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We also determined the effect of LPS on luteinizing hormone (LH) release.
We also determined the effect of marker registration on the measured SV displacement and its impact on margin design.
We not only employed pre-treatment and along with treatment approach, but also determined the effect of antioxidants at different time points of treatment.
We also determined the effect of pH on the reduction of Fe III) with S IV) in seawater.
Furthermore, we also determined the effect of priming on the biodistribution of 177Lu-octreotate to evaluate the effect on the therapeutic window.
We have also determined the effect of thymectomy on levels of PB cells containing signal joint TCR delta excision circles (TRECs), a molecular marker of thymus emigrants that have divided few times after leaving the thymus.
We therefore also determined the effect of BI-2536 treatment on MDM2 protein levels and found that inhibition of PLK-1 did not affect the levels of the MDM2 protein (Fig. 6a, b).
We also determined the effect of curcumin on VEGF gene expression in the cells.
We also determined the effect of curcumin on tumor vascularization by staining for the endothelial specific antigen CD31.
Thus, we also determined the effect of mitomycin C and camptothecin on HuR and PTB subcellular localization by immunofluorescence.
In line with these findings, we have also determined the effect over time of different iota-carrageenan concentrations on viral replication of infected MDCK cells (Figure 1C F).
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