Barely Significant
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“showed a trend”

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In the literature

For HIV-positive individuals in Southeast Asia, baseline CD4 count <350 cells/mm 3 showed a trend toward increased risk of any anal HR-HPV persistence, while antiretroviral therapy use and plasma HIV-RNA had no association with any anal HR-HPV persistence ( 34 ), whereas, in the same region, another investigation revealed that CD4 + count, HIV-RNA, or use of combination antiretroviral therapy were not significantly associated with the prevalence of anal HR-HPV types in HIV-positive MSM.
Moreover, after TRPM7 was disrupted, it showed a trend consistent with OIP5-AS1 and CD147 , that is, the level of apoptosis was significantly increased, which was confirmed by apoptosis flow cytometry and western blot ( Figures 6I–L ). 3.7 OIP5-AS1/CD147/TRPM7 axis promotes apoptosis by impairing PI3K-Akt signaling Notably, the western blot results showed that the p-AKT protein level was significantly reduced, but there was no significant difference in AKT protein expression after si-OIP5-AS1 both in AGS and MKN-45 cells.
CON2 showed a trend in accordance with the hypothesis for \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\frac{{AFiso}_{max}}{{MVIC}_{pre}}$$\end{document} AFiso max MVIC pre with − 18% lower values; however, it missed significance ( p = 0.168).
Acute single MW showed a trend of anxiety but did not result in depressive-like behaviors. a The schedule of open field test (OFT), elevated plus maze test (EPM) and tail suspension test (TST) after MW exposure. b – c Time in center of mice during OFT (n = 12). d – e Time in open/closed arm of mice during EPM (n = 15). f Time of freezing/immobile/mobile of mice during TST (n = 15).
This finding showed a trend towards a higher blood transfusion despite not reaching statistical significance and it contrasted with much of the literature on TEG-guided transfusion in cirrhosis patients that demonstrated a decrease in blood product utilization [ 9 , 10 ].