Evidence map›Paper›PMID 32561641›Full record

ArticleThe Journal of biological chemistry2020

An astrocyte cell line that differentially propagates murine prions.

Waqas Tahir, Basant Abdulrahman, Dalia H Abdelaziz, Simrika Thapa, Rupali Walia, Hermann M Schätzl

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Astrocyte in prion disease: a double-edged sword.Neural regeneration research · 2022
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Neuroinflammation in Prion Disease.International journal of molecular sciences · 2021
    Review
  14. Article
  15. Review
  16. Microglia in Prion Diseases: Angels or Demons?International journal of molecular sciences · 2020
    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

6 authors at 1 institution in 2 countries.

Waqas TahirDepartment of Comparative Biology & Experimental Medicine, Faculty of Veterinary Medicine, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0003-3030-5625
Basant AbdulrahmanDepartment of Comparative Biology & Experimental Medicine, Faculty of Veterinary Medicine, University of Calgary, Calgary, Alberta, Canada.
Dalia H AbdelazizDepartment of Comparative Biology & Experimental Medicine, Faculty of Veterinary Medicine, University of Calgary, Calgary, Alberta, Canada.
Simrika ThapaDepartment of Comparative Biology & Experimental Medicine, Faculty of Veterinary Medicine, University of Calgary, Calgary, Alberta, Canada.
Rupali WaliaDepartment of Comparative Biology & Experimental Medicine, Faculty of Veterinary Medicine, University of Calgary, Calgary, Alberta, Canada.
Hermann M SchätzlDepartment of Comparative Biology & Experimental Medicine, Faculty of Veterinary Medicine, University of Calgary, Calgary, Alberta, Canada hschaetz@ucalgary.ca.ORCID 0000-0003-4972-8740
University of Calgary · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prion diseases are fatal infectious neurodegenerative disorders in human and animals caused by misfolding of the cellular prion protein (PrP

Indexed as

AnimalsAstrocytesCell LineGene ExpressionHumansMicePrion DiseasesProtein Aggregation, PathologicalPrPC ProteinsPrPSc ProteinsPrPC ProteinsPrPSc Proteinsastrocyteastrocytesbovine spongiform encephalopathyC8D1ACreutzfeldt–Jakob diseaseneurodegenerationneurodegenerative diseaseprionprion diseaseprion infectionprion strainprotein misfoldingscrapie

Identifiers

PMID32561641
PMCPMC7450132
OpenAlexW3036186700

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.