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The devices measured in this experiment are back-gated and dual-gated etched graphene devices.
All three progress variables measured in this experiment are shown: H+ (top), Fetot(middle), SO42- (bottom).
All the enzymes measured in this experiment increased after inflection point.
The same can be said for most of the blood hormones that were measured in this experiment.
The spectra of various powder samples such as CuCl2, NaCl and ZnS were measured in this experiment.
Although the digestive process in fish is not studied as much as in mammals, the enzyme profile measured in this experiment is a good physiological indicator of feed utilization.
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There may be hidden costs of this response that we were unable to measure in this experiment.
Therefore, using C data we conclude that creatine is not present at concentrations that we can measure in this experiment.
Although the timing and lengths of the resulting segments were not measured in these experiments, this suggests that the schedule, once established, is relatively refractory to new input.
Table 1 reports the hemodynamic parameters measured in this set of experiments.
Taking together all eight mediators measured in this series of experiments, it was possible for each of the trial subjects to establish a fingerprint-like cytokine pattern, which showed considerable stability over the whole observation period, as can be derived from the mean values plus confidence intervals shown in Figures 1, 2, 3, 4, 5, 6, 7, 8.
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