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Such observations could not be explained by increased caloric consumption since male and female RGS9 KO mice demonstrated equivalent daily food intake as compared to their respective WT littermates.
All mice demonstrated equivalent levels of exogenous BCR-ABL expression, thus precluding any effect from transgene expression changes with age.
Tem1/endosialin KO vs WT mice demonstrated equivalent survival and tumor growth when implanted with intracranial GBM xenografts, although Tem1/endosialin KO tumors were significantly more vascular than the WT counterparts.
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No animals included in further DNA and RNA analysis received a NEC score higher than 2. QRT-PCR demonstrated equivalent TLR4 and iNOS mRNA levels in mice with NEC as compared to mice without NEC (Figure 2).
When mice immunised with ChAd63/MVA were challenged with live Plasmodium berghei sporozoites, microneedle-mediated ChAd63.ME-TRAP priming demonstrated equivalent protective efficacy as did ID immunisation.
Freshly isolated cells demonstrated equivalent suppression between these CD62LHI and CD62LLO Treg subsets (Figure 2A, p≥0.25 for each cell ratio, 3 6 mice per group).
The study groups demonstrated equivalent improvement on all six outcomes.
These populations demonstrated equivalent performance in fitness assays.
These results demonstrated equivalent virologic suppression between the two regimens.
Saline-treated PAI-1−/− mice demonstrated significantly less IL-13 than similarly treated WT mice (p < 0.05).
Further, S. pneumoniae infected-PAI-1−/− mice demonstrated significantly higher plasmin activity than infected WT mice (p = 0.04).
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