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The measurements were taken using two experimental sets one with a grating for better resolution at high energies (a) and the other with a better resolution at low energies (b).
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A set of 198 experimental data was generated using two experimental designs.
A family of model parameters was estimated using nine experimental training sets compiled from different cell-lines and laboratories.
We use seven experimental cycling data sets for model fitting and validation, six of them derived from PHEV drive cycles.
Two experimental sets were conducted for the differentiation assay.
Two experimental sets were conducted for myelination assay.
The two experimental sets we report generated complementary results.
The model was validated by using three tier experimental set ups 1) ischemia in the vascular bed 2) secondary ischemia in endothelial cells (EC) and cardiomyocyte cells cultured on ischemic vascular bed and 3) secondary ischemia created in caprine cardiac tissues by placing them on ischemic vascular bed.
The results are validated using two sets of experimental data involving different sets of fluorescent proteins.
Subsequently, the simulator was verified using two sets of experimental results.
The proposed algorithm was tested using two sets of experimental data.
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