Evidence map›Paper›PMID 35163535›Full record

ArticleInternational journal of molecular sciences2022

SARM1 Ablation Is Protective and Preserves Spatial Vision in an In Vivo Mouse Model of Retinal Ganglion Cell Degeneration.

Laura K Finnegan, Naomi Chadderton, Paul F Kenna, Arpad Palfi, Michael Carty, Andrew G Bowie, Sophia Millington-Ward, G Jane Farrar

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

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  14. From Bench to Bed: The Current Genome Editing Therapies for Glaucoma.Frontiers in cell and developmental biology · 2022
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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

8 authors at 1 institution in 1 country.

Laura K FinneganDepartment of Genetics, The School of Genetics and Microbiology, Trinity College Dublin, D02 VF25 Dublin, Ireland.ORCID 0000-0002-3395-1211
Naomi ChaddertonDepartment of Genetics, The School of Genetics and Microbiology, Trinity College Dublin, D02 VF25 Dublin, Ireland.ORCID 0000-0002-1684-1598
Paul F KennaDepartment of Genetics, The School of Genetics and Microbiology, Trinity College Dublin, D02 VF25 Dublin, Ireland.
Arpad PalfiDepartment of Genetics, The School of Genetics and Microbiology, Trinity College Dublin, D02 VF25 Dublin, Ireland.
Michael CartyTrinity Biomedical Sciences Institute, The School of Biochemistry and Immunology, Trinity College Dublin, D02 R590 Dublin, Ireland.
Andrew G BowieTrinity Biomedical Sciences Institute, The School of Biochemistry and Immunology, Trinity College Dublin, D02 R590 Dublin, Ireland.
Sophia Millington-WardDepartment of Genetics, The School of Genetics and Microbiology, Trinity College Dublin, D02 VF25 Dublin, Ireland.
G Jane FarrarDepartment of Genetics, The School of Genetics and Microbiology, Trinity College Dublin, D02 VF25 Dublin, Ireland.
Trinity College Dublin · IE

Funding

Fighting Blindness Ireland - Health Research Board of Ireland - Health Research Charities Ireland MRCG-2012-4Fighting Blindness Ireland - Health Research Board of Ireland - Health Research Charities Ireland MRCG-2016-14Health Research Board of Ireland HRAPOR-2015-1140Irish Research Council GOIPG/2017/1631Science Foundation Ireland 16/IA/4376Science Foundation Ireland 16/IA/4452
6 · The paper itself

Abstract

The challenge of developing gene therapies for genetic forms of blindness is heightened by the heterogeneity of these conditions. However, mechanistic commonalities indicate key pathways that may be targeted in a gene-independent approach. Mitochondrial dysfunction and axon degeneration are common features of many neurodegenerative conditions including retinal degenerations. Here we explore the neuroprotective effect afforded by the absence of sterile alpha and Toll/interleukin-1 receptor motif-containing 1 (SARM1), a prodegenerative NADase, in a rotenone-induced mouse model of retinal ganglion cell loss and visual dysfunction.

Indexed as

AnimalsArmadillo Domain ProteinsCells, CulturedCytoskeletal ProteinsDisease Models, AnimalEnergy MetabolismFemaleFibroblastsGene Knockout TechniquesMaleMiceMice, Inbred C57BLMitochondriaOxygen ConsumptionPrimary Cell CultureRetinal DegenerationArmadillo Domain ProteinsCytoskeletal ProteinsRotenoneSARM1 protein, mouseaxon degenerationNAD+NADaseretinal degenerationsterile alpha and Toll/interleukin-1 receptor motif-containing 1 (SARM1)

Identifiers

PMID35163535
PMCPMC8835928
OpenAlexW4210774799

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.