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File:Sendai Virus organ infection specificity.png

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Recombinant SeV constructs (1ร—107 TCID50/100 ยตl) were injected intratumorally. 48 h post injection the mice were sacrificed, tumors were removed and indicator cultures (Vero cells) were infected with lysates from frozen tissue sections. Fluorescence microscopy pictures of the infected Vero cells were
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Martina Zimmermann, Sorin Armeanu-Ebinger, Sascha Bossow, Johanna Lampe, Irina Smirnow, Andrea Schenk, Sebastian Lange, Thomas S. Weiss, Wolfgang Neubert, Ulrich M. Lauer, and Michael Bitzer
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Intratumoral and intra-organ spread of recombinant SeV virions in vivo in a hepatoma xenograft murine model.
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Attenuated and Protease-Profile Modified Sendai Virus Vectors as a New Tool for Virotherapy of Solid Tumors
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taken 72 hpi. Shown are representative picture for each animal.
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File:Sendai Virus organ infection specificity.png
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Murine respirovirus

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