Evidence map›Paper›PMID 33420492›Full record

ArticleNature cell biology2021

Loss of the fragile X syndrome protein FMRP results in misregulation of nonsense-mediated mRNA decay.

Tatsuaki Kurosaki, Naoto Imamachi, Christoph Pröschel, Shuhei Mitsutomi, Rina Nagao, Nobuyoshi Akimitsu, Lynne E Maquat

Open access · greenAbstract read
In one paragraph

Article in Nature cell biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
9.7field-weighted citation impact, top 1% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

  1. Variable expression ofProceedings of the National Academy of Sciences of the United States of America · 2024
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  18. Ribosomes in RNA Granules Are Stalled on mRNA Sequences That Are Consensus Sites for FMRP Association.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
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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

7 authors at 3 institutions in 2 countries.

Tatsuaki KurosakiDepartment of Biochemistry and Biophysics, School of Medicine and Dentistry, University of Rochester, Rochester, NY, USA.
Naoto ImamachiIsotope Science Center, The University of Tokyo, Tokyo, Japan.
Christoph PröschelDepartment of Biomedical Genetics, School of Medicine and Dentistry, University of Rochester, Rochester, NY, USA.
Shuhei MitsutomiDepartment of Biochemistry and Biophysics, School of Medicine and Dentistry, University of Rochester, Rochester, NY, USA.
Rina NagaoDepartment of Biochemistry and Biophysics, School of Medicine and Dentistry, University of Rochester, Rochester, NY, USA.
Nobuyoshi AkimitsuIsotope Science Center, The University of Tokyo, Tokyo, Japan.
Lynne E MaquatDepartment of Biochemistry and Biophysics, School of Medicine and Dentistry, University of Rochester, Rochester, NY, USA. lynne_maquat@urmc.rochester.edu.ORCID http://orcid.org/0000-0002-2789-2075
University of Rochester · USThe University of Tokyo · JPUniversity of Rochester Medical Center · US

Funding

REGULATION OF SELENOPROTEIN RNA METABOLISMR01GM059614 · NIGMS · UNIVERSITY OF ROCHESTER · PI MAQUAT, LYNNE E · 1999 to 2022
$9.1M
iPSC-derived astrocytes to model Vanishing White Matter DiseaseR21NS104878 · NINDS · UNIVERSITY OF ROCHESTER · PI PROSCHEL, CHRISTOPH · 2018 to 2019
$452k
NIGMS NIH HHS R01 GM059614NINDS NIH HHS R21 NS104878
6 · The paper itself

Abstract

Loss of the fragile X protein FMRP is a leading cause of intellectual disability and autism

Indexed as

Gene DeletionNonsense Mediated mRNA DecayTranscriptomeCase-Control StudiesCells, CulturedFibroblastsFragile X Messenger Ribonucleoprotein 1Fragile X SyndromeHumansInduced Pluripotent Stem CellsNeuroblastomaNeuronsRNA-SeqTrans-ActivatorsFMR1 protein, humanFragile X Messenger Ribonucleoprotein 1Trans-Activators

Identifiers

PMID33420492
PMCPMC8273690
OpenAlexW3119237440

What OpenQuestion holds

Textmetadata
LicenceTDM
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.