Aydar Uatay
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Aydar Uatay has a total of 9 co-authors. Here are the top co-authors by number of shared publications:
Christina Surulescu
2 shared publications- Anna Zhigun
School of Mathematics and Physics, Queen’s University Belfast, Belfast, Northern Ireland, UK
1 shared publication Christian Stinner
Felix-Klein-Zentrum für Mathematik, Technische Universität Kaiserslautern, Paul-Ehrlich-Str. 31, 67663 Kaiserslautern, Germany
1 shared publication- Holly Kimko
Clinical Pharmacology & Quantitative Pharmacology, AstraZeneca, Gaithersburg, MD 20878, USA
1 shared publication - Linda Irons
Department of Biomedical Engineering, Yale University, New Haven, USA
1 shared publication - Louis Gall
Clinical Pharmacology and Quantitative Pharmacology, Clinical Pharmacology and Safety Sciences, R&D, AstraZeneca
1 shared publication
Latest Publications
- 26 October 2023
- Published by Elsevier in Journal of Pharmaceutical Sciences
- Vol. 113 (1) , 11-21
Physiological Indirect Response Model to Omics-Powered Quantitative Systems Pharmacology Model
- 26 October 2023
- Published by Elsevier in Journal of Pharmaceutical Sciences
- Vol. 113 (1) , 11-21
Physiological Indirect Response Model to Omics-Powered Quantitative Systems Pharmacology Model
- Open Access
A Stochastic Modelling Framework for Single Cell Migration: Coupling Contractility and Focal Adhesions
The interaction of the actin cytoskeleton with cell–substrate adhesions is necessary for cell migration. While the trajectories of motile cells have a stochastic character, investigations of cell motility mechanisms rarely elaborate on the origins of the observed randomness. Here, guided by a few fundamental attributes of cell motility, I construct a minimal stochastic cell migration model from ground-up. The resulting model couples a deterministic actomyosin contractility mechanism with stochastic cell–substrate adhesion kinetics, and yields a well-defined piecewise deterministic process. Numerical simulations reproduce several experimentally observed results, including anomalous diffusion, tactic migration and contact guidance. This work provides a basis for the development of cell–cell collision and population migration models.
Open AccessA Stochastic Modelling Framework for Single Cell Migration: Coupling Contractility and Focal Adhesions
The interaction of the actin cytoskeleton with cell–substrate adhesions is necessary for cell migration. While the trajectories of motile cells have a stochastic character, investigations of cell motility mechanisms rarely elaborate on the origins of the observed randomness. Here, guided by a few fundamental attributes of cell motility, I construct a minimal stochastic cell migration model from ground-up. The resulting model couples a deterministic actomyosin contractility mechanism with stochastic cell–substrate adhesion kinetics, and yields a well-defined piecewise deterministic process. Numerical simulations reproduce several experimentally observed results, including anomalous diffusion, tactic migration and contact guidance. This work provides a basis for the development of cell–cell collision and population migration models.
- 7 November 2016
- Published by Springer Nature in Zeitschrift für angewandte Mathematik und Physik
- Vol. 67 (6) , 146
Global existence for a degenerate haptotaxis model of cancer invasion
- 7 November 2016
- Published by Springer Nature in Zeitschrift für angewandte Mathematik und Physik
- Vol. 67 (6) , 146
Global existence for a degenerate haptotaxis model of cancer invasion
- 12 October 2016
- Published by World Scientific Pub Co Pte Ltd in Mathematical Models and Methods in Applied Sciences
- Vol. 26 (11) , 2163-2201
Global existence for a go-or-grow multiscale model for tumor invasion with therapy
- 12 October 2016
- Published by World Scientific Pub Co Pte Ltd in Mathematical Models and Methods in Applied Sciences
- Vol. 26 (11) , 2163-2201
Global existence for a go-or-grow multiscale model for tumor invasion with therapy