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Although the primary MDA-MB-231 xenograft was unavailable for examination, mesenteric deposits in the spleen and mesentery of the same mouse were examined (Table 2).
Two slides per mouse were examined.
Three hippocampal slices per mouse were examined to reach an average value of CA3 region.
Foci of mPIN PPARγ KO mouse were examined by electron microscopy.
KOGs with single-exon coding sequences in the mouse were examined for mis-assembly.
The tumour incidence and the number and the size of tumours per mouse were examined for 21 weeks.
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The mice were sacrificed after each mouse was examined for body composition, physical performance and metabolic parameters, and various tissues were harvested.
Their biodistribution in tumor bearing mouse was examined along with their antitumor activity against murine leukemia L1210 cell line.
Furthermore, the metabolic pathway of DTNs-AS1411 in mouse is examined via SPECT/CT technology.
Each stained slide for each mouse was examined under microscope (Olympus, Japan).
All mice were examined by an examiner (MS) masked to infection status and serotype.
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