The numerical examples show that the regularised models exhibit all of the desired features: mesh insensitivity, imperfection size insensitivity and description of size effects.
Because of the difficulty to suggest a single model which exhibits all properties of non-Newtonian fluids, they cannot be described as simply as Newtonian fluids.
The model (2) exhibits all possible outcomes of oncolytic virus infection, i.e., no effect on the tumor (domains I and II in Fig. 1), stabilization or reduction of the tumor load (domains IV and V), and complete elimination of the tumor (domain VIII).
Thus, the availability of an in vitro erythropoiesis model, which exhibits all stages of RBC development, would be a powerful tool for investigating the factors and molecular mechanisms involved in proliferation and differentiation of human erythroid cells under normal and pathophysiologic conditions.
Our model, in contrast to the previously published models of oncolytic virus-tumor interaction, exhibits all possible outcomes of oncolytic virus infection, i.e., no effect on the tumor, stabilization or reduction of the tumor load, and complete elimination of the tumor.
The figure shows that no single model exhibits the lowest RMSE values for all scenarios, as the LCAR model performs best in this regard for six scenarios and second best in the remaining three, while the LM model has the lowest values for three scenarios.
The mouse model described above is unique because it exhibits all three proteinopathies clinically associated with AD, DLB, and PD.
The tensor model proves to exhibit all the flow modes found in the molecular model.
The standard model exhibit large error in all cases and is not recommended.
However, none of these models can completely exhibit all that is observed clinically and account the full course of infection.
