Evidence map›Paper›PMID 42509725›Full record

ArticleBiomolecules2026

Mouse Model of Fast-Channel Genetic Myasthenic Syndrome Carrying

Richard G Webster, Susan Maxwell, Yin Y Dong

Abstract read
In one paragraph

Article in Biomolecules, 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

3 authors.

Richard G WebsterNuffield Department of Clinical Neurosciences, University of Oxford, Oxford OX3 9DS, UK.ORCID 0000-0001-7893-1348
Susan MaxwellNuffield Department of Clinical Neurosciences, University of Oxford, Oxford OX3 9DS, UK.ORCID 0009-0009-6514-149X
Yin Y DongNuffield Department of Clinical Neurosciences, University of Oxford, Oxford OX3 9DS, UK.ORCID 0000-0001-8600-6988

Funding

UK Research and Innovation MR/S007180/1UK Research and Innovation MR/Z504099/1
6 · The paper itself

Abstract

Fast-channel genetic myasthenic syndromes (FCGMSs) are caused by genetic variants in muscle nicotinic acetylcholine receptor (AChR) subunits that reduce channel open times and impair neuromuscular transmission. Among these, the

Indexed as

MutationMyasthenic Syndromes, CongenitalReceptors, NicotinicAnimalsDisease Models, AnimalFemaleGene Knock-In TechniquesMaleMiceMice, Inbred C57BLNeuromuscular JunctionSynaptic TransmissionReceptors, Nicotinicacetylcholine receptorfast channel genetic myasthenic syndromemouse model

Identifiers

PMID42509725
PMCPMC13406490

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.