ArticleNanophotonics (Berlin, Germany)2019
Fluorescence imaging with tailored light.
Article in Nanophotonics (Berlin, Germany), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 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
12 citing papers in PubMed.
- Multiplane 2.5D microscopy for high-throughput high-resolution tissue imaging.Journal of biomedical optics · 2025Article
- High-Fidelity Computational Microscopy via Feature-Domain Phase Retrieval.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025Article
- Out-of-focus signal rejection forBiomedical optics express · 2025Article
- Highly sensitive volumetric single-molecule imaging.Nanophotonics (Berlin, Germany) · 2024Article
- AIEgens-Doped Photonic Crystals for High Sensitivity Fluorescence Detection of Tumor Markers.Biosensors · 2023Article
- Fluorescein-derived carbon dots with chitin-targeting for ultrafast and superstable fluorescent imaging of fungi.Nanophotonics (Berlin, Germany) · 2022Article
- Incoherent superposition of polychromatic light enables single-shot nondiffracting light-sheet microscopy.Optics express · 2021Article
- 2.5D microscopy with polarization independent SLM for enhanced detection efficiency and aberration correction.Optics express · 2021Article
- 2.5D microscopy: Fast, high-throughput imaging via volumetric projection for quantitative subcellular analysis.ACS photonics · 2021Article
- Single-shot, shadowless total internal reflection fluorescence microscopy via annular fiber bundle.Optics letters · 2020Article
- Instantaneous non-diffracting light-sheet generation by controlling spatial coherence.Optics communications · 2020Article
- Optimizing the performance of multiline-scanning confocal microscopy.Journal of physics D: Applied physics · 2020Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
Abstract
Fluorescence microscopy has long been a valuable tool for biological and medical imaging. Control of optical parameters such as the amplitude, phase, polarization and propagation angle of light gives fluorescence imaging great capabilities ranging from super-resolution imaging to long-term real-time observation of living organisms. In this review, we discuss current fluorescence imaging techniques in terms of the use of tailored or structured light for the sample illumination and fluorescence detection, providing a clear overview of their working principles and capabilities.
Identifiers
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.