Evidence map›Paper›PMID 36192156›Full record

ArticleeNeuro

Axonal Domain Structure as a Putative Identifier of Neuron-Specific Vulnerability to Oxidative Stress in Cultured Neurons.

Samuel Burke, Louis-Eric Trudeau

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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 30% 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. Article
  3. Review
  4. Article
  5. Review
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

2 authors at 1 institution in 1 country.

Samuel BurkeDepartment of Pharmacology and Physiology, Faculty of Medicine, Université de Montréal, Montreal, Quebec, H3T 1J4, Canada.ORCID https://orcid.org/0000-0002-7363-5133
Louis-Eric TrudeauDepartment of Pharmacology and Physiology, Faculty of Medicine, Université de Montréal, Montreal, Quebec, H3T 1J4, Canada louis-eric.trudeau@umontreal.ca.ORCID https://orcid.org/0000-0003-4684-1377
SNC-Lavalin (Canada) · CA

Funding

CIHR
6 · The paper itself

Abstract

Several populations of neurons are purported to degenerate in Parkinson's disease (PD). One current hypothesis suggests that vulnerable neurons in PD share common characteristics including projecting to voluminous territories and having extremely long and branched axonal domains with large numbers of neurotransmitter release sites. In this study, we used a mouse

Indexed as

Parkinson DiseaseSynaptotagmin IAnimalsCholinergic AgentsDopamineDopaminergic NeuronsHydrogen PeroxideMiceNeurotransmitter AgentsOxidative StressSerotoninCholinergic AgentsDopamineHydrogen PeroxideNeurotransmitter AgentsSerotoninSynaptotagmin Iaxon branchingaxon terminalsdopamineParkinson’svulnerability

Identifiers

PMID36192156
PMCPMC9595591
OpenAlexW4300819254

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.