Evidence map›Paper›PMID 30429220›Full record

ArticleThe Journal of biological chemistry2019

MAPK- and glycogen synthase kinase 3-mediated phosphorylation regulates the DEAD-box protein modulator Gle1 for control of stress granule dynamics.

Aditi, Aaron C Mason, Manisha Sharma, T Renee Dawson, Susan R Wente

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

19 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. SARS-CoV-2 nsp14 induces the mCommunications biology · 2025
    Article
  3. Advances in the understanding of nuclear pore complexes in human diseases.Journal of cancer research and clinical oncology · 2024
    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

5 authors at 1 institution in 1 country.

AditiFrom the Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, Tennessee 37240-7935.
Aaron C MasonFrom the Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, Tennessee 37240-7935.
Manisha SharmaFrom the Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, Tennessee 37240-7935.
T Renee DawsonFrom the Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, Tennessee 37240-7935.
Susan R WenteFrom the Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, Tennessee 37240-7935 susan.wente@vanderbilt.edu.
Vanderbilt University · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI STACIE B DUSETZINA · 1995 to 2026
$172.8M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ALVIN C POWERS · 2012 to 2026
$29.3M
Shop Module CoreP30EY008126 · NEI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI David J. Calkins · 1989 to 2026
$19.6M
Vanderbilt Mouse Metabolic Physiology CenterU24DK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2001 to 2015
$14.9M
Vanderbilt Mouse Metabolic Phenotyping CenterU2CDK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2016 to 2021
$6.3M
Molecular Analysis of Nuclear Pore Complex FunctionR37GM051219 · NIGMS · VANDERBILT UNIVERSITY · PI WENTE, SUSAN R. · 2010 to 2019
$5.6M
LTQ Orbitrap XL ETD Hybrid FT High Resolution Mass SpectrometerS10RR027714 · NCRR · VANDERBILT UNIVERSITY · PI HACHEY, DAVID L · 2010 to 2010
$479k
NCI NIH HHS P30 CA068485NCRR NIH HHS S10 RR027714NEI NIH HHS P30 EY008126NIDDK NIH HHS P30 DK020593NIDDK NIH HHS P30 DK058404NIDDK NIH HHS U24 DK059637NIDDK NIH HHS U2C DK059637NIGMS NIH HHS R37 GM051219
6 · The paper itself

Abstract

Rapid expression of critical stress response factors is a key survival strategy for diseased or stressed cells. During cell stress, translation is inhibited, and a pre-existing pool of cytoplasmic mRNA-protein complexes reversibly assembles into cytoplasmic stress granules (SGs). Gle1 is a conserved modulator of RNA-dependent DEAD-box proteins required for mRNA export, translation, and stress responses. Proper Gle1 function is critical as reflected by some human diseases such as developmental and neurodegenerative disorders and some cancers linked to

Indexed as

Adenosine TriphosphatasesCytoplasmic GranulesDEAD-box RNA HelicasesGlycogen Synthase Kinase 3HeLa CellsHumansMitogen-Activated Protein KinasesNucleocytoplasmic Transport ProteinsPhosphorylationRNA, MessengerAdenosine TriphosphatasesDDX3X protein, humanDEAD-box RNA HelicasesGle1 protein, humanGlycogen Synthase Kinase 3Mitogen-Activated Protein KinasesNucleocytoplasmic Transport ProteinsRNA, MessengerDDX3DEAD-box proteinsGle1glycogen synthase kinase 3 (GSK-3)mitogen-activated protein kinase (MAPK)neurodegenerationphosphorylationpost-translational modification (PTM)stress granulestress responsetranslation regulation

Identifiers

PMID30429220
PMCPMC6333882
OpenAlexW2900605974

What OpenQuestion holds

Textmetadata
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.