At least 50 nuclei from each condition were analyzed.
We selected one representative student from each condition and analyzed their log data.
Data from each condition baseline subtracted.
We constructed for each individual subject statistical contrasts by subtracting null events from each condition.
For each participant, logistic functions were fitted to the data from each condition.
Three fields were chosen from each condition and data were analyzed by Student's t-test.
One mouse from each condition (treated or not with TSA) was sacrificed at various time points.
For our event-related design, we intermixed the stimuli from each condition as follows.
For the morphometric assay, 25 cells from each condition in 3 different fields were included in the analysis.
A 50% contribution from each condition suggested an equal chance that foci from either condition formed the cluster.
We collected and analyzed supernatants from each condition during the suppression assay in order to determine sCD25 production at 48 and 96 h time points (Figure 3).
