Through a microarray analysis, we discovered that the miR-205 gene (MIR205HG) was consistently overexpressed upon TMPRSS4 downregulation.
In the microarray analysis, we evaluated three conditions at several concentrations of S-PRG eluate: 0% versus 6.3%, 0% versus 12.5%, and 0% versus 25.0%.
MEK1/2 activity is essential for the effect of Ca2+ and using microarray analysis, we have identified c-Fos as an early Ca2+ response gene.
Although biclustering has been almost exclusively applied to DNA microarray analysis, we present that biclustering can be successfully applied to the PMG problem.
Thus, using microarray analysis, we identified a small set of genes that may be used as biomarkers for discriminating V from Zn.
Using transcriptome microarray analysis, we identified IL-33 as a key cytokine up-regulated in the inflamed skin of urushiol-challenged mice.
Before carrying out our microarray analysis, we used RT-PCR to assess the expression of OsDMAS1 and OsVIT2 to confirm the effects of excess Fe and deficiency treatments.
Using microarray analysis, we showed >100 genes to be differentially expressed in tGLI1-expressing compared with GLI1-expressing GBM cells, although both cell types expressed equal levels of known GLI1-regulated genes, such as PTCH1.
To validate the data obtained by microarray analysis, we randomly sampled 14 of the 37 candidate genes and compared their expression levels in both Rio and BTx623 by performing quantitative reverse transcription polymerase chain reaction (qRT-PCR; Fig. 2a).
Prior to microarray analysis, we first examined the Fir1 knockdown efficiency using qRT-PCR assay and found that Fir1 mRNA expression decreased dramatically in both part 1 and part 2 (Fig. 4C).
To validate the results of the microarray analysis, we focused on several genes associated with ICM, mES, EpiSC, hES [34].
