Pages that link to "Item:Q2321123"

The following pages link to Global Boundedness in a quasilinear fully parabolic chemotaxis system with indirect signal production (Q2321123):

Displaying 42 items.

• A quasilinear predator-prey model with indirect prey-taxis (Q1981909) (← links)
• Asymptotic stability in a chemotaxis-competition system with indirect signal production (Q1995537) (← links)
• On a fully parabolic singular chemotaxis-(growth) system with indirect signal production or consumption (Q2026413) (← links)
• Boundedness in a quasilinear chemotaxis model with logistic growth and indirect signal production (Q2064649) (← links)
• Boundedness and long-time behavior for a two-dimensional quasilinear chemotaxis system with indirect signal consumption (Q2071838) (← links)
• Global solvability in a Keller-Segel-growth system with indirect signal production (Q2079853) (← links)
• On a quasilinear fully parabolic attraction or repulsion chemotaxis system with nonlinear signal production (Q2081983) (← links)
• Emergence of lager densities in chemotaxis system with indirect signal production and non-radial symmetry case (Q2083327) (← links)
• Boundedness of solutions in a quasilinear chemo-repulsion system with nonlinear signal production (Q2085642) (← links)
• Boundedness in a fully parabolic attraction-repulsion chemotaxis system with nonlinear diffusion and signal-dependent sensitivity (Q2113913) (← links)
• On a two-species chemotaxis-competition system with indirect signal consumption (Q2116225) (← links)
• On an exponentially decaying diffusive chemotaxis system with indirect signals (Q2136183) (← links)
• Global weak solutions in a three-dimensional Keller-Segel-Navier-Stokes system with indirect signal production (Q2152763) (← links)
• Boundedness and large-time behavior for a two-dimensional quasilinear chemotaxis-growth system with indirect signal consumption (Q2185807) (← links)
• Boundedness in a fully parabolic quasilinear repulsion chemotaxis model of higher dimension (Q2194708) (← links)
• Global boundedness in the higher-dimensional chemotaxis system with indirect signal production and rotational flux (Q2213688) (← links)
• Boundedness in a three-dimensional two-species chemotaxis system with two chemicals (Q2301332) (← links)
• Global boundedness of weak solutions for a three-dimensional chemotaxis-Stokes system with nonlinear diffusion and rotation (Q2304455) (← links)
• A quasilinear fully parabolic chemotaxis system with indirect signal production and logistic source (Q2314843) (← links)
• On a three-dimensional quasilinear Keller-Segel-Stokes system with indirect signal production (Q2678890) (← links)
• Boundedness in a chemotaxis-fluid system involving a gradient-dependent flux limitation and indirect signal production mechanism (Q2683676) (← links)
• Blow-up prevention by logistic source in an \(N\)-D chemotaxis-convection model of capillary-sprout growth during tumor angiogenesis (Q2699512) (← 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)
• Global existence of a quasilinear chemotaxis model with signal-dependent motility and indirect signal production mechanism (Q5884853) (← links)
• (Q6070492) (← links)
• Global boundedness in a 3D quasilinear Keller-Segel-Stokes system with nonlinear sensitivity and indirect signal production (Q6105317) (← links)
• Boundedness and weak stabilization in a degenerate chemotaxis model arising from tumor invasion (Q6111019) (← links)
• Boundedness in a three-component quasilinear chemotaxis system on alopecia areata (Q6120367) (← links)
• Nonlinear transmission exponent for boundedness of solutions to a chemotaxis system with indirect signal production (Q6141023) (← links)
• Global dynamics in a chemotaxis system involving nonlinear indirect signal secretion and logistic source (Q6180856) (← links)
• Global boundedness for a chemotaxis system involving nonlinear indirect consumption mechanism (Q6192457) (← links)
• Global boundedness and asymptotic behavior in a chemotaxis system with signal‐dependent motility and indirect signal absorption (Q6198831) (← links)
• Global Classical Solutions to a Predator-Prey Model with Nonlinear Indirect Chemotaxis Mechanism (Q6492274) (← links)
• Global dynamics for a two-species chemotaxis system with loop (Q6495908) (← links)
• Global boundedness in an attraction-repulsion chemotaxis system involving nonlinear indirect signal mechanism (Q6542903) (← links)
• Boundedness in an attraction-repulsion chemotaxis system with both nonlinear signal production and consumption (Q6595501) (← links)
• Global smooth solutions in a chemotaxis system modeling immune response to a solid tumor (Q6602161) (← links)
• Global existence and uniform boundedness to a bi-attraction chemotaxis system with nonlinear indirect signal mechanisms (Q6611459) (← links)
• Global stabilization in a Keller-Segel-growth system with indirect signal production (Q6615296) (← links)
• Radial blow-up in quasilinear Keller-Segel systems: approaching the full picture (Q6633352) (← links)
• Analysis of global dynamics in an attraction-repulsion model with nonlinear indirect signal and logistic source (Q6637353) (← links)