Evidence map›Paper›PMID 34819667›Full record

ArticleNature2021

Aldehyde-driven transcriptional stress triggers an anorexic DNA damage response.

Lee Mulderrig, Juan I Garaycoechea, Zewen K Tuong, Christopher L Millington, Felix A Dingler, John R Ferdinand, Liam Gaul, John A Tadross, Mark J Arends, Stephen O'Rahilly and 3 more

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Nature, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
16.0field-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

75 citing papers in PubMed, 134 citations in OpenAlex.

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  19. A health-system-scale, episode-resolved multimodal atlas of cancer cachexia.medRxiv : the preprint server for health sciences · 2025
    Article
  20. Article

15 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 6 institutions in 2 countries.

Lee Mulderrig *MRC Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Oxford, UK.
Juan I Garaycoechea *Hubrecht Institute, Utrecht, The Netherlands.
Zewen K TuongMolecular Immunity Unit, Department of Medicine, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-6735-6808
Christopher L MillingtonMRC Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Oxford, UK.
Felix A DinglerMRC Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Oxford, UK.ORCID http://orcid.org/0000-0002-6297-2986
John R FerdinandMolecular Immunity Unit, Department of Medicine, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0003-0936-0128
Liam GaulThe Francis Crick Institute, London, UK.ORCID http://orcid.org/0000-0002-3159-8127
John A TadrossMRC Metabolic Diseases Unit, Wellcome Trust-Medical Research Council Institute of Metabolic Science, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-8424-1252
Mark J ArendsDivision of Pathology, University of Edinburgh, Cancer Research UK Edinburgh Centre, IGMM, Edinburgh, UK.ORCID http://orcid.org/0000-0002-6826-8770
Stephen O'RahillyMRC Metabolic Diseases Unit, Wellcome Trust-Medical Research Council Institute of Metabolic Science, University of Cambridge, Cambridge, UK.
Gerry P CrossanMRC Laboratory of Molecular Biology, Cambridge, UK.ORCID http://orcid.org/0000-0002-7974-009X
Menna R ClatworthyMolecular Immunity Unit, Department of Medicine, University of Cambridge, Cambridge, UK.
Ketan J PatelMRC Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Oxford, UK. ketan.patel@imm.ox.ac.uk.
University of Cambridge · GBMRC Laboratory of Molecular Biology · GBJohn Radcliffe Hospital · GBEdinburgh Cancer Research · GBHubrecht Institute for Developmental Biology and Stem Cell Research · NLThe Francis Crick Institute · GB

Funding

Medical Research Council MC_U105178811Medical Research Council MC_UP_1201/18Medical Research Council MC_UU_00016/17Medical Research Council MC_UU_12012/1Medical Research Council MR/N024907/1Medical Research Council MR/S035842/1MRF_ MRF-104-0006-S-MULDEWellcome Trust 106202/Z/14/ZWellcome Trust FC001166
6 · The paper itself

Abstract

Endogenous DNA damage can perturb transcription, triggering a multifaceted cellular response that repairs the damage, degrades RNA polymerase II and shuts down global transcription

Indexed as

Cockayne SyndromeDNA DamageAlcohol DehydrogenaseAnimalsBrainCachexiaDisease Models, AnimalDNA Repair EnzymesFemaleFormaldehydeGrowth Differentiation Factor 15Kidney Tubules, ProximalMaleMicePoly-ADP-Ribose Binding ProteinsRenal InsufficiencyAdh5 protein, mouseAlcohol DehydrogenaseDNA Repair EnzymesErcc6 protein, mouseFormaldehydeGdf15 protein, mouseGrowth Differentiation Factor 15Poly-ADP-Ribose Binding Proteins

Identifiers

PMID34819667
OpenAlexW3216063992

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.