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The agent could then be tested in the sample in a short study of 2 4 weeks using the appropriate biomarkers for the predicted mechanism of action and potential adverse effects.
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The results for all serological markers tested in the samples and for the statistical analysis according to three analyzed variables (sex, age group and geographical origin of the samples) are shown in Table 1.
Specificity and sensitivity was tested in the samples of PI and controls for RIS and for PSQI separately.
Developed equations were then tested in a validation sample; FFM predicted by previously published equations were tested in the total sample.
First, the configural model was tested in the overall sample.
HIV positive prevalence was 7.0% of those tested in the total sample.
Models B and E were also tested in the French sample.
These models included all of the covariates that were tested in the UN sample and tested the outcomes WHtR, BMI, and BMI ≥ 30.
Cytonuclear disequilibrium (CND) was tested in the S23 sample after recoding the mitochondrial haplotypes as N versus S "mitotypes".
Different contents of PBDEs were tested in the tested samples and the total contents ranged from 25.0 ng g−1 to 194.0 ng g−1.
Major ions including Ca2+, Mg2+, Na+, K+, Cl−, SO4 2− and NO3 − were tested in the extracted samples.
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