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. 2015 Mar 19;4(7):e1014760. doi: 10.1080/2162402X.2015.1014760

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© 2015 The Author(s). Published with license by Taylor & Francis

© Karin Schilbach, Mohammed Alkhaled, Christian Welker, Franziska Eckert, Gregor Blank, Hendrik Ziegler, Marco Sterk, Friederike Müller, Katja Sonntag, Thomas Wieder, Heidi Braumüller, Julia Schmitt5, Matthias Eyrich, Sabine Schleicher, Christian Seitz, Annika Erbacher, Bernd J Pichler, Hartmut Müller, Robert Tighe, Annick Lim, Stephen D Gillies, Wolfgang Strittmatter, Martin Röcken, and Rupert Handgretinger

This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.

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Figure 6. — In vivo expression and organization of desmin as a marker of myogenic differentiation in A204 RMS. (A) Histologic slides from tumors (n = 3/cohort) of all cohorts (FcIL-7, NHS-IL12/FcIL-7, or NHS-IL12/IL-2MAB602 treated) were stained for desmin (scale bars: 200 µm) and analyzed by a pathologist (B) in a blinded manner. LT: long-term treatment; ST: short-term treatment.