Sentence examples for supplementary half from inspiring English sources

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A surgical level of anaesthesia was maintained by supplementary half doses of ketamine and xylazine injected every 45 min.

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Each supplementary half-run produced between 16 and 21% new contigs for a second half-run, and between 5 and 7% for a third half-run (Additional file 3).

In this 'vocal non-vocal'vocal non-vocalductest melodic excerpts of orchestral music (popular operas, oratorios, ballets and symphonies) were presented in randomized order (Supplementary Table S1): half the source compositions from which the excerpts were drawn contained human voices, while the remaining half were entirely orchestral, however no voices were present in the excerpts presented.

Expression levels of six3, otx2, and tbx3 were not significantly different in animal caps treated with SB43+DM versus those injected with Noggin RNA, wherea s rax, pax6, and lhx2 expression was about half (supplementary material Fig. S2).

Neither osmostress nor anisomycin altered p57 half live (Supplementary Figure S2A), albeit this was under the control of the proteosome as previously reported (Supplementary Figure S2B; Kamura et al, 2003).

Thus, there is a significant relationship between the variation in thickness as well as the overlap length with the yielding effect in the connection zone of the supplementary plates with the half-ring, and some values are not recommended to be employed in thickness and overlap.

To explore this within the present sample we performed a split-half validation (Supplementary material and Supplementary Fig. 3).

To study mRNA half-life (Supplementary Fig S7A), asynchronous HeLa Kyoto cells were treated with 5 μg/ml actinomycin D (Sigma) and cells were harvested at the indicated time points after drug treatment for RNA analysis.

To test whether the levels and consistency of dual AAV-mediated transduction obtained can be improved by varying the ratio between the 5′-and 3′-half vectors, we injected subretinally C57BL/6 mice with dual AAV TS and hybrid AK vectors with different doses of 5′-and 3′-half vectors (supplementary Fig S6).

We found that a small number of genes (n = 92) had statistically significant differences in mRNA decay rates between MC1 (129S6/SvEvTac) and MC2-B6 (cells/6J) ES cells (FDR <0.05 and >2-fold change of half-life) (Supplementary Table S5) and only 10 of these genes overlapped with strain-specific signature genes.

Furthermore, knockdown of HuR decreased levels of lincRNA-p21 in the absence or presence of ING1b, suggesting that effects of ING1b overexpression on lincRNA-p21 occur independently of HuR, consistent with ING1b knockdown increasing lincRNA-p21 half-life (Supplementary Figure S1E).

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