Sentence examples for mouse epithelial network from inspiring English sources

In the case of the mouse epithelial network shown in Figure 1A, Tc = 1.53 gives the CD4/CD8SP ratio of 2∶1 (2.09±0.06) (Fig. 3).

Interestingly if at day 50 of simulation is reestablished the normal mouse epithelial network, the selection process and proportions of thymocyte populations normalize after seven weeks.

After 200 days of simulation, the average number of thymocytes in the lattice was around 16950 cells, two times the number of cells obtained with the mouse epithelial network.

The CD4SP over CD8SP cell ratio as a function of Tc also follows a decay in a power law, as we found using the mouse epithelial network, but with the exponent a = −20.5.

The number of cells in each thymocyte subset is closer to that in the mouse epithelial network: 4.7% (419.8±42.4 cells) of DN cells, 84% (7559.4±128.8 cells) of DP cells, 11.4% (230.4±8.75 cells cells and 789.3±16.0 cells cells) of SP cells, and 0.9% (83.9±4.35 cells) of cells that are selected and leave the lattice.

To compare the results obtained with the mouse epithelial network, we also evaluated the dynamics of the model with a human epithelial network derived from data obtained experimentally in our laboratory, by immunolabeling a histological section of a normal child thymic tissue with a pan-cytokeratin antibody.

The results shown herein indicate that the thymus architecture is important in determination of the duration of the TCR signal; simulations performed with mouse and human epithelial networks provide different CD4∶CD8 ratios, using the same set of parameters.

Here, our analysis of distinct human and mouse epithelial subtypes has highlighted potential miRNA networks responsible for governing lineage commitment and differentiation in mammary tissue.

After 6 weeks, an epithelial network was evident in those mice injected with WT epithelium (Fig. 5B) but not in those injected with RIP140 KO epithelium (Fig. 5C) or in control mice (Fig. 5A).

In this respect, we showed that simulations made using a mathematically-devised random epithelial network presented a specific dynamics that differed from those observed for the experimental mouse or human epithelial networks.

Figure 7 shows that the temporal evolution of the thymocyte subsets upon interaction with the random epithelial network assume different dynamics, when compared with the results of interactions with the mouse and human epithelial networks (seen in Figs. 2D and 6C, respectively).