Evidence map›Paper›PMID 24506781›Full record

ReviewNucleic acid therapeutics2014

Exon-skipping antisense oligonucleotides to correct missplicing in neurogenetic diseases.

Kavitha Siva, Giuseppina Covello, Michela A Denti

Abstract readReview
In one paragraph

Review in Nucleic acid therapeutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing 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

38 citing papers in PubMed.

  1. Review
  2. CRISPR-Based Gene Therapy for Brain Disease.Molecular neurobiology · 2026
    Review
  3. Splice Modulation Studies Using Reporter Mice.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Exon Skipping Through Chimeric AntisenseNucleic acid therapeutics · 2022
    Article
  12. Targeted exon skipping ofMolecular therapy. Nucleic acids · 2022
    Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. 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

3 authors.

Kavitha Siva1 Center for Integrative Biology (CIBIO), University of Trento , Trento, Italy .
Giuseppina Covello
Michela A Denti

Funding

Telethon GGP08244
6 · The paper itself

Abstract

Alternative splicing is an important regulator of the transcriptome. However, mutations may cause alteration of splicing patterns, which in turn leads to disease. During the past 10 years, exon skipping has been looked upon as a powerful tool for correction of missplicing in disease and progress has been made towards clinical trials. In this review, we discuss the use of antisense oligonucleotides to correct splicing defects through exon skipping, with a special focus on diseases affecting the nervous system, and the latest stage achieved in its progress.

Indexed as

AnimalsAtaxia TelangiectasiaBlood-Brain BarrierCongenital Disorders of GlycosylationCystsDrug Delivery SystemsExonsFrontotemporal DementiaGenetic Diseases, InbornHereditary Central Nervous System Demyelinating DiseasesHumansMuscular Dystrophy, DuchenneMutationNervous System DiseasesNeurofibromatosesNiemann-Pick Disease, Type COligonucleotides, AntisensePhosphotransferases (Phosphomutases)

Identifiers

PMID24506781
PMCPMC3922311

What OpenQuestion holds

Textmetadata
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.