On the unsteady Darcy-Forchheimer-Brinkman equation in local and nonlocal tumor growth models
DOI10.1142/S0218202519500325zbMATH Open1425.35076arXiv1812.08872WikidataQ127751464 ScholiaQ127751464MaRDI QIDQ4973296FDOQ4973296
Authors: Marvin Fritz, E. A. B. F. Lima, J. Tinsley Oden, B. Wohlmuth
Publication date: 3 December 2019
Published in: M\(^3\)AS. Mathematical Models \& Methods in Applied Sciences (Search for Journal in Brave)
Full work available at URL: https://arxiv.org/abs/1812.08872
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Cited In (18)
- Strong well-posedness and inverse identification problem of a non-local phase field tumour model with degenerate mobilities
- Tumor evolution models of phase-field type with nonlocal effects and angiogenesis
- An asymptotic analysis and numerical simulation of a prostate tumor growth model via the generalized moving least squares approximation combined with semi-implicit time integration
- Local and nonlocal phase-field models of tumor growth and invasion due to ECM degradation
- Existence and uniqueness of solution to unsteady Darcy-Brinkman problem with Korteweg stress for modelling miscible porous media flow
- Improvement of nonlocal Pennes heat transfer equation in fractal dimensions in the analysis of tumor growth
- Parameter identification for nonlocal phase field models for tumor growth via optimal control and asymptotic analysis
- Modeling and simulation of vascular tumors embedded in evolving capillary networks
- Time-fractional Cahn-Hilliard equation: well-posedness, degeneracy, and numerical solutions
- On a nonlocal Cahn–Hilliard model permitting sharp interfaces
- On a class of non-local phase-field models for tumor growth with possibly singular potentials, chemotaxis, and active transport
- Cahn-Hilliard-Brinkman systems for tumour growth
- On a phase field model of Cahn-Hilliard type for tumour growth with mechanical effects
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- Nonlocal Cahn-Hilliard-Hele-Shaw systems with singular potential and degenerate mobility
- Stability and error analysis of structure-preserving schemes for a diffuse-interface tumor growth model
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