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Expression levels of several Yap1/p73 and Yap1/TEAD1 target genes were monitored by quantitative reverse transcription-polymerase chain reaction (RT-PCR).
The GUS expression patterns within transgenic lines for these genes were monitored in rice at three sequential stages of pollen development (Fig. 2c-g).
Expression of a selected set of 20 genes were monitored and validated through real-time PCR for specific induction during early and late stage of interaction in three rice genotypes.
Expression patterns of the selected genes were monitored.
Cytoplasmic lipid droplet accumulation and mRNA expression for adipogenesis-related genes were monitored.
The expression patterns of 17 of those genes were monitored by real-time PCR.
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Expression of various bone important genes was monitored by real-time RT-PCR.
Expression of EC specification and marker genes was monitored by quantitative PCR, western, immunocytochemistry, and flow cytometry.
The response of 5 genes was monitored resulting in expression increase with the dose of radiation received.
In order to address this question, the expression pattern of some stress marker genes was monitored.
The false discovery rate for selected genes was monitored and controlled by calculating the q value.
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