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To assess inherent differences in gene expression between the two species, the differential gene expression of naïve N. giraulti compared to naïve N. vitripennis expression was identified as well (Additional file 1: Table S2 and Additional file 2).
Thus, differential gene expression was identified as a significant) group effect p-value<0.001 p-value<0.001tive splicing andalternativent tisplicingbeset interastion (p-value<0.001).
A change in gene expression was identified as significant if the false discovery rate was less than 0.05, meaning that fewer than 5% of false findings would be expected among the genes declared to be differentially expressed.
Only genes whose expression was identified as being significantly changed at P = 0.01 were retained.
Slug expression was identified as positive if nuclear staining was observed, as described with Snail expression.
Using Thbs1 gene expression as a marker, the molecule responsible for the gene expression was identified as AMP.
Similar(25)
Lumens with negative hCD31 expression were identified as invading murine blood vessels.
In EHCC, 14 factors including EGFR expression were identified as significantly prognostic by univariate analysis.
In IHCC, 13 factors including EGFR expression were identified as significantly prognostic by univariate analysis.
A Luminal phenotype and ER expression are identified as major determinants of ATRA sensitivity.
Absence of A-type lamin expression is identified as a novel marker for undifferentiated ES cells (Constantinescu et al., 2006).
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