| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10899433 | Cancer Letters | 2016 | 8 Pages |
Abstract
Our results reveal that CRC TIC can be propagated under conditions previously thought to induce their elimination. This phenotypic plasticity allows addressing primary human CRC TIC properties in experimental settings based on adherent cell growth.
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Authors
Taronish D. Dubash, Christopher M. Hoffmann, Felix Oppel, Klara M. Giessler, Sarah Weber, Sebastian M. Dieter, Jennifer Hüllein, Thorsten Zenz, Friederike Herbst, Claudia Scholl, Wilko Weichert, Wiebke Werft, Axel Benner, Manfred Schmidt,