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Compared with results achieved in Table 15 it should be noted that the error rate increased from 4.55% to 16% and all other metrics showed poorer results, excepting RAM and CPU, which remained stable.
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Among the 10 patients treated, CR or CR with incomplete blood count recovery (CRi) was achieved in 50% (Table 1).
It is necessary to point out that the complete genome-scale metabolic model reconstructions cannot be automatically achieved in MicrobesFlux (Table 1) yet.
A higher PR (58.4%) was achieved in Group 1 (Table 2).
R0 resection could be achieved in all patients (Table 2) and all patients were uneventfully recovered.
Higher productivities were always achieved in F medium (Table 4) irrespective of the habitat of origin of the strains.
Despite MV and lung insult by Pam3CSK4, hemodynamic stability and adequate blood oxygenation were achieved in our model (Table 1).
The blood sampling has been designed to determine drug concentrations at various time points to describe whether pharmacokinetic/pharmacodynamic targets are achieved in individual patients (Table 1).
We have also examined the scope of the alkene component using acetanilide 5 f, and, again, complete branch selectivity was achieved in all cases (Table 3).
By analysing three different cutting levels for each valid sample, the minimum useful area (2.5 mm) for quantitative analysis was achieved in all patients (Table 1).
Under negative misspecifications of the distribution of the prognostic factor, empirical power was improved in comparison to doing nothing but 80% power was not achieved in all cases (Table 3).
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CEO of Professional Science Editing for Scientists @ prosciediting.com