ReviewJournal of microscopy2026
Review of expansion microscopy combined with advanced imaging modalities.
Review in Journal of microscopy, 2026. 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.
- Modern RNA Quantification Methods: From RT-qPCR to Advanced Microscopy.The journal of physical chemistry. B · 2026Review
- Visualising viral interactions and mechanisms at the nanoscale with expansion microscopy.Npj viruses · 2026Review
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
No grant is acknowledged in the PubMed record.
Abstract
Expansion microscopy (ExM) is a powerful high-resolution imaging technique that enhances the spatial resolution of conventional light microscopy by physically enlarging biological specimens by embedding and cross-linking them in a swellable polymer network. This review explores the combination of ExM with commonly used advanced fluorescence imaging modalities, including light sheet fluorescence microscopy (LSFM), stimulated emission depletion (STED), structured illumination microscopy (SIM), single-molecule localisation microscopy (SMLM), and computational super-resolution radial fluctuations (SRRF) to push the boundaries of achievable resolution in biological imaging. By integrating ExM with these optical and analytical approaches, researchers can visualise subcellular structures and molecular complexes with unprecedented clarity, enabling the study of intricate biological processes that are otherwise inaccessible with conventional light microscopy methods. The review covers the theoretical resolutions attainable with each combined technique, example biological questions they can address, and key considerations for optimising their use. Together, these advancements offer novel insights into nanoscale cellular and subcellular structures, opening new avenues for exploration in fields such as neuroscience, cancer research, and developmental biology.
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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.