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. 2010 Nov 29;191(5):1029–1041. doi: 10.1083/jcb.201007008

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© 2010 Biswas et al.

This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).

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Figure 7. — In vivo two-photon time-lapse microscopy and automated cell tracking in wild-type and morphant embryos. (A–D) Cell trajectories determined from time-lapse sequences from Tg(h2afv:GFP) transgenic embryos. Time lapses were collected from wild-type embryos (A), pcdh19 morphants (B), ncad morphants (C), and embryos coinjected with subthreshold doses of pcdh19 and ncad morpholinos (D). Bar, 50 µm. Anterior is to the left. (E–G) Graphs show the mean instantaneous cell velocities (E) and the mean cell velocities along the anteroposterior (F) and mediolateral axis (G). Error bars represent SEM.