Evidence map›Paper›PMID 35269468›Full record

ArticleCells2022

The Neurotoxicity of Vesicles Secreted by ALS Patient Myotubes Is Specific to Exosome-Like and Not Larger Subtypes.

Ekene Anakor, Vanessa Milla, Owen Connolly, Cecile Martinat, Pierre Francois Pradat, Julie Dumonceaux, William Duddy, Stephanie Duguez

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review of the Pathology of Muscle in Amyotrophic Lateral Sclerosis.International journal of molecular sciences · 2026
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Analysis of translatomic changes in theFrontiers in neurology · 2024
    Article
  13. Aberrant evoked calcium signaling and nAChR cluster morphology in aFrontiers in cell and developmental biology · 2024
    Article
  14. Review
  15. The Cellular and Molecular Signature of ALS in Muscle.Journal of personalized medicine · 2022
    Review
  16. Review
  17. Pathogenic Extracellular Vesicle (EV) Signaling in Amyotrophic Lateral Sclerosis (ALS).Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2022
    Review
  18. 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

8 authors at 3 institutions in 2 countries.

Ekene AnakorPersonalised Medicine Centre, Biomedical Sciences Research Institute, Ulster University, Derry-Londonderry BT47 6SB, UK.ORCID 0000-0003-1809-4933
Vanessa MillaPersonalised Medicine Centre, Biomedical Sciences Research Institute, Ulster University, Derry-Londonderry BT47 6SB, UK.
Owen ConnollyPersonalised Medicine Centre, Biomedical Sciences Research Institute, Ulster University, Derry-Londonderry BT47 6SB, UK.
Cecile MartinatI-STEM, INSERM/UEVE UMR 861, AFM, 91100 Corbeil-Essones, France.ORCID 0000-0002-5234-1064
Pierre Francois PradatPersonalised Medicine Centre, Biomedical Sciences Research Institute, Ulster University, Derry-Londonderry BT47 6SB, UK.
Julie DumonceauxPersonalised Medicine Centre, Biomedical Sciences Research Institute, Ulster University, Derry-Londonderry BT47 6SB, UK.ORCID 0000-0002-2052-9361
William DuddyPersonalised Medicine Centre, Biomedical Sciences Research Institute, Ulster University, Derry-Londonderry BT47 6SB, UK.ORCID 0000-0003-2239-9094
Stephanie DuguezPersonalised Medicine Centre, Biomedical Sciences Research Institute, Ulster University, Derry-Londonderry BT47 6SB, UK.ORCID 0000-0001-6510-5426
University of Ulster · GBCentre National de la Recherche Scientifique · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extracellular vesicles can mediate communication between tissues, affecting the physiological conditions of recipient cells. They are increasingly investigated in Amyotrophic Lateral Sclerosis, the most common form of Motor Neurone Disease, as transporters of misfolded proteins including SOD1, FUS, TDP43, or other neurotoxic elements, such as the dipeptide repeats resulting from

Indexed as

Amyotrophic Lateral SclerosisExosomesExtracellular VesiclesNeurotoxicity SyndromesHumansMotor NeuronsMuscle Fibers, Skeletalcell–cell communicationectosomesexosomesmotor neurone diseases

Identifiers

PMID35269468
PMCPMC8909615
OpenAlexW4214708490

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.