Pages that link to "Item:Q1707304"
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The following pages link to Singular structure formation in a degenerate haptotaxis model involving myopic diffusion (Q1707304):
Displaying 30 items.
- Singular structure formation in a degenerate haptotaxis model involving myopic diffusion (Q1707304) (← links)
- Global boundedness of classical solutions to a two species cancer invasion haptotaxis model with tissue remodeling (Q2009311) (← links)
- Global weak solutions to an oncolytic viral therapy model with doubly haptotactic terms (Q2025878) (← links)
- Global classical solutions to an oncolytic viral therapy model with triply haptotactic terms (Q2026546) (← links)
- Modeling multiple taxis: tumor invasion with phenotypic heterogeneity, haptotaxis, and unilateral interspecies repellence (Q2026618) (← links)
- Analysis of a two-dimensional triply haptotactic model with a fusogenic oncolytic virus and syncytia (Q2035753) (← links)
- Dampening effects on global boundedness and asymptotic behavior in an oncolytic virotherapy model (Q2054010) (← links)
- Dampening effects on global boundedness in a quartic haptotactic model with fusogenic oncolytic virus and syncytia (Q2096964) (← links)
- A critical virus production rate for blow-up suppression in a haptotaxis model for oncolytic virotherapy (Q2188508) (← links)
- Boundedness in a haptotactic cross-diffusion system modeling oncolytic virotherapy (Q2208440) (← links)
- Critical mass for infinite-time blow-up in a haptotaxis system with nonlinear zero-order interaction (Q2229257) (← links)
- Global classical solutions to a doubly haptotactic cross-diffusion system modeling oncolytic virotherapy (Q2297246) (← links)
- Refined regularity and stabilization properties in a degenerate haptotaxis system (Q2309179) (← links)
- Dampening effect of logistic source in a two-dimensional haptotaxis system with nonlinear zero-order interaction (Q2657693) (← links)
- Global boundedness in an oncolytic virotherapy model with generalized logistic source (Q2679221) (← links)
- Asymptotic behavior of solutions to a tumor angiogenesis model with chemotaxis–haptotaxis (Q4973287) (← links)
- Global solvability in a two-species chemotaxis system with logistic source (Q4987861) (← links)
- A critical virus production rate for efficiency of oncolytic virotherapy (Q5056748) (← links)
- Global solutions to a haptotaxis system with a potentially degenerate diffusion tensor in two and three dimensions (Q5060031) (← links)
- Chemotaxis and cross-diffusion models in complex environments: Models and analytic problems toward a multiscale vision (Q5083464) (← links)
- Global generalized solutions for a two-species chemotaxis system with tensor-valued sensitivity and logistic source (Q5104589) (← links)
- Asymptotic stability of exogenous chemotaxis systems with physical boundary conditions (Q5157419) (← links)
- Modeling glioma invasion with anisotropy- and hypoxia-triggered motility enhancement: From subcellular dynamics to macroscopic PDEs with multiple taxis (Q5164207) (← links)
- Asymptotic stability of spatial homogeneity in a haptotaxis model for oncolytic virotherapy (Q5861961) (← links)
- Global weak solutions in a three-dimensional two-species cancer invasion haptotaxis model without cell proliferation (Q5884846) (← links)
- Boundedness in a two-dimensional two-species cancer invasion haptotaxis model without cell proliferation (Q6102488) (← 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)
- Stabilization despite pervasive strong cross-degeneracies in a nonlinear diffusion model for migration–consumption interaction (Q6169637) (← links)
- Global dynamics for a two-species chemotaxis system with loop (Q6495908) (← links)
