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Scanning electron microscopy revealed that this culminates in the formation of structures that anchor monocyte adhesion.
Confocal microscopy revealed that the droplets emerged directly after addition of fuel.
Visualization of cultures by light microscopy revealed that cells were completely confluent after two days in GM (Fig. 5e).
Electron microscopy revealed that ptrn-1 null mutants have fewer MTs and abnormal MT organization in the PLM neuron.
Transmission electron microscopy revealed that these particles were aggregates of rod-like HAp nanocrystals, whereas scanning electron microscopy revealed that these particles ultimately formed into larger aggregates.
Scanning electron microscopy revealed that non-porous microparticles with a smooth surface were prepared.
The images taken by electron microscopy revealed that the treated samples maintained their submicrofibrous morphology.
Optical microscopy revealed that the stir zone consisted of micro-scale mechanical inter-locks.
The immunofluorescence using confocal microscopy revealed that Dorin M is produced in the tick hemocytes.
Confocal microscopy revealed that LCP NPs were largely localized in hepatocytes not Kupffer cells.
Scanning electron microscopy revealed that caffeine crystals were homogeneously dispersed onto oral film matrix.
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