qRT-PCR data were calculated using the comparative Ct method (Life Technologies).
Data were calculated using the MIT Sloan Management Review tool kit for Kane et al., "Moving Beyond Marketing"; see "2014 Social Business Interactive Tool," 2014, https://sloanreview.mit.edu.edu
Relative permeability data were calculated using the new models and the model results were compared with experimental data measured using a steady-state technique.
All the data were calculated using the MOE 2014.09 package.
Statistically significant data were calculated using the signed rank test (p < 0.01), and agreement analysis was calculated using Cohen's kappa.
The P values of cell cycle data were calculated using Chi-square test.
Data were calculated using the delta-delta-Ct method, where the GAPDH mRNA levels were used as a normalization control.
After the reaction, cycle threshold (CT) data were calculated using fixed threshold settings, and the mean CT was determined from the triplicate PCR results.
mRNA expression data were calculated using the Livak method [36], and data are presented as the fold change of the gene of interest, relative to that of control animals.
Descriptive statistics of socio-demographic variables and clinical data were calculated using frequencies and percentages, while the outcomes in FA in the different ROIs were calculated by means and standard deviations.
Gas sorption analyzer was carried out using Quantachrome Instruments and adsorption data were calculated using multipoint BET to provide a specific surface area, adsorption desorption isotherm, and BJH desorption to provide pore size and volume.
