Evidence map›Paper›PMID 35688821›Full record

ArticleNature communications2022

Excess ribosomal protein production unbalances translation in a model of Fragile X Syndrome.

Sang S Seo, Susana R Louros, Natasha Anstey, Miguel A Gonzalez-Lozano, Callista B Harper, Nicholas C Verity, Owen Dando, Sophie R Thomson, Jennifer C Darnell, Peter C Kind and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
9.4field-weighted citation impact, top 2% 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

34 citing papers in PubMed, 52 citations in OpenAlex.

  1. Review
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  6. bioRxiv : the preprint server for biology · 2026
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  11. Review
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  14. Neuronal processes contain the essential components for the late steps of ribosome biogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  15. Article
  16. Ribogenesis shaping the brain.Nature cell biology · 2025
    Article
  17. Article
  18. Article
  19. Article
  20. eNeuro · 2025
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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 2 institutions in 2 countries.

Sang S Seo *Centre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, UK.
Susana R Louros *Centre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, UK.
Natasha AnsteyCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, UK.
Miguel A Gonzalez-LozanoDepartment of Molecular and Cellular Neurobiology, Center for Neurogenomics and Cognitive Research, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.ORCID 0000-0002-7837-151X
Callista B HarperCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, UK.
Nicholas C VerityCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, UK.
Owen DandoCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, UK.ORCID 0000-0002-6269-6408
Sophie R ThomsonCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, UK.
Jennifer C DarnellCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, UK.
Peter C KindCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, UK.
Ka Wan LiDepartment of Molecular and Cellular Neurobiology, Center for Neurogenomics and Cognitive Research, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.ORCID 0000-0001-6983-5055
Emily K OsterweilCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, UK. Emily.osterweil@ed.ac.uk.ORCID 0000-0003-0582-2284
University of Edinburgh · GBVrije Universiteit Amsterdam · NL

Funding

Medical Research Council MR/M006336/1Medical Research Council MR/S026312/1Wellcome TrustWellcome Trust 104116/Z/14/ZWellcome Trust 219556/Z/19/Z
6 · The paper itself

Abstract

Dysregulated protein synthesis is a core pathogenic mechanism in Fragile X Syndrome (FX). The mGluR Theory of FX predicts that pathological synaptic changes arise from the excessive translation of mRNAs downstream of mGlu

Indexed as

Fragile X SyndromeReceptors, Metabotropic GlutamateAnimalsDisease Models, AnimalFragile X Messenger Ribonucleoprotein 1HippocampusMiceMice, Inbred C57BLMice, KnockoutRibosomal ProteinsFmr1 protein, mouseFragile X Messenger Ribonucleoprotein 1Receptors, Metabotropic GlutamateRibosomal Proteins

Identifiers

PMID35688821
PMCPMC9187743
OpenAlexW4281725500

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.