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To calculate the mean of the polarization angle, we chose three time points before and after wounding, per cell (time points 0, 10 and 18 min before wounding and time points 10, 18 and 28 min after wounding, respectively).
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ADER runtime is reduced by performing only one Cauchy Kowalewski (C K) procedure per cell per time step and by using the Differential Transform Method for high-order derivatives.
Investigating further, the scientists chose 20 factors that seemed to have the most potential for creating neurons and subsequently delivered activated versions of those genes — one gene per cell — this time looking to see if the genes changed the cells' molecular nature.
We further optimized loading conditions by altering AuNP concentration (per cell) and time of incubation.
Figure 6 The system-wide PF utility versus time for K = 16 and N t = N r = 2. Figure 7 The average achievable sum rate per cell versus time for K = 16 and N t = N r = 2.
Intuitively, this product represents the number of mutations generated per cell division time in a population of cells.
Hence, we decided to describe the decrease in the number of RIF per cell over time with a biexponential model.
In these calculations, the rate of division (average division per cell per time point) can be determined directly for the entire experiment by counting the divisions for a given population.
During this time the measured fluorescence intensities showed large variations (mean cMEF: 2.18*106 ± 41.9%), probably indicating variations in virus protein content per cell over time of infection.
Venn diagrams of the differentially expressed genes per cell line, time point and treatment showing overlap of genes between the different conditions.
Pearson correlation was used to evaluate a possible correlation between PML-NBs frequency per cell and time after exposure and between age and focus formation.
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