Evidence map›Paper›PMID 24530702›Full record

ArticleJournal of neuroscience methods2014

Morphological analysis of neuromuscular junction development and degeneration in rodent lumbrical muscles.

James N Sleigh, Robert W Burgess, Thomas H Gillingwater, M Zameel Cader

Open access · greenAbstract read
In one paragraph

Article in Journal of neuroscience methods, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.1field-weighted citation impact, top 7% 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

49 citing papers in PubMed, 90 citations in OpenAlex.

  1. The neuropathy-causingbioRxiv : the preprint server for biology · 2026
    Article
  2. Junctions in Jeopardy: the neuromuscular junction is a selective pathological target in Charcot-Marie-Tooth disease.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Review
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  13. Neuronal signaling · 2023
    Article
  14. Article
  15. Article
  16. Axon Initial Segments Are Required for Efficient Motor Neuron Axon Regeneration and Functional Recovery of Synapses.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  17. Article
  18. Review
  19. Ankyrin-dependent NaCurrent biology : CB · 2021
    Article
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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

4 authors at 4 institutions in 2 countries.

James N SleighNuffield Department of Clinical Neurosciences, University of Oxford, John Radcliffe Hospital, Oxford OX3 9DU, UK; The Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Oxford OX3 9DS, UK.
Robert W BurgessThe Jackson Laboratory, Bar Harbor, ME 04609, USA.
Thomas H GillingwaterCentre for Integrative Physiology & Euan MacDonald Centre for Motor Neurone Disease Research, University of Edinburgh, Edinburgh EH8 9XD, UK.
M Zameel CaderNuffield Department of Clinical Neurosciences, University of Oxford, John Radcliffe Hospital, Oxford OX3 9DU, UK; The Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Oxford OX3 9DS, UK. Electronic address: zameel.cader@ndcn.ox.ac.uk.
Jackson Laboratory · USJohn Radcliffe Hospital · GBUniversity of Edinburgh · GBUniversity of Oxford · GB

Funding

Genetics of the Neuromuscular Junction: Mechanisms and Disease ModelsR01NS054154 · NINDS · JACKSON LABORATORY · PI BURGESS, ROBERT W. · 2006 to 2019
$6.0M
The Genetics of the Neuromuscular Junction: Mechanisms and Disease ModelsR37NS054154 · NINDS · JACKSON LABORATORY · PI Robert W. Burgess · 2020 to 2026
$5.9M
Genetics of the Neuromuscular Junction: Mechanisms and Disease ModelsR56NS054154 · NINDS · JACKSON LABORATORY · PI BURGESS, ROBERT W. · 2015 to 2015
$613k
An Animal Model of LRSAM1 Peripheral NeuropathyR03NS079677 · NINDS · JACKSON LABORATORY · PI BURGESS, ROBERT W. · 2012 to 2013
$177k
Medical Research Council G0601887NINDS NIH HHS NS054154NINDS NIH HHS NS079677NINDS NIH HHS R01 NS054154NINDS NIH HHS R03 NS079677NINDS NIH HHS R37 NS054154NINDS NIH HHS R56 NS054154
6 · The paper itself

Abstract

backgroundThe neuromuscular junction (NMJ) is a specialised synapse formed between a lower motor neuron and a skeletal muscle fibre, and is an early pathological target in numerous nervous system disorders, including amyotrophic lateral sclerosis (ALS), Charcot-Marie-Tooth disease (CMT), and spinal muscular atrophy (SMA). Being able to accurately visualise and quantitatively characterise the NMJ in rodent models of neurological conditions, particularly during the early stages of disease, is thus of clear importance. NEW

methodWe present a method for dissection of rodent deep lumbrical muscles located in the hind-paw, and describe how to perform immunofluorescent morphological analysis of their NMJs.

resultsThese techniques allow the temporal assessment of a number of developmental and pathological NMJ phenotypes in lumbrical muscles. COMPARISON WITH EXISTING

methodsSmall muscles, such as the distal hind-limb lumbrical muscles, possess a major advantage over larger muscles, such as gastrocnemius, in that they can be whole-mounted and the entire innervation pattern visualised. This reduces preparation time and ambiguity when evaluating important neuromuscular phenotypes.

conclusionsTogether, these methods will allow the reader to perform a detailed and accurate analysis of the neuromuscular system in rodent models of disease in order to identify pertinent features of neuropathology.

Indexed as

Age FactorsAnimalsAnimals, NewbornBungarotoxinsDisease Models, AnimalGlycine-tRNA LigaseIn Vitro TechniquesLumbosacral RegionMembrane GlycoproteinsMice, Inbred C57BLMice, TransgenicMuscle DenervationNerve Tissue ProteinsNeuromuscular JunctionNeuromuscular Junction DiseasesOptical ImagingBungarotoxinsGlycine-tRNA LigaseMembrane GlycoproteinsNerve Tissue ProteinsSv2a protein, mouseLower motor neuronLumbrical muscleNeurodegenerationNeurodevelopmentNeuromuscular diseaseNeuromuscular junction (NMJ)

Identifiers

PMID24530702
PMCPMC4120659
OpenAlexW1996331201

What OpenQuestion holds

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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.