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The significant increase in transcripts for transcription and translation machinery in fungal host cells seems to be related to virus replication.
Transcription profiling across many generations revealed an increase in transcripts from genes expressed during spermatogenesis that correlated with a transgenerational increase in H3K4me2 levels in the promoters of these genes [ 34].
The increase in transcripts observed in mmi1W112A was comparable to that observed in erh1∆ (Fig. 6b).
We note that previous transcriptome studies with Yersinia spp. cultured in human plasma reported an increase in transcripts encoding proteins involved in iron uptake [18], [19].
Recently, DNA microarray analysis of Drosophila S2 cells infected with Wolbachia demonstrated an increase in transcripts belonging to the Toll and Imd immune signaling pathways, and the antimicrobial peptides attacin and diptericin [71].
We observed a decrease in transcripts that include exon 8, and an increase in transcripts that skip exons 7 and 8, relative to APP transcripts from the control cells (Figure 6C).
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Their products, 10-deacetylbaccatin III and baccatin III, respectively, accumulate within 6 h of the initial increase in transcript abundance.
Subsequent to excision, a wound signal induces promoter activity, which results in an increase in transcript and protein levels (Fig. 2d f).
A significant increase in transcript levels of ent-kaurene oxidase genes that are involved in gibberellin synthesis occurs in maize seedlings treated with H. seropedicae [38].
The rofA-containing chimera displayed a substantial increase in transcript abundance relative to wt Alab49.
Some increase in transcript levels by 7 days after inoculation was evident for Nbs2-Rdg2a but not for Nbs1-Rdg2a (Figure 2C).
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