Moreover, it applies perfectly to the contribution of the defined five metrics for characterizing routes in a hybrid network in order to reduce end-to-end delay and determine the best path, while at the same time satisfying the QoS requirements.
Although intestinal Cr absorption in humans has not been well characterized, potential routes for Cr absorption into systemic circulation include paracellular movement by solvent drag transport, or via basolateral Cr transport by the monocarboxylate transporter 12 (MCT12).
The optimal path length characterized the shortest route from an origin to destination.
We characterize this route choice behavior in the face of uncertain travel times with the notion of probabilistic user equilibrium (PUE).
Existing Proportional-Switch Adjustment Process (PSAP) models have been extensively investigated to characterize travelers' route choice behaviors; PSAP has concise structure and intuitive behavior rule.
Further work is needed to more precisely characterize the route(s) of exposure.
The same events also characterize the route of clathrin-independent endocytic vesicles.
To characterize the route of sucrose movement, we performed dye transport studies, examining elongated internodes at the stage when sucrose begins to significantly accumulate within stems.
From Figure 3, we can see that the following categories primarily characterize the route from hMSC to hOST: 20 (cytokine activity), 27 (heparin binding), 46 (oxygen and reactive oxygen species metabolism), 52 (protein kinase activity), and 69 (translation initiation factor activity).
