Evidence map›Paper›PMID 36672271›Full record

ArticleCells2023

Abnormal Cellular Phenotypes Induced by Three

Nathalie Vadrot, Flavie Ader, Maryline Moulin, Marie Merlant, Françoise Chapon, Estelle Gandjbakhch, Fabien Labombarda, Pascale Maragnes, Patricia Réant, Caroline Rooryck and 5 more

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
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

15 authors at 8 institutions in 1 country.

Nathalie VadrotBasic and Translational Myology Laboratory, Université Paris Cité, BFA, UMR 8251, CNRS, F-75013 Paris, France.
Flavie AderAPHP-Sorbonne Université, Unité Fonctionnelle de Cardiogénétique et Myogénétique Moléculaire, Service de Biochimie Métabolique, HU Pitié Salpêtrière-Charles Foix, F-75013 Paris, France.ORCID 0000-0001-7891-3385
Maryline MoulinBasic and Translational Myology Laboratory, Université Paris Cité, BFA, UMR 8251, CNRS, F-75013 Paris, France.ORCID 0000-0002-1851-8727
Marie MerlantBasic and Translational Myology Laboratory, Université Paris Cité, BFA, UMR 8251, CNRS, F-75013 Paris, France.
Françoise ChaponService d'anatomopathologie, CHU de Caen, F-14000 Caen, France.
Estelle GandjbakhchINSERM, UMR_S 1166, Sorbonne Université, F-75005 Paris, France.
Fabien LabombardaService de Cardiologie, CHU de Caen, Université de Caen Normandie, F-14000 Caen, France.
Pascale MaragnesCardiologie pédiatrique, Service de pédiatrie, CHU de Caen, F-14000 Caen, France.
Patricia RéantService de Cardiologie, Hôpital Haut Lévêque, CHU de Bordeaux, INSERM 1045, Université de Bordeaux, F-33000 Bordeaux, France.
Caroline RooryckService de Génétique Médicale, CHU Bordeaux, F-33000 Bordeaux, France.ORCID 0000-0002-9789-3591
Vincent ProbstCentre de référence des maladies rythmiques cardiaques, CHU de Nantes, F-44000 Nantes, France.ORCID 0000-0002-5492-8619
Erwan DonalCentre Cardio-Pneumologique, CHU de Rennes Hôpital de Pontchaillou, F-35000 Rennes, France.
Pascale RichardAPHP-Sorbonne Université, Unité Fonctionnelle de Cardiogénétique et Myogénétique Moléculaire, Service de Biochimie Métabolique, HU Pitié Salpêtrière-Charles Foix, F-75013 Paris, France.
Ana FerreiroBasic and Translational Myology Laboratory, Université Paris Cité, BFA, UMR 8251, CNRS, F-75013 Paris, France.ORCID 0000-0003-2806-5386
Brigitte BuendiaBasic and Translational Myology Laboratory, Université Paris Cité, BFA, UMR 8251, CNRS, F-75013 Paris, France.
Centre National de la Recherche Scientifique · FRCentre Hospitalier Universitaire de Caen Normandie · FRInserm · FRCentre Hospitalier Universitaire de Bordeaux · FRCentre Hospitalier Universitaire de Nantes · FRDélégation Paris 5 · FRHôpital Pontchaillou · FRUniversité de Bordeaux · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A single missense variant of the

Indexed as

CardiomyopathiesChromosomesAnimalsChromatinCyclic N-OxidesFemaleHumansMaleMicePhenotype3,3,5,5-tetramethyl-1-pyrroline N-oxideChromatinCyclic N-Oxidescardiomyopathychromatin-associated proteinsE2F1 regulationgenderLAP2 proteinsnuclear alterationsTMPO gene

Identifiers

PMID36672271
PMCPMC9857342
OpenAlexW4316663404

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.