Data for local cooling alone were normalized to baseline; total vasoconstriction response (local cooling + NA) was normalized to baseline.
Data were normalized to baseline values and expressed as percentage as mean±s.e.m deviation.
The final signal was normalized to baseline fluorescence F 0), as [F t)s − F 0)]/F(0) [65], [65].
Responses were normalized to baseline and statistics were based on values obtained during the last 5 minutes of recording (Fig. 2a,b).
Data shown was normalized to baseline (before plasticity induction).
For LTP experiments post-tetanic responses were normalized to baseline.
Responses were normalized to baseline, and data were analyzed using ANOVA.
Typically PSPs are normalized to baseline responses to allow for comparisons across slices and across animals.
For analysis of LTP experiments, post-tetanic responses were normalized to baseline as is standard in this field.
Fluorescence intensity was normalized to baseline (average of all pre-bleach measurements) and plotted as a function of time.
