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. 2011 Dec 1;22(23):4527–4538. doi: 10.1091/mbc.E11-08-0739

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© 2011 DiPetrillo and Smith. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0).

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FIGURE 5: — Calcium-mediated motility phenotypes of single and double dynein mutants. (A) Table listing each cell strain used in this study along with the associated structural defect, ability to photoaccumulate (which is quantified in B), percentage of cells able to convert to the symmetric waveform, and the average symmetric beat frequency for those cells that are able to photoshock. (B) The fold change in the concentration of cells at the light-exposed edge of the Petri dish used in the photoaccumulation assay. Time points were taken at 0, 5, 15, 30, 60, 120, and 180 min, and the fold change compared with the 0-min time point was plotted. See Materials and Methods for details of quantification.