Pages that link to "Item:Q3058200"
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The following pages link to Absence of collapse in a parabolic chemotaxis system with signal-dependent sensitivity (Q3058200):
Displaying 50 items.
- Global existence and asymptotic behavior in a two-species chemotaxis system with logistic source (Q1989445) (← links)
- Boundedness in the higher dimensional attraction-repulsion chemotaxis-growth system (Q2012694) (← links)
- Global solutions of a Keller-Segel system with saturated logarithmic sensitivity function (Q2018436) (← links)
- Global existence and boundedness to a two-species chemotaxis-competition model with singular sensitivity (Q2021691) (← links)
- Boundedness and stability in a chemotaxis-growth model with indirect attractant production and signal-dependent sensitivity (Q2023048) (← links)
- Keller-Segel chemotaxis models: a review (Q2026547) (← links)
- The Keller-Segel system of parabolic-parabolic type in homogeneous Besov spaces framework (Q2048599) (← links)
- Finite-time blow-up in a higher-dimensional quasilinear parabolic-elliptic chemotaxis system with space dependent logistic source (Q2050878) (← links)
- Global existence in a chemotaxis system with singular sensitivity and signal production (Q2064500) (← links)
- Boundedness in a quasilinear chemotaxis model with logistic growth and indirect signal production (Q2064649) (← links)
- Global well-posedness in a chemotaxis system with oxygen consumption (Q2075877) (← links)
- Dynamics and pattern formation in a cross-diffusion model with stage structure for predators (Q2090368) (← links)
- The small-convection limit in a two-dimensional chemotaxis-Navier-Stokes system with density-dependent motion (Q2101101) (← links)
- Global existence and asymptotic stability of solutions to a forager-exploiter model with logistic source (Q2105244) (← links)
- Boundedness in a quasilinear attraction-repulsion chemotaxis system with nonlinear sensitivity and logistic source (Q2108340) (← links)
- Boundedness and global stability of the predator-prey model with prey-taxis and competition (Q2113909) (← links)
- Boundedness in a fully parabolic attraction-repulsion chemotaxis system with nonlinear diffusion and signal-dependent sensitivity (Q2113913) (← links)
- Boundedness of solutions in a fully parabolic quasilinear chemotaxis model with two species and two chemicals (Q2119700) (← links)
- A new result for global solvability in a singular chemotaxis-growth system with indirect signal production (Q2172472) (← links)
- Boundedness and stabilization in a two-species chemotaxis system with signal absorption (Q2203515) (← links)
- Global boundedness in a three-dimensional chemotaxis-haptotaxis model (Q2203941) (← links)
- Boundedness and stabilization enforced by mild saturation of taxis in a producer-scrounger model (Q2215479) (← links)
- A new result for the global existence (and boundedness) and regularity of a three-dimensional Keller-Segel-Navier-Stokes system modeling coral fertilization (Q2216042) (← links)
- Boundedness in a parabolic-parabolic chemotaxis system with nonlinear diffusion (Q2253944) (← links)
- Global well-posedness and zero diffusion limit of classical solutions to 3D conservation laws arising in chemotaxis (Q2253946) (← links)
- Global solvability and large-time behavior to a three-dimensional chemotaxis-Stokes system modeling coral fertilization (Q2287218) (← links)
- Analysis of a chemotaxis model with indirect signal absorption (Q2314014) (← links)
- Stabilization in three-dimensional chemotaxis-growth model with indirect attractant production (Q2317487) (← links)
- Global classical solutions in a Keller-Segel(-Navier)-Stokes system modeling coral fertilization (Q2323830) (← links)
- Global boundedness of solutions to a two-species chemotaxis system (Q2342152) (← links)
- Global boundedness in a quasilinear chemotaxis system with signal-dependent sensitivity (Q2347152) (← links)
- Boundedness in a fully parabolic chemotaxis system with strongly singular sensitivity (Q2349468) (← links)
- Global weak solutions for the three-dimensional chemotaxis-Navier-Stokes system with nonlinear diffusion (Q2355411) (← links)
- On a class of Keller-Segel chemotaxis systems with cross-diffusion (Q2355430) (← links)
- Global boundedness in a quasilinear chemotaxis system with general density-signal governed sensitivity (Q2358720) (← links)
- Global solutions in the species competitive chemotaxis system with inequal diffusion rates (Q2398550) (← links)
- Convergence rate estimates of a two-species chemotaxis system with two indirect signal production and logistic source in three dimensions (Q2402763) (← links)
- On the multi-dimensional advective Lotka-Volterra competition systems (Q2406520) (← links)
- An optimal result for global existence and boundedness in a three-dimensional Keller-Segel-Stokes system with nonlinear diffusion (Q2416364) (← links)
- Finite-time blow-up in a quasilinear chemotaxis system with an external signal consumption (Q2422550) (← links)
- On a quasilinear parabolic-elliptic chemotaxis system with logistic source (Q2437984) (← links)
- Global boundedness to a parabolic-parabolic chemotaxis model with nonlinear diffusion and singular sensitivity (Q2633728) (← links)
- Dynamics and pattern formations in a three-species predator-prey model with two prey-taxis (Q2633780) (← links)
- Global existence of solutions and uniform persistence of a diffusive predator-prey model with prey-taxis (Q2634205) (← links)
- Boundedness in prey-taxis system with rotational flux terms (Q2658656) (← links)
- Global classical solutions of Keller-Segel-(Navier)-Stokes system with nonlinear motility functions (Q2673002) (← links)
- Dynamics in two-predator and one-prey models with signal-dependent motility (Q2692808) (← links)
- Global existence and blow up of solutions of quasilinear chemotaxis system (Q2795386) (← links)
- Stabilization and convergence rate in a chemotaxis system with consumption of chemoattractant (Q2943422) (← links)
- Boundedness in chemotaxis systems with rotational flux terms (Q2953718) (← links)
