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Polymorphisms in PPAR genes are shown to influence the activity of these receptors.
Mutations in histone encoding genes are shown to be associated with >70% of DIPG cases.
The results of qPCR related to expression changes of these genes are shown in Fig. 6.
The primers used to amplify promoters, terminators, and genes are shown in Table 2.
The gene-specific primers designed from the 3'UTR of rice genes are shown in Table 1.
Three rice genes are shown to be involved histone H3K9 deacetylation (SRT701) and methylation (SDG714) in transposon repression.
Representative genes are shown in the heatmap (Figure 1A).
Primer sequences for target genes are shown in Table S3.
Polymorphisms detected in these genes are shown in Table S5.
Results for individual genes are shown in Figure 1.
The primer sequences for the respective genes are shown in Table 1.
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