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Images were obtained by classical microscopy analysis (Leica DMRE microscope) of both ventricles.
Images were obtained by classical microscopy analysis (Leica DMRE microscope) of ventricles and interventricular septum at 20×.
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Infected tissues were observed by classical microscopy following hematoxylin-eosin staining.
By fluorescence microscopy analysis, EBD uptake into muscle fibers was visualized by red emission.
We then tracked nucleolin localization at different time points of infection, by confocal microscopy analysis.
Migration of NCC was evaluated by florescence microscopy analysis.
The morphological studies of the prepared samples are observed by scanning electron microscopy analysis.
Structural analysis by transmission electron microscopy analysis further confirmed the formation of crystalline CoSb3 nanoparticles with high purity.
It contains less than 2% of contaminating structures as judged by microscopy analysis.
Infection efficiencies were evaluated by using confocal microscopy analysis.
Classical histological and electron microscopy analysis revealed major lesions, characterized by cellular disorganization in the follicles, increasing intercellular spaces and the absence of the basal lamina in diseased tissues (Figure 1F and 1H, and Figure 2B) compared to healthy tissues (Figure 1G and Figure 2A).
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