Pages that link to "Item:Q457841"
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The following pages link to Nondegeneracy of blow-up points for the parabolic Keller-Segel system (Q457841):
Displaying 50 items.
- Chemotaxis can prevent thresholds on population density (Q256845) (← links)
- Lower bounds for blow-up in a parabolic-parabolic Keller-Segel system (Q260908) (← links)
- Boundedness in a multi-dimensional chemotaxis-haptotaxis model with nonlinear diffusion (Q285105) (← links)
- Boundedness in a quasilinear chemotaxis-haptotaxis system with logistic source (Q294043) (← links)
- Type II blowup in a doubly parabolic Keller-Segel system in two dimensions (Q329692) (← links)
- Boundedness of solutions to a quasilinear parabolic-parabolic Keller-Segel system with a logistic source (Q491824) (← links)
- Global classical small-data solutions for a three-dimensional chemotaxis Navier-Stokes system involving matrix-valued sensitivities (Q502264) (← links)
- Boundedness and large time behavior of an attraction-repulsion chemotaxis model with logistic source (Q503018) (← links)
- Blow-up behavior of solutions to a degenerate parabolic-parabolic Keller-Segel system (Q514356) (← 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)
- Boundedness of solutions to a fully parabolic Keller-Segel system with nonlinear sensitivity (Q524106) (← links)
- Blow-up for a three dimensional Keller-Segel model with consumption of chemoattractant (Q683801) (← links)
- Global stability of prey-taxis systems (Q729904) (← links)
- Global existence and boundedness of a chemotaxis model with indirect production and general kinetic function (Q777341) (← links)
- Boundedness in the higher-dimensional chemotaxis-haptotaxis model with nonlinear diffusion (Q890222) (← links)
- Boundedness and decay enforced by quadratic degradation in a three-dimensional chemotaxis-fluid system (Q894905) (← links)
- Explicit lower bound of blow-up time in a fully parabolic chemotaxis system with nonlinear cross-diffusion (Q905930) (← links)
- Global dynamics for a diffusive predator-prey model with prey-taxis and classical Lotka-Volterra kinetics (Q1681018) (← links)
- How strong a logistic damping can prevent blow-up for the minimal Keller-Segel chemotaxis system? (Q1684822) (← links)
- Global classical solution to a chemotaxis consumption model with singular sensitivity (Q1698379) (← links)
- Global existence of solutions to an \(n\)-dimensional parabolic-parabolic system for chemotaxis with logistic-type growth and superlinear production (Q1704393) (← links)
- Global classical solutions to the Keller-Segel-Navier-Stokes system with matrix-valued sensitivity (Q1706571) (← links)
- The fast signal diffusion limit in a Keller-Segel system (Q1728019) (← links)
- Boundedness and stabilization in a two-species chemotaxis-competition system with signal-dependent diffusion and sensitivity (Q1737546) (← links)
- A blow-up result for a quasilinear chemotaxis system with logistic source in higher dimensions (Q1748318) (← links)
- Eventual smoothness of generalized solutions to a singular chemotaxis-Stokes system in 2D (Q1753217) (← links)
- Global existence and boundedness in a chemorepulsion system with superlinear diffusion (Q1791660) (← links)
- Global dynamics of a quasilinear chemotaxis model arising from tumor invasion (Q1994846) (← links)
- Blow-up profiles and life beyond blow-up in the fully parabolic Keller-Segel system (Q1996481) (← links)
- Global solutions for chemotaxis-Navier-Stokes system with Robin boundary conditions (Q2003939) (← links)
- Global bounded weak solutions and asymptotic behavior to a chemotaxis-Stokes model with non-Newtonian filtration slow diffusion (Q2020209) (← links)
- Global boundedness and stability of solutions for prey-taxis model with handling and searching predators (Q2025907) (← links)
- Boundedness and stabilization of solutions to a chemotaxis May-Nowak model (Q2026471) (← links)
- Keller-Segel chemotaxis models: a review (Q2026547) (← links)
- Modeling multiple taxis: tumor invasion with phenotypic heterogeneity, haptotaxis, and unilateral interspecies repellence (Q2026618) (← links)
- Global boundedness of solutions to the two-dimensional forager-exploiter model with logistic source (Q2030807) (← links)
- The Keller-Segel system with logistic growth and signal-dependent motility (Q2033546) (← links)
- To what extent is cross-diffusion controllable in a two-dimensional chemotaxis-(Navier-)Stokes system modeling coral fertilization (Q2048712) (← links)
- Global existence of strong solution to the chemotaxis-shallow water system with vacuum in a bounded domain (Q2051755) (← links)
- Global boundedness for a chemotaxis-competition system with signal dependent sensitivity and loop (Q2055164) (← links)
- Global boundedness of a diffusive prey-predator model with indirect prey-taxis and predator-taxis (Q2059973) (← links)
- Time periodic solution to a two-species chemotaxis-Stokes system with \(p\)-Laplacian diffusion (Q2062576) (← links)
- Global boundedness for a \(N\)-dimensional two species cancer invasion haptotaxis model with tissue remodeling (Q2064499) (← links)
- On a quasilinear fully parabolic two-species chemotaxis system with two chemicals (Q2064501) (← links)
- Approaching logarithmic singularities in quasilinear chemotaxis-consumption systems with signal-dependent sensitivities (Q2081942) (← links)
- Boundedness of a chemotaxis-convection model describing tumor-induced angiogenesis (Q2088154) (← links)
- Global solutions to a Keller-Segel-consumption system involving singularly signal-dependent motilities in domains of arbitrary dimension (Q2101062) (← links)
- Boundedness in a quasilinear chemotaxis-haptotaxis model of parabolic-parabolic-ODE type (Q2108363) (← links)
