We clearly show that the measured electrical signal is due to TJ-related barrier tissue formation rather than simple cell coverage; the presence of cells on the active area of the OECT does not modify the transistor response to gate pulse voltage unless the cells present barrier properties.
Thus, the relation between the processing efficiency of StAR protein in mitochondria and the steroidogenic activity in cells of the active form of StAR has not been fully clarified.
The overall mean staining intensity of the cells of the active group animals was 30.47%, whereas that of the sham group was 21.78% (P <.0001).
Only after the shoot tip became yellow did the cytoplasm became less intensely stained compared to that in cells of the active growth regions.
As this is the rate-limiting enzyme in 5-FU catabolism, high enzyme levels would be expected to reduce exposure of cells to the active forms of 5-FU.
This excision efficiency may be easily improved by longer exposure of cells to the active Cre-recombinase.
In our algorithm, the cell size of the active BSs is expanded as much as needed which does not necessarily correspond with the maximum cell size.
The algorithm developed in[10] is similar to ours, but it is assumed that the cell size of the active (non-sleeping) BSs is maximized.
Notably, the polymeric nanoparticle formulation achieved greater tumour retention, resulting in prolonged exposure of cancer cells to the active drug.
The highest expression found in all cell lines tested of the active protein forms of MMP-2 and -11 was detected in BeWo cells.
