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Several polymerase chain reaction (PCR) primers have been designed to detect this species; however, a comparative assessment of their accuracy has not been conducted.
A molecular diagnosis test was designed to detect this mutation and was used to show that it is still present in Cyprus Island.
Our analysis is designed to detect this slip-deficient area by summing the seismic slip (white areas in Fig. 8); however, we cannot extract the hidden source area using earthquakes with slips larger than the relative plate displacement (Fig. 8b).
Based on theoretical analysis of PEC technique, three different probes, including a differential hall probe, a differential coil probe, and a two-stage differential coil probe are designed to detect this kind of defects.
Due to the prevailing assumption that two devices exist at the same time in a rogue AP attack, the current IDS systems have not been designed to detect this type of attack where the legitimate AP is taken over by the attacker.
We have no evidence to suggest that any patients suffered harm, but our study was not designed to detect this.
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To confirm the higher level of methylation in the GABARAPL1 promoter in BC, the same experiment was repeated using primers (MC2) designed to detect the 5′-UTR 5′-UTR of this gene.
This study was designed to detect the positive difference in PONV incidence between groups; however, study hypothesis was declined.
However this study is designed to detect the timing of the presence of transcripts, as assessed by hybridization.
This assay is designed to detect the biologically active natural and recombinant human TGF-β1.
This study was designed to detect the superiority of 1% octanediol product compared with a placebo.
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