Evidence map›Paper›PMID 31685979›Full record

ArticleCell death and differentiation2020

Impaired cellular bioenergetics caused by GBA1 depletion sensitizes neurons to calcium overload.

Nicoletta Plotegher, Dany Perocheau, Ruggero Ferrazza, Giulia Massaro, Gauri Bhosale, Federico Zambon, Ahad A Rahim, Graziano Guella, Simon N Waddington, Gyorgy Szabadkai and 1 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Cell death and differentiation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Mitochondrial CaBiomolecules · 2026
    Review
  4. Review
  5. Article
  6. Review
  7. Unifying biology of neurodegeneration in lysosomal storage diseases.Journal of inherited metabolic disease · 2025
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Gaucher disease - more than just a rare lipid storage disease.Journal of molecular medicine (Berlin, Germany) · 2022
    Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Mitochondrial bioenergetics and neurodegeneration: aNeural regeneration research · 2021
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 3 countries.

Nicoletta PlotegherCell and Developmental Biology Department, University College London, London, WC1E6XA, UK.
Dany PerocheauInstitute for Women's Health, University College London, London, WC1E6HU, UK.
Ruggero FerrazzaDepartment of Physics, University of Trento, 38123, Povo (TN), Italy.
Giulia MassaroSchool of Pharmacy, University College London, London, WC1N1AX, UK.ORCID http://orcid.org/0000-0002-5986-6082
Gauri BhosaleCell and Developmental Biology Department, University College London, London, WC1E6XA, UK.
Federico ZambonCell and Developmental Biology Department, University College London, London, WC1E6XA, UK.
Ahad A RahimSchool of Pharmacy, University College London, London, WC1N1AX, UK.
Graziano GuellaDepartment of Physics, University of Trento, 38123, Povo (TN), Italy.
Simon N WaddingtonInstitute for Women's Health, University College London, London, WC1E6HU, UK.ORCID http://orcid.org/0000-0003-4970-4730
Gyorgy SzabadkaiCell and Developmental Biology Department, University College London, London, WC1E6XA, UK.ORCID http://orcid.org/0000-0002-3006-3577
Michael R DuchenCell and Developmental Biology Department, University College London, London, WC1E6XA, UK. m.duchen@ucl.ac.uk.ORCID http://orcid.org/0000-0003-2548-4294
University College London · GBUniversity of Padua · ITUniversity of Trento · ITMRC Laboratory for Molecular Cell Biology · GBUniversity of the Witwatersrand · ZA

Funding

Biotechnology and Biological Sciences Research Council BB/L502145/1Medical Research Council G1000709Medical Research Council MR/N019075/1Medical Research Council MR/N026101/1Medical Research Council MR/P026494/1Medical Research Council MR/R015325/1Medical Research Council MR/R025134/1Medical Research Council MR/S009434/1Medical Research Council MR/S036784/1Wellcome Trust
6 · The paper itself

Abstract

Heterozygous mutations of the lysosomal enzyme glucocerebrosidase (GBA1) represent the major genetic risk for Parkinson's disease (PD), while homozygous GBA1 mutations cause Gaucher disease, a lysosomal storage disorder, which may involve severe neurodegeneration. We have previously demonstrated impaired autophagy and proteasomal degradation pathways and mitochondrial dysfunction in neurons from GBA1 knockout (gba1

Indexed as

Energy MetabolismAdenosine DiphosphateAdenosine TriphosphateAnimalsBrainCalciumFree RadicalsGlucosylceramidaseGlutamic AcidHomeostasisLipid MetabolismMembrane Potential, MitochondrialMice, KnockoutMitochondriaNeuronsReceptors, GlutamateAdenosine DiphosphateAdenosine TriphosphateCalciumFree RadicalsGlucosylceramidaseGlutamic AcidReceptors, Glutamate

Identifiers

PMID31685979
PMCPMC7206133
OpenAlexW2984768884

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.