ReviewMethods (San Diego, Calif.)2006
Imaging the division process in living tissue culture cells.
Review in Methods (San Diego, Calif.), 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
32 citing papers in PubMed.
- A Dispersive Image Scanning Microscope for Multi-color High-resolution Imaging.ACS photonics · 2026Article
- Three-dimensional label-free morphology of CD8 + T cells as a sepsis biomarker.Light, science & applications · 2023Article
- Near single-photon imaging in the shortwave infrared using homodyne detection.Proceedings of the National Academy of Sciences of the United States of America · 2023Article
- Quantitative understanding of HepaRG cells during drug-induced intrahepatic cholestasis through changes in bile canaliculi dynamics.Pharmacology research & perspectives · 2022Article
- Dose-Extreme Mechanics Letters · 2021Article
- Imaging mitotic processes in three dimensions with lattice light-sheet microscopy.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2021Review
- Long-term Brillouin imaging of live cells with reduced absorption-mediated damage at 660 nm wavelength.Biomedical optics express · 2019Article
- The Effect of Surface Charges on the Cellular Uptake of Liposomes Investigated by Live Cell Imaging.Pharmaceutical research · 2017Article
- Visualizing the Early Stages of Phagocytosis.Journal of visualized experiments : JoVE · 2017Article
- Automated microbeam observation environment for biological analysis-Custom portable environmental control applied to a vertical microbeam system.Sensors and actuators. B, Chemical · 2017Article
- Contractile dynamics change before morphological cues during fluorescence [corrected] illumination.Scientific reports · 2015Article
- Light-induced cell damage in live-cell super-resolution microscopy.Scientific reports · 2015Article
- Hybrid random walk-linear discriminant analysis method for unwrapping quantitative phase microscopy images of biological samples.Journal of biomedical optics · 2015Article
- Live-cell mass profiling: an emerging approach in quantitative biophysics.Nature methods · 2014Article
- Lattice light-sheet microscopy: imaging molecules to embryos at high spatiotemporal resolution.Science (New York, N.Y.) · 2014Article
- Noninvasive imaging beyond the diffraction limit of 3D dynamics in thickly fluorescent specimens.Cell · 2012Article
- Predictive-focus illumination for reducing photodamage in live-cell microscopy.Journal of microscopy · 2012Article
- Caspase activity is not required for the mitotic checkpoint or mitotic slippage in human cells.Molecular biology of the cell · 2011Article
- Rapid three-dimensional isotropic imaging of living cells using Bessel beam plane illumination.Nature methods · 2011Article
- P38 mitogen-activated protein kinase activity is required during mitosis for timely satisfaction of the mitotic checkpoint but not for the fidelity of chromosome segregation.Molecular biology of the cell · 2010Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
We detail some of the pitfalls encountered when following live cultured somatic cells by light microscopy during mitosis. Principle difficulties in this methodology arise from the necessity to compromise between maintaining the health of the cell while achieving the appropriate temporal and spatial resolutions required for the study. Although the quality of the data collected from fixed cells is restricted only by the quality of the imaging system and the optical properties of the specimen, the major limiting factor when viewing live cells is radiation damage induced during illumination. We discuss practical considerations for minimizing this damage, and for maintaining the general health of the cell, while it is being followed by multi-mode or multi-dimensional light microscopy.
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What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.