Evidence map›Paper›PMID 31737985›Full record

ArticleAging cell2020

Deficiency in the DNA repair protein ERCC1 triggers a link between senescence and apoptosis in human fibroblasts and mouse skin.

Dong Eun Kim, Martijn E T Dollé, Wilbert P Vermeij, Akos Gyenis, Katharina Vogel, Jan H J Hoeijmakers, Christopher D Wiley, Albert R Davalos, Paul Hasty, Pierre-Yves Desprez and 1 more

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

43 citing papers in PubMed, 64 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

11 authors at 5 institutions in 3 countries.

Dong Eun KimBuck Institute for Research on Aging, Novato, CA, USA.ORCID 0000-0002-2681-3320
Martijn E T DolléCentre for Health Protection Research, National Institute of Public Health and the Environment (RIVM), Bilthoven, The Netherlands.
Wilbert P VermeijDepartment of Molecular Genetics, Erasmus University Medical Center, Rotterdam, The Netherlands.
Akos GyenisCECAD Forschungszentrum, Köln, Germany.
Katharina VogelCECAD Forschungszentrum, Köln, Germany.
Jan H J HoeijmakersDepartment of Molecular Genetics, Erasmus University Medical Center, Rotterdam, The Netherlands.
Christopher D WileyBuck Institute for Research on Aging, Novato, CA, USA.
Albert R DavalosBuck Institute for Research on Aging, Novato, CA, USA.
Paul HastyDepartment of Molecular Medicine, Sam and Ann Barshop Institute for Longevity and Aging Studies, University of Texas Health Science Center, San Antonio, TX, USA.ORCID 0000-0003-3046-0131
Pierre-Yves DesprezBuck Institute for Research on Aging, Novato, CA, USA.
Judith CampisiBuck Institute for Research on Aging, Novato, CA, USA.
Buck Institute for Research on Aging · USCologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases · DEErasmus MC · NLNational Institute for Public Health and the Environment · NLThe University of Texas Health Science Center at San Antonio · US

Funding

THE IMPACT OF CELLULAR DEFENSE ON THE ROLE OF Ku80 IN GENOME MAINTENANCE AND LONGP01AG017242 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI VIJG, JAN · 1999 to 2023
$46.1M
San Antonio OAIC - Research Education Component (REC)P30AG044271 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Adam Salmon, Elena Volpi · 2015 to 2026
$14.1M
CELLULAR SENESCENCE AND CONTROL OF GENE EXPRESSIONR37AG009909 · NIA · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI CAMPISI, JUDITH · 1995 to 2015
$7.6M
Cellular senescence and control of gene expressionR56AG009909 · NIA · BUCK INSTITUTE FOR RESEARCH ON AGING · PI CAMPISI, JUDITH · 2017 to 2017
$592k
NIA NIH HHS P01 AG017242NIA NIH HHS P30 AG044271NIA NIH HHS R37 AG009909NIA NIH HHS R56 AG009909
6 · The paper itself

Abstract

ERCC1 (excision repair cross complementing-group 1) is a mammalian endonuclease that incises the damaged strand of DNA during nucleotide excision repair and interstrand cross-link repair. Ercc1

Indexed as

AnimalsApoptosisCells, CulturedCellular SenescenceDNA-Binding ProteinsEndonucleasesFibroblastsGene Knockdown TechniquesHumansMiceMice, Inbred C57BLMice, TransgenicPhenotypeSignal TransductionSkinStem CellsDNA-Binding ProteinsEndonucleasesERCC1 protein, humanErcc1 protein, mouseTNF protein, humanTnf protein, mouseTumor Necrosis Factor-alphaTumor Suppressor Protein p53agingcell deathDNA damage repairsenescence-associated secretory phenotypetumor necrosis factor α

Identifiers

PMID31737985
PMCPMC7059167
OpenAlexW2984736033

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.