Gene Expression Landscape of Chronic Myeloid Leukemia K562 Cells Overexpressing the Tumor Suppressor Gene PTPRG.

This study concerns the analysis of the modulation of Chronic Myeloid Leukemia (CML) cell model K562 transcriptome following transfection with the tumor suppressor gene encoding for Protein Tyrosine Phosphatase Receptor Type G (PTPRG) and treatment with the tyrosine kinase inhibitor (TKI) Imatinib. Specifically, we aimed at identifying genes whose level of expression is altered by PTPRG modulation and Imatinib concentration. Statistical tests as differential expression analysis (DEA) supported by gene set enrichment analysis (GSEA) and modern methods of ontological term analysis are presented along with some results of current interest for forthcoming experimental research in the field of the transcriptomic landscape of CML.

Multi-fidelity surrogate modeling through hybrid machine learning for biomechanical and finite element analysis of soft tissues.

Biomechanical simulation enables medical researchers to study complex mechano-biological conditions, although for soft tissue modeling, it may apply highly nonlinear multi-physics theories commonly implemented by expensive finite element (FE) solvers. This is a significantly time-consuming process on a regular computer and completely inefficient in urgent situations. One remedy is to first generate a dataset of the possible inputs and outputs of the solver in order to then train an efficient machine learning (ML) model, i.

A backward pre-stressing algorithm for efficient finite element implementation of in vivo material and geometrical parameters into fibril-reinforced mixture models of articular cartilage.

Classical continuum mechanics has been widely used for implementation of the material models of articular cartilage (AC) mainly with the aid of the finite element (FE) method, which, in many cases, considers the stress-free configuration as the initial configuration. On the contrary, the AC experimental tests typically begin with the pre-stressed state of both material and geometrical properties. Indeed, imposing the initial pre-stress onto AC models with the in vivo values as the initial state would result in nonphysiologically expansion of the FE mesh due to the soft nature of AC.

Simulation of cardiac electrophysiology on next-generation high-performance computers.

Models of cardiac electrophysiology consist of a system of partial differential equations (PDEs) coupled with a system of ordinary differential equations representing cell membrane dynamics. Current software to solve such models does not provide the required computational speed for practical applications. One reason for this is that little use is made of recent developments in adaptive numerical algorithms for solving systems of PDEs.