Evidence map›Paper›PMID 32151030›Full record

ArticleInternational journal of molecular sciences2020

Combined Dendritic and Axonal Deterioration Are Responsible for Motoneuronopathy in Patient-Derived Neuronal Cell Models of Chorea-Acanthocytosis.

Hannes Glaß, Patrick Neumann, Arun Pal, Peter Reinhardt, Alexander Storch, Jared Sterneckert, Andreas Hermann

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-weighted citation impact, top 29% 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

14 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. The Diverse Neuromuscular Spectrum of VPS13A Disease.Annals of clinical and translational neurology · 2026
    Article
  3. Article
  4. A chorea-acanthocytosis patient with novel mutations in the VPS13A gene without acanthocyte.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Yeast as a Model to Find New Drugs and Drug Targets forInternational journal of molecular sciences · 2022
    Review
  11. Article
  12. Unraveling the Spatiotemporal Distribution of VPS13A in the Mouse Brain.International journal of molecular sciences · 2021
    Article
  13. Article
  14. 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

7 authors at 5 institutions in 1 country.

Hannes GlaßSection for Translational Neurodegeneration "Albrecht Kossel", Department of Neurology, Universitätsmedizin Rostock, 18057 Rostock, Germany.
Patrick NeumannDivision of Neurodegenerative Diseases, Department of Neurology, Technische Universität Dresden, 01307 Dresden, Germany.
Arun PalDivision of Neurodegenerative Diseases, Department of Neurology, Technische Universität Dresden, 01307 Dresden, Germany.
Peter ReinhardtCenter for Regenerative Therapies Dresden (CRTD), Technische Universität Dresden, 01307 Dresden, Germany.
Alexander StorchDepartment of Neurology, University of Rostock, 18147 Rostock, Germany.
Jared SterneckertDepartment of Neurology, Städtisches Klinikum Dresden, 01129 Dresden, Germany.
Andreas HermannSection for Translational Neurodegeneration "Albrecht Kossel", Department of Neurology, Universitätsmedizin Rostock, 18057 Rostock, Germany.
German Center for Neurodegenerative Diseases · DEStädtisches Klinikum Dresden · DEAbbVie (Germany) · DETechnische Universität Dresden · DEUniversitätsmedizin Rostock · DE

Funding

Advocacy for Neuroacanthocytosis Patients -Bundesministerium für Bildung und Forschung FKZ:01GM1303Deutsche Forschungsgemeinschaft DFG EXC 168Deutsche Forschungsgemeinschaft DFG FZT 111Hermann and Lilly Schilling-Stiftung für medizinische Forschung im Stifterverband -
6 · The paper itself

Abstract

Chorea acanthocytosis (ChAc), an ultra-rare devastating neurodegenerative disease, is caused by mutations in the

Indexed as

MutationAdultAxonsCells, CulturedDendritesFemaleHumansInduced Pluripotent Stem CellsLysosomesMiddle AgedMitochondriaModels, BiologicalMotor Neuron DiseaseNeuroacanthocytosisNeuronsVesicular Transport ProteinsVesicular Transport ProteinsVPS13A protein, humanChorea Acanthocytosis (ChAc)human induced pluripotent stem cells (iPSC)lysosomesmicrofluidic chambers (MFCs)mitochondriamotoneurons (MN)organelle trafficking

Identifiers

PMID32151030
PMCPMC7084777
OpenAlexW3010113402

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.