Evidence map›Paper›PMID 28194442›Full record

ArticleJCI insight2017

Redirecting

Dominic J Gessler, Danning Li, Hongxia Xu, Qin Su, Julio Sanmiguel, Serafettin Tuncer, Constance Moore, Jean King, Reuben Matalon, Guangping Gao

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
4.5field-weighted citation impact, top 5% of its field
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

54 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
  2. The Emerging Role of N-Acetylaspartate in Cancer.International journal of molecular sciences · 2026
    Review
  3. Article
  4. Article
  5. Stem cell and gene therapies for leukodystrophies.Molecular therapy. Methods & clinical development · 2025
    Review
  6. Current clinical applications of AAV-mediated gene therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Neurosurgical gene therapy for central nervous system diseases.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2024
    Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. AAV9-mediated SH3TC2 gene replacement therapy targeted to Schwann cells for the treatment of CMT4C.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 3 countries.

Dominic J GesslerDepartment of Microbiology and Physiological Systems.
Danning LiHorae Gene Therapy Center, University of Massachusetts, Worcester, Massachusetts, USA.
Hongxia XuHorae Gene Therapy Center, University of Massachusetts, Worcester, Massachusetts, USA.
Qin SuHorae Gene Therapy Center, University of Massachusetts, Worcester, Massachusetts, USA.
Julio SanmiguelHorae Gene Therapy Center, University of Massachusetts, Worcester, Massachusetts, USA.
Serafettin TuncerHeinrich Heine University, Medical School, Duesseldorf, Germany.
Constance MooreCenter for Comparative Neuroimaging, Department of Psychiatry, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Jean KingCenter for Comparative Neuroimaging, Department of Psychiatry, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Reuben MatalonUniversity of Texas Medical Branch, Galveston, USA.
Guangping GaoDepartment of Microbiology and Physiological Systems.
Heinrich Heine University Düsseldorf · DEState Key Laboratory of BiotherapyThe University of Texas Medical Branch at Galveston · USUniversity Hospital Heidelberg · DE

Funding

Viral escape from AAV expressed transgenesP01AI100263 · NIAID · SCRIPPS FLORIDA · PI FARZAN, MICHAEL R. · 2012 to 2016
$11.9M
Viral Vector CoreP01HL131471 · NHLBI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI FLOTTE, TERENCE R. · 2016 to 2020
$11.3M
Oligodendrocyte-focused rAAV gene therapy strategies for Canavan disease and LeukodystrophiesR01NS076991 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Guangping Gao · 2012 to 2026
$5.7M
NHLBI NIH HHS P01 HL131471NIAID NIH HHS P01 AI100263NINDS NIH HHS R01 NS076991
6 · The paper itself

Abstract

Canavan disease (CD) is a debilitating and lethal leukodystrophy caused by mutations in the aspartoacylase (

Indexed as

AmidohydrolasesAnimalsAspartic AcidBlood-Brain BarrierCanavan DiseaseCentral Nervous SystemDependovirusDisease Models, AnimalGenetic TherapyGenetic VectorsHumansMiceOligodendrogliaAmidohydrolasesAspartic AcidaspartoacylaseN-acetylaspartate

Identifiers

PMID28194442
PMCPMC5291725
OpenAlexW2587002666

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.