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Data were calculated as a discrimination task from each averaged waveform.
Tissue distribution data were calculated as percent injected dose per gram (%ID/g) applying a suitable algorithm.
All data were calculated as means ± SD and multiple group comparisons were performed using one-way ANOVA, followed by the post hoc Tukey's test for comparisons.
Data were calculated as means ± SD.
Data were calculated as Mean ± SEM.
All numerical data were calculated as means and standard deviations.
The data were calculated as the mean Fluorescence intensity.
Spectrogram [30] and power spectral density [7] of acceleration data were calculated as described previously.
Relative expression data were calculated as described by Livak and Schmittgen [49].
Data were calculated as percentage of stimulated untransfected cells and expressed as mean ± SEM.
Data were calculated as percentage over unstimulated cells and expressed as means ± SEM.
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