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Global Weak Solutions in a PDE-ODE System Modeling Multiscale Cancer Cell Invasion

https://doi.org/10.1137/13094058x
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Holder Estimates for Local Solutions of Some Doubly Nonlinear Degenerate Parabolic Equations
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Global Solutions of Some Chemotaxis and Angiogenesis Systems in High Space Dimensions
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Multiscale agent-based cancer modeling
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Multiscale modelling and nonlinear simulation of vascular tumour growth
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How Far Can Chemotactic Cross-diffusion Enforce Exceeding Carrying Capacities?
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Function and interactions of integrins
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Boundedness vs. blow-up in a chemotaxis system
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Finite-time blowup and global-in-time unbounded solutions to a parabolic–parabolic quasilinear Keller–Segel system in higher dimensions
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Energy-type estimates and global solvability in a two-dimensional chemotaxis–haptotaxis model with remodeling of non-diffusible attractant
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Global existence of classical solutions to a combined chemotaxis–haptotaxis model with logistic source
inferredcites →https://doi.org/10.1016/j.jmaa.2010.02.015openalex-snapshot
A density-dependent chemotaxis–haptotaxis system modeling cancer invasion
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Mathematical modelling, analysis and numerical simulations for the influence of heat shock proteins on tumour invasion
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Finite-time blow-up in the higher-dimensional parabolic–parabolic Keller–Segel system
inferredcites →https://doi.org/10.1016/j.nonrwa.2010.06.027openalex-snapshot
Global existence for a haptotaxis model of cancer invasion with tissue remodeling
inferredcites →https://doi.org/10.1016/s0362-546x(01)00815-xopenalex-snapshot
Exponential attractor for a chemotaxis-growth system of equations
inferredcites →https://doi.org/10.1023/a:1006667303583openalex-snapshot
Alterations in proteolytic activity at low pH and its association with invasion: A theoretical model
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Role of integrins in cell invasion and migration
inferredcites →https://doi.org/10.1080/03605300903473426openalex-snapshot
Boundedness in the Higher-Dimensional Parabolic-Parabolic Chemotaxis System with Logistic Source
inferredcites →https://doi.org/10.1080/03605302.2011.591865openalex-snapshot
Global Large-Data Solutions in a Chemotaxis-(Navier–)Stokes System Modeling Cellular Swimming in Fluid Drops
inferredcites →https://doi.org/10.1080/03605309708821314openalex-snapshot
Heat kernels and maximal l p —l q estimates for parabolic evolution equations
inferredcites →https://doi.org/10.1080/10273660008833042openalex-snapshot
Mathematical Modelling of Tumour Invasion and Metastasis
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Global solution for a chemotactic–haptotactic model of cancer invasion
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Finite-time blow-up in a quasilinear system of chemotaxis
inferredcites →https://doi.org/10.1088/1478-3975/6/1/016008openalex-snapshot
Multi-scale modelling of cancer cell intravasation: the role of cadherins in metastasis
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Linear and Quasi-linear Equations of Parabolic Type
inferredcites →https://doi.org/10.1093/imammb/dqq011openalex-snapshot
'Go or Grow': the key to the emergence of invasion in tumour progression?
