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Individual heavy metal in soil and plant samples was measured for control along with treatments.
Cell survival (C) and caspase-3-like activity (D) were measured for control (Randsi) or Apaf1 (Apafsi) silencing in the presence or absence of Doxo (1 µmol/L) and SVT016426 treatment (SVT; 5 µmol/L) (mean ± SD, n = 3).
For quantification of (Golgi surface area)/ total cell surface area) 98 cells were measured for control conditions and 88 for knock down conditions.
Cutoff was calculated for each dilution using equation Cutoff = X*SDf, where X is average and SD is standard deviation values measured for control serum, and f is SD multiplier corresponding to the confidence level 95% and number of replicates [51].
Direct clinic revenue was measured for control and scribe visits.
As with untreated embryos, this value was also significantly lower than that measured for control embryos (P < 0.0001).
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In their study heat and cold pain thresholds measured for controls are remarkably different from current physiological values [18] and therefore create the impression that the migraine patients' data are pathological.
Service contacts were not measured for the control group.
Previously isolated DNA samples were measured for quality control and concentration using a Nanodrop spectrophotometer.
A total of 20 cells were measured for each control and OLFM1 treatment.
CAEPs were also measured for a control group of 11 age-matched, normal-hearing (NH) children.
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