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The VAS modifications, the number of attacks and the number of analgesics taken during the study are shown in Figure 1 for the patients diagnosed with ETTH.
However, as already stated in Section 1, if duty-cycle techniques are adopted within the proposed CRT-based scheme (or any other splitting techniques) without modifications, the number of packets lost greatly increases.
As a result of alternative splicing, point-mutations, degradations and co- and post-translational modifications, the number of protein species [1] of a proteome exceeds by far the number of protein-coding genes of the corresponding genome.
In the last years several models have been suggested to estimate the logarithm of the folding rate and structural parameters such as the contact order along with its modifications, the number of contacts, or the protein "effective length" [3], [7], [19] [23].
To quantify the Fpg-sensitive modifications, the number of SSBs was subtracted, whereas the background levels observed with untreated controls were subtracted in all cases.
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VAS modification, the number of attacks and the number of analgesics taken during the study are shown in Figure 2 for the patients diagnosed with MO.
It is also worthy to point out that after the modification, the number of elements under the threshold of 2 %–4 % is more than doubled.
Study of the blood compatibility of Ar plasma surface-modified PS showed an initial increase in the number of adhered platelets to the surface and then decreased by increasing exposure time (Figure 5). Figure 6 depicts that after O2 plasma surface modification, the number of adhered platelets onto the surface decreased.
However, using Lumley et al.'s weighted modification, the number of copies is basically irrelevant because the data set size is only doubled for any weights [ 31].
We expect the level of statistical significance will depend on the type of modification, the number of modifications applied, and the percentage of patients excluded from final efficacy analysis.
The following information was collected at each infusion: the initial infusion rate, the number and proportion of patients with an infusion modification and the reasons for modification; the number and proportion of patients who completed the 1000-mg dose; and the total infusion times among those who completed the 1000-mg dose.
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