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In conclusion, we identified miRNAs and evaluated their expression patterns in Ae. albopictus upon DENV-2 infection using Illumina sequencing.
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Coexpression between two genes can be quantified by a measure evaluating how similar their expression patterns are across the biological samples.
Some had their expression patterns evaluated by real-time PCR along the entire time course of phytohormone treatment (SCBGLR1023D05.g [CA117725], SCJLHR1028C12.g [CA106117], SCEQRT1024E12.g [CA132523], SCQGLR1062E12.g [Cand4203] and SCRULR1020D11.g [Cand5940]) and presented consistent results.
In parallel, we evaluated the expression patterns of late stage ECM molecules including Col10a1, Ibsp and Dmp1 by qRT-PCR (Figure 3).
We also evaluated gene expression patterns and activated pathways associated with RANK and RANKL expression.
Twenty-one cellular loci were evaluated for expression patterns consistent with the allele effects.
In this study, we evaluated the expression patterns and functional significance of SOCS2 in PCa.
Moreover, we evaluated the expression patterns of selected miRNAs in different sugarcane tissues/organs (see next section).
We evaluated gene expression patterns from cultured rat primary hepatocytes after a 24-hr incubation with methapyrilene (MP).
In the present study, we evaluated miRNA expression patterns in the serum from the circulating blood derived from multiple myeloma patients, MGUS patients and controls.
We evaluated the expression patterns of 11 targeted PcNLP genes by qRT-PCR at different time points after infection by P. capsici.
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