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Our results showed clearly the expression of these genes was not significantly different from that of WT (Additional file 5: Figure S5A).
Clearly, the expression of harmful bystander effects impacts the long-term outcome of therapeutic irradiation.
The expression correlations that we have observed between inflammatory and zinc genes are very noteworthy, but clearly the expression of other genes may also correlate.
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However, more detailed studies combining quantitative RT-PCR and Western blot using multiple cell lines and a large number of incubation times will be necessary to clearly define the expression of TRF2 after DNA damage.
These findings clearly demonstrate the expression of meprinβ protein in podocytes of rat glomeruli.
Overexpression of miR-24 clearly decreased the expression of DHFR protein, with a potency that was comparable to control DHFR-siRNA, independent of the presence of functional p53.
While we could clearly demonstrate the expression of G2019S LRRK2 in nigral dopaminergic neurons, this was not possible for WT or R1441C LRRK2 mice.
Clearly, blocking the expression of c-Fos with ASO abrogates phospholipid synthesis activation to similar rates as those found in WT animals (C57BL/6J WT) whereas SO has no effect.
The results clearly showed the expression of this CSCs marker in all four examined cell lines.
Gel separation of the digested products clearly demonstrated the expression of both germacrene A synthases in roots and trichomes.
As shown in Figure 2, knockdown of IRE1a clearly increased the expression of BMP2 in C2C12 cells and BMSC cells.
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