Pages that link to "Item:Q2830977"

The following pages link to To the exclusion of blow-up in a three-dimensional chemotaxis-growth model with indirect attractant production (Q2830977):

Displaying 29 items.

• Mass Threshold for Infinite-time Blowup in a Chemotaxis Model with Split Population (Q5003315) (← links)
• Global solvability and asymptotic stabilization in a three-dimensional Keller–Segel–Navier–Stokes system with indirect signal production (Q5024428) (← 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)
• Chemotaxis and cross-diffusion models in complex environments: Models and analytic problems toward a multiscale vision (Q5083464) (← links)
• (Q5096712) (← 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 boundedness and decay property of a three-dimensional Keller–Segel–Stokes system modeling coral fertilization (Q5229271) (← links)
• Hilbert method toward a multiscale analysis from kinetic to macroscopic models for active particles (Q5272436) (← links)
• Global existence of a quasilinear chemotaxis model with signal-dependent motility and indirect signal production mechanism (Q5884853) (← links)
• Global existence and boundedness in a chemotaxis system with indirect nonlinear signal production (Q6058362) (← links)
• Boundedness on a fully parabolic singular chemotaxis system with indirect signal production and logistic source (Q6062920) (← links)
• Global boundedness and large time behavior in a chemotaxis system with indirect signal consumption (Q6079014) (← links)
• Finite element analysis of chemotaxis-growth model with indirect attractant production and logistic source (Q6106709) (← links)
• Boundedness in a higher-dimensional singular chemotaxis-growth system with indirect signal production (Q6165408) (← 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 boundedness in an attraction-repulsion chemotaxis system involving nonlinear indirect signal mechanism (Q6542903) (← links)
• Boundedness and stability for an indirect signal absorption chemotaxis system with signal-dependent motility (Q6546782) (← links)
• Dirac-type aggregation with full mass in a chemotaxis model (Q6553094) (← links)
• Global boundedness and asymptotic behavior of the chemotaxis system for alopecia areata with singular sensitivity (Q6568879) (← links)
• Global classical solutions to an indirect chemotaxis-consumption model with signal-dependent degenerate diffusion and logistic source (Q6604894) (← links)
• Global existence and uniform boundedness to a bi-attraction chemotaxis system with nonlinear indirect signal mechanisms (Q6611459) (← links)
• Eventual smoothness in a chemotaxis-Navier-Stokes system with indirect signal production involving Dirichlet signal boundary condition (Q6613005) (← links)
• Global stabilization in a Keller-Segel-growth system with indirect signal production (Q6615296) (← links)
• Global boundedness in a chemotaxis system with signal-dependent motility and indirect signal consumption and logistic source (Q6615616) (← links)
• Negligibility of haptotaxis on global dynamics in a chemotaxis-haptotaxis system with indirect signal production (Q6615809) (← links)
• Global dynamics for a class of chemotaxis systems with density-suppressed motility and nonlinear indirect signal consumption (Q6667546) (← links)