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FLO8 expression showed no difference in the tested strains.
This variation may due to the difference in the tested organisms and the method used to assess antimicrobial activity (Janssen et al., [ 20]).
There was no significant difference in the tested endpoints between these two groups, so only the CTRL group was shown in this study.
Since there is little apparent difference in the tested metabolic parameters between Lepr +/+ and Lepr db/+ mice, we chose to focus on the Lepr +/+ and Lepr db/db genotypes for subsequent experiments.
Compared with other similar reports [ 9, 24– 26], the extremely higher co-infection rate found by both assays might be due to the difference in the tested population and possible nosocomial infections in the hospital.
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These values disregard age-specific differences in the tested functions as previously mentioned.
Moreover, there were no significant differences in the tested oxidative stress biomarkers between CLRE-treated animals and Silymarin-treated animals.
Also, there were no major differences in the tested datasets between GATA3 transcription factor binding in T47D and MCF7 cells (Additional file 1: Figures S8-S10).
Moreover, there were significant differences in the tested IL-1 β level between AND HD (G5) and AV (G3), at a value of 52.07 ± 0.71 (pg/mL).
Since sclerosing adenosis and ADH are believed to constitute distinct precursors of invasive breast carcinoma, we attempted to investigate potential differences in the tested parameters.
Differences observed in the tested isolates' pathogenicity and abundance on roots and in soil have also been experienced by others.
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