inferredcites →https://doi.org/10.1101/cshperspect.a005074openalex-snapshot
Integrins in Cell Migration
inferredcites →https://doi.org/10.1115/1.3424338openalex-snapshot
Navier Stokes Equations: Theory and Numerical Analysis
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Global Existence of Classical Solutions for a Haptotaxis Model
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A Combined Chemotaxis-haptotaxis System: The Role of Logistic Source
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A Chemotaxis-Haptotaxis Model: The Roles of Nonlinear Diffusion and Logistic Source
inferredcites →https://doi.org/10.1142/s0218202510004301openalex-snapshot
BOUNDEDNESS OF SOLUTIONS OF A HAPTOTAXIS MODEL
inferredcites →https://doi.org/10.1142/s0218202510004775openalex-snapshot
ASYMPTOTIC BEHAVIOR OF GLOBAL SOLUTIONS TO A MODEL OF CELL INVASION
inferredcites →https://doi.org/10.1142/s0218202511500175openalex-snapshot
A MULTISCALE APPROACH TO CELL MIGRATION IN TISSUE NETWORKS
inferredcites →https://doi.org/10.1142/s0218202512500480openalex-snapshot
CONVERGENCE OF A CANCER INVASION MODEL TO A LOGISTIC CHEMOTAXIS MODEL
inferredcites →https://doi.org/10.1142/s0218202514500249openalex-snapshot
On a class of multiscale cancer cell migration models: Well-posedness in less regular function spaces
inferredcites →https://doi.org/10.1529/biophysj.107.114678openalex-snapshot
Modeling the Influence of the E-Cadherin-β-Catenin Pathway in Cancer Cell Invasion: A Multiscale Approach
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On a multiscale model involving cell contractivity and its effects on tumor invasion

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Mathematical Research for Models Which is Related to Chemotaxis System
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Solvability of Solid Tumor Invasion Model
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Global Boundedness and Asymptotic Stability of Solutions in a Forager-Exploiter Model with Logistic Source
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Global existence and decay for a chemotaxis-growth system with generalized volume-filling effect and sublinear secretion
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Global existence for a degenerate haptotaxis model of cancer invasion
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Boundedness and large-time behavior for a two-dimensional quasilinear chemotaxis-growth system with indirect signal consumption
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Global existence and boundedness of a chemotaxis model with indirect production and general kinetic function
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Boundedness in the higher-dimensional fully parabolic chemotaxis-competition system with loop
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Global existence for a class of chemotaxis systems with signal-dependent motility, indirect signal production and generalized logistic source
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On a fully parabolic chemotaxis system with source term and periodic asymptotic behavior
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Nonlocal adhesion models for two cancer cell phenotypes in a multidimensional bounded domain
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On a two-species chemotaxis-competition system with indirect signal consumption
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Boundedness and stabilization in a quasilinear forager–exploiter model with volume-filling effects
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Global existence and asymptotic stability of solutions to a forager–exploiter model with logistic source
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Global boundedness in an oncolytic virotherapy model with generalized logistic source
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Global existence and boundedness of solutions to a two-species chemotaxis-competition system with singular sensitivity and indirect signal production
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Boundedness in a two-dimensional two-species cancer invasion haptotaxis model without cell proliferation
