a The survey response rate is shown indicating that most of the invited participants completed the survey.
Fig. 3 A MIP image from the initial SPECT study (0.5 h after administration of the therapy commenced) for one subject is shown, indicating the location of the calibration flask (yellow arrow) relative to the subject.
HMGB1 and UBF-1 contain multiple HMG-box motifs, although only one is shown (indicated by decimal in Fig. 1).
(B ) Quantification of cells from (A ) is shown indicating the number of cells with detectable Mic60 or Mic27 foci, as indicated.
We hope this explAnation clarifiedited questions raised by the reversion.
In Figure 2, the estimated trend is shown, indicating a general decrease in incidence rates over time; however, with periods of local increase.
A 'summary of results' table is shown indicating the number of genes found for each dataset/tissue selected on the search page.
In Figure 3D, the number of colonies is shown, indicating clearly that, among MFH2003 cells, SP, but not MP, cells had the potential for spherical colony formation.
However, many adherent cells were detected in the pool of cells transfected with Cas9 and the four FUT8 sgRNAs (Fig. 3B, only sgRNA3_F is shown), indicating Cas9-mediated functional knockout of FUT8 in these cells.
Below the MS/MS spectra, the alignment between the Sanger (top) and TIGR (below) annotation is shown, indicating that the identified sequence was only annotated as part of the Aspartate transaminase gene in the TIGR dataset (underlined).
In Figure 1 the cytotoxicity of extracts at 100 μg/ml is shown, indicating that these soft corals demonstrated potent cytotoxicity by killing more than 90% of the cells.
