<p>(A) Confirmation of microarray data by examining 16 genes selected from the list of up- or down-regulated genes based on our microarray analysis using total RNA extracted from 3 months old <i>Tg-I</i> liver. (B–D) Analysis of the expression of these 16 genes in different transgenic lines at different ages. Gene expression was analyzed by qPCR using gene specific primers and was expressed as fold change after normalization against <i>elf1a</i>. The value of CK was set as 1. CK: wild type adult liver control. *: <i>p</i><0.05, **: <i>p</i><0.01.</p
<p>Several genes involved in different processes were measured by qPCR in order to determine express...
<p>A total of 30 genes, including (A) 10 downregulated, (B) 10 upregulated, and (C) 10 unigenes with...
Data were normalized to gapdh as the reference gene and presented as a fold change between the Selec...
<p>The summary was based on the qPCR data shown in <a href="http://www.plosone.org/article/info:doi/...
The expression levels of the selected genes were compared between microarray and qPCR analysis. For ...
<p>QPCR data indicated as mean ± SD, where * indicates p<0.05, and ** indicates p<0.01.</p><p>The ex...
<p>Validation of changes in mRNA expression by quantitative real-time RT-PCR (qRT-PCR) for genes rep...
<p>qPCR analysis was performed on 7 genes to confirm the transcript abundance seen with the microarr...
<p>Log ratio of microarray fold change expression of the selected 20 up and down regulated genes ass...
<p>A. Validation of gene expression changes by qPCR The expression profiles of seven representative ...
<p>The expression of selected target genes was determined in surgically collected samples (A) and in...
<p>Bars represent the mean ± SD of fold change relative to growth medium control. At least 3 indepen...
RT-qPCR was used to measure expression of 61 genes extracted by microarray analysis. Among the genes...
<p>The log<sub>10</sub> values of the real-time RT-qPCR were plotted against the microarray analysis...
<p>Gene expression was measured in blood cell RNA using qRT-PCR to validate the microarray measureme...
<p>Several genes involved in different processes were measured by qPCR in order to determine express...
<p>A total of 30 genes, including (A) 10 downregulated, (B) 10 upregulated, and (C) 10 unigenes with...
Data were normalized to gapdh as the reference gene and presented as a fold change between the Selec...
<p>The summary was based on the qPCR data shown in <a href="http://www.plosone.org/article/info:doi/...
The expression levels of the selected genes were compared between microarray and qPCR analysis. For ...
<p>QPCR data indicated as mean ± SD, where * indicates p<0.05, and ** indicates p<0.01.</p><p>The ex...
<p>Validation of changes in mRNA expression by quantitative real-time RT-PCR (qRT-PCR) for genes rep...
<p>qPCR analysis was performed on 7 genes to confirm the transcript abundance seen with the microarr...
<p>Log ratio of microarray fold change expression of the selected 20 up and down regulated genes ass...
<p>A. Validation of gene expression changes by qPCR The expression profiles of seven representative ...
<p>The expression of selected target genes was determined in surgically collected samples (A) and in...
<p>Bars represent the mean ± SD of fold change relative to growth medium control. At least 3 indepen...
RT-qPCR was used to measure expression of 61 genes extracted by microarray analysis. Among the genes...
<p>The log<sub>10</sub> values of the real-time RT-qPCR were plotted against the microarray analysis...
<p>Gene expression was measured in blood cell RNA using qRT-PCR to validate the microarray measureme...
<p>Several genes involved in different processes were measured by qPCR in order to determine express...
<p>A total of 30 genes, including (A) 10 downregulated, (B) 10 upregulated, and (C) 10 unigenes with...
Data were normalized to gapdh as the reference gene and presented as a fold change between the Selec...