Evidence map›Paper›PMID 32033983›Full record

ArticleeNeuro

Sex-Specific Differences in Motor-Unit Remodeling in a Mouse Model of ALS.

Éric Martineau, Adriana Di Polo, Christine Vande Velde, Richard Robitaille

Open access · goldAbstract read
In one paragraph

Article in eNeuro. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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  4. The Neuromuscular Junction: A Shared Vulnerability in Aging and Disease.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Review
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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 3 institutions in 1 country.

Éric MartineauDépartement de neurosciences, Université de Montréal, Montréal, Québec H3C 3J7, Canada eric.martineau.3@umontreal.ca.ORCID 0000-0002-5503-0798
Adriana Di PoloDépartement de neurosciences, Université de Montréal, Montréal, Québec H3C 3J7, Canada.ORCID 0000-0003-1430-0760
Christine Vande VeldeDépartement de neurosciences, Université de Montréal, Montréal, Québec H3C 3J7, Canada.ORCID 0000-0001-5926-1529
Richard RobitailleDépartement de neurosciences, Université de Montréal, Montréal, Québec H3C 3J7, Canada.
Centre Hospitalier de l’Université de Montréal · CACentre Hospitalier Universitaire Sainte-Justine · CAUniversité de Montréal · CA

Funding

CIHR MOP-111070CIHR PJT-376483
6 · The paper itself

Abstract

Progressive loss of neuromuscular junctions (NMJs) is an early event in amyotrophic lateral sclerosis (ALS), preceding the global degeneration of motor axons and being accompanied by new axonal sprouting within the same axonal arbor. Some aspects of ALS onset and progression seem to be affected by sex in animal models of the disease. However, whether there are sex-specific differences in the pattern or time course of NMJ loss and repair within single motor axons remains unknown. We performed further analysis of a previously published

Indexed as

Amyotrophic Lateral SclerosisAnimalsDisease Models, AnimalFemaleMaleMiceMice, TransgenicMotor NeuronsNeuromuscular JunctionSuperoxide DismutaseSuperoxide Dismutase-1Superoxide DismutaseSuperoxide Dismutase-1amyotrophic lateral sclerosismotor-unitneuromuscular junctionreinnervationsex-specific differencessuperoxide dismutase

Identifiers

PMID32033983
PMCPMC7044502
OpenAlexW3005421933

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.