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. 2017 May;46(5):659–670.

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Copyright© Iranian Public Health Association & Tehran University of Medical Sciences

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 6: — The effect of siRNA snail1 on MDA-MB-468 migration. A confluent monolayer of MDA-MB-468 cells was scratched and then treated with snail1-siRNA. After 24 and 48 h, the scratch area was observed and photographed by microscopy. (a) Images at 0 h after transfection of snail1 siRNA and without transfection of snail1 (control). (b) Images at 24 h after transfection of snail1 siRNA and control. (c) Images at 48 h after transfection of snail1 siRNA and control. (d) The quantity was normalized the scratch area between 0 and 48 h against the scratch area at time zero and expressed as number of the migratory rate of MDA-MB-468 cells incubated with the control. Data are presented as means ± SD. (n=3); **** P<0.0001 versus control.