Evidence map›Paper›PMID 36170200›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Prevention of ribosome collision-induced neuromuscular degeneration by SARS CoV-2-encoded Nsp1.

Xingjun Wang, Suman Rimal, Ishaq Tantray, Ji Geng, Sunil Bhurtel, Tejinder Pal Khaket, Wen Li, Zhe Han, Bingwei Lu

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. The peptidoglycan ofScience translational medicine · 2025
    Article
  4. Review
  5. Ribosome stalling duringPNAS nexus · 2024
    Article
  6. Article
  7. Article
  8. 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

9 authors at 2 institutions in 1 country.

Xingjun WangDepartment of Pathology, Stanford University School of Medicine, Stanford, CA 94350.ORCID 0000-0002-8862-3864
Suman RimalDepartment of Pathology, Stanford University School of Medicine, Stanford, CA 94350.
Ishaq TantrayDepartment of Pathology, Stanford University School of Medicine, Stanford, CA 94350.
Ji GengDepartment of Pathology, Stanford University School of Medicine, Stanford, CA 94350.
Sunil BhurtelDepartment of Pathology, Stanford University School of Medicine, Stanford, CA 94350.
Tejinder Pal KhaketDepartment of Pathology, Stanford University School of Medicine, Stanford, CA 94350.ORCID 0000-0001-5605-1307
Wen LiDepartment of Pathology, Stanford University School of Medicine, Stanford, CA 94350.ORCID 0000-0002-6458-1364
Zhe HanCenter for Precision Disease Modeling, Department of Medicine, University of Maryland School of Medicine, Baltimore, MD 21201.
Bingwei LuDepartment of Pathology, Stanford University School of Medicine, Stanford, CA 94350.ORCID 0000-0002-5807-7014
Stanford University · USUniversity of Maryland, Baltimore · US

Funding

Molecular Genetic Analysis of TORC1 and TORC2 Signaling in Neuronal MaintenanceR01NS084412 · NINDS · STANFORD UNIVERSITY · PI Bingwei Lu · 2014 to 2026
$4.9M
Genetic Control of Neural Stem Cell HomeostasisR01NS083417 · NINDS · STANFORD UNIVERSITY · PI LU, BINGWEI · 2013 to 2022
$3.5M
Modeling Nephrotic Syndrome in Drosophila NephrocytesR01DK098410 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI HAN, ZHE · 2014 to 2022
$3.3M
INCLUDE19-Ancestral roles of histone-modifying genes in heart development and diseaseR01HL134940 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI HAN, ZHE · 2017 to 2020
$2.4M
Mitochondrial inner membrane architecture in skeletal muscle pathophysiologyR01AR074875 · NIAMS · STANFORD UNIVERSITY · PI LU, BINGWEI · 2019 to 2023
$2.0M
NHLBI NIH HHS R01 HL134940NIAMS NIH HHS R01 AR074875NIDDK NIH HHS R01 DK098410NINDS NIH HHS R01 NS083417NINDS NIH HHS R01 NS084412
6 · The paper itself

Abstract

An overarching goal of aging and age-related neurodegenerative disease research is to discover effective therapeutic strategies applicable to a broad spectrum of neurodegenerative diseases. Little is known about the extent to which targetable pathogenic mechanisms are shared among these seemingly diverse diseases. Translational control is critical for maintaining proteostasis during aging. Gaining control of the translation machinery is also crucial in the battle between viruses and their hosts. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the causative agent of the ongoing COVID-19 pandemic. Here, we show that overexpression of SARS-CoV-2-encoded nonstructural protein 1 (Nsp1) robustly rescued neuromuscular degeneration and behavioral phenotypes in

Indexed as

COVID-19Neurodegenerative DiseasesRibosomesRNA-Dependent RNA PolymeraseViral Nonstructural ProteinsAlzheimer DiseaseAmyotrophic Lateral SclerosisAnimalsDrosophilaHumansPandemicsParkinson DiseaseProto-Oncogene Proteins c-aktRNA, MessengerSARS-CoV-2Nsp1 protein, SARS coronavirusProto-Oncogene Proteins c-aktRNA-Dependent RNA PolymeraseRNA, MessengerViral Nonstructural ProteinsAlzheimer’s diseaseNsp1ribosome-associated quality controlribosome collisionSARS-CoV-2

Identifiers

PMID36170200
PMCPMC9586304
OpenAlexW4297457570

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.