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The scanning electron microscopy and atomic force microscopy studies indicate the presence of smooth, crack-free, uniform layers, with densely packed crystal grains on the silicon surface.
Atomic force microscopy studies indicate that the thickness of patterned GO can be controlled by adjusting the concentration of the GO dispersion.
Dynamic light scattering and transmission electron microscopy studies indicate that the carboxylate-terminated nanocarriers (20 nm) sequester LDL (22 nm), resulting in complexes with a diameter of 60 90 nm, but neutral ethoxy-terminated nanocarriers do not retain LDL.
X-ray scattering and transmission electron microscopy studies indicate the formation of an intercalated morphology in the nanocomposites due to favorable interactions between the polymer matrix and the clay.
Microscopy studies indicate that for 4 h of contact time, bacteria exhibit inner damage and even lysis, however, no morphological changes are detected because of the short timeframes used.
Electron microscopy studies indicate that cardiac (RyR2) channels could interact among themselves as they are physically connected in organized arrays at the terminal cisternae of SR [4].
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The atomic resolution electron microscopy studies indicated that the hardening kinetics was related to the formation of the nano-particles and location of the doped atoms.
Transmission electron microscopy studies indicated that this behaviour was due to the preferential location of silicates in the PBS phase than in the PLA phase.
Electron microscopy studies indicated that the interphase boundary interaction was highest in the clay with intermediate hydrophobicity but decreased with clays of higher or lower hydrophobicity.
Fluorescent microscopy studies indicated that fluorescein isothiocyanate labeled insulin when administered in solution, as well as when loaded into MCT1 or MCT2 SNEDDS, localized within the intercellular space of the Caco-2 cell monolayer, indicating transport by paracellular diffusion.
Confocal microscopy studies indicated that the lipophilic CL targets the endoplasmic reticulum (ER) of live cells, where it could be functioned as a fluorescent chemosensor for visualization of Cys in this organelle.
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