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Subjects were required to submit overnight fasting blood samples utilized for the different metabolic parameters.
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Genomic DNA was extracted from whole blood samples, utilizing the salting out method.
While in those with regular menstrual cycles, blood samples were obtained during the follicular phase of the cycle, except for samples utilized for the assay of progesterone that performed in the day 21 of the cycle (luteal phase).
* Samples utilized for 2D-gel elctrophoresis N/A = not available.
Their blood samples were utilized for ICC as confocal control specimens but not were used for FCM.
a = Asthma sample utilized for HRQOL comparisons across disease clusters.
b = Asthma sample utilized for HRQOL comparisons across disease categories.
Another limitation is that we measured the biomarkers such as PS-PLA1 and glycerol LPLs in the blood samples taken from the arterial sheaths, while the venous blood samples are ordinarily utilized for the similar clinical studies.
The collected blood samples were utilized immediately for the preparation of thin blood smears and were then kept at −20°C until DNA extraction.
Only endogenous 25(OH)D2 and/or 25(OH)D3 contained in human blood samples should be utilized for this purpose.
For blood samples, we utilized the tool Cn.
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