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Global boundedness and large time behavior in a chemotaxis system with indirect signal consumption
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Global bounded solution of a forager–exploiter model with logistic sources and different taxis mechanisms
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Boundedness and large-time behavior in a chemotaxis system with signal-dependent motility arising from tumor invasion
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Global dynamics in a competitive chemotaxis–(Navier)–Stokes system with indirect signal consumption
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Global dynamics of a pursuit–evasion predator–prey model with alarm signal
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Global boundedness in a three-dimensional chemotaxis-Stokes system with double chemical signals and quadratic damping effects
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Global boundedness and asymptotic behavior of a predator–prey chemotaxis model
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A subcritical mass criterion for boundedness in a chemotaxis system with indirect signal production and signal-dependent motility
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Global Boundedness of Solutions to a Food Chain Model with Nonlinear Taxis Sensitivity
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Global Dynamics for a Class of Chemotaxis Systems with Density-Suppressed Motility and Nonlinear Indirect Signal Consumption
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Global Weak Solutions in a Haptotactic Cross-Diffusion System Modeling Oncolytic Virotherapy with Nonlinear Diffusion
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Global Solvability and Boundedness for an Indirect Absorption Keller-Segel System with Signal-Dependent Motility and Logistic Source
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Global Solvability for a Three-Dimensional Doubly Haptotactic System with Porous Medium Diffusion
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Global Solvability and Uniform Boundedness of Classical Solution for Chemotaxis System of Immune Responses to Solid Tumors
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Boundedness and Stability in a Chemotaxis-Growth Model with Indirect Attractant Production and Signal-Dependent Sensitivity
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Global Classical Solutions to an Oncolytic Viral Therapy Model with Triply Haptotactic Terms
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Boundedness in a Quasilinear Chemotaxis Model with Logistic Growth and Indirect Signal Production
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The Global Existence of Bounded Weak Solutions to a Degenerate Haptotaxis and Diffusion Model of Cancer Invasion
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Boundedness and Stabilization in a Stage-Structured Predator–Prey Model with Two Taxis Mechanisms
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Global Boundedness of a Two-species Parabolic Keller-Segel System with Gradient-dependent Singular Sensitivity and Indirect Signal Production
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Tumor Evolution Models of Phase-Field Type with Nonlocal Effects and Angiogenesis
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Chemotactic Feedback Controls Patterning in Hybrid Tumor–Stroma Model
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Boundedness and stabilization in a two-species competition system with density-dependent motility and indirect signal production
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Stability in a Two-dimensional Keller-Segel-Navier-Stokes System
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Blow-Up Phenomena of a Cancer Invasion Model with Nonlinear Diffusion and Haptotaxis Term
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Global existence and boundedness in a chemotaxis system with indirect nonlinear signal production
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Global solvability of a two-species attraction-repulsion chemotaxis system with singular sensitivity
