Evidence map›Paper›PMID 39137772›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2024

Full-length dystrophin gene therapy for Duchenne muscular dystrophy.

Dongsheng Duan

Abstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

1 author.

Dongsheng DuanDepartment of Molecular Microbiology and Immunology and Department of Neurology, School of Medicine, Department of Biomedical Sciences, College of Veterinary Medicine; Department of Chemical and Biomedical Engineering, College of Engineering, University of Missouri, Columbia, MO 65212, USA. Electronic address: duand@missouri.edu.

Funding

Mechanism of immune response to muscle-directed AAV gene transferR01AI177600 · NIAID · INDIANA UNIVERSITY INDIANAPOLIS · PI Dongsheng Duan, Roland W. Herzog · 2023 to 2026
$3.1M
CRISPR editing therapy for Duchenne muscular dystrophyR01NS131416 · NINDS · UNIVERSITY OF MISSOURI-COLUMBIA · PI Dongsheng Duan · 2023 to 2026
$2.2M
Development of optimized AAVrh74 vectors for gene therapy of muscular dystrophiesR21AR081018 · NIAMS · UNIVERSITY OF FLORIDA · PI DUAN, DONGSHENG, SRIVASTAVA, ARUN · 2023 to 2024
$377k
NIAID NIH HHS R01 AI177600NIAMS NIH HHS R21 AR081018NINDS NIH HHS R01 NS131416
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

DystrophinGenetic TherapyGenetic VectorsMuscular Dystrophy, DuchenneAnimalsDisease Models, AnimalHumansDystrophin

Identifiers

PMID39137772
PMCPMC11403215

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.