<p>Relative transcription levels were measured by RT-qPCR, in <i>A</i>. <i>niger</i> N400 sampled 2 hours after mycelium transfer to minimal medium with 100 mM D-sorbitol (reference), 5 mM L-rhamnose or 5 mM D-fructose. Transcript levels are relative to reference sample (D-sorbitol 100 mM), indicated with an asterisk. Results are given as relative transcript ratios in logarithmic scale (lg(10)). The values provided in the figures correspond to two biological replicates per culture condition. Error bars are means of three technical replicates.</p
<p>A standard curve was constructed and used to calculate the transcript copies per mL of sample and...
<p>The miRNA levels were normalized to an internal control (actin) and expressed relative to the val...
<p>For each gene, expression induction is represented as a ratio of its relative expression at 1, 3 ...
<p>Cells were grown in glucose MCGC media, and mRNA levels were measured by RT-qPCR as described in ...
<p>A standard curve was constructed and used to calculate the transcript copies per mL of sample and...
<p>Log<sub>2</sub> fold changes of transcript levels measured with DNA microarrays (x-axis) and RT-q...
a<p>Total RNA samples were prepared from <i>F. verticillioides</i> wild-type strain grown on DL medi...
<p>Actin was used as a reference gene, and the calibrating sample was mycelial RNA. Red indicates up...
<p>Log<sub>2</sub> fold-changes of transcript levels measured with DNA microarrays (x-axis) and RT-q...
Relative expression levels of selected ten genes and 18S as an internal reference detected by RT-qPC...
<p>The values indicate changes relative to the levels of mRNA transcripts in <i>Sphingobium yanoikuy...
The proper design of DNA microarray experiments requires knowledge of biological and technical varia...
<p>Relative transcript abundance was measured by quantitative real-time PCR (qRT-PCR) and normalized...
<p>Abundance values (average of log2 MII/MI from three biological replicates) and transcripts with s...
<p>Relative expression measured with RNA-Seq and RT-qPCR for 6 genes including 3 glutathione S-trans...
<p>A standard curve was constructed and used to calculate the transcript copies per mL of sample and...
<p>The miRNA levels were normalized to an internal control (actin) and expressed relative to the val...
<p>For each gene, expression induction is represented as a ratio of its relative expression at 1, 3 ...
<p>Cells were grown in glucose MCGC media, and mRNA levels were measured by RT-qPCR as described in ...
<p>A standard curve was constructed and used to calculate the transcript copies per mL of sample and...
<p>Log<sub>2</sub> fold changes of transcript levels measured with DNA microarrays (x-axis) and RT-q...
a<p>Total RNA samples were prepared from <i>F. verticillioides</i> wild-type strain grown on DL medi...
<p>Actin was used as a reference gene, and the calibrating sample was mycelial RNA. Red indicates up...
<p>Log<sub>2</sub> fold-changes of transcript levels measured with DNA microarrays (x-axis) and RT-q...
Relative expression levels of selected ten genes and 18S as an internal reference detected by RT-qPC...
<p>The values indicate changes relative to the levels of mRNA transcripts in <i>Sphingobium yanoikuy...
The proper design of DNA microarray experiments requires knowledge of biological and technical varia...
<p>Relative transcript abundance was measured by quantitative real-time PCR (qRT-PCR) and normalized...
<p>Abundance values (average of log2 MII/MI from three biological replicates) and transcripts with s...
<p>Relative expression measured with RNA-Seq and RT-qPCR for 6 genes including 3 glutathione S-trans...
<p>A standard curve was constructed and used to calculate the transcript copies per mL of sample and...
<p>The miRNA levels were normalized to an internal control (actin) and expressed relative to the val...
<p>For each gene, expression induction is represented as a ratio of its relative expression at 1, 3 ...