Abstract
Time-lapse fluorescence microscopy is one of the main tools used to image subcellular structures in living cells. Yet for decades it has been applied primarily to in vitro model systems. Thanks to the most recent advancements in intravital microscopy, this approach has finally been extended to live rodents. This represents a major breakthrough that will provide unprecedented new opportunities to study mammalian cell biology in vivo and has already provided new insight in the fields of neurobiology, immunology, and cancer biology.
| Original language | English |
|---|---|
| Pages (from-to) | 969-979 |
| Number of pages | 11 |
| Journal | Journal of Cell Biology |
| Volume | 201 |
| Issue number | 7 |
| DOIs | |
| Publication status | Published - Jun 2013 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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