uveniles were dissociated in pools of 15 polyps. Prior dissociation were labeled for 30 min with EdU (100uM, 2%DMSO) over several time points after feeding, and then dissociated and fixed using Trypsi
Modeling and in silico simulations are of major conceptual and applicative interest in studying the cell cycle and proliferation in eukaryotic cells. In this paper, we present a cell cycle checkpoint-
This dataset contains images of Arabidopsis shoot apical meristems expressing the KRP4-mCherry, CDT1a-CFP and acyl-YFP reporters. These images have been used to study how cell cycle progression is coo
