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Fig. 4 a Whole-body PET maximum intensity projection of Balb/c nu/nu mice bearing an AR47J tumour on the right flank 1 h PI of 68Ga-labelled tracers.
The next day, cells were harvested, counted and injected subcutaneously in the flank, 1 × 106 cells per C57BL/6 mouse (n = 4), in 100 μl PBS.
One week after the last vaccination, mice received subcutaneous B16/LT tumor challenge in the right flank (1 × 10 cells/mouse).
The body areas treated were: thorax (7 patients), knee (3), thigh external side (2), leg external side (1), groin (1), foot (2), left flank (1), finger (2) and wrist (1).
TGBC2TKB cells transfected with Smo siRNA or non-targeting control siRNA were s.c. implanted into the flank (1 × 10 cells in PBS per mouse) of nude mice (n = 5 in each treatment group).
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Residents of seven buildings that flank 418 and 420 State Street were evacuated from their homes.
To assess in vivo effects, mice bearing established subcutaneous flank CT26 tumors were intravenously injected with ST8/pSEndo or ST8/pSGFP.
The in vivo antitumor activity of formulations was evaluated in the right flank HepG2 cancer cell in nude mice.
On the desert flank, 2RTR advanced with the 7th Armoured Brigade group.
AMC-HN9 cells were injected subcutaneously into each flank (5 × 10 per flank).
In the opossum genome, USM flanks ARID5A while 14 tandem copies of MSMB flank FAM21C and ANUBL1.
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