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Using the expression data from the study, we performed WGCNA after regressing out principal components of overall expression and single-nucleotide polymorphisms (to reduce population stratification effects).
In all RA patients included in the study, we performed cell cytometry analyses the same day of blood extraction for microarray analysis.
The study we performed is not the first using flow cytometry to determine antimicrobial susceptibility.
Continuing the study, we performed tests to confirm pro-antioxidant activity.
Lastly, following the completion of this single ascending-dose segment of the study, we performed a multiple ascending-dose evaluation.
The study we performed focuses on the removal of bilirubin in hepatic failure patients with a ventricular assist device (VAD).
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In this part of the study, we perform two set of experiments.
As a novel feature of the study, we perform such a temporal-dependent analysis in our in silico experiments.
The studies we performed in zebrafish revealed that human MPZ-MCS3 directs reporter-gene expression in the hindbrain and spinal column in positions consistent with oligodendrocytes.
All the studies we performed were in vitro with cell lines and as such, no IACUC or approval was necessary.
The study is not without limitations, most of which are the same with those of the studies we performed in other biomedical fields [ 10, 11].
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