Evidence map›Paper›PMID 39264859›Full record

ArticleNucleic acid therapeutics2024

Antisense Oligonucleotide STK-002 Increases OPA1 in Retina and Improves Mitochondrial Function in Autosomal Dominant Optic Atrophy Cells.

Aditya Venkatesh, Taylor McKenty, Syed Ali, Donna Sonntag, Shobha Ravipaty, Yanyan Cui, Deirdre Slate, Qian Lin, Anne Christiansen, Sarah Jacobson and 11 more

Abstract read
In one paragraph

Article in Nucleic acid therapeutics, 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
–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

11 citing papers in PubMed.

  1. The Versatile Applications of Antisense Oligonucleotides in Modern Medicine.International journal of molecular sciences · 2026
    Review
  2. Rhesus macaques with anProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Therapies for Mitochondrial Disease: Past, Present, and Future.Journal of inherited metabolic disease · 2025
    Review
  10. Review
  11. 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

21 authors.

Aditya VenkateshStoke Therapeutics, Bedford, Massachusetts, USA.ORCID 0000-0002-9809-3414
Taylor McKentyStoke Therapeutics, Bedford, Massachusetts, USA.
Syed AliStoke Therapeutics, Bedford, Massachusetts, USA.
Donna SonntagStoke Therapeutics, Bedford, Massachusetts, USA.
Shobha RavipatyStoke Therapeutics, Bedford, Massachusetts, USA.
Yanyan CuiStoke Therapeutics, Bedford, Massachusetts, USA.
Deirdre SlateStoke Therapeutics, Bedford, Massachusetts, USA.
Qian LinStoke Therapeutics, Bedford, Massachusetts, USA.
Anne ChristiansenStoke Therapeutics, Bedford, Massachusetts, USA.
Sarah JacobsonStoke Therapeutics, Bedford, Massachusetts, USA.
Jacob KachStoke Therapeutics, Bedford, Massachusetts, USA.
Kian Huat LimStoke Therapeutics, Bedford, Massachusetts, USA.
Vaishnavi SrinivasanStoke Therapeutics, Bedford, Massachusetts, USA.
Boris ZinshteynStoke Therapeutics, Bedford, Massachusetts, USA.
Isabel AznarezStoke Therapeutics, Bedford, Massachusetts, USA.
Laryssa A HurynOphthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, USA.
Zhiyu LiOphthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, USA.
Robert B HufnagelOphthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, USA.
Gene LiauStoke Therapeutics, Bedford, Massachusetts, USA.
Karen AndersonStoke Therapeutics, Bedford, Massachusetts, USA.
Jeff HogerStoke Therapeutics, Bedford, Massachusetts, USA.

Funding

NEI NIH HHS
6 · The paper itself

Abstract

Autosomal dominant optic atrophy (ADOA) is an inherited optic neuropathy most frequently associated with

Indexed as

GTP PhosphohydrolasesMacaca fascicularisMitochondriaOligonucleotides, AntisenseOptic Atrophy, Autosomal DominantRetinaAnimalsExonsFibroblastsHumansMutationRabbitsGTP PhosphohydrolasesOligonucleotides, AntisenseOPA1 protein, humanADOAASOexon splicinghaploinsufficiencymRNAOPA1

Identifiers

PMID39264859
PMCPMC11564677

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.