<p>MDMs were stimulated with TLR2/1L (black bars) or IFN-γ (gray bars) for 2, 6, and 24 hours and <b>(A)</b> S100A12, <b>(B)</b> GBP1, and <b>(C)</b> IL15 expression is assessed by RNAseq (left) and quantitative PCR (qPCR) (right). RNAseq results are represented as FC determined by normalized counts in stimulated MDMs versus counts in media control for each time point. Quantitative PCR (qPCR) results were determined by calculating relative arbitrary units using ΔΔCT analysis and normalizing to housekeeping gene. Data are represented as mean FC ± SEM, <i>n</i> = 5.</p
<p>Twenty-two genes were arbitrary selected, from highly up-regulated to highly down-regulated conti...
Aim: Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) is still the “gold stand...
<p>The mean fold changes for each group were compared in the bar chart for eight high to medium fold...
<p>Twenty-five genes that whose expression was significantly different in the control and treatment ...
<p>The same RNA used for RNAseq was used for qPCR. The ΔΔCt method was used for calculation of gene ...
Five genes were selected to verify RNA-Seq results using qRT-PCR. Graphs on the left (A, C, E, G, I,...
<p>Expression levels of 26 randomly selected genes in the four samples used in this study were detec...
<p>Relative expression levels of genes determined by RNAseq to be differentially expressed <i>in viv...
<p>The expression profiles of 10 UP and 10 DOWN contigs (randomly selected) were analysed by qPCR to...
<p>RT-qPCR was used to validate the RNA sequencing data using total RNA isolated from mock-infected ...
<p>(<b>A</b>) qPCR assessment of genes showing statistically significant difference on the microarra...
<p>Bar plots of Log2ChangeFold of the subset of genes chosen to validate the RNASeq (red) pattern of...
<p>(a) Comparisons of changes in miRNAs targets involved in the KEGG pathway. (b) Fold changes of ge...
<p>Results of qPCR were presented in histograms, and results of RNA-Seq were listed in the embedded ...
<p>A. miRNA expression in tumour tissue from mice with LLC that received RNase A therapy. The expres...
<p>Twenty-two genes were arbitrary selected, from highly up-regulated to highly down-regulated conti...
Aim: Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) is still the “gold stand...
<p>The mean fold changes for each group were compared in the bar chart for eight high to medium fold...
<p>Twenty-five genes that whose expression was significantly different in the control and treatment ...
<p>The same RNA used for RNAseq was used for qPCR. The ΔΔCt method was used for calculation of gene ...
Five genes were selected to verify RNA-Seq results using qRT-PCR. Graphs on the left (A, C, E, G, I,...
<p>Expression levels of 26 randomly selected genes in the four samples used in this study were detec...
<p>Relative expression levels of genes determined by RNAseq to be differentially expressed <i>in viv...
<p>The expression profiles of 10 UP and 10 DOWN contigs (randomly selected) were analysed by qPCR to...
<p>RT-qPCR was used to validate the RNA sequencing data using total RNA isolated from mock-infected ...
<p>(<b>A</b>) qPCR assessment of genes showing statistically significant difference on the microarra...
<p>Bar plots of Log2ChangeFold of the subset of genes chosen to validate the RNASeq (red) pattern of...
<p>(a) Comparisons of changes in miRNAs targets involved in the KEGG pathway. (b) Fold changes of ge...
<p>Results of qPCR were presented in histograms, and results of RNA-Seq were listed in the embedded ...
<p>A. miRNA expression in tumour tissue from mice with LLC that received RNase A therapy. The expres...
<p>Twenty-two genes were arbitrary selected, from highly up-regulated to highly down-regulated conti...
Aim: Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) is still the “gold stand...
<p>The mean fold changes for each group were compared in the bar chart for eight high to medium fold...