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Global existence of classical solutions to a chemotaxis-haptotaxis model
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Global solvability of a class of reaction–diffusion systems with cross-diffusion
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Finite-time blow-up of solutions to a cancer invasion mathematical model with haptotaxis effects
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Global boundedness in a three-dimensional chemotaxis–haptotaxis model
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An easy to implement numerical framework for a cancer invasion mathematical model with two distinct cancer sub-populations
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On a Parabolic–Elliptic system with chemotaxis and logistic type growth
inferred← citeshttps://doi.org/10.1016/j.jde.2017.06.034openalex-snapshot
Boundedness and global solvability to a chemotaxis model with nonlinear diffusion
inferred← citeshttps://doi.org/10.1016/j.jde.2018.01.027openalex-snapshot
Global existence and stabilization in a degenerate chemotaxis-Stokes system with mildly strong diffusion enhancement
inferred← citeshttps://doi.org/10.1016/j.jde.2018.02.031openalex-snapshot
Global solvability and boundedness to a coupled chemotaxis-fluid model with arbitrary porous medium diffusion
inferred← citeshttps://doi.org/10.1016/j.jde.2018.08.018openalex-snapshot
Large time behavior of solutions to a fully parabolic chemotaxis–haptotaxis model in N dimensions
inferred← citeshttps://doi.org/10.1016/j.jde.2018.12.019openalex-snapshot
Global classical solvability and generic infinite-time blow-up in quasilinear Keller–Segel systems with bounded sensitivities
inferred← citeshttps://doi.org/10.1016/j.jde.2019.10.046openalex-snapshot
Global classical solutions to a doubly haptotactic cross-diffusion system modeling oncolytic virotherapy
inferred← citeshttps://doi.org/10.1016/j.jde.2019.11.078openalex-snapshot
Boundedness of weak solutions of a chemotaxis-Stokes system with slow p-Laplacian diffusion
inferred← citeshttps://doi.org/10.1016/j.jde.2020.03.018openalex-snapshot
Global classical solutions and convergence to a mathematical model for cancer cells invasion and metastatic spread
inferred← citeshttps://doi.org/10.1016/j.jde.2020.04.039openalex-snapshot
Large time behavior in a three-dimensional degenerate chemotaxis-Stokes system modeling coral fertilization
inferred← citeshttps://doi.org/10.1016/j.jde.2020.05.008openalex-snapshot
Global boundedness and large time behavior of a chemotaxis system with indirect signal absorption
inferred← citeshttps://doi.org/10.1016/j.jde.2020.05.018openalex-snapshot
Boundedness and asymptotics of a reaction-diffusion system with density-dependent motility
inferred← citeshttps://doi.org/10.1016/j.jde.2020.07.032openalex-snapshot
Boundedness in a haptotactic cross-diffusion system modeling oncolytic virotherapy
inferred← citeshttps://doi.org/10.1016/j.jde.2021.04.020openalex-snapshot
Global bounded weak solutions for a chemotaxis-Stokes system with nonlinear diffusion and rotation
inferred← citeshttps://doi.org/10.1016/j.jde.2021.10.020openalex-snapshot
The role of local kinetics in a three-component chemotaxis model for Alopecia Areata
inferred← citeshttps://doi.org/10.1016/j.jde.2022.06.007openalex-snapshot
Global dynamics of a three-species spatial food chain model
inferred← citeshttps://doi.org/10.1016/j.jde.2022.07.044openalex-snapshot
A new result for global solvability in a singular chemotaxis-growth system with indirect signal production
inferred← citeshttps://doi.org/10.1016/j.jde.2022.08.018openalex-snapshot
Long time behavior of a parabolic p-Laplacian equation coupled to a compartmental ODE system with an induction threshold phenomenon
inferred← citeshttps://doi.org/10.1016/j.jde.2022.08.032openalex-snapshot
Global classical solutions to a higher-dimensional doubly haptotactic cross-diffusion system modeling oncolytic virotherapy
inferred← citeshttps://doi.org/10.1016/j.jde.2022.12.004openalex-snapshot
Global dynamics for a chemotaxis consumption system with signal-dependent motility and logistic source
inferred← citeshttps://doi.org/10.1016/j.jde.2023.02.063openalex-snapshot
