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Both constructs demonstrated significant KD, however the shEZR-1 consistentlynsistently achieved higher ezrin KD (>90%) and was used for the majority of experiments.
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shRNA constructs demonstrating significant enrichment (log2-fc > 0.3 and P < 0.01) in the Alexa488-high-intensity fraction were extracted (1,276 genes; Supplementary Table S1).
Both groups demonstrated significant decreases in platelet aggregation, and a decline in plasma protein S when compared with baseline.
Both groups, however, demonstrated significant RT benefits for multisensory VS orienting cues.
Both groups also demonstrated significant improvements in SRT.
Of the six a priori construct hypotheses, five demonstrated significant correlations in the expected directions.
Parallel reporter gene assays of the nine constructs demonstrated a significant difference in basal transcription rate, in SH-SY5Y cells, between pGL3b −1.1/−0.6 kb and the other β-syn promoter constructs, which had minimal or negligible activity above background (Figure 1B).
Both hospital and reference laboratory subgroups demonstrated significant heterogeneity.
These electrodes demonstrated significant improvement both in capacity retentions and rate capabilities.
Weighted principal component and unweighted composite scores were derived from individual tests.Both treatment groups demonstrated significant improvement on both composite scores.
Some target compounds demonstrated significant inhibitory activities against both cell lines.
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