ArticleBiosensors2025
Cell Observation and Analysis with a Three-Dimensional Optical Wave Field Microscope.
Article in Biosensors, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 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
2 citing papers in PubMed.
- Macrophage volume analysis and real-time monitoring by digital holography.Journal of biomedical optics · 2026Article
- Uptake mechanisms and functions of isolated mitochondria in mesenchymal stromal cells.Scientific reports · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
Abstract
Cell observation is crucial in life science research, and advancements in microscopy are essential for deciphering biological phenomena. These technological developments have significantly enhanced our understanding of cellular mechanisms and processes. Light, characterized by its wave-like properties, is fundamental to scientific observation. Recently, new technologies have been developed to detect changes in light wavelengths upon illumination, using them as signals for visualization. Three-dimensional optical wave field microscopy (3D-OWFM), a recent innovation in optimal imaging, leverages the wave properties of light to capture objects without labels, invasive procedures, or direct contact, thus facilitating non-invasive observation. In this study, we observed and analyzed mammalian cell structure and behaviors using 3D-OWFM. The 3D-OWFM revealed the intrinsic structure of the cells, including the cytoplasm and nucleus, with high clarity. The optical path difference (OPD) intensity effectively highlighted nuclear complexity. Furthermore, time-lapse imaging captured cell division process through variations in OPD signal intensity. These findings indicate that 3D-OWFM has significant potential for cell observation, offering insights not attainable with conventional microscopes.
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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.