Evidence map›Paper›PMID 38321198›Full record

ArticleGene therapy2024

Gene therapy corrects the neurological deficits of mice with sialidosis.

Wuh-Liang Hwu, Karine Chang, Yu-Han Liu, Hao-Chun Wang, Ni-Chung Lee, Yin-Hsiu Chien

Abstract read
PubMed Publisher
In one paragraph

Article in Gene therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. AAV-mediated gene therapy for sialidosis.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    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

6 authors.

Wuh-Liang HwuDepartment of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan, ROC. hwuwlntu@ntu.edu.tw.ORCID 0000-0001-6690-4879
Karine ChangDepartment of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan, ROC.
Yu-Han LiuDepartment of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan, ROC.ORCID 0000-0001-6091-5550
Hao-Chun WangDepartment of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan, ROC.
Ni-Chung LeeDepartment of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan, ROC.
Yin-Hsiu ChienDepartment of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan, ROC.ORCID 0000-0001-8802-5728

Funding

National Taiwan University Hospital (NTUH) MS501
6 · The paper itself

Abstract

Patients with sialidosis (mucolipidosis type I) type I typically present with myoclonus, seizures, ataxia, cherry-red spots, and blindness because of mutations in the neuraminidase 1 (NEU1) gene. Currently, there is no treatment for sialidosis. In this study, we developed an adeno-associated virus (AAV)-mediated gene therapy for a Neu1 knockout (Neu1

Indexed as

DependovirusDisease Models, AnimalGenetic TherapyGenetic VectorsMice, KnockoutMucolipidosesNeuraminidaseAnimalsBrainCathepsin AHumansMiceCathepsin ANeu1 protein, mouseNeuraminidase

Identifiers

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.