For the subsequent off-line analysis, we considered the first second (i.e., 1 s of EEG recordings) as period of interest (POI) for the initial decision-making processes.
Along this line of analysis, we cannot help but ask: What are pseudo-existentials, if they are not genuine existentials (i.e., thing-existentials)? How do we explain the differences between them?
Using line intensity analysis we found that GFP-APC only colocalized with F-actin at the leading edge in the presence of Cdc42V12 (Fig. 5(i) panel g).
Regarding cell line proliferation analysis, we showed that RAB25 expression increased cell proliferation, whereas Amornphimolthan et al. [ 26] found no impact on cell proliferation.
This data resulted as a consequence of our broader MA line mutational analysis; we conservatively identified natural isolate SNPs as those sites in unique genomic regions with ≥6X unanimous HTS data reporting the progenitor SNP in the MA line natural isolate (PB306, HK104, PB800) and derivative MA line HTS data.
When the presence of pericentric cohesin was scored in the myc-Scc1 HeLa cell line by immunofluorescence analysis, we did not see a significant reduction in the number of Scc1-myc-positive mitotic cells upon drug treatment (Figure 5C).
Further to elucidate the classification of MCF10A, which is the most widely-used putatively normal breast cell line in array analysis, we examined the expression values of KT14, KT8/18 and KT19 (Fig. 2A and 2B) and CD104.
To perform line-by-line coding and narrative analysis, we imported all course participants' journals into NVivo (QSR International, Burlington, MA), a textual analysis software program that facilitated coding and analysis (Richards, 2006).
In order to verify the role of ANXA1-FPR interaction in MIA PaCa-2 and PANC-1 cell migration and invasiveness, we first assessed FPR expression in these cell lines by cytofluorimetric analysis: we found that FPR-1 and FPR-2 were expressed in both cell lines.
For the purposes of identifying CAD-silenced lines for further analysis we visually screened leaf blades and sheaths for reddish brown discoloration and also stained sectioned leaves and stems with phloroglucinol-HCl.
Using multiple transgenic reporter lines to facilitate analysis, we report LepRb colocalization with POMC-EGFP neurons, with neurons that express PPG/GLP1 and with neurons that express CCK but not with other energy balance-associated populations that contain NPY, BDNF, CART, nesfatin, catecholamines, GABA, acetylcholine, PrRP, or nNOS.