Pursuit-evasion dynamics for Bazykin-type predator-prey model with indirect predator taxis
inferred← citeshttps://doi.org/10.1016/j.jde.2023.11.015openalex-snapshot
Boundedness of solutions for parabolic-elliptic predator-prey chemotaxis-fluid system with logistic source term
inferred← citeshttps://doi.org/10.1016/j.jde.2024.09.027openalex-snapshot
Global dynamics for a two-species chemotaxis-competition system with loop and nonlocal kinetics
inferred← citeshttps://doi.org/10.1016/j.jde.2024.12.045openalex-snapshot
Blow-up prevention by subquadratic and quadratic degradations in a three-dimensional Keller–Segel–Stokes system with indirect signal production
inferred← citeshttps://doi.org/10.1016/j.jde.2025.02.023openalex-snapshot
Existence of weak solutions for a volume-filling model of cell invasion into extracellular matrix
inferred← citeshttps://doi.org/10.1016/j.jde.2025.113625openalex-snapshot
Global existence for Lotka-Volterra models of predation and competition with diffusion and predator/competitor taxis in the spatial dimension n = 2,3
inferred← citeshttps://doi.org/10.1016/j.jde.2025.113913openalex-snapshot
Global existence and eventual smoothness of a nutrient consumption system involving local sensing and proliferation
inferred← citeshttps://doi.org/10.1016/j.jde.2025.113991openalex-snapshot
Global well-posedness to a parabolic-degenerate angiogenesis system
inferred← citeshttps://doi.org/10.1016/j.jfranklin.2026.109087openalex-snapshot
Sampled-data boundary stabilization of non-strict-feedback PDE-ODE cascades with distributed delays
inferred← citeshttps://doi.org/10.1016/j.jmaa.2018.03.052openalex-snapshot
Blow-up profiles and refined extensibility criteria in quasilinear Keller–Segel systems
inferred← citeshttps://doi.org/10.1016/j.jmaa.2019.123474openalex-snapshot
Analysis of a chemotaxis-convection model of capillary-sprout growth during tumor angiogenesis
inferred← citeshttps://doi.org/10.1016/j.jmaa.2020.124231openalex-snapshot
A new (and optimal) result for the boundedness of a solution of a quasilinear chemotaxis–haptotaxis model (with a logistic source)
inferred← citeshttps://doi.org/10.1016/j.jmaa.2020.124249openalex-snapshot
Viability in a non-local population model structured by size and spatial position
inferred← citeshttps://doi.org/10.1016/j.jmaa.2020.124665openalex-snapshot
Global bounded solution to a chemotaxis-convection model of capillary-sprout growth during tumor angiogenesis
inferred← citeshttps://doi.org/10.1016/j.jmaa.2021.125027openalex-snapshot
Homogenization and solvability in a chemotaxis-convection angiogenesis model with leakage boundary conditions
inferred← citeshttps://doi.org/10.1016/j.jmaa.2021.125078openalex-snapshot
Boundedness in a two-species chemotaxis system with nonlinear sensitivity and signal secretion
inferred← citeshttps://doi.org/10.1016/j.jmaa.2021.125299openalex-snapshot
Global classical solutions in a chemotaxis(-Navier)-Stokes system with indirect signal production
inferred← citeshttps://doi.org/10.1016/j.jmaa.2021.125545openalex-snapshot
Boundedness of weak solutions in a 3D chemotaxis-Stokes system with nonlinear doubly degenerate diffusion
inferred← citeshttps://doi.org/10.1016/j.jmaa.2021.125820openalex-snapshot
Global boundedness of a diffusive prey-predator model with indirect prey-taxis and predator-taxis
inferred← citeshttps://doi.org/10.1016/j.jmaa.2021.125825openalex-snapshot
Boundedness and stabilization in a two-species chemotaxis-competition system with indirect signal production
inferred← citeshttps://doi.org/10.1016/j.jmaa.2022.126793openalex-snapshot
Asymptotic behavior in a forager-exploiter model with nonlinear resource consumption with/without general logistic sources
inferred← citeshttps://doi.org/10.1016/j.jmaa.2023.127595openalex-snapshot
Global bounded weak solutions in a two-dimensional Keller-Segel-Navier-Stokes system with indirect signal production and nonlinear diffusion
inferred← citeshttps://doi.org/10.1016/j.jmaa.2024.128546openalex-snapshot
Boundedness and stabilization in a two-species chemotaxis-competition system with signal-dependent sensitivities and indirect signal consumption
inferred← citeshttps://doi.org/10.1016/j.jmaa.2024.128948openalex-snapshot
Dynamic behavior in a pursuit-evasion system with signaling mechanism
