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Paper · 41998758

WFS1 gene delivery rescues visual function in a mouse model of Wolfram syndrome.

Jagodzinska J and 7 others. Acta Neuropathol Commun, 2026. Cited by 0 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. WFS1 gene delivery rescues visual function in a mouse model of Wolfram syndrome. Papers, record 41998758. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/41998758

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title
WFS1 gene delivery rescues visual function in a mouse model of Wolfram syndrome.
PubMed
Journal
Acta Neuropathol Commun
PubMed
Year
2026
PubMed
Publication types
Journal Article, Research Support, Non-U.S. Gov't
PubMed
Citations, by iCite
0
iCite
Revised in PubMed
2026-08-13
PubMed

Authors8

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

OrderAuthorForenameKindORCID iD
1Jagodzinska JJolanta
2Péquignot MMarie
3Sarzi EEmmanuelle
4Quiles MMélanie
5Cazevieille CChantal
6Müller AAgnès
7Koks SSulev
8Delettre CCécile

Source PubMed

Topics15

NLM's MeSH indexing of the paper, its major topics first.

MeSH termMajor
Wolfram SyndromeMajor topic
Membrane ProteinsMajor topic
Genetic TherapyMajor topic
Animals
Disease Models, Animal
Mice, Knockout
Humans
Retinal Ganglion Cells
Mice
Gene Therapy Agents
Mice, Inbred C57BL
Visual Acuity
Gene Transfer Techniques
Dependovirus
Male

Source PubMed

Grants2

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

Grant, as the record writes itAgencyCountryNIH projectStated by
R15075FFRPHRegion OccitaniePubMed
R17025FFAFM TelethonPubMed

Source PubMed

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References85

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

OrderPMIDTitleJournalYearIn PapersSource
127,395,765WFS1 in Optic Neuropathies: Mutation Findings in Nonsyndromic Optic Atrophy and Assessment of Clinical Severity.Ophthalmology2016https://conductscience.org/library/papers/27395765PubMed
215,557,474Rapid quantification of adult and developing mouse spatial vision using a virtual optomotor system.Invest Ophthalmol Vis Sci2004https://conductscience.org/library/papers/15557474PubMed
335,469,785WFS1-Associated Optic Neuropathy: Genotype-Phenotype Correlations and Disease Progression.Am J Ophthalmol2022https://conductscience.org/library/papers/35469785PubMed
421,051,915Simple and efficient: validation of a cotton wick electrode for animal electroretinography.Ophthalmic Res2011https://conductscience.org/library/papers/21051915PubMed
59,491,819Predisposition of Wolfram syndrome heterozygotes to psychiatric illness.Mol Psychiatry1998https://conductscience.org/library/papers/9491819PubMed
623,358,189A comprehensive review of retinal gene therapy.Mol Ther2013https://conductscience.org/library/papers/23358189PubMed
77,894,760Four cases of Wolfram syndrome: ophthalmologic findings and complications.Bull Soc Belge Ophtalmol1994https://conductscience.org/library/papers/7894760PubMed
82,721,980Incomplete Wolfram syndrome: clinical and electrophysiologic study of two familial cases.Graefes Arch Clin Exp Ophthalmol1989https://conductscience.org/library/papers/2721980PubMed
934,415,265Long-Term Follow-Up After Unilateral Intravitreal Gene Therapy for Leber Hereditary Optic Neuropathy: The RESTORE Study.J Neuroophthalmol2021https://conductscience.org/library/papers/34415265PubMed
1020,160,352Wolfram syndrome 1 gene negatively regulates ER stress signaling in rodent and human cells.J Clin Invest2010https://conductscience.org/library/papers/20160352PubMed

Cited by1

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 0 citations.

PMIDTitleJournalYearIn Papers
42,793,043Comorbid Auditory and Visual Dysfunction: From Pathogenic Genes to Gene Therapy.Genes (Basel)2026https://conductscience.org/library/papers/42793043

Source PubMed

Genes0

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

None in this release.

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed
2026-11-06
PubMed
iCite
2026-11-05
iCite
PMC's ID file
2026-11-05
PMC's ID file
NIH RePORTER's grant and paper links
2026-11-01
NIH RePORTER's grant and paper links
Trials
2026-11-12
Gene search
2026-11-11
Pipelines
2026-09-18

Sources 11

  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • HGNCCC0
  • iCiteCC BY 4.0
  • NCBI GenePublic domain (US government)
  • NIH RePORTER's grant and paper linksPublic domain
  • Open TargetsCC0 1.0
  • PMC's ID filePublic domain (US government)
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • HGNCCC0: https://www.genenames.org/about/license/
  • iCiteCC BY 4.0
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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