Evidence map›Paper›PMID 40201548›Full record

ArticleJournal of biomedical optics2025

LED-based multicolor extended resolution transmission fluorescence microscopy.

Huaiyuan Zhang, Yiting Hu, Xingwei Pu, Shizheng Zhang, Yi He, Kun Chen, Ziji Liu

Abstract read
In one paragraph

Article in Journal of biomedical optics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Huaiyuan ZhangUniversity of Electronic Science and Technology of China, School of Optoelectronic Science and Engineering, Chengdu, China.
Yiting HuUniversity of Electronic Science and Technology of China, School of Optoelectronic Science and Engineering, Chengdu, China.
Xingwei PuUniversity of Electronic Science and Technology of China, School of Optoelectronic Science and Engineering, Chengdu, China.
Shizheng ZhangUniversity of Electronic Science and Technology of China, School of Optoelectronic Science and Engineering, Chengdu, China.
Yi HeUniversity of Electronic Science and Technology of China, School of Optoelectronic Science and Engineering, Chengdu, China.
Kun ChenUniversity of Electronic Science and Technology of China, School of Optoelectronic Science and Engineering, Chengdu, China.
Ziji LiuUniversity of Electronic Science and Technology of China, School of Optoelectronic Science and Engineering, Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Significance: The multiplexing capabilities of fluorescence imaging are enhanced by its exceptional molecular specificity with diverse fluorescent probes, making it a powerful tool for studying complex biological structures, organization, and functions. Recent advances in super-resolution fluorescence microscopy have further revolutionized our ability to explore biology and related fields. However, current multicolor super-resolution fluorescence imaging systems often come with high costs and bulky designs. Aim: We present a multicolor extended resolution fluorescence imaging system that uses light-emitting diode to simplify the optical path, make the design more compact, and reduce system costs. Approach: This multicolor extended resolution fluorescence imaging system is based on structured illumination, utilizing a simple diffraction unit positioned between the light source and the sample in a wide-field microscope. Notably, this design could be easily integrated into standard widefield microscopes as a convenient add-on unit, enabling extended resolution imaging. Results: Our system demonstrates concurrent extended resolved imaging of three-color microsphere beads and successfully showcases multicolor extended resolution fluorescence imaging of biological tissue samples, revealing intricate structural details. Conclusions: This system provides a structurally simple, cost-effective alternative to traditional microscopes, offering flexible multicolor extended resolution fluorescence imaging and potential applications in multimodal imaging.

Indexed as

LightingAnimalsEquipment DesignHumansMicroscopy, FluorescenceMicrospheresfluorescence imaginglight-emitting diodestructured illumination microscopy

Identifiers

PMID40201548
PMCPMC11977515

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.