Evidence map›Paper›PMID 38151240›Full record

ArticleJournal of the American Chemical Society2024

Cellular Visualization of G-Quadruplex RNA via Fluorescence- Lifetime Imaging Microscopy.

Jenna Robinson, Stine G Stenspil, Karolina Maleckaite, Molly Bartlett, Marco Di Antonio, Ramon Vilar, Marina K Kuimova

Open access · hybridAbstract read
In one paragraph

Article in Journal of the American Chemical Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
6.3field-weighted citation impact, top 3% of its field
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

11 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Light-Activated Molecules Targeting G-Quadruplex Nucleic Acids.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025
    Review
  8. Review
  9. Review
  10. Article
  11. 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

7 authors at 3 institutions in 1 country.

Jenna RobinsonDepartment of Chemistry, Molecular Science Research Hub, Imperial College London, 82 Wood Lane, London W12 0BZ, U.K.
Stine G StenspilDepartment of Chemistry, Molecular Science Research Hub, Imperial College London, 82 Wood Lane, London W12 0BZ, U.K.ORCID 0000-0002-0252-6829
Karolina MaleckaiteDepartment of Chemistry, Molecular Science Research Hub, Imperial College London, 82 Wood Lane, London W12 0BZ, U.K.ORCID 0000-0002-4992-9158
Molly BartlettDepartment of Chemistry, Molecular Science Research Hub, Imperial College London, 82 Wood Lane, London W12 0BZ, U.K.
Marco Di AntonioDepartment of Chemistry, Molecular Science Research Hub, Imperial College London, 82 Wood Lane, London W12 0BZ, U.K.ORCID 0000-0002-7321-1867
Ramon VilarDepartment of Chemistry, Molecular Science Research Hub, Imperial College London, 82 Wood Lane, London W12 0BZ, U.K.ORCID 0000-0003-2992-199X
Marina K KuimovaDepartment of Chemistry, Molecular Science Research Hub, Imperial College London, 82 Wood Lane, London W12 0BZ, U.K.ORCID 0000-0003-2383-6014
Imperial College London · GBInstitute of Structural and Molecular Biology · GBThe Francis Crick Institute · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Over the past decade, appreciation of the roles of G-quadruplex (G4) structures in cellular regulation and maintenance has rapidly grown, making the establishment of robust methods to visualize G4s increasingly important. Fluorescent probes are commonly used for G4 detection in vitro; however, achieving sufficient selectivity to detect G4s in a dense and structurally diverse cellular environment is challenging. The use of fluorescent probes for G4 detection is further complicated by variations of probe uptake into cells, which may affect fluorescence intensity independently of G4 abundance. In this work, we report an alternative small-molecule approach to visualize G4s that does not rely on fluorescence intensity switch-on and, thus, does not require the use of molecules with exclusive G4 binding selectivity. Specifically, we have developed a novel thiazole orange derivative,

Indexed as

Fluorescent DyesG-QuadruplexesCytoplasmMicroscopy, FluorescenceRNAFluorescent DyesRNA

Identifiers

PMID38151240
PMCPMC10786036
OpenAlexW4390274152

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.