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Using time lapse video microscopy, we demonstrated that an applied DC EF directs migration of the EPCs toward the cathode.
Using high-resolution transmission electron microscopy, we demonstrated that the films were not a unique amorphous phase.
In vivo, using high resolution intravital microscopy, we demonstrated that Dox-CTSL upon an external heat-trigger delivered 3-fold higher Dox quantity to tumors than TSL.
Using fluorescence microscopy and transmission and scanning electron microscopy, we demonstrated that Ehrlichia was transported through the filopodia of macrophages during early stages of infection.
Using light and electron microscopy, we demonstrated that driver pathways of different origin can synaptically interact on single thalamocortical cells.
By confocal laser microscopy, we demonstrated a considerably reduced number of peroxisomes in neuronal processes that contained phosphorylated tau in pre-tangles (Fig. 4).
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Using confocal microscopy, we demonstrate that FLTX1 colocalizes with estrogen receptor α (ERα).
Using transmission electron microscopy, we demonstrate that porcine aortic endothelial cells take up GaN-based nanoparticles suspended in the growth medium.
Using Raman spectroscopy and electron microscopy, we demonstrate that initial thermal annealing of SWNT significantly improves their dispersion in PS.
By means of electron and confocal microscopy, we demonstrate that the in vivo findings were reproduced in vitro by incubating human epithelial cell lines with H. pylori products/virulence factors.
Combining the use of the new colocalization algorithm with image restoration and time-lapse confocal microscopy, we demonstrate the presence of MEK in mitochondria of HeLa and MEF cells and that MEK localization in the organelle is favored in proliferative conditions.
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