Evidence map›Paper›PMID 36528626›Full record

ArticleNature communications2022

Translation factor eIF5a is essential for IFNγ production and cell cycle regulation in primary CD8

Thomas C J Tan, Van Kelly, Xiaoyan Zou, David Wright, Tony Ly, Rose Zamoyska

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 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

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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

6 authors at 3 institutions in 1 country.

Thomas C J TanInstitute of Immunology and Infection Research, University of Edinburgh, Ashworth Laboratories, Charlotte Auerbach Road, Edinburgh, EH9 3FL, UK.ORCID 0000-0001-9892-7098
Van KellyWellcome Trust Centre for Cell Biology, University of Edinburgh, Michael Swann Building, Max Born Crescent, Edinburgh, EH9 3BF, UK.ORCID 0000-0002-2663-7160
Xiaoyan ZouInstitute of Immunology and Infection Research, University of Edinburgh, Ashworth Laboratories, Charlotte Auerbach Road, Edinburgh, EH9 3FL, UK.
David WrightInstitute of Immunology and Infection Research, University of Edinburgh, Ashworth Laboratories, Charlotte Auerbach Road, Edinburgh, EH9 3FL, UK.ORCID 0000-0001-8666-4155
Tony LyWellcome Trust Centre for Cell Biology, University of Edinburgh, Michael Swann Building, Max Born Crescent, Edinburgh, EH9 3BF, UK.ORCID 0000-0002-8650-5215
Rose ZamoyskaInstitute of Immunology and Infection Research, University of Edinburgh, Ashworth Laboratories, Charlotte Auerbach Road, Edinburgh, EH9 3FL, UK. Rose.Zamoyska@ed.ac.uk.ORCID 0000-0001-9816-2638
University of Edinburgh · GBUniversity of Dundee · GBWellcome Centre for Cell Biology · GB

Funding

Wellcome Trust 205014/Z/16/ZWellcome Trust 20611/Z/17/ZWellcome Trust 206211/Z/17/ZWellcome Trust WT205014/Z/16/Z
6 · The paper itself

Abstract

Control of mRNA translation adjusts protein production rapidly and facilitates local cellular responses to environmental conditions. Traditionally initiation of translation is considered to be a major translational control point, however, control of peptide elongation is also important. Here we show that the function of the elongation factor, eIF5a, is regulated dynamically in naïve CD8

Indexed as

CD8-Positive T-LymphocytesPeptide Chain Elongation, TranslationalCell CyclePeptide Elongation FactorsPeptide Initiation FactorsPeptidesPeptide Elongation FactorsPeptide Initiation FactorsPeptides

Identifiers

PMID36528626
PMCPMC9759561
OpenAlexW4313324133

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.