File:Rac1-Dependent-Collective-Cell-Migration-Is-Required-for-Specification-of-the-Anterior-Posterior-pbio.1000442.s023.ogv
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Rac1-Dependent-Collective-Cell-Migration-Is-Required-for-Specification-of-the-Anterior-Posterior-pbio.1000442.s023.ogv (Ogg Theora video file, length 8.0 s, 570 × 215 pixels, 229 kbps, file size: 224 KB)
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[edit]DescriptionRac1-Dependent-Collective-Cell-Migration-Is-Required-for-Specification-of-the-Anterior-Posterior-pbio.1000442.s023.ogv |
English: Absence of cell movement and long cellular projections in Rac1 VE-deleted embryos. The Rac1 VE-deleted embryo was dissected on e5.6 and imaged for 4 h 20 min. Frames are 10 min apart. A stack of 22 slices was taken, at 2 µm per slice. The embryo had developed overnight to a degree similar to wild-type embryos. Individual cells were pseudocolored in order to visualize their trajectories. The cell tracking was made using individual confocal images of each stack in order to increase the accuracy of the cell contours. |
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Source | Video S11 from Migeotte I, Omelchenko T, Hall A, Anderson K (2010). "Rac1-Dependent Collective Cell Migration Is Required for Specification of the Anterior-Posterior Body Axis of the Mouse". PLOS Biology. DOI:10.1371/journal.pbio.1000442. PMID 20689803. PMC: 2914637. | ||
Author | Migeotte I, Omelchenko T, Hall A, Anderson K | ||
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![]() ![]() This file is licensed under the Creative Commons Attribution 3.0 Unported license.
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Date/Time | Thumbnail | Dimensions | User | Comment | |
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current | 00:02, 19 October 2016 | 8.0 s, 570 × 215 (224 KB) | 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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Author | Migeotte I, Omelchenko T, Hall A, Anderson K |
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Usage terms | http://creativecommons.org/licenses/by/3.0/ |
Image title | Absence of cell movement and long cellular projections in Rac1 VE-deleted embryos. The Rac1 VE-deleted embryo was dissected on e5.6 and imaged for 4 h 20 min. Frames are 10 min apart. A stack of 22 slices was taken, at 2 µm per slice. The embryo had developed overnight to a degree similar to wild-type embryos. Individual cells were pseudocolored in order to visualize their trajectories. The cell tracking was made using individual confocal images of each stack in order to increase the accuracy of the cell contours. |
Software used | Xiph.Org libtheora 1.1 20090822 (Thusnelda) |
Date and time of digitizing | 2010-08 |