Results are shown as target gene mRNA levels normalized to Gapdh mRNA levels. Data are as the mean ± SEM. *P (PDF)</p
<p>Data were analyzed by the 2<sup>–ΔΔCt</sup> method using GAPDH as a reference gene. The results a...
<p>Data from qPCR are shown as means ± standard error (SE) of three replicates. RPKM from RNA-seq ar...
<p>Target RNA relative expression levels were given as ratios of GAPDH transcript levels in the same...
RT-qPCR was performed on the 61 genes extracted from microarray analysis. Only the 12 genes that wer...
<p>Expression levels of 26 randomly selected genes in the four samples used in this study were detec...
RT-qPCR was used to measure expression of 61 genes extracted by microarray analysis. Among the genes...
<p>Expression level of <i>CCNA1</i> gene was assessed by qRT-PCR. Quantification of mRNA relative qu...
<p>The data are shown as the mean ± SEM (n = 7 for small follicle group, n = 4 for large follicle gr...
<p>The expression values generated by RNA-seq (red) or qPCR (blu) for eleven selected genes using th...
<p>Values are given in the form of RT-qPCR threshold cycle numbers (Ct values), mean ± SD (n = 6), *...
<p>*p<0.05, ** p 0.01 vs. controls (Wt group). <b>(A)</b> <i>Igf1;</i> <b>(B), (C), (D), (E), (F)</b...
Sequences of primers used for RT-qPCR to assess the expression of the indicated genes.</p
<p>Gene expression characteristics for the 10 evaluable mRNA targets investigated with qPCR in 187 F...
Five genes were selected to verify RNA-Seq results using qRT-PCR. Graphs on the left (A, C, E, G, I,...
<p>Gene specific primers for RT-qPCR were mentioned in <a href="http://www.plosone.org/article/info:...
<p>Data were analyzed by the 2<sup>–ΔΔCt</sup> method using GAPDH as a reference gene. The results a...
<p>Data from qPCR are shown as means ± standard error (SE) of three replicates. RPKM from RNA-seq ar...
<p>Target RNA relative expression levels were given as ratios of GAPDH transcript levels in the same...
RT-qPCR was performed on the 61 genes extracted from microarray analysis. Only the 12 genes that wer...
<p>Expression levels of 26 randomly selected genes in the four samples used in this study were detec...
RT-qPCR was used to measure expression of 61 genes extracted by microarray analysis. Among the genes...
<p>Expression level of <i>CCNA1</i> gene was assessed by qRT-PCR. Quantification of mRNA relative qu...
<p>The data are shown as the mean ± SEM (n = 7 for small follicle group, n = 4 for large follicle gr...
<p>The expression values generated by RNA-seq (red) or qPCR (blu) for eleven selected genes using th...
<p>Values are given in the form of RT-qPCR threshold cycle numbers (Ct values), mean ± SD (n = 6), *...
<p>*p<0.05, ** p 0.01 vs. controls (Wt group). <b>(A)</b> <i>Igf1;</i> <b>(B), (C), (D), (E), (F)</b...
Sequences of primers used for RT-qPCR to assess the expression of the indicated genes.</p
<p>Gene expression characteristics for the 10 evaluable mRNA targets investigated with qPCR in 187 F...
Five genes were selected to verify RNA-Seq results using qRT-PCR. Graphs on the left (A, C, E, G, I,...
<p>Gene specific primers for RT-qPCR were mentioned in <a href="http://www.plosone.org/article/info:...
<p>Data were analyzed by the 2<sup>–ΔΔCt</sup> method using GAPDH as a reference gene. The results a...
<p>Data from qPCR are shown as means ± standard error (SE) of three replicates. RPKM from RNA-seq ar...
<p>Target RNA relative expression levels were given as ratios of GAPDH transcript levels in the same...
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