<p>The presence of fungal RNA in the mixed transcriptome samples (COM: compatible, INC: incompatible interactions) was examined by qRT-PCR using artificial mixed transcriptome samples at several fungal RNA concentrations (0, 0.5, 1, 3, 5, 10, 20, 30, 40 and 100%). Crossing point (CP) values represent the point at which the amount of the amplified fungal actin reached a fixed threshold. High CP values indicate low abundance of fungal RNAs. The means and standard errors of CP values of three technical replicates are shown for each sample.</p
International audienceAbstract Quantitative real-time PCR (qPCR) is increasingly used to detect Pneu...
In order to determine if living fungi of phytosanitary concern are present in wood or to evaluate th...
Fungi constitute an important group in soil biological diversity and functioning. However, character...
<p>RNAs were extracted from H99, H4, S48B and S68B for qRT-PCR analysis. Two independent samples wer...
Fungi are nearly ubiquitous in the environment. There are currently accepted methods to quantify fun...
<p>For each deletion, one transformant of the NRRL 13383 background was analysed. Columns show calcu...
Background: Fungal load quantification is a critical component of fungal community analyses. Limitat...
Background: A critical step in the RT-qPCR workflow for studying gene expression is data normalizati...
Fungal infections, ranging from superficial to life-threatening infections, represent a major public...
<p><i>C</i>. <i>ribicola tubulin</i> transcript was used as the calibrator for normalization of inpu...
To enable quantification of mycelial abundance in mixed-species environments, eight new TaqMan® real...
<p>For each gene, expression induction is represented as a ratio of its relative expression at 1, 3 ...
Fungi constitute an important group in soil biological diversity and functioning. However, character...
Quantitative real-time PCR (qRT-PCR), used in conjunction with reverse transcriptase, has been appli...
(A) DNA was isolated from a range of urinary volumes in male and female subjects (n = 3 each) and as...
International audienceAbstract Quantitative real-time PCR (qPCR) is increasingly used to detect Pneu...
In order to determine if living fungi of phytosanitary concern are present in wood or to evaluate th...
Fungi constitute an important group in soil biological diversity and functioning. However, character...
<p>RNAs were extracted from H99, H4, S48B and S68B for qRT-PCR analysis. Two independent samples wer...
Fungi are nearly ubiquitous in the environment. There are currently accepted methods to quantify fun...
<p>For each deletion, one transformant of the NRRL 13383 background was analysed. Columns show calcu...
Background: Fungal load quantification is a critical component of fungal community analyses. Limitat...
Background: A critical step in the RT-qPCR workflow for studying gene expression is data normalizati...
Fungal infections, ranging from superficial to life-threatening infections, represent a major public...
<p><i>C</i>. <i>ribicola tubulin</i> transcript was used as the calibrator for normalization of inpu...
To enable quantification of mycelial abundance in mixed-species environments, eight new TaqMan® real...
<p>For each gene, expression induction is represented as a ratio of its relative expression at 1, 3 ...
Fungi constitute an important group in soil biological diversity and functioning. However, character...
Quantitative real-time PCR (qRT-PCR), used in conjunction with reverse transcriptase, has been appli...
(A) DNA was isolated from a range of urinary volumes in male and female subjects (n = 3 each) and as...
International audienceAbstract Quantitative real-time PCR (qPCR) is increasingly used to detect Pneu...
In order to determine if living fungi of phytosanitary concern are present in wood or to evaluate th...
Fungi constitute an important group in soil biological diversity and functioning. However, character...