Pages that link to "Item:Q2427277"
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The following pages link to On the global existence of solutions to an aggregation model (Q2427277):
Displaying 50 items.
- On the boundedness and decay of solutions for a chemotaxis-haptotaxis system with nonlinear diffusion (Q256196) (← links)
- Boundedness and decay property in a three-dimensional Keller-Segel-Stokes system involving tensor-valued sensitivity with saturation (Q281644) (← links)
- Global existence and uniform boundedness of smooth solutions to a parabolic-parabolic chemotaxis system with nonlinear diffusion (Q283421) (← links)
- Boundedness in a quasilinear chemotaxis-haptotaxis system with logistic source (Q294043) (← links)
- Global boundedness in a quasilinear attraction-repulsion chemotaxis model with nonlinear sensitivity (Q294110) (← links)
- Boundedness and blow up in the higher-dimensional attraction-repulsion chemotaxis system with nonlinear diffusion (Q306238) (← links)
- Global dynamics in a fully parabolic chemotaxis system with logistic source (Q321614) (← links)
- Global existence and boundedness in a Keller-Segel-(Navier-)Stokes system with signal-dependent sensitivity (Q335438) (← links)
- Boundedness in a parabolic-parabolic quasilinear chemotaxis system with logistic source (Q379754) (← links)
- Uniqueness for Keller-Segel-type chemotaxis models (Q379814) (← links)
- Boundedness of the attraction-repulsion Keller-Segel system (Q465239) (← links)
- Global existence of classical solutions to an acid-mediated invasion model for tumor-stromal interactions (Q470836) (← links)
- Global existence to a higher-dimensional quasilinear chemotaxis system with consumption of chemoattractant (Q493566) (← links)
- Parabolic elliptic type Keller-Segel system on the whole space case (Q495813) (← links)
- Boundedness in a three-dimensional chemotaxis-haptotaxis model with nonlinear diffusion (Q514389) (← links)
- Existence and uniqueness of solutions of degenerate chemotaxis system (Q514782) (← links)
- Boundary layer analysis from the Keller-Segel system to the aggregation system in one space dimension (Q519550) (← links)
- Global solutions to a chemotaxis model with consumption of chemoattractant (Q520494) (← links)
- Convergence of global and bounded solutions of a two-species chemotaxis model with a logistic source (Q521493) (← links)
- Global boundedness in a two-competing-species chemotaxis system with two chemicals (Q522543) (← links)
- The variational formulation of the fully parabolic Keller-Segel system with degenerate diffusion (Q526023) (← links)
- Global existence for a haptotaxis model of cancer invasion with tissue remodeling (Q611260) (← links)
- Existence and uniqueness of solutions of predator-prey type model with mixed boundary conditions (Q645009) (← links)
- Boundedness in a quasilinear parabolic-parabolic Keller-Segel system with subcritical sensitivity (Q649778) (← 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, blowup and critical mass phenomenon in competing chemotaxis (Q888195) (← links)
- A density-dependent chemotaxis-haptotaxis system modeling cancer invasion (Q968855) (← links)
- Global existence of classical solutions to a predator-prey model with nonlinear prey-taxis (Q974624) (← links)
- Global existence of classical solutions to a combined chemotaxis-haptotaxis model with logistic source (Q1018160) (← links)
- Chemotaxis effect vs. logistic damping on boundedness in the 2-D minimal Keller-Segel model (Q1657937) (← links)
- Boundedness and large time behavior in a two-dimensional Keller-Segel-Navier-Stokes system with signal-dependent diffusion and sensitivity (Q1661125) (← links)
- Global dynamics in a two-species chemotaxis-competition system with two signals (Q1661127) (← links)
- Boundedness in a chemotaxis model with exponentially decaying diffusivity and consumption of chemoattractant (Q1667680) (← links)
- Inter-species competition and chemorepulsion (Q1684828) (← links)
- Boundedness and asymptotic stability of solutions to a two-species chemotaxis system with consumption of chemoattractant (Q1688667) (← links)
- Global classical solution to a chemotaxis consumption model with singular sensitivity (Q1698379) (← links)
- Global classical solvability and generic infinite-time blow-up in quasilinear Keller-Segel systems with bounded sensitivities (Q1733221) (← links)
- Blow-up profiles and refined extensibility criteria in quasilinear Keller-Segel systems (Q1747080) (← links)
- Boundedness in a three-dimensional Keller-Segel-Stokes system involving tensor-valued sensitivity with saturation (Q1755942) (← links)
- Existence and uniqueness of global classical solutions to a two dimensional two species cancer invasion haptotaxis model (Q1756887) (← links)
- Global existence and boundedness in a chemorepulsion system with superlinear diffusion (Q1791660) (← links)
- Vanishing cross-diffusion limit in a Keller-Segel system with additional cross-diffusion (Q1985821) (← links)
- Global boundedness of classical solutions to a two species cancer invasion haptotaxis model with tissue remodeling (Q2009311) (← links)
- Boundedness and finite-time blow-up in a chemotaxis system with nonlinear signal production (Q2025392) (← links)
- Global boundedness and stability of solutions for prey-taxis model with handling and searching predators (Q2025907) (← links)
- Keller-Segel chemotaxis models: a review (Q2026547) (← links)
- Global boundedness of the fully parabolic Keller-Segel system with signal-dependent motilities (Q2040626) (← links)
- Boundedness and stabilization in the chemotaxis consumption model with signal-dependent motility (Q2046488) (← links)
- Boundedness and stabilization in a two-species chemotaxis-competition system with indirect signal production (Q2059978) (← links)
