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Histological analysis showed a large number of mononuclear cells had accumulated under the inoculation of pIL-6.
Raman spectral analysis showed a large 2D peak shift of up to −11 comparedpared with that of flat graphene on silicon wafers.
Similarly, far-Western analysis showed a large number of bands associated with MET phosphorylation status (Fig. 6B).
Our analysis showed a large increase in levels of expression from day 7 to day 42 for these genes (19 fold change; Figure 3B) in iCT animals and a similar, but less pronounced effect, was seen in the iWT frogs (Figure 3B).
Spectrophotometric analysis showed a large 230 nm component, potentially salt carryover.
Urine analysis showed a large amount of blood and 1+ protein without cast.
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The additional multilevel analysis showed a larger difference in costs (€6038; 95 % CI 4543 7533) between those experiencing AEs compared to those without AEs when the ICU costs were included.
Subgroup analysis showed a larger therapeutic effect for A. paniculata extract (HMPL-004) relative to placebo in patients who were currently failing oral mesalamine, and a smaller and non-significant effect relative to placebo among patients not receiving mesalamine.
This analysis shows a large variation of loss for different control structures and that a control structure evaluation is necessary to collect the benefits from a RTO system.
As illustrated in Figure 8, the sliding window analysis shows a large, highly significant eye position effect developing after the eye movement to target.
Additionally, our analysis shows a large number of effects not yet tested experimentally.
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