Pages that link to "Item:Q3058200"
From MaRDI portal
The following pages link to Absence of collapse in a parabolic chemotaxis system with signal-dependent sensitivity (Q3058200):
Displaying 37 items.
- Global solutions in a fully parabolic chemotaxis system with singular sensitivity (Q3067820) (← links)
- Mathematical analysis of a model of chemotaxis arising from morphogenesis (Q3225047) (← links)
- Boundedness and large time behavior in a quasilinear chemotaxis model for tumor invasion (Q4569328) (← links)
- Boundedness of classical solutions for a chemotaxis system with general sensitivity function (Q4622824) (← links)
- Dynamics and pattern formation of a diffusive predator–prey model with predator-taxis (Q4630537) (← links)
- The full Keller–Segel model is well-posed on nonsmooth domains (Q4639613) (← links)
- Chemotaxis Effect on Algae by Inorganic Polymer Flocculants: Backward Bifurcations and Traveling Wave Solutions (Q4647442) (← links)
- Classical solution of a PDE system stemming from auxin transport model for leaf venation (Q4959733) (← links)
- On the global existence and qualitative behaviour of one-dimensional solutions to a model for urban crime (Q5056790) (← links)
- A predator–prey model with taxis mechanisms and stage structure for the predator (Q5113313) (← links)
- Global existence and uniqueness of solutions to a chemotaxis system (Q5140816) (← links)
- Boundedness and global stability of a diffusive prey–predator model with prey-taxis (Q5164917) (← links)
- Stability and Bifurcation in a Predator–Prey System with Prey-Taxis (Q5222621) (← links)
- Boundedness of solutions to parabolic-elliptic Keller-Segel systems with signal-dependent sensitivity (Q5246804) (← links)
- Global existence of solutions for a fully parabolic chemotaxis system with consumption of chemoattractant and logistic source (Q5248796) (← links)
- Toward a mathematical theory of Keller–Segel models of pattern formation in biological tissues (Q5265465) (← links)
- Boundedness and stabilization in a two-species chemotaxis system with two chemicals (Q5919123) (← links)
- Boundedness and stabilization in a two-species chemotaxis system with two chemicals (Q5919281) (← links)
- Boundedness on a fully parabolic singular chemotaxis system with indirect signal production and logistic source (Q6062920) (← links)
- An attraction‐repulsion chemotaxis system with logistic source (Q6065007) (← links)
- Dynamics of a chemotaxis-May-Nowak model with volume filling sensitivity (Q6112129) (← links)
- Global boundedness in a two-dimensional chemotaxis system with nonlinear diffusion and singular sensitivity (Q6119529) (← links)
- A note to the global solvability of a chemotaxis-Navier-Stokes system with density-suppressed motility (Q6130248) (← links)
- Global well‐posedness and uniform boundedness of a higher dimensional crime model with a logistic source term (Q6141510) (← links)
- Boundedness and large-time behavior in a chemotaxis system with signal-dependent motility arising from tumor invasion (Q6153633) (← links)
- Boundedness in a higher-dimensional singular chemotaxis-growth system with indirect signal production (Q6165408) (← links)
- Spatiotemporal dynamics and bifurcation analysis of a generalized two-prey one-predator system with diffusion and double prey-taxes (Q6538894) (← links)
- Asymptotic behavior in a two-species chemotaxis system with Lotka-Volterra type competition and two signals (Q6539301) (← links)
- Dynamical analysis of a diffusive population-toxicant model with toxicant-taxis in polluted aquatic environments (Q6566675) (← links)
- Boundedness and stabilization in a haptotaxis model of oncolytic virotherapy with nonlinear sensitivity (Q6569354) (← links)
- Global classical solutions in a self-consistent chemotaxis(-Navier)-Stokes system. (Q6584410) (← links)
- Global solvability and asymptotic behavior of solutions for a fully parabolic nutrient taxis system (Q6597591) (← links)
- Global bounded solutions and large time behavior of a chemotaxis system with flux limitation (Q6632174) (← links)
- Global existence in a fully parabolic attraction-repulsion chemotaxis system with singular sensitivities and proliferation (Q6632958) (← links)
- Boundedness and asymptotic stability of solutions in an alopecia areata chemotaxis system with signal-dependent sensitivity (Q6638330) (← links)
- Eventual smoothness and stabilization of global weak solutions to a chemotaxis system with sublinear consumption of chemoattractant (Q6642462) (← links)
- Study on a growth-expansion model with chemotaxis in nutrient-replete environments (Q6669908) (← links)
