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401 protocols using prism for windows

1

Serological Analysis of SARS-CoV-2 Antibodies

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Questionnaire results were calculated using the unpaired t‐test. The NAbs titer was visualized using PRISM for Windows (v.7.0; GraphPad Software, San Diego, CA, USA). All statistical analyses were performed using SPSS for Windows (v.12.0; SPSS, Inc., Chicago, IL, USA) and PRISM for Windows (v.7.0; GraphPad Software, San Diego, CA, USA). No adjustment of multiple comparisons was made. All reported p values were two‐sided, and p < 0.05 was considered significant.
Correlations between NAbs and sVNT were analyzed using Pearson correlation coefficients. The Spearman's rank correlation coefficient was used to analyze correlations between NAbs, sVNT, and POCT‐sVNT. All data presented were derived from two independent experiments.
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2

Oxidative Stress Modulation in Tissues

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Data are expressed as the mean ± standard error of the mean (SEM). Two-way ANOVA (with Bonferroni correction for comparison of multiple means) was used for comparisons of concentration–relaxation curves (Prism for Windows, version 9, GraphPad Software Inc., San Diego, CA, USA). One-way ANOVA (with Bonferroni correction for comparison of multiple means) was used for comparisons of XO/XDH as well as DMPO-positive protein levels (Prism for Windows, version 9, GraphPad Software Inc., CA, USA). All values passed a normality test (alpha = 0.05 in D’Agostino–Pearson tests, and Shapiro–Wilk tests for smaller numbers of values). We considered p-values < 0.05 as statistically significant. The number of measurements in the different assays may vary since not all animals were used in all assays.
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3

Antidiabetic Effects of Novel Compound

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Results are expressed as the means ± SEM. Two-way ANOVA (with Bonferroni's correction for comparison of multiple means) was used for comparisons of concentration-relaxation curves (Prism for Windows, version 6.05, GraphPad Software Inc.). One-way ANOVA (with Bonferroni's or Dunn's correction for comparison of multiple means), or, where appropriate, an equivalent non-parametric test (Dunn / Kruskal-Wallis multiple comparison) was used for comparisons of weight gain, blood glucose, HbA1c levels, other serum parameters, such as insulin, triglycerides and methylglyoxal levels, histological data, aortic ROS formation, protein and mRNA expression, cardiac and whole blood oxidative stress and mitochondrial ALDH-2 activity (SigmaStat for Windows, version 3.5, Systat Software Inc.). Correlations between fasting blood glucose, HbA1c and endothelial function, oxidative burst were analyzed by linear regression analysis (Prism for Windows, version 6.05, GraphPad Software Inc.). p values < 0.05 were considered as statistically significant. The number of replicates in the different assays may vary since not all animals were used in all assays and some values were excluded when they exceeded a deviation of 2xSD from the means.
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4

Organ Weight and Efficacy Data Analysis

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For organ weight data in toxicity study, analysis of covariance with Student’s t test was performed using terminal body weight as covariate [42 (link)], unless non-parametric methods were applied. The treatment comparisons were made on adjusted group means in order to allow for differences in body weight that might influence the organ weights. Significant differences between the groups compared were calculated using GraphPad Prism for Windows version 5.03, GraphPad Software, San Diego, CA, USA, and expressed as * p < 0.05.
Regarding efficacy study, data were expressed as means ± standard errors of the means. Statistical analysis was used to determine whether there were significant differences in BAL total and differential cell counts and BAL cytokine levels between SET-M33 (0.5, 2 and 5 mg/kg) or budesonide (1 mg/kg)-treated LPS-challenged animals and vehicle-treated LPS-challenged animals. Statistical analysis was also performed to compare vehicle-treated LPS-challenged animals with vehicle-treated saline-challenged animals. Statistical analysis was performed using the Student’s t-test with GraphPad Prism for Windows version 5.03, GraphPad Software, San Diego, CA, USA. The levels of statistical significance are indicated in the legends of the figures.
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5

Evaluating QOL Outcomes in Chronic Conditions

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Continuous variables were presented as median and standard deviation. Categorical variables were presented as number and percentage. Paired student's t-test or 2-way ANOVA test was used to study the relationship between continuous variables of baseline and follow-up data. The QOL was compared using Wilcoxon matched-pairs signed rank test. A p value of <0.05 was considered significant. All statistical analyses were performed using PRISM for Windows.
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6

Statistical Analysis of Experimental Data

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Statistical analyses were conducted using Prism for windows (version 7). Data are expressed as mean values with their standard errors. Statistical significance of differences was evaluated by Student's t test or by ANOVA, followed by the Tukey's multiple comparison test. P < 0•05 was considered as the level of significance.
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7

Effects of Therapeutic Intervention Assessed

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The data from each experiment are presented as mean ± standard error of the mean (SEM) and were analyzed by Prism for Windows (version 8.0, GraphPad Software Inc., USA). Multiple comparisons were performed by one-way analysis of variance (ANOVA) with Newman–Keuls posttests. P-values less than 0.05 were considered to be statistically significant.
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8

Statistical Analysis of Biological Data

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GraphPad Prism for Windows was applied for all statistical analysis. The data are shown as means ± SEM. Mann-Whitney test or one-way analysis of variance (ANOVA) was used to assess the significance of difference as indicated in the figure legends, and the following P values were applied: *P < 0.05, **P < 0.01, and ***P < 0.001. Detailed information about statistical analysis, including tests and values used, and the number of experiments is provided in the figure legends.
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9

Cardiac Electrophysiology and Echocardiography

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All data are expressed as means ± standard deviation. For whole‐cell patch‐clamp electrophysiology data, the sample sizes (n) indicate the numbers of cells recorded and mice (i.e., total number of cells recorded/total number of mice used). Statistical analyses were performed using Prism for Windows (version 9; GraphPad Software, La Jolla, CA) and OriginPro (version 7.5, OriginLab, Northampton, MA). The D’Agostino‐Pearson test was used to test the normality of all electrophysiology and echocardiography data and the distributions were found to be normal in all cases except for the APD50 values with DTX‐K in WT mice and the echocardiographic measurements of LVPWd in WT mice and LVAWd in KO mice. For comparisons involving two groups, either paired or unpaired two‐tailed Student's t‐tests were employed as appropriate. The action potential duration data were also analyzed using nested (i.e., hierarchical) t‐tests and no significant differences were identified between animals of the same genotype.
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10

Noise-Induced Hearing Loss Treatment

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Results are expressed as means ± SEM. We applied two-way ANOVA (with Tukey’s correction for comparison of multiple means) for comparisons of all parameters as the experimental setup contained two variables per group (noise exposure and drug treatment). We used Prism for Windows, version 8.1, GraphPad Software Inc., for statistical analyses. p-Values < 0.05 were considered statistically significant, and symbols of significance are explained in the figure legends.
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