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The percentage of γδ T cells expressing IL-17 in WT infected mice was considerably higher than the percentage of CD4+ T cells.
Although there were no changes in the expression levels of any of the three NOS isoforms, NOS activity in neocortex of mutant mice was considerably increased compared with control neocortex.
As illustrated in figure 1B, the rate of human T cell reconstitution in DRAG mice was considerably higher than in control mice, since 14 out of 15 (93.3%) DRAG mice developed human T cells by 25 weeks post-infusion with HSC as compared to only 4 out of 11 (36.4%) control littermates developing human T cells.
Additionally, Ttr expression in colon from WT mice was considerably lower than in Hsf/V30M mice.
As was expected for nocturnal animals, the activity of mice was considerably higher during the scotophase than during the photophase.
Of note, however, protection in the Bak− / − BCL-2tg mice was considerably more robust (>90%), suggesting that TCR-activated apoptosis involves a Bak-specific component.
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Treated with DFP and DFO + DFP mice were considerably increased in lipid peroxidative markers.
The reason is because of the great deal of effort put into the former two models and that the studies in humans and mice are considerably more relevant to our own health.
Interestingly, subordinate mice were considerably more often involved in self-directed Grooming activity than dominants.
The adipocytes from AC3−/− mice were considerably larger than those from AC3+/+ mice (Figure 3A and 3B).
Therefore, the incidence of osteogenic tumors in Pol β Tg mice is considerably higher than incidences cited in the literature.
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