Evidence map›Paper›PMID 37014866›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2023

Heterozygosity for cervid S138N polymorphism results in subclinical CWD in gene-targeted mice and progressive inhibition of prion conversion.

Maria I Arifin, Lech Kaczmarczyk, Doris Zeng, Samia Hannaoui, Chi Lee, Sheng Chun Chang, Gordon Mitchell, Debbie McKenzie, Michael Beekes, Walker Jackson and 1 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

17 citing papers in PubMed, 32 citations in OpenAlex.

  1. A Neuronal Cell Line Model for Studying Camel Prions.Pathogens (Basel, Switzerland) · 2026
    Article
  2. Article
  3. Prion shedding is reduced by chronic wasting disease vaccination.bioRxiv : the preprint server for biology · 2025
    Article
  4. Review
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  15. Article
  16. Propagation of PrPCommunications biology · 2023
    Article
  17. 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

11 authors at 5 institutions in 3 countries.

Maria I ArifinFaculty of Veterinary Medicine and Hotchkiss Brain Institute, University of Calgary, Alberta T2N 4Z6, Canada.ORCID 0000-0003-2042-3492
Lech KaczmarczykDepartment of Clinical and Experimental Medicine, Wallenberg Center for Molecular Medicine, Linköping University, Linköping 581 83, Sweden.ORCID 0000-0003-2747-3134
Doris ZengFaculty of Veterinary Medicine and Hotchkiss Brain Institute, University of Calgary, Alberta T2N 4Z6, Canada.ORCID 0009-0002-2512-6227
Samia HannaouiFaculty of Veterinary Medicine and Hotchkiss Brain Institute, University of Calgary, Alberta T2N 4Z6, Canada.
Chi LeeFaculty of Veterinary Medicine and Hotchkiss Brain Institute, University of Calgary, Alberta T2N 4Z6, Canada.
Sheng Chun ChangFaculty of Veterinary Medicine and Hotchkiss Brain Institute, University of Calgary, Alberta T2N 4Z6, Canada.
Gordon MitchellNational and World Organisation for Animal Health Reference Laboratory for Scrapie and Chronic Wasting Disease, Canadian Food Inspection Agency, Ontario K1A 0Y9, Canada.ORCID 0009-0002-6257-7617
Debbie McKenzieDepartment of Biological Sciences and Centre for Prions and Protein Folding Diseases, University of Alberta, Alberta T6G 2M8, Canada.ORCID 0000-0002-9291-6977
Michael BeekesPrion and Prionoid Research Unit, Centre for Biological Threats and Special Pathogens, Robert Koch Institute, Berlin 13353, Germany.ORCID 0000-0002-6454-6657
Walker JacksonDepartment of Clinical and Experimental Medicine, Wallenberg Center for Molecular Medicine, Linköping University, Linköping 581 83, Sweden.
Sabine GilchFaculty of Veterinary Medicine and Hotchkiss Brain Institute, University of Calgary, Alberta T2N 4Z6, Canada.ORCID 0000-0001-5923-3464
University of Calgary · CALinköping University · SECanadian Food Inspection Agency · CARobert Koch Institute · DEUniversity of Alberta · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prions are proteinaceous infectious particles that replicate by structural conversion of the host-encoded cellular prion protein (PrP

Indexed as

DeerPrion DiseasesPrionsReindeerWasting Disease, ChronicAnimalsMiceMice, TransgenicPrion ProteinsPrion ProteinsPrionschronic wasting diseasegene-targeted mouse modelpmcaprionprion protein polymorphism

Identifiers

PMID37014866
PMCPMC10104538
OpenAlexW4362522171

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.