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A priori, one may expect expression to be higher in female than male tissues.
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If the miRNAs are regulated by endogenous FOXO activity, one may expect their expression to be sensitive to the status of AKT in the same cells.
As may be expected, expression of the genes for ROS scavenging enzymes is upregulated in plants under abiotic stress [ 7].
If Symbiodinium spp. use their photosynthetic capabilities to maintain residence within the intracellular habitat (but are "parasitic" in other aspects of their life history), then we may expect different types of genetic expression profiles than if the host is somehow controlling the association (e.g. [ 32, 62]).
Because human, mouse, rat and cow are placental mammals, one may expect some similarity between orthologous gene expression profiles.
If shared cis-regulatory regions were critical to coordinated expression evolution, we may expect that the genes would tend to be on the same stand.
As one may expect, proteins associated with cell proliferation changed in expression upon FUS knockdown.
However, we may expect that different genes, depending on their peculiar expression profile are represented by clusters of different sizes or are not represented at all.
Therefore, we may expect a priori that some imprinted loci would show sex-dependent expression.
Additionally, we may expect that Grh will be upregulated in response to injury, while knockdown of Grh expression may undermine epithelial integrity and inhibit wound healing.
Patients may expect a scan.
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