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The location and penetration characteristics of nanoparticles in the arterial vessel wall were visualized using confocal laser scanning microscopy and transmission electron microscopy (TEM).
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Mineralization of the arterial wall was visualized by both von Kossa method and alizarin red staining (Fig. 1 b-f).
Plant cell walls were visualized by propidium iodide staining (red).
The IVC was examined where its vessel walls were visualized best, preferably no further than 3 cm caudal to the junction of the right atrium [ 12, 13, 21– 21].
The measurements listed were obtained after a well-defined, continuous interface of the anterior and posterior walls was visualized.
The wall segments were visualized from two-dimensional images taken from the parasternal long axis and from the basal and midpapillary short axes.
Through the uterine wall, embryos were visualized, and plasmids (0.5 2.0 μg/μL for each) were injected into the lateral ventricle through a glass capillary.
Through the uterine wall, embryos were visualized, and plasmids (1.5 µg/µl for each) were injected into the lateral ventricle through a glass capillary.
Finally, small intraluminal details such as thrombus, stent malapposition, guide-wires and vessel wall dissection were visualized by 3D IV-OCT and compared to conventional 2D images.
Incision was performed (3 mm) and the underlying chest wall and intercostal spaces were visualized.
The branches of the portal veins were visualized with hyperechoic walls and hepatic veins, characterized by numerous anechoic tubular structures.
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