Figure 2a , depicts a marked difference in the diestrus phase duration within the DMPA-treated group before and after administration, showing a highly significant difference ( p <0.0001).
Excerpts
Correlation between all Smads in the ALS samples was highly significant (Fig. 1B ), with Smad1 and 5 being the strongest (Pearson coefficient of 0.88, P < 0.0001).
The analysis of blood loss showed that the median (IQR) total blood loss was 575 mL (375, 875) in the NTA group compared to 450 mL (325, 675) in the TA group, a highly significant difference (p < 0.0001 Mann-Whitney test).
monodon , Amidostomum anseris , and Quasiamidostomum fulicae ), gave highly significant results (P < 0.0001) with respect to both males and females.
Parasite inbreeding The analysis of the monoclonal samples (n = 136) showed a highly significant overall LD ( I A s = 0.51, p < 0.0001) indicating a clonal population.
In particular, when WF was used as source of survival and growth stimuli the difference was extremely significant (CTR vs KR, in WF p < 0.0001).
As evaluated with ANOVA for repeated measures, the difference was highly significant ( P < 0.0001).
Relationship between ALT and LIC in patients with TI Liver enzymes (ALT) showed a highly significant coefficient of correlation with LIC in a subset of patients with TI (R=0.78; P <0.0001), depicted in Fig. 6 .
Highly significant up-regulation was observed in CIN III, CC, and TB categories ( p < 1 × 10 −4 ), consistent with activation of proliferative and inflammatory oncogenic miRNA programs.
Overall differences across histopathologic categories were highly significant (Kruskal–Wallis p < 0.0001), and there was a strong monotonic increase in OCNI across the ordered categories from benign to malignant disease (Jonckheere–Terpstra p < 0.0001).
Statistically, there was an extremely significant increase ( p = 0.0001) in lesion scores in the cecal tissue of the CP group compared to the CN group.
[ 99m Tc] TcO4 − (Pertechnetate) A highly significant effect of both the cell line and radioactivity concentration on cellular DNA fragmentation was observed (two-way ANOVA: p < 0.0001 for both factors), indicating that chemoresistance correlates with radioresistance.
The increase in the image intensity of globus pallidus was quite significant between healthy controls and HE patients ( p < 0.0001 ) .
Differences in green-red channel ratiometric pixel intensities between front and back were highly significant ( Figure 10G,M ; p<0.0001, Mann–Whitney test).
The difference in OS between the LTS and STS patients was highly significant (HR = 0.03, 95% confidence interval (CI) 0.01–0.07; p < 0.0001) (Fig. 1 B).
The fitted model was extremely significant ( F = 61.47 and p < 0.0001).
The data indicate that the regression model is highly significant ( p < 0.0001), with a non-significant lack-of-fit term ( P = 0.9490 > 0.05), demonstrating a good fit and low experimental error.
Modelling of PAS 1 and PAS 2 effects on MEP amplitudes Computational modelling of the PAS 1 and PAS 2 effects on the absolute MEP amplitude raw data as a function of time revealed highly significant differences between PAS 1 and PAS 2 MEP functions ( P < 0.0001) ( Fig 5 ).
The enrichment was highly significant compared to random control regions ( P = 0.0001) and decreased with distance from the genetic variants ( Supplementary Dataset S4 ).
The effect of adapting speed using row-scrambled videos was highly significant (F (2, 8) = 22.79, p = 0.0001, n = 5).
The antibody increase was highly significant ( p < 0.0001), with a 28-fold GMC increase (95% CI: 17–43-fold) ( Figure 2 B).
Conversely, the treatment caused a highly significant ( p < 0.0001) decrease in Pol, Tax, and HBZ expression with respect to the untreated control in PB2/NO-IL-2 cells.
The minor allele frequency of rs2607474 in the methylated group was significantly lower than that in the unmethylated group (p = 0.0004, setting α = 0.05, 1-βpower = 0.946) and the frequency of the GG homozygote was significantly higher in the methylated group than in the unmethylated group (p = 0.013). Risk associated with rs2607474 GG homozygote for DAPK and CDH1 methylation Overall, rs2607474 GG homozygote conferred a highly significant increased risk for the development of DAPK methylation (OR, 2.43; 95%CI, 1.60-3.69; p < 0.0001; Table 4 ).
The difference in MIC between the two agents against the standard isolate was highly significant ( p < 0.0001), whereas the difference in MBC was not statistically significant ( p = 0.1030).
Between groups analysis (PCOS, T2D and controls) showed a highly significant difference between the groups ( F = 63.43, p < 0.0001).