Evidence map›Paper›PMID 40575297›Full record

ReviewJACS Au2025

Advancing Multicolor Super-Resolution Volume Imaging: Illuminating Complex Cellular Dynamics.

Navid Rabiee, Xun Lan

Abstract readReview
In one paragraph

Review in JACS Au, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Vimentin Intermediate Filaments: A Paradigm Shift From Static Structure to Dynamic Cytoplasmic Network.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
  2. Article
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

2 authors.

Navid RabieeDepartment of Basic Medical Science, School of Medicine, Tsinghua University, 100084 Beijing, China.ORCID https://orcid.org/0000-0002-6945-8541
Xun LanDepartment of Basic Medical Science, School of Medicine, Tsinghua University, 100084 Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The rapidly evolving field of live-cell super-resolution imaging has transformed our understanding of cellular structures and dynamic biological processes. This perspective delves into the importance and challenges of multicolor super-resolution volume imaging in the context of living cells, where the ability to visualize multiple molecular species simultaneously across three dimensions is critical for deciphering complex cellular functions. While recent innovations have made significant strides, challenges such as temporal and spatial resolution limits, photobleaching, and depth of field remain significant obstacles. This work explores emerging strategies aimed at overcoming these technical barriers, including the development of novel fluorophores, advanced computational techniques leveraging artificial intelligence, and hardware innovations in imaging systems. By addressing these challenges, the field is poised to move toward a future where high-precision, multicolor live-cell volume imaging becomes routine, enabling real-time visualization of intricate molecular interactions. The conclusion emphasizes that we are on the brink of a new frontier in cellular imaging, one that promises to revolutionize biological research and disease treatment by providing unprecedented access to the molecular mechanisms governing life at its most fundamental level.

Indexed as

cellular dynamicscomputational techniqueslive-cell imagingmulticolor fluorescencesuper-resolution imaging

Identifiers

PMID40575297
PMCPMC12188487

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.