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Therefore we independently tested the expression levels of a panel of mitotic regulators that were identified as differentially expressed in the H' vs H analysis.
Therefore, we tested the expression levels of these two genes in their most functionally relevant tissues: SALL1 in kidneys and PTEN in the bone marrow.
We tested the expression levels of 12 randomly selected genes by qRT-PCR analysis (six specifically deregulated genes were chosen on each microarray list).
We tested the expression levels of probes that overlapped with endo-siRNA reads.
We first tested the expression levels of canine BRCA2 in mammary gland and mammary tumor samples by qRT-PCR.
In this study, we first tested the expression levels of miR-1 and miR-133a using needle biopsies of PCa (n=15) and non-PCa (n=17) tissues.
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The ability to perform cell-by-cell analysis allowed us to test the hypothesis that expression level alters the observed responses.
We selected a number of genes that had roles in transcriptional regulation, development and signal transduction and tested the expression level of these genes using quantitative RT-PCR.
Since previous yeast two hybrid results indicated possible interaction of SNAP29 with other members of the EHD family [12], we also tested the expression level and intracellular localization of other EHDs in the absence of SNAP29.
Therefore, we tested the expression level of miR-29a using the hepatoma cell lines which were reported with different metastasis potential as a model, such as MHCC-97H and MHCC-97L [24].
To further confirm that hsf1-R206S, F256S cells had enhanced basal activation of Hsf1 at 25°C, we tested the expression level of numerous known transcriptional targets of Hsf1 in these cells.
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