Evidence map›Paper›PMID 38812789›Full record

ArticleFrontiers in cellular neuroscience2024

Synaptic defects in a drosophila model of muscular dystrophy.

Jessica M Sidisky, Alex Winters, Russell Caratenuto, Daniel T Babcock

Abstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Jessica M SidiskyDepartment of Biological Sciences, Lehigh University, Bethlehem, PA, United States.
Alex Winters *Department of Biological Sciences, Lehigh University, Bethlehem, PA, United States.
Russell Caratenuto *Department of Biological Sciences, Lehigh University, Bethlehem, PA, United States.
Daniel T BabcockDepartment of Biological Sciences, Lehigh University, Bethlehem, PA, United States.

Funding

Regulation of Synaptic Dysfunction and Maintenance with age using DrosophilaR01NS110727 · NINDS · LEHIGH UNIVERSITY · PI BABCOCK, DANIEL T. · 2019 to 2023
$1.7M
NINDS NIH HHS R01 NS110727
6 · The paper itself

Abstract

Muscular dystrophies are a devastating class of diseases that result in a progressive loss of muscle integrity. Duchenne Muscular Dystrophy, the most prevalent form of Muscular Dystrophy, is due to the loss of functional Dystrophin. While much is known regarding destruction of muscle tissue in these diseases, much less is known regarding the synaptic defects that also occur in these diseases. Synaptic defects are also among the earliest hallmarks of neurodegenerative diseases, including the neuromuscular disease Amyotrophic Lateral Sclerosis (ALS). Our current study investigates synaptic defects within adult muscle tissues as well as presynaptic motor neurons in Drosophila

Indexed as

degenerationdystrophinflightneuromuscular junctionpostsynapticpresynaptic

Identifiers

PMID38812789
PMCPMC11133739

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.