File:Adhesion-molecule-periplakin-is-involved-in-cellular-movement-and-attachment-in-pharyngeal-squamous-1471-2121-12-41-S4.ogv
Adhesion-molecule-periplakin-is-involved-in-cellular-movement-and-attachment-in-pharyngeal-squamous-1471-2121-12-41-S4.ogv (Ogg Theora video file, length 15 s, 328 × 328 pixels, 1.11 Mbps, file size: 1.91 MB)
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[edit]DescriptionAdhesion-molecule-periplakin-is-involved-in-cellular-movement-and-attachment-in-pharyngeal-squamous-1471-2121-12-41-S4.ogv |
English: siRNA against PPL reduces cell migration in D562 cells. D562 cells were transfected with either control siRNA (Additional file 3) or PPL siRNA (Additional file 4). After 24 h, cells were seeded on glass-bottomed dishes and incubated for another 24 h. Images were analyzed by time-lapse confocal laser scanning microscopy using a laser-scanning confocal microscope. Frames were taken every 5 min for 24 h. |
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Source | Tonoike Y, Matsushita K, Tomonaga T, Katada K, Tanaka N, Shimada H, Nakatani Y, Okamoto Y, Nomura F (2011). "Adhesion molecule periplakin is involved in cellular movement and attachment in pharyngeal squamous cancer cells". BMC Cell Biology. DOI:10.1186/1471-2121-12-41. PMID 21951621. PMC: 3195110. | ||
Author | Tonoike Y, Matsushita K, Tomonaga T, Katada K, Tanaka N, Shimada H, Nakatani Y, Okamoto Y, Nomura F | ||
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This file is licensed under the Creative Commons Attribution 2.0 Generic license.
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current | 20:57, 6 December 2012 | 15 s, 328 × 328 (1.91 MB) | Open Access Media Importer Bot (talk | contribs) | Automatically uploaded media file from Open Access source. Please report problems or suggestions here. |
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Short title | Additional file 4 |
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Author | Tonoike Y, Matsushita K, Tomonaga T, Katada K, Tanaka N, Shimada H, Nakatani Y, Okamoto Y, Nomura F |
Usage terms | http://creativecommons.org/licenses/by/2.0/ |
Image title | siRNA against PPL reduces cell migration in D562 cells. D562 cells were transfected with either control siRNA (Additional file 3) or PPL siRNA (Additional file 4). After 24 h, cells were seeded on glass-bottomed dishes and incubated for another 24 h. Images were analyzed by time-lapse confocal laser scanning microscopy using a laser-scanning confocal microscope. Frames were taken every 5 min for 24 h. |
Software used | Xiph.Org libtheora 1.1 20090822 (Thusnelda) |
Date and time of digitizing | 2011 |