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Statistically significant main effects were further analyzed using ANOVAs.
These effects were further strengthened by intra-VLO injection of TSA.
Such protective effects were further identified in FA- and IRI-induced AKI models (Fig. 6), suggesting that HQH is a broad-spectrum nephroprotective agent for AKI.
Significant main or interaction effects were further pursued by appropriate post-hoc tests that were corrected for multiple comparisons, if required.
In the model, the NCI effects were further partitioned into additive and dominance nuclear-cytoplasmic interaction components.
The down-regulation of these genes was verified using qPCR, and downstream effects were further tested using NR activity assays.
Wind-chill effects were further simulated for lowland and upland environments, and related to ovine-specific thermal tolerance limits.
EMME improved visual search and enhanced interpretation of relevant information for those novel stimuli compared to the control group; these effects were further moderated by the specific display.
These concurrent reference frame facilitation/interference effects were further enhanced when the current and to-be-imagined environments were more similar.
The coupling effects were further demonstrated with anti-phase synchronization of relaxation, and phase and identical synchronization of chaotic current oscillations.
These effects were further supported by down-regulation of NF-κB and reduction of colonic TNF-α, IL-10, TP and serum 5-HT levels.
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