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Administration of OVV did not result in any additional photodynamic damage to normal mouse foot tissue.
As shown in Figure 4C, injection of OVV to HPPH-treated mice did not result in any additional damage to normal mouse foot tissue after exposure to light.
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In the present study, further characterization of the overall pseudogene transcriptional profile of M. leprae in the nu/ nu mouse foot pad granulomatous tissue by global DNA array and RT-PCR analyses demonstrated that not only does M. leprae possess the highest number of pseudogenes/genome it also possesses the highest rate of bacterial pseudogene transcription documented to date.
The effects of OV treatment on normal tissue phototoxicity was examined using the mouse foot response assay.
Normal tissue phototoxicity following PDT-OV treatment was studied using the mouse foot response assay.
The mouse foot response assay was performed on non-tumour-bearing A/J mice to assess normal tissue phototoxicity in vivo as described previously (Pandey et al, 1991).
Foot tissue was preserved in 95% ethanol.
The foot contains its own type of mucus-secreting cells that were likely incorporated into our foot tissue transcriptome.
Skin reactions on irradiated mouse feet were used to measure the radiosensitization of normal tissues by misonidazole (MISO).
Pollitt may be kidding about the mouse feet.
By 2010, researchers at Stanford had shown that mouse connective tissue cells could be reprogrammed directly into neurons, bypassing the pluripotent state.
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