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Unconfined compressive strength test was further performed with 50 × 100 mm cylindrical specimens moulded in plastic moulds and then stored under the curing storage condition with a curing chamber that can maintain the temperature of 25 °C and 100%% of relative humidity immediately adjacent to the cylinders until desirable testing times of 3, 7 and 28 days as presented in ASTM D 4832.
Maximum adsorption was achieved with a ratio of 1 9, as compared to 1 11, which was attributed to a lack of stability in the latter; hence, the adsorption experiments were further performed with beads prepared by using the ratio 1 9 (Fig. 2).
All analyses were further performed with these transformed values.
Cell cycle analysis was further performed with HepB3 cells transected with miR-221 mimic and inhibitor.
Data analysis was further performed with Genespring software version 7.0 (Silicon Genetics).
GLM was further performed with population structure (Q matrix) integrated as covariate to correct for the effects of population substructure.
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We further performed experiments with the same protocol as applied for results in Table 6 but with a reduced set of features by each of the three feature selection strategies (cf. Section 5).
We further performed comparisons with earlier reports.
Then we further performed bisulfite sequencing with genomic DNAs extracted from NPs and rNP-iPS cells.
We further performed karyotype analysis with the first 4 CAFs (data not shown).
Pairwise comparisons were further performed when necessary, with the significant level adjusted by the Bonferroni method.
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