Evidence map›Paper›PMID 41300342›Full record

ArticleBiology2025

Characterising PMP22-Proximal Partners in a Schwann Cell Model of Charcot-Marie-Tooth Disease Type1A.

Ian Holt, Nicholas Emery, Monte A Gates, Sharon J Brown, Sally L Shirran, Heidi R Fuller

Abstract read
In one paragraph

Article in Biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Ian HoltWolfson Centre for Inherited Neuromuscular Disease, TORCH Centre, RJAH Orthopaedic Hospital, Oswestry SY10 7AG, UK.
Nicholas EmeryWolfson Centre for Inherited Neuromuscular Disease, TORCH Centre, RJAH Orthopaedic Hospital, Oswestry SY10 7AG, UK.
Monte A GatesSchool of Medicine, Keele University, Keele ST5 5BG, UK.
Sharon J BrownWolfson Centre for Inherited Neuromuscular Disease, TORCH Centre, RJAH Orthopaedic Hospital, Oswestry SY10 7AG, UK.ORCID 0000-0001-9671-7054
Sally L ShirranBSRC Mass Spectrometry and Proteomics Facility, University of St Andrews, St Andrews KY16 9ST, UK.ORCID 0000-0003-3516-3507
Heidi R FullerWolfson Centre for Inherited Neuromuscular Disease, TORCH Centre, RJAH Orthopaedic Hospital, Oswestry SY10 7AG, UK.ORCID 0000-0002-2858-869X

Funding

Orthopaedic Institute, UK RPG193
6 · The paper itself

Abstract

Charcot-Marie-Tooth disease type 1A (CMT1A) is a hereditary condition caused by the duplication of the

Indexed as

BioID2Charcot-Marie-Tooth disease 1AITGA2ITGA7PMP22proteomicsSchwann cells

Identifiers

PMID41300342
PMCPMC12650596

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.