Using transmission electron microscopy, we observed changes in the cytoplasm and peripheral vesicles.
From a combination of confocal microscopy and transmission electron microscopy, we observed that the released pA disrupts the cell membrane.
Using transmission electron microscopy we observed that the diterpene induced a delay in the progression of cell division.
By means of scanning electron microscopy, we observed indeed that the mutant parasites had a rougher, more heterogeneous surface, with apparently larger knobs, when compared to the wild-type parasites (Fig. 4B).
Using video-light microscopy, we observed the decrease in flagella beating frequency and severe changes in the lateral flange and in the general aspect of the cell.
Through further analysis via microplate reader, as well as confocal and wide-field epi-fluorescence microscopy, we observed non-specific binding of PI in viable filamentous cyanobacteria.
Using two-photon intravital imaging and transmission electron microscopy, we observed the existence of preferred sites for neutrophil entrance into the endothelial cell monolayer and exit from the basement membrane and pericyte sheath during neutrophil extravasation, namely, hotspots I and II, by elucidating distinctive roles of LFA-1 and Mac-1.
Using scanning electron microscopy, we observed that as early as two weeks after insult, a few immature hair cells, demonstrating the characteristic immature morphology indicative of regeneration, could be seen in the utricle.
Using in situ transmission electron microscopy, we observed the nucleation and growth of graphene bilayer edges (BLE) with "fractional nanotube -like structure from the reactionanotube -likemonolayer edgestructure
Employing scanning electron microscopy, we observed that addition of MWCNT led to a transition from dispersed to interconnected morphology for the blends with PS as minor phase (PP PS/50 50 and PP PS/90 10).
