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To validate the transcriptional pattern identified by microarray analysis, expression of 42 differentially expressed genes was analyzed using RT-PCR.
Combining the results of pathway enrichment analysis, expression of target genes and hormone measurement, these differentially expressed miRNAs in anestrus are indicated to participate in attenuation of ovarian activity by regulating the pathways relating to hormone secretion and follicular development.
Combining the results of pathway enrichment analysis, expression of target genes and hormone measurement, we suggest that these differentially expressed miRNAs in anestrus might participate in attenuation of ovarian activity by regulating the above pathways.
In the tumor analysis, expression of Noxa was seen in all biopsies.
Fig. 4 Real-time PCR analysis expression of the eight genes before and after interaction with epithelial cells.
However, the analysis expression of such (p^{ast}) in Theorem 3 may not be the optimal result.
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For analysis, expression levels of the housekeeping gene rp49 were used as an RNA loading control.
Class comparison analysis: expression levels of tissue-selective T-UCRs.
Using GO_BP terms to start, we conducted gene co-expression analysis of expression profiles of PrCa.
Northern blot analysis demonstrated expression of the variant mRNAs.
Fig. 5 RT-PCR analysis of expression of drought-responsive genes in OsWRKY11-ox and OsWRKY11-kd plants.
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