@inbook{10268,
  abstract     = {The analysis of dynamic cellular processes such as plant cytokinesis stands and falls with live-cell time-lapse confocal imaging. Conventional approaches to time-lapse imaging of cell division in Arabidopsis root tips are tedious and have low throughput. Here, we describe a protocol for long-term time-lapse simultaneous imaging of multiple root tips on a vertical-stage confocal microscope with automated root tracking. We also provide modifications of the basic protocol to implement this imaging method in the analysis of genetic, pharmacological or laser ablation wounding-mediated experimental manipulations. Our method dramatically improves the efficiency of cell division time-lapse imaging by increasing the throughput, while reducing the person-hour requirements of such experiments.},
  author       = {Hörmayer, Lukas and Friml, Jiří and Glanc, Matous},
  booktitle    = {Plant Cell Division},
  isbn         = {978-1-0716-1743-4},
  issn         = {1940-6029},
  pages        = {105--114},
  publisher    = {Humana Press},
  title        = {{Automated time-lapse imaging and manipulation of cell divisions in Arabidopsis roots by vertical-stage confocal microscopy}},
  doi          = {10.1007/978-1-0716-1744-1_6},
  volume       = {2382},
  year         = {2021},
}