Pages that link to "Item:Q4933526"

The following pages link to Boundedness in the Higher-Dimensional Parabolic-Parabolic Chemotaxis System with Logistic Source (Q4933526):

Displaying 50 items.

• Small-signal solutions to a nonlocal cross-diffusion model for interaction of scroungers with rapidly diffusing foragers (Q6102912) (← links)
• Global and bounded solution to a quasilinear parabolic-elliptic pursuit-evasion system in \(N\)-dimensional domains (Q6111124) (← links)
• Global boundedness in a Keller-Segel system with flux limitation and logistic source (Q6112526) (← links)
• Boundedness in a three-component quasilinear chemotaxis system on alopecia areata (Q6120367) (← links)
• Global existence and asymptotic behavior in a two-species chemotaxis system with signal production (Q6120369) (← links)
• Properties of given and detected unbounded solutions to a class of chemotaxis models (Q6124720) (← links)
• How far do indirect signal production mechanisms influence regularity in the three-dimensional Keller–Segel–Navier–Stokes system? (Q6125055) (← links)
• Global boundedness and asymptotic stabilization in a chemotaxis system with density-suppressed motility and nonlinear signal production (Q6126787) (← links)
• Strong convergence of weighted gradients in parabolic equations and applications to global generalized solvability of cross-diffusive systems (Q6133322) (← links)
• Acceleration of propagation in a chemotaxis‐growth system with slowly decaying initial data (Q6135065) (← links)
• On the existence of solutions for a parabolic‐elliptic chemotaxis model with flux limitation and logistic source (Q6139315) (← links)
• Stationary and oscillatory patterns of a food chain model with diffusion and predator‐taxis (Q6139334) (← links)
• On a quasilinear fully parabolic predator-prey model with indirect pursuit-evasion interaction (Q6139528) (← links)
• Global existence of solutions in two-species chemotaxis system with two chemicals with sub-logistic sources in 2d (Q6141020) (← links)
• Boundedness through nonlocal dampening effects in a fully parabolic chemotaxis model with sub and superquadratic growth (Q6142543) (← links)
• Boundedness and stabilization in a three-species chemotaxis-competition system (Q6150490) (← links)
• Global existence of solutions in some chemotaxis systems with sub-logistic source under nonlinear Neumann boundary conditions in 2d (Q6153607) (← links)
• Boundedness and large-time behavior in a chemotaxis system with signal-dependent motility arising from tumor invasion (Q6153633) (← links)
• Improvement of conditions for global boundedness in a predator-prey system with pursuit-evasion interaction (Q6154498) (← links)
• Boundedness of solutions to a chemotaxis-haptotaxis model with nonlocal terms (Q6154863) (← links)
• Strong solutions to a nonlinear stochastic aggregation-diffusion equation (Q6154987) (← links)
• Global boundedness of weak solutions for an attraction-repulsion chemotaxis system with p-Laplacian diffusion and nonlinear production (Q6155163) (← links)
• The role of logistic damping in a class of chemotaxis systems with density-dependent motility and indirect signal absorption (Q6155166) (← links)
• Global solutions to a chemotaxis-May-Nowak model with arbitrary superlinear degradation (Q6155171) (← links)
• Global solvability and large time behavior in a two-species chemotaxis-consumption model (Q6155174) (← links)
• Finite-time blow-up in the Cauchy problem of a Keller-Segel system with logistic source (Q6155178) (← links)
• Global existence and boundedness for an \(N\)-dimensional parabolic-elliptic chemotaxis-fluid system with indirect pursuit-evasion (Q6155329) (← links)
• Existence and boundedness of solutions for a parabolic-elliptic predator-prey chemotaxis system (Q6156556) (← links)
• Boundedness and asymptotic behavior in a quasilinear chemotaxis system for alopecia areata (Q6158270) (← links)
• Possible points of blow-up in chemotaxis systems with spatially heterogeneous logistic source (Q6158280) (← links)
• Blow-up solutions of a chemotaxis model with nonlocal effects (Q6158296) (← links)
• Traveling wave solutions for a two-species competitive Keller-Segel chemotaxis system (Q6158307) (← links)
• Smoothness effects of a quadratic damping term of mixed type on a chemotaxis-type system modeling propagation of urban crime (Q6158323) (← links)
• Boundedness in a two-dimensional attraction-repulsion Navier-Stokes system with consumption of chemoattractant and sub-quadratic degradation (Q6158324) (← links)
• Stabilization in a chemotaxis-May-Nowak model with exposed state (Q6164080) (← links)
• Boundedness in a higher-dimensional singular chemotaxis-growth system with indirect signal production (Q6165408) (← links)
• Global solvability in a two-dimensional singular chemotaxis-fluid system with indirect signal production or consumption (Q6165618) (← links)
• On a two-species attraction-repulsion chemotaxis system with nonlocal terms (Q6166007) (← links)
• Boundedness and large time behavior of solutions of a higher-dimensional haptotactic system modeling oncolytic virotherapy (Q6166572) (← links)
• Chemotaxis and reactions in biology (Q6172686) (← links)
• The spatial and temporal effects of Fog–Haze pollution on the influenza transmission (Q6174916) (← links)
• Combined effects of nonlinear diffusion and gradient-dependent flux limitation on a chemotaxis-haptotaxis model (Q6180873) (← links)
• A repertoire of repulsive Keller–Segel models with logarithmic sensitivity: Derivation, traveling waves, and quasi‐stationary dynamics (Q6182196) (← links)
• Global boundedness and large time behavior in a signal-dependent motility system with nonlinear signal consumption (Q6183943) (← links)
• Nutrient control for a viscous Cahn-Hilliard-Keller-Segel model with logistic source describing tumor growth (Q6189963) (← links)
• Dynamics in a parabolic-elliptic chemotaxis system with logistic source involving exponents depending on the spatial variables (Q6192454) (← links)
• Global boundedness for a chemotaxis system involving nonlinear indirect consumption mechanism (Q6192457) (← links)
• Global existence, boundedness and asymptotic behavior of classical solutions to a fully parabolic two-species chemotaxis-competition model with singular sensitivity (Q6193751) (← links)
• On the global well‐posedness for the 2D incompressible Keller‐Segel‐Navier‐Stokes equations (Q6194373) (← links)
• Global boundedness and asymptotic behavior in a chemotaxis system with signal‐dependent motility and indirect signal absorption (Q6198831) (← links)