Evidence map›Paper›PMID 30105628›Full record

ArticleJournal of molecular neuroscience : MN2018

Neuromuscular Junction Morphology and Gene Dysregulation in the Wobbler Model of Spinal Neurodegeneration.

Whitney A Ratliff, Jessica N Saykally, Michael J Kane, Bruce A Citron

Open access · greenAbstract read
In one paragraph

Article in Journal of molecular neuroscience : MN, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Cyanobacteria, Cyanotoxins, and Neurodegenerative Diseases:International journal of molecular sciences · 2021
    Review
  5. Article
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 1 institution in 1 country.

Whitney A RatliffLaboratory of Molecular Biology, Research and Development, Bay Pines VA Healthcare System, 151, Bldg. 22, Rm. 123, 10000 Bay Pines Blvd., Bay Pines, FL, 33744, USA.
Jessica N SaykallyLaboratory of Molecular Biology, Research and Development, Bay Pines VA Healthcare System, 151, Bldg. 22, Rm. 123, 10000 Bay Pines Blvd., Bay Pines, FL, 33744, USA.
Michael J KaneLaboratory of Molecular Biology, Research and Development, Bay Pines VA Healthcare System, 151, Bldg. 22, Rm. 123, 10000 Bay Pines Blvd., Bay Pines, FL, 33744, USA.
Bruce A CitronLaboratory of Molecular Biology, Research and Development, Bay Pines VA Healthcare System, 151, Bldg. 22, Rm. 123, 10000 Bay Pines Blvd., Bay Pines, FL, 33744, USA. bruce.citron@va.gov.ORCID http://orcid.org/0000-0002-4384-9755
University of South Florida · US

Funding

Department of Defense W81XWH-16-1-0626Department of Veterans Affairs I01RX001520Florida Department of Health 4KB14RRD VA I01 RX001520
6 · The paper itself

Abstract

Amyotrophic lateral sclerosis (ALS) is the most common adult-onset neuromuscular disease for which there is currently no effective treatment. The progression of ALS includes loss of motor neurons controlling the voluntary muscles, with much of this loss occurring at the neuromuscular junction. In an effort to better understand changes at the neuromuscular junction, we utilized the wobbler mouse model of motor neuron loss. We examined biceps and end plate morphologies and monitored selected factors involved in end plate function. Structural volumes were determined from 3D reconstructions that were generated for the end plates. Wobbler mice exhibited size reductions of both the muscle fibers and the end plates within the biceps, and we found that the end plate volumes were the most sensitive indicator of the degeneration. Concurrently, we found increases in calcitonin gene-related peptide (CGRP) and its receptor in wobbler biceps and spinal cord. We also found increases in gene expression of two acetylcholine receptors within the wobbler biceps, which may be a result of altered CGRP/CALCRL (calcitonin receptor-like receptor) expression.

Indexed as

AnimalsCalcitonin Gene-Related PeptideMiceMotor EndplateMotor NeuronsNeurodegenerative DiseasesReceptors, CholinergicVesicular Transport ProteinsCalcitonin Gene-Related PeptideReceptors, CholinergicVesicular Transport ProteinsVps54 protein, mouseCalcitonin gene-related peptide (CGRP)End plateMotor neuron diseaseNeuromuscular junctionWobbler mice

Identifiers

PMID30105628
PMCPMC6684170
OpenAlexW2885505788

What OpenQuestion holds

Textmetadata
LicenceTDM
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.