inferred← citeshttps://doi.org/10.1016/j.jmaa.2025.129290openalex-snapshot
Nonlinear generation index of bounded solutions in a chemotaxis system with indirect signal, density-suppressed motility and generalized logistic source
inferred← citeshttps://doi.org/10.1016/j.jmaa.2025.129346openalex-snapshot
Global boundedness of Lotka-Volterra competition system with cross-diffusion
inferred← citeshttps://doi.org/10.1016/j.jmaa.2025.129426openalex-snapshot
Global existence for a three-species predator-prey model with slow p-Laplacian diffusion
inferred← citeshttps://doi.org/10.1016/j.jmaa.2025.129473openalex-snapshot
Boundedness and global existence in a higher-dimensional parabolic-elliptic-ODE chemotaxis-haptotaxis model with remodeling of non-diffusible attractant
inferred← citeshttps://doi.org/10.1016/j.jmaa.2025.129522openalex-snapshot
On a mathematical model for tissue regeneration
inferred← citeshttps://doi.org/10.1016/j.jmaa.2025.129747openalex-snapshot
Boundedness of solutions to an alarm-taxis model with/without growth sources
inferred← citeshttps://doi.org/10.1016/j.jmaa.2025.129961openalex-snapshot
Global boundedness in a three-dimensional alarm-taxis system
inferred← citeshttps://doi.org/10.1016/j.jmaa.2025.130387openalex-snapshot
An eco-epidemiological model with prey-taxis and “slow” diffusion: global existence, boundedness and novel dynamics
inferred← citeshttps://doi.org/10.1016/j.jmaa.2026.130928openalex-snapshot
Global existence of classical solutions to high-dimensional urban crime models with competition
inferred← citeshttps://doi.org/10.1016/j.jmaa.2026.131054openalex-snapshot
Long time dynamics analysis of the Cauchy problem for the Chaplain-Lolas model
inferred← citeshttps://doi.org/10.1016/j.jtbi.2019.110088openalex-snapshot
Glioma invasion and its interplay with nervous tissue and therapy: A multiscale model
inferred← citeshttps://doi.org/10.1016/j.matcom.2025.06.014openalex-snapshot
Modeling the impact of Allee effect, herd behavior and harvesting on kelp beds: A cross-diffusion-ODE dynamical approach
inferred← citeshttps://doi.org/10.1016/j.matpur.2017.11.002openalex-snapshot
Singular structure formation in a degenerate haptotaxis model involving myopic diffusion
inferred← citeshttps://doi.org/10.1016/j.mbs.2026.109747openalex-snapshot
Global dynamics of an intraguild predation predator–prey model with density-dependent velocity suppression
inferred← citeshttps://doi.org/10.1016/j.na.2017.06.003openalex-snapshot
Existence of global bounded classical solution to a quasilinear attraction–repulsion chemotaxis system with logistic source
inferred← citeshttps://doi.org/10.1016/j.na.2020.111870openalex-snapshot
A critical virus production rate for blow-up suppression in a haptotaxis model for oncolytic virotherapy
inferred← citeshttps://doi.org/10.1016/j.na.2020.111923openalex-snapshot
Boundedness and convergence of constant equilibria in a two-species chemotaxis-competition system with loop
inferred← citeshttps://doi.org/10.1016/j.na.2021.112750openalex-snapshot
Existence and global asymptotic stability in a fractional double parabolic chemotaxis system with logistic source
inferred← citeshttps://doi.org/10.1016/j.nonrwa.2014.08.008openalex-snapshot
A stochastic multiscale model for acid mediated cancer invasion
inferred← citeshttps://doi.org/10.1016/j.nonrwa.2018.07.028openalex-snapshot
Global dynamics for an attraction–repulsion chemotaxis–(Navier)–Stokes system with logistic source
inferred← citeshttps://doi.org/10.1016/j.nonrwa.2018.09.019openalex-snapshot
Global solvability and large time behavior to a chemotaxis–haptotaxis model with nonlinear diffusion
inferred← citeshttps://doi.org/10.1016/j.nonrwa.2019.05.015openalex-snapshot
Global existence and boundedness of classical solutions to a forager–exploiter model with volume-filling effects
inferred← citeshttps://doi.org/10.1016/j.nonrwa.2019.103079openalex-snapshot
Global existence and asymptotic stability in a predator–prey chemotaxis model
inferred← citeshttps://doi.org/10.1016/j.nonrwa.2020.103276openalex-snapshot
Global weak solutions to an oncolytic viral therapy model with doubly haptotactic terms
inferred← citeshttps://doi.org/10.1016/j.nonrwa.2021.103374openalex-snapshot
