N42 cells were transfected with scramble control or Pgrmc1 siRNA. Bars represent mean ± SEM. (*Significantly different from scramble control, ppp<0.0001).</p
<p>The mean fold changes for each group were compared in the bar chart for eight high to medium fold...
cDNA from cells as in S2C was analysed by qPCR. Data is represented as gene expression relative to a...
<p>(A) GR loading at the MMTV promoter array (white arrow) in the 3617 cell line (single cell analys...
N42 cells were transfected with scramble control or Pgrmc1 siRNA. Bars represent mean ± SEM. (*Signi...
Primers used for QPCR validation of targets identified on microarrays to be significantly regulated ...
Bars represent mean ± SEM. (aSignificantly different from cells with control vector treated with veh...
N42 cells were treated with 10 μM AG-205 for 24 h before harvesting. Bars represent mean ± SEM. (*Si...
<p>Validation by RT-qPCR of the microarray-based differentially expressed genes between line 6 and l...
<p>The quercetin (Q) regulated genes Cyp4a14, Cyp4a10, Acot3, Car (Nr1i3) and Por, compared to the c...
RT-qPCR was performed on the 61 genes extracted from microarray analysis. Only the 12 genes that wer...
The expression levels of the selected genes were compared between microarray and qPCR analysis. For ...
<p>(A) Quantitative RT-PCR of a subset of markers with RNA isolated from ctrl and <i>Tfap2c<sup>−/−<...
<p>The same RNA used for Agilent microarrays was examined by QRTPCR. All fold changes were calculate...
<p>For the evaluation, we selected the most highly expressed genes involved in both DNA damage and p...
<p>Selected qPCR of genes that were 1.5 fold or more changed by RSV treatment in the microarray (RSV...
<p>The mean fold changes for each group were compared in the bar chart for eight high to medium fold...
cDNA from cells as in S2C was analysed by qPCR. Data is represented as gene expression relative to a...
<p>(A) GR loading at the MMTV promoter array (white arrow) in the 3617 cell line (single cell analys...
N42 cells were transfected with scramble control or Pgrmc1 siRNA. Bars represent mean ± SEM. (*Signi...
Primers used for QPCR validation of targets identified on microarrays to be significantly regulated ...
Bars represent mean ± SEM. (aSignificantly different from cells with control vector treated with veh...
N42 cells were treated with 10 μM AG-205 for 24 h before harvesting. Bars represent mean ± SEM. (*Si...
<p>Validation by RT-qPCR of the microarray-based differentially expressed genes between line 6 and l...
<p>The quercetin (Q) regulated genes Cyp4a14, Cyp4a10, Acot3, Car (Nr1i3) and Por, compared to the c...
RT-qPCR was performed on the 61 genes extracted from microarray analysis. Only the 12 genes that wer...
The expression levels of the selected genes were compared between microarray and qPCR analysis. For ...
<p>(A) Quantitative RT-PCR of a subset of markers with RNA isolated from ctrl and <i>Tfap2c<sup>−/−<...
<p>The same RNA used for Agilent microarrays was examined by QRTPCR. All fold changes were calculate...
<p>For the evaluation, we selected the most highly expressed genes involved in both DNA damage and p...
<p>Selected qPCR of genes that were 1.5 fold or more changed by RSV treatment in the microarray (RSV...
<p>The mean fold changes for each group were compared in the bar chart for eight high to medium fold...
cDNA from cells as in S2C was analysed by qPCR. Data is represented as gene expression relative to a...
<p>(A) GR loading at the MMTV promoter array (white arrow) in the 3617 cell line (single cell analys...