Evidence map›Paper›PMID 39625536›Full record

ArticleCellular and molecular life sciences : CMLS2024

Potential compensatory mechanisms preserving cardiac function in myotubular myopathy.

Alix Simon, Nadège Diedhiou, David Reiss, Marie Goret, Erwan Grandgirard, Jocelyn Laporte

Abstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. OXPHOS complex deficiency in congenital myopathy: A systematic review.European journal of clinical investigation · 2025
    Pooled it
  2. Article
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

6 authors.

Alix SimonInstitute of Genetics and Molecular and Cellular Biology (IGBMC), INSERM U1258, CNRS UMR7104, University of Strasbourg, 1 rue Laurent Fries, Illkirch, 67404, France.
Nadège DiedhiouInstitute of Genetics and Molecular and Cellular Biology (IGBMC), INSERM U1258, CNRS UMR7104, University of Strasbourg, 1 rue Laurent Fries, Illkirch, 67404, France.
David ReissInstitute of Genetics and Molecular and Cellular Biology (IGBMC), INSERM U1258, CNRS UMR7104, University of Strasbourg, 1 rue Laurent Fries, Illkirch, 67404, France.
Marie GoretInstitute of Genetics and Molecular and Cellular Biology (IGBMC), INSERM U1258, CNRS UMR7104, University of Strasbourg, 1 rue Laurent Fries, Illkirch, 67404, France.
Erwan GrandgirardInstitute of Genetics and Molecular and Cellular Biology (IGBMC), INSERM U1258, CNRS UMR7104, University of Strasbourg, 1 rue Laurent Fries, Illkirch, 67404, France.
Jocelyn LaporteInstitute of Genetics and Molecular and Cellular Biology (IGBMC), INSERM U1258, CNRS UMR7104, University of Strasbourg, 1 rue Laurent Fries, Illkirch, 67404, France. jocelyn@igbmc.fr.ORCID http://orcid.org/0000-0001-8256-5862

Funding

AFM-Téléthon 22734AFM-Téléthon 23933Agence Nationale de la Recherche ANR-10-IDEX-0002Agence Nationale de la Recherche ANR-17-EURE-0023Agence Nationale de la Recherche ANR-20-SFRI-0012Fondation pour la Recherche Médicale EQU201903007992Muscular Dystrophy Association 576154
6 · The paper itself

Abstract

X-Linked myotubular myopathy (XLMTM) is characterized by severe skeletal muscle weakness and reduced life expectancy. The pathomechanism and the impact of non-muscular defects affecting survival, such as liver dysfunction, are poorly understood. Here, we investigated organ-specific effects of XLMTM using the Mtm1

Indexed as

Muscle, SkeletalMyocardiumMyopathies, Structural, CongenitalProtein Tyrosine Phosphatases, Non-ReceptorAnimalsCell AdhesionDisease Models, AnimalDynamin IILiverMaleMiceMice, Inbred C57BLDNM2 protein, mouseDynamin IImyotubularinProtein Tyrosine Phosphatases, Non-ReceptorCentronuclear myopathyDynaminIntegrinMyotubularinOmicsPhosphoinositides

Identifiers

PMID39625536
PMCPMC11615164

What Socratic 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 Socratic graph.