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The experimental laboratory mice were arbitrarily divided in six groups each containing six mice.
Then, mice were arbitrarily placed in control (n=10) and NaPaC-treated group (n=10).
Since the mice were arbitrarily labeled, we used the permutation of mouse identities that gave the smallest value of D JS between two groups.
When tumors reached a volume of 200 mm, the mice were arbitrarily assigned to different groups (n = 6 each) to receive intratumoural injections of 10 PFU Ad-NDRG2, Ad-LacZ, or PBS.
Based on our observations of mammary tumor development [ 21], MMT mice were arbitrarily stratified into three age groups for purpose of experiment, including: 20 to 35 days (hyperplastic lesion), 53 to 87 days (mammary intraepithelial neoplasms (MIN), a premalignant stage), and 98 to 170 days (malignant stage) and compared with control MT and MUC1.Tg mice.
Mice were arbitrarily placed in the groups of treatment.
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For the qPCR analysis: mRNA levels were standardized to cyclophilin; expression in the PPARα-null mice was arbitrarily set to 1. Significance was determined by a Bayesian t-test (array data) or unpaired student's t-test (qPCR data), * = p-value <0.05.
For these mice, threshold was arbitrarily assigned to be 95 dB SPL.
For mice that did not receive conditioning in Experiments 1 and 7, baseline preference scores were arbitrarily calculated as the time spent by each mouse in the aspen environment minus the time spent by each mouse in the paper environment.
Eight yeasts representing the four groups were arbitrarily selected, and their effects on EAE model mice were examined.
These concentrations were arbitrarily chosen.
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