Pages that link to "Item:Q3451747"
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The following pages link to Large Time Behavior in a Multidimensional Chemotaxis-Haptotaxis Model with Slow Signal Diffusion (Q3451747):
Displaying 47 items.
- A critical virus production rate for efficiency of oncolytic virotherapy (Q5056748) (← links)
- Does indirectness of signal production reduce the explosion-supporting potential in chemotaxis–haptotaxis systems? Global classical solvability in a class of models for cancer invasion (and more) (Q5056753) (← links)
- (Q5081609) (← links)
- Dynamics of a predator–prey system with nonlinear prey-taxis (Q5089482) (← links)
- (Q5096712) (← links)
- Global generalized solutions for a two-species chemotaxis system with tensor-valued sensitivity and logistic source (Q5104589) (← links)
- Critical mass on the Keller-Segel system with signal-dependent motility (Q5119238) (← links)
- Global solvability and stabilization to a cancer invasion model with remodelling of ECM (Q5130935) (← links)
- Global solvability and asymptotic behavior in a two-species chemotaxis system with Lotka–Volterra competitive kinetics (Q5164225) (← links)
- Negligibility of haptotaxis effect in a chemotaxis–haptotaxis model (Q5164239) (← links)
- A quasilinear parabolic–elliptic chemotaxis-growth system with nonlinear secretion (Q5207774) (← links)
- A new result for 2D boundedness of solutions to a chemotaxis–haptotaxis model with/without sub-logistic source (Q5243473) (← links)
- Asymptotic stability of spatial homogeneity in a haptotaxis model for oncolytic virotherapy (Q5861961) (← links)
- Asymptotic dynamics and spatial patterns of a ratio-dependent predator–prey system with prey-taxis (Q5862265) (← links)
- Global weak solutions in a three-dimensional two-species cancer invasion haptotaxis model without cell proliferation (Q5884846) (← links)
- Global boundedness of weak solutions to a chemotaxis-haptotaxis model with \(p\)-Laplacian diffusion (Q6054930) (← links)
- Asymptotic behavior of a three-dimensional haptotactic cross-diffusion system modeling oncolytic virotherapy (Q6057512) (← links)
- Global existence in a two-species chemotaxis system with signal-dependent sensitivity and logistic source (Q6070664) (← links)
- Global boundedness and large time behavior in a chemotaxis system with indirect signal consumption (Q6079014) (← links)
- Global solvability, pattern formation and stability to a chemotaxis-haptotaxis model with porous medium diffusion (Q6079310) (← links)
- Some further progress for boundedness of solutions to a quasilinear higher-dimensional chemotaxis-haptotaxis model with nonlinear diffusion (Q6091068) (← links)
- Large time behavior of solutions to a chemotaxis system with singular sensitivity and logistic source (Q6093981) (← links)
- Asymptotic stabilization in a three-dimensional Keller-Segel-Stokes system with indirect signal production and subquadratic degradation (Q6094873) (← links)
- Qualitative properties for a three-species food chain model with cross-diffusion and intra-specific competition (Q6097005) (← links)
- Boundedness in a two-dimensional two-species cancer invasion haptotaxis model without cell proliferation (Q6102488) (← links)
- Asymptotic behaviour in a doubly haptotactic cross-diffusion model for oncolytic virotherapy (Q6111246) (← links)
- Dynamics of a chemotaxis-May-Nowak model with volume filling sensitivity (Q6112129) (← links)
- Global existence and asymptotic behavior in a two-species chemotaxis system with signal production (Q6120369) (← links)
- Global boundedness and asymptotic stabilization in a chemotaxis system with density-suppressed motility and nonlinear signal production (Q6126787) (← links)
- On a mathematical model for cancer invasion with repellent pH-taxis and nonlocal intraspecific interaction (Q6153643) (← links)
- Boundedness of solutions to a chemotaxis-haptotaxis model with nonlocal terms (Q6154863) (← links)
- On a Parabolic-ODE chemotaxis system with periodic asymptotic behavior (Q6175078) (← links)
- Boundedness and asymptotic stability in a predator-prey system with density-dependent motilities (Q6192459) (← links)
- Global boundedness and asymptotic behavior in a chemotaxis system with signal‐dependent motility and indirect signal absorption (Q6198831) (← links)
- On small-data solution of the chemotaxis-SIS epidemic system with bilinear incidence rate (Q6490192) (← links)
- Blow-up prevention by logistic damping in a chemotaxis-May-Nowak model for virus infection (Q6542424) (← links)
- Qualitative behavior of solutions for a chemotaxis-haptotaxis system with gradient-dependent flux-limitation (Q6549360) (← links)
- A quasilinear chemotaxis-haptotaxis system: existence and blow-up results (Q6584922) (← links)
- Global strong solution and periodic dynamic behavior to Chaplain-Lolas model (Q6612565) (← links)
- Global boundedness and asymptotic behavior in a double haptotaxis model for oncolytic virotherapy (Q6614323) (← links)
- Negligibility of haptotaxis on global dynamics in a chemotaxis-haptotaxis system with indirect signal production (Q6615809) (← links)
- Critical exponent to a cancer invasion model with nonlinear diffusion (Q6632821) (← links)
- Global boundedness and asymptotic stability for a food chain model with nonlinear diffusion (Q6632826) (← links)
- Large time behavior of solution to a quasilinear chemotaxis model describing tumor angiogenesis with/without logistic source (Q6641250) (← links)
- Dynamic behavior in a pursuit-evasion system with signaling mechanism (Q6648766) (← links)
- Global dynamics for a class of chemotaxis systems with density-suppressed motility and nonlinear indirect signal consumption (Q6667546) (← links)
- Study on a growth-expansion model with chemotaxis in nutrient-replete environments (Q6669908) (← links)