Global well-posedness to a chemotaxis-Stokes system
inferred← citeshttps://doi.org/10.1016/j.nonrwa.2021.103447openalex-snapshot
Boundedness and large time behavior for a chemotaxis system with signal-dependent motility and indirect signal consumption
inferred← citeshttps://doi.org/10.1016/j.nonrwa.2022.103521openalex-snapshot
Boundedness and global stability of the predator–prey model with prey-taxis and competition
inferred← citeshttps://doi.org/10.1016/j.nonrwa.2022.103703openalex-snapshot
Global existence in a food chain model consisting of two competitive preys, one predator and chemotaxis
inferred← citeshttps://doi.org/10.1016/j.nonrwa.2023.103898openalex-snapshot
Global weak solution for a chemotaxis Navier–Stokes system with p -Laplacian diffusion and singular sensitivity
inferred← citeshttps://doi.org/10.1016/j.nonrwa.2023.103912openalex-snapshot
Smoothness effects of a quadratic damping term of mixed type on a chemotaxis-type system modeling propagation of urban crime
inferred← citeshttps://doi.org/10.1016/j.nonrwa.2023.103969openalex-snapshot
Boundedness on a fully parabolic singular chemotaxis system with indirect signal production and logistic source
inferred← citeshttps://doi.org/10.1016/j.nonrwa.2023.104017openalex-snapshot
Global dynamics of a three-species spatial food chain model with alarm-taxis and logistic source
inferred← citeshttps://doi.org/10.1016/j.nonrwa.2024.104119openalex-snapshot
Global boundedness and stability of a predator–prey model with alarm-taxis
inferred← citeshttps://doi.org/10.1016/j.nonrwa.2025.104415openalex-snapshot
Global boundedness in a two-dimensional chemotaxis-Navier–Stokes system with double chemical signals and nonlinear diffusion
inferred← citeshttps://doi.org/10.1016/j.nonrwa.2025.104436openalex-snapshot
Dynamics in a two-species system with common dynamical resources and general competition term
inferred← citeshttps://doi.org/10.1016/j.nonrwa.2025.104516openalex-snapshot
Global existence of weak solutions to a cell migration and (de)differentiation model with double haptotaxis in the context of tissue regeneration
inferred← citeshttps://doi.org/10.1016/j.nonrwa.2025.104520openalex-snapshot
A note on the logistic damping effect to ensure the global solvability of the chemotaxis system with degenerate signal-dependent motility
inferred← citeshttps://doi.org/10.1016/j.nonrwa.2026.104679openalex-snapshot
Boundedness and large time behavior in a parabolic-parabolic-elliptic forager-exploiter model with competitive kinetics
inferred← citeshttps://doi.org/10.1016/j.physd.2025.134654openalex-snapshot
Dynamic behavior of taxis-driven intraguild predation model of three species with BD functional response
inferred← citeshttps://doi.org/10.1016/j.rinam.2024.100450openalex-snapshot
Global boundedness and asymptotic behavior of the chemotaxis system for alopecia areata with singular sensitivity
inferred← citeshttps://doi.org/10.1016/j.rinam.2024.100473openalex-snapshot
Boundedness and asymptotic behavior in a quasilinear chemotaxis system with nonlinear diffusion and singular sensitivity for alopecia areata
inferred← citeshttps://doi.org/10.1016/j.rinam.2025.100602openalex-snapshot
Global boundedness of a three-species spatial intraguild predation model with alarm-taxis
inferred← citeshttps://doi.org/10.1017/prm.2020.97openalex-snapshot
Asymptotic stability of spatial homogeneity in a haptotaxis model for oncolytic virotherapy
inferred← citeshttps://doi.org/10.1017/prm.2022.24openalex-snapshot
Asymptotic behaviour in a doubly haptotactic cross-diffusion model for oncolytic virotherapy
inferred← citeshttps://doi.org/10.1017/s0956792520000236openalex-snapshot
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)
inferred← citeshttps://doi.org/10.1063/1.5010681openalex-snapshot
Persistence property in a two-species chemotaxis system with two signals
inferred← citeshttps://doi.org/10.1063/5.0097126openalex-snapshot
Global weak solutions in a three-dimensional two-species cancer invasion haptotaxis model without cell proliferation
inferred← citeshttps://doi.org/10.1063/5.0145255openalex-snapshot
Global asymptotic stability in a two-dimensional chemotaxis model arising from tumor invasion
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