Evidence map›Paper›PMID 29491143›Full record

ArticleThe Journal of biological chemistry2018

Hairy and enhancer of split 1 (HES1) protects cells from endoplasmic reticulum stress-induced apoptosis through repression of

Ji Eun Lee, William Morrison, Julie Hollien

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

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  4. Epithelial Endoplasmic Reticulum Stress Enhances the Risk of Muc5b-associated Lung Fibrosis.American journal of respiratory cell and molecular biology · 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

3 authors at 1 institution in 1 country.

Ji Eun LeeFrom the Department of Biology and the Center for Cell and Genome Science, University of Utah, Salt Lake City, Utah 84112.
William MorrisonFrom the Department of Biology and the Center for Cell and Genome Science, University of Utah, Salt Lake City, Utah 84112.
Julie HollienFrom the Department of Biology and the Center for Cell and Genome Science, University of Utah, Salt Lake City, Utah 84112 hollien@biology.utah.edu.
University of Utah · US

Funding

Regulation of mRNA decay and metabolism during endoplasmic reticulum stressR35GM119540 · NIGMS · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI HOLLIEN, JULIE · 2016 to 2025
$3.1M
NIGMS NIH HHS R35 GM119540
6 · The paper itself

Abstract

Disruption in endoplasmic reticulum (ER) function, termed ER stress, occurs in many diseases, including neurodegenerative disorders, diabetes, and cancer. Cells respond to ER stress with the unfolded protein response (UPR), which triggers a broad transcriptional program to restore and enhance ER function. Here, we found that ER stress up-regulates the mRNA encoding the developmentally regulated transcriptional repressor hairy and enhancer of split 1 (

Indexed as

ApoptosisEndoplasmic Reticulum StressAnimalsCell LineDown-RegulationDrosophila melanogasterHEK293 CellsHumansMicePromoter Regions, GeneticProtein Phosphatase 1RNA, MessengerTranscription Factor HES-1Unfolded Protein ResponseUp-RegulationHES1 protein, humanHes1 protein, mousePPP1R15A protein, humanPpp1r15a protein, mouseProtein Phosphatase 1RNA, MessengerTranscription Factor HES-1apoptosisER quality controltranscription regulationtranscription repressorunfolded protein response (UPR)

Identifiers

PMID29491143
PMCPMC5912459
OpenAlexW2793728773

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.