Sentence examples for each groups were identified from inspiring English sources

For in vitro studies, average of the results obtained was determined in order to construct a graph, whereby IC50 of each groups were identified, respectively.

Significant variables of the models and craniofacial structures of each group were identified by one-way analysis of variance (ANOVA) at a significance level of P < 0.05.

Significant variables of models and craniofacial structures of each group were identified by comparing the measurements using one-way analysis of variance (ANOVA) at a significance level of P < 0.05.

The TFs potentially regulating maximum number of genes in each group were identified.

The survey samples for each group were identified and recruited following different protocols.

First, genes present in at least two samples belonging to each group were identified.

The DEGs in the caecum for each group were identified, and the statistics are shown in Table S9.

At the end of each treatment, animals of each group were identified, weighed, and subsequently euthanized by inhalation of carbon dioxide.

A total of 502 subjects from each group were identified and following matching showed no significant differences in any of the covariates existed between the two groups.

For a comprehensive analysis of similarities between the receptor fingerprints of the different IPL areas, we performed a hierarchical cluster analysis (Fig. 8 A ). Three groups with similar receptor distributions within each group were identified: a rostroventral group with areas PFt, PFop, and PFcm; a middle group of areas PF and PFm; and a caudal group consisting of areas PGa and PGp.

Overrepresented GO terms for each group were identified using a hypergeometric test using the GOstats package (Beißbarth and Speed 2004) in R. Culicidae orthologous protein sequences of the genes of interest were retrieved from orthoDB and fragmented sequences were removed manually.