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Gene transcript levels in brain are generally consistent with gene dosage.
CTB8 transcriptional activator controls cercosporin production by controlling gene transcript levels.
Reverse Transcription quantitative real-time PCR (RT-qPCR) is applied to quantify gene transcript levels in a wide range of investigations.
Relative gene transcript levels were calculated using the 2-ΔΔCT method.
The 2−ΔΔCTmethod was used to determine the relative gene transcript levels with the mean value of triplicate experiments.
There were also changes in alcohol dehydrogenase (ADH) and glutamine synthetase (GS) gene transcript levels in response to HS exposure.
To determine whether the follicle environment modulates oocyte-specific gene transcript levels in cultured oocytes and polar bodies (PBs).
To study these effects, we developed a real-time qPCR assays useful for measuring both p53 and cdkn1a gene transcript levels in liver.
Transcriptome analysis has the advantage of being able to quantify changes in gene transcript levels at different developmental stages in wild-type species, their mutants, and cultivars with different genetic backgrounds.
This requires the implicit assumption that gene expression directly mirrors gene transcript levels.
The same was found in the present analysis of gene transcript levels.
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