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To compare ambient PM2.5 PM10, NO, NO2 and ozone concentrations between the two exposure scenarios (road test and clean room), we compared these concentrations obtained from fixed measuring stations, close to the location of the road test and the clean room test.
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The results of GLC from Gaussian dispersion models as National Standard of China and those from the dispersion modeling system show that the concentrations obtained from these two distinctly different methods are of the same order of magnitude.
As illustrated in Table 1, the concentrations obtained using these two different methods were found to differ by only ±10% except for 3′-SL (−38%).
Therefore, reduced breakdown of bradykinin in the tubes without gel results in lower concentrations of des-Arg-bradykinin for these individuals compared to the concentrations obtained in tubes with gel separator.
Pharmacokinetic analysis revealed dose-related plasma concentrations for transdermal treatments, bracketing the concentrations obtained from nicotine gum.
For long-term stability evaluation, the concentrations obtained after 121 days were compared with initial concentrations.
In that work, the juice was diluted to simulate the concentrations obtained from the mills.
However, the daily means of the exposure concentrations from the personal samples followed the concentrations obtained from the area samples.
As shown in Fig. 3, linear regression analysis of these PICP concentrations obtained by both methods revealed a significant relationship (R2 = 0.9914).
Figure 1A, B illustrates Kaplan Meier survival analysis for these biomarkers including concentrations obtained at the last follow-up visit or the follow-up visit preceding an event.
We also estimated apo B100 using published prediction equations [ 23, 33] and compared predicted values from these equations with concentrations obtained from direct biochemical measurements.
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