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Molecular imaging provides a unique opportunity to image the tumor microenvironment, which is challenging by more invasive means.
Molecular imaging also provides a unique opportunity to image the tumor microenvironment, which is challenging by more invasive means.
By combining the powerful synchrotron X-ray source and fast switching between white (for X-ray diffraction) and monochromatic (for absorption imaging) modes, this technique provides the high-pressure community with a unique opportunity to image the three-dimensional volume, texture, and microstructure of materials under high pressure and temperature.
The combination of a fluorescent calcium sensor, delivered virally to optically accessible SMG neurons, provides a first opportunity to image PRV live in vivo to explore both connectivity and activity.
The advent of radiology as a diagnostic aid provided the first opportunity to image internal tumors non-invasively, and progress over the past three decades has resulted in a wide array of non-invasive, live-tissue imaging options [1], [2], [3], [4].
MIBG offers a unique opportunity to image NBL with highly sensitive and specific tracers.
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More importantly, magnetic resonance molecular imaging presents opportunities to image directly the biological processes of vascular disease at the molecular and cellular levels [ 4, 5].
These probes thus offer new opportunities to image molecular and cellular dynamics.
The translucency of zebrafish larval tissues has offered us a unique opportunity to live image how the wound inflammatory response impacts on adjacent pre-neoplastic or cancer cells and reveals some interesting insights.
To maximize imaging efficiency, this gap provides the opportunity to acquire images that are relatively unaffected by contrast accumulation in the hepatocytes.
Since we could obtain both CLSM and TEM images of the same specimen, the tail fin infection model provided the opportunity to correlate images generated by these 2 types of microscopy.
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