<p>Expression analysis of NER, cell cycle regulation and DNA damage detection factors in LB1 silenced and control cells. mRNA from Sc and shLB1 U-2 OS cells was prepared at 3 days after silencing and analyzed by qRT-PCR using GAPDH as a reference gene. The change in expression of a specific gene was considered significant if the “fold change” was higher than 1.7 or lower than 0.6.</p
<p>RT–PCR analysis was performed on total RNA isolated from WT and WTΔRad26 cells (<b>A</b>) followi...
<p>Expression of indicated genes was assayed by QPCR analysis (Gli1, Gli3, n = 8; Gli2, MEF2C, n = 6...
<p>Bars represent fold increase (or decrease) with respect to untreated controls ± SEM for 10 indepe...
<p>(A) Relative expression of the marker of pluripotency Nanog and Nucleostemin (NST) determined by ...
<p>qRT-PCR was performed on mRNA isolated from quadriceps muscle of <i>Cfl2</i> KO mice and compared...
<p>For each gene: fold values (FC) and p value obtained in p43−/− mice versus respective controls. S...
Quantitative RT-PCR was performed as described in Materials and methods in presence or absence of BC...
<p>Real Time RT-PCR was performed to analyse the expression of the six genes. Fold change in express...
<p>(A) Relative quantity of RNAs extracted from control and FXR1 KD cells are estimated by using qRT...
The expression levels of the selected genes were compared between microarray and qPCR analysis. For ...
The cell division cycle is regulated through both transcriptional and post-transcriptional mechanism...
<p>Total RNA isolated from MCF-7 cells with acute and chronic exposure to H<sub>2</sub>O<sub>2</sub>...
<p>A. The protein levels of LB1, LB2, and LA and C were assayed by immunoblotting at day 3 after ele...
<p>The expression of genes in each group was normalized to the control group. Data were collected fr...
RT-qPCR was used to measure expression of 61 genes extracted by microarray analysis. Among the genes...
<p>RT–PCR analysis was performed on total RNA isolated from WT and WTΔRad26 cells (<b>A</b>) followi...
<p>Expression of indicated genes was assayed by QPCR analysis (Gli1, Gli3, n = 8; Gli2, MEF2C, n = 6...
<p>Bars represent fold increase (or decrease) with respect to untreated controls ± SEM for 10 indepe...
<p>(A) Relative expression of the marker of pluripotency Nanog and Nucleostemin (NST) determined by ...
<p>qRT-PCR was performed on mRNA isolated from quadriceps muscle of <i>Cfl2</i> KO mice and compared...
<p>For each gene: fold values (FC) and p value obtained in p43−/− mice versus respective controls. S...
Quantitative RT-PCR was performed as described in Materials and methods in presence or absence of BC...
<p>Real Time RT-PCR was performed to analyse the expression of the six genes. Fold change in express...
<p>(A) Relative quantity of RNAs extracted from control and FXR1 KD cells are estimated by using qRT...
The expression levels of the selected genes were compared between microarray and qPCR analysis. For ...
The cell division cycle is regulated through both transcriptional and post-transcriptional mechanism...
<p>Total RNA isolated from MCF-7 cells with acute and chronic exposure to H<sub>2</sub>O<sub>2</sub>...
<p>A. The protein levels of LB1, LB2, and LA and C were assayed by immunoblotting at day 3 after ele...
<p>The expression of genes in each group was normalized to the control group. Data were collected fr...
RT-qPCR was used to measure expression of 61 genes extracted by microarray analysis. Among the genes...
<p>RT–PCR analysis was performed on total RNA isolated from WT and WTΔRad26 cells (<b>A</b>) followi...
<p>Expression of indicated genes was assayed by QPCR analysis (Gli1, Gli3, n = 8; Gli2, MEF2C, n = 6...
<p>Bars represent fold increase (or decrease) with respect to untreated controls ± SEM for 10 indepe...