Tibiae from twenty five 11 week old female C57BL/6 mice were separated into 2 preservation groups.
(C) 10 mice were separated into Small Tumor group (n = 4) and Large Tumor group (n = 6), p-value < 0.01 with student's two-tail t-test.
In the present study, male APPswe/PS1dE9 transgenic mice were separated from dam and pups 3 h per day from postnatal day 2 to day 21.
The mandibles of E12.5 mice were separated into SMG epithelium (bud), invaginating OE connected to the SMG (stalk), and OE distant from the SMG through laser micro-dissection, and the gene expression profiles of these three specimen types were then compared via RNA sequencing (RNA-seq) (Fig. 1b and Supplementary Data 1).
To this end, Balb/c mice were separated into four groups (12 mice/each group).
When the tumor reached about 40 mm3, the mice were separated randomly in several groups.
A1R Hz mice were separated into groups described above and challenged with cocaine.
After weaning, male and female mice were separated and were housed 4 5 per cage until 2 months of age.
At 50 days of age mice were separated into Drug Treatment (DRUG) and Vehicle Control (CTRL) groups.
By shifting the light:dark cycles mice were separated into two groups, one phase advanced and the other phase delayed.
Thirteen male WT mice and eleven DAT-KO mice were separated into individual cages, and surgically implanted with electrodes and electromyographic (EMG) wires.
