Visualizing spatiotemporal dynamics of multicellular cell-cycle progression.

By A. Sakaue-Sawano, H. Kurokawa, T. Morimura, A. Hanyu, H. Hama, Hatsuki Osawa, S. Kashiwagi, K. Fukami, T. Miyata, H. Miyoshi and 4 more. Cell, 2008

2,105 citations recorded by the source corpus.

Subfields: Biophysics, Cell Biology

View Paper: https://www.semanticscholar.org/paper/e0a34e2287fc23f409278aa5771719b8c22d1623

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Citations in the corpus

The Cell-Cycle State of Stem Cells Determines Cell Fate Propensity (2014, positive): “Sorting by FACS FACS was performed as described before (Sakaue-Sawano et al., 2008).”
Fluorescent proteins and their applications in imaging living cells and tissues. (2010, methodology): “A vivid example of this is the technique developed for the realtime monitoring of cell cycle progression in living tissues, named Fucci (370).”
The growing and glowing toolbox of fluorescent and photoactive proteins (2016, background): “This new indicator could be combined with the previously reported visible FP-based FUCCI for imaging cell cycle progression in two distinct cell types [41].”
IRF4 Transcription Factor-Dependent CD11b+ Dendritic Cells in Human and Mouse Control Mucosal IL-17 Cytokine Responses (2013, methodology): “By using Fucci-492 mice where cells in S, G2, and M phases of the cell cycle are fluorescent (Sakaue-Sawano et al., 2008), we observed that 5%–7% of lung CD103+ DCs and CD11b+CD24+ cells were in active cell cycle compared to 3% of CD11b+CD24 cells (Figure 1E).”
A cell cycle-dependent regulatory circuit composed of 53BP1-RIF1 and BRCA1-CtIP controls DNA repair pathway choice. (2013, methodology): “To purify G1 cells in cycling cultures, we took advantage of the Fucci system, which is based on fluorescent proteins with fragments of CDT1 and Geminin, for the G1 and S/G2 reporters, respectively (Sakaue-Sawano et al., 2008) (Figure 1A).”
Scale: a chemical approach for fluorescence imaging and reconstruction of transparent mouse brain (2011, positive): “To observe directly proliferating NSCs (PNSCs), we employed the Fucci (fluorescent ubiquitination-based cell cycle indicator) techniqu”
A subcellular map of the human proteome (2017, methodology): “First, we stained selected proteins with an observed SCV in the U-2 OS FUCCI [fluorescence ubiquitination cell cycle indicator (47)] cell line, which allows monitoring of the cell cycle; by this method, we verified a cell cycle–dependent expression of 64 proteins, including, for example, ANLN (Fig.”