Evidence map›Paper›PMID 36951542›Full record

ArticleeLife2023

UBQLN2 restrains the domesticated retrotransposon PEG10 to maintain neuronal health in ALS.

Holly H Black, Jessica L Hanson, Julia E Roberts, Shannon N Leslie, Will Campodonico, Christopher C Ebmeier, G Aaron Holling, Jian Wei Tay, Autumn M Matthews, Elizabeth Ung and 2 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

25 citing papers in PubMed, 33 citations in OpenAlex.

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  15. Viruses and neurodegeneration: a growing concern.Journal of translational medicine · 2025
    Review
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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

12 authors at 1 institution in 1 country.

Holly H Black *Department of Biochemistry, University of Colorado Boulder, Boulder, United States.ORCID 0000-0002-1383-136X
Jessica L Hanson *Institute for Behavioral Genetics, University of Colorado Boulder, Boulder, United States.ORCID 0000-0001-9165-930X
Julia E RobertsDepartment of Biochemistry, University of Colorado Boulder, Boulder, United States.
Shannon N LeslieDepartment of Biochemistry, University of Colorado Boulder, Boulder, United States.
Will CampodonicoDepartment of Biochemistry, University of Colorado Boulder, Boulder, United States.ORCID 0000-0002-9098-5266
Christopher C EbmeierDepartment of Biochemistry, University of Colorado Boulder, Boulder, United States.ORCID 0000-0001-7940-6190
G Aaron HollingDepartment of Biochemistry, University of Colorado Boulder, Boulder, United States.
Jian Wei TayBiofrontiers Institute, University of Colorado Boulder, Boulder, United States.ORCID 0000-0002-8634-5039
Autumn M MatthewsDepartment of Biochemistry, University of Colorado Boulder, Boulder, United States.
Elizabeth UngDepartment of Biochemistry, University of Colorado Boulder, Boulder, United States.
Cristina I LauDepartment of Biochemistry, University of Colorado Boulder, Boulder, United States.ORCID 0000-0003-0850-9963
Alexandra M WhiteleyDepartment of Biochemistry, University of Colorado Boulder, Boulder, United States.ORCID 0000-0002-4144-7605
University of Colorado Boulder · US

Funding

Research Training: Mental Health Behavior GeneticsT32MH016880 · NIMH · UNIVERSITY OF COLORADO AT BOULDER · PI Naomi P. Friedman, Matthew Charles Keller · 1985 to 2026
$5.3M
Training in Translational Research of Lung, Head and Neck CancerT32CA174648 · NCI · UNIVERSITY OF COLORADO DENVER · PI KARAM, SANA D · 2013 to 2022
$4.2M
Predoctoral Training Program in Signaling and Cellular Regulation INCLUDE Down Syndrome SupplementT32GM142607 · NIGMS · UNIVERSITY OF COLORADO · PI Sabrina Leigh Spencer, Tin Tin Su · 2021 to 2026
$3.6M
NCI NIH HHS T32 CA174648NCI NIH HHS T32CA174648NIGMS NIH HHS T32 GM142607NIGMS NIH HHS T32GM142607NIMH NIH HHS T32 MH016880
6 · The paper itself

Abstract

Amyotrophic Lateral Sclerosis (ALS) is a fatal neurodegenerative disease characterized by progressive motor neuron dysfunction and loss. A portion of ALS cases are caused by mutation of the proteasome shuttle factor

Indexed as

Amyotrophic Lateral SclerosisNeurodegenerative DiseasesAdaptor Proteins, Signal TransducingApoptosis Regulatory ProteinsAutophagy-Related ProteinsCell Cycle ProteinsDNA-Binding ProteinsHumansMotor NeuronsMutationRetroelementsRNA-Binding ProteinsUbiquitinsAdaptor Proteins, Signal TransducingApoptosis Regulatory ProteinsAutophagy-Related ProteinsCell Cycle ProteinsDNA-Binding ProteinsPEG10 protein, humanRetroelementsRNA-Binding ProteinsUbiquitinsUBQLN2 protein, humanALScell biologydomesticated retrotransposonhumanneurosciencePEG10proteomicsubiquilinUBQLN2

Identifiers

PMID36951542
PMCPMC10076021
OpenAlexW4360600527

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.