with singular sensitivity and indirect signal production (Q2677643) (← links)
• Global boundedness in an oncolytic virotherapy model with generalized logistic source (Q2679221) (← links)
• On a two-species competitive predator-prey system with density-dependent diffusion (Q2694126) (← links)
• Pursuit-evasion dynamics for Bazykin-type predator-prey model with indirect predator taxis (Q2700651) (← links)
• To the exclusion of blow-up in a three-dimensional chemotaxis-growth model with indirect attractant production (Q2830977) (← links)
• Global existence for a go-or-grow multiscale model for tumor invasion with therapy (Q2830979) (← links)
• A quasilinear chemotaxis-haptotaxis model: The roles of nonlinear diffusion and logistic source (Q2978111) (← links)
• Global Very Weak Solutions to a Chemotaxis-Fluid System with Nonlinear Diffusion (Q3176429) (← links)
• On a class of multiscale cancer cell migration models: Well-posedness in less regular function spaces (Q3191255) (← links)
• Large Time Behavior in a Multidimensional Chemotaxis-Haptotaxis Model with Slow Signal Diffusion (Q3451747) (← links)
• Global Existence and Uniform Boundedness of Smooth Solutions to a Cross-Diffusion System with Equal Diffusion Rates (Q3467556) (← links)
• Persistence property in a two-species chemotaxis system with two signals (Q4599484) (← links)
• Global boundedness of solutions to a chemotaxis–haptotaxis model with tissue remodeling (Q4630535) (← links)
• Local and nonlocal phase-field models of tumor growth and invasion due to ECM degradation (Q4973281) (← links)
• Asymptotic behavior of solutions to a tumor angiogenesis model with chemotaxis–haptotaxis (Q4973287) (← links)
• On the unsteady Darcy–Forchheimer–Brinkman equation in local and nonlocal tumor growth models (Q4973296) (← links)
• Effects of signal-dependent motilities in a Keller–Segel-type reaction–diffusion system (Q4977915) (← links)
• A New Result for Global Solvability of a Two Species Cancer Invasion Haptotaxis Model with Tissue Remodeling (Q5020856) (← links)
• Does indirectness of signal production reduce the explosion-supporting potential in chemotaxis–haptotaxis systems? Global classical solvability in a class of models for cancer invasion (and more) (Q5056753) (← links)
• Dynamics of a predator–prey system with nonlinear prey-taxis (Q5089482) (← links)
• (Q5096712) (← links)
• Boundedness and asymptotic stability in a chemotaxis model with indirect signal production and logistic source (Q5101654) (← links)
• On a two-species chemotaxis system with indirect signal production and general competition terms (Q5104588) (← links)
• Mathematical Research for Models Which is Related to Chemotaxis System (Q5110837) (← links)
• Global bounded solution of the higher-dimensional forager–exploiter model with/without growth sources (Q5127161) (← links)
• Global solvability and stabilization to a cancer invasion model with remodelling of ECM (Q5130935) (← links)
• Can simultaneous density-determined enhancement of diffusion and cross-diffusion foster boundedness in Keller–Segel type systems involving signal-dependent motilities? (Q5136539) (← links)
• Toward a mathematical theory of Keller–Segel models of pattern formation in biological tissues (Q5265465) (← links)
• On a structured multiscale model for acid-mediated tumor invasion: The effects of adhesion and proliferation (Q5272437) (← links)
• Asymptotic stability of spatial homogeneity in a haptotaxis model for oncolytic virotherapy (Q5861961) (← links)
• Global weak solutions in a three-dimensional two-species cancer invasion haptotaxis model without cell proliferation (Q5884846) (← links)
• Boundedness and stabilization in a two-species chemotaxis system with two chemicals (Q5919281) (← links)