Predicting red blood cell transport and capillary hemodynamics in angiogenic and tumor vascular networks in silico.

Also, experimental determination of vasculature-scale “lumped” parameters does not reveal hemodynamic variations within a capillary vessel that are physiologically highly significant.

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Due to the heterogeneity of the diameter, flow rate, and hematocrit distributions in the networks, a clear trend of the nonlinear diameter dependence of the viscosity effect is not seen for the A and T networks.

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