Evidence map›Paper›PMID 38725905›Full record

ReviewRSC chemical biology2024

Pseudouridine and

Lyana L Y Ho, Gabriel H A Schiess, Pâmella Miranda, Gerald Weber, Kira Astakhova

Abstract readReview
In one paragraph

Review in RSC chemical biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Review
  3. RNA therapeutic targeting of recalcitrant and rare cancers.Exploration of targeted anti-tumor therapy · 2026
    Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Recent Advances and Prospects in RNA Drug Development.International journal of molecular sciences · 2024
    Review
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

5 authors.

Lyana L Y HoTechnical University of Denmark 2800 Kongens Lyngby Denmark kiraas@kemi.dtu.dk.
Gabriel H A SchiessDepartamento de Física, Universidade Federal de Minas Gerais Belo Horizonte MG Brazil.
Pâmella MirandaDepartamento de Física, Universidade Federal de Minas Gerais Belo Horizonte MG Brazil.
Gerald WeberDepartamento de Física, Universidade Federal de Minas Gerais Belo Horizonte MG Brazil.ORCID https://orcid.org/0000-0002-2935-1571
Kira AstakhovaTechnical University of Denmark 2800 Kongens Lyngby Denmark kiraas@kemi.dtu.dk.ORCID https://orcid.org/0000-0003-4878-0301

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Modified nucleosides are integral to modern drug development, serving as crucial building blocks for creating safer, more potent, and more precisely targeted therapeutic interventions. Nucleobase modifications often confer antiviral and anti-cancer activity as monomers. When incorporated into nucleic acid oligomers, they increase stability against degradation by enzymes, enhancing the drugs' lifespan within the body. Moreover, modification strategies can mitigate potential toxic effects and reduce immunogenicity, making drugs safer and better tolerated. Particularly,

Identifiers

PMID38725905
PMCPMC11078203

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.