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Synchronizing chromosome segregation by flux-dependent force equalization at kinetochores

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Academic year: 2019

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Figure 1.  Phenotypic analyses of CLASP, KLP10A, and CLASP/KLP10A RNAi in Drosophila S2 cells
Table I.  Summary of measured mitotic parameters Experiment Metaphase flux
Figure 2.  Analysis of chromosome and spindle dynamics during anaphase. (a–c) S2 cells stably expressing GFP–-tubulin (green) and CID-mCherry (red)  were used to track kinetochore movement and spindle elongation during anaphase
Figure  3.  Analysis  of  chromosome  segregation  during  anaphase. (a  and  b)  S2  cells  stably  expressing  low  levels  of  GFP–-tubulin  (green)  and  CID- CID-mCherry (red) were used to track tubulin speckle movement (white broken lines) relative
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