Evidence map›Paper›PMID 42201138›Full record

ReviewMuscles (Basel, Switzerland)2026

Beyond Membrane Remodeling: Organelle Crosstalk and Convergent Pathology in Centronuclear Myopathy.

Bana Abolibdeh, Charles H Williams

Abstract readReview
In one paragraph

Review in Muscles (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Bana AbolibdehDepartment of Medicine, Michigan State University College of Human Medicine, East Lansing, MI 48824, USA.ORCID 0000-0002-2265-9207
Charles H WilliamsDepartment of Medicine, Michigan State University College of Human Medicine, East Lansing, MI 48824, USA.ORCID 0000-0002-0331-5652

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Centronuclear myopathy (CNM) is a genetically heterogenous congenital myopathy traditionally classified as a membrane remodeling disorder. Emerging evidence reveals that centronuclear myopathy mutations converge upon common cellular dysfunction extending beyond membrane trafficking. This review proposes a unified model positioning CNM as a disorder of impaired organelle communication and structural crosstalk. We focus on how mutations in Myotubularin1 (

Indexed as

centronuclear myopathy (CNM)cytoskeletal instabilityDynamin 2 (DNM2)mitochondriaMyotubularin 1 (MTM1)reactive oxygen species (ROS)t-tubule/triadX-linked myotubular myopathy (XLMTM)

Identifiers

PMID42201138
PMCPMC13214784

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.