Codon 219 polymorphism of PRNP in healthy Caucasians and Creutzfeldt-Jakob disease patients.

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.

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.

Who cites it

15 citing papers in PubMed.

1. Yeast Prions: Discovery, Nature, Cellular Manipulation and Implication.Journal of microbiology and biotechnology · 2025
   Review
2. First Report of Polymorphisms and Genetic Characteristics ofAnimals : an open access journal from MDPI · 2024
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3. Prion protein E219K polymorphism: from the discovery of the KANNO blood group to interventions for human prion disease.Frontiers in neurology · 2024
   Review
4. The first report of polymorphisms of the prion protein gene (Frontiers in veterinary science · 2023
   Article
5. Structural basis for the complete resistance of the human prion protein mutant G127V to prion disease.Scientific reports · 2018
   Article
6. Prion-like protein gene (PRND) polymorphisms associated with scrapie susceptibility in Korean native black goats.PloS one · 2018
   Article
7. Epidemiological characteristics of human prion diseases.Infectious diseases of poverty · 2016
   Review
8. Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene.BMJ open · 2014
   Article
9. Genetic studies in human prion diseases.Journal of Korean medical science · 2014
   Review
10. Multiple substitutions of methionine 129 in human prion protein reveal its importance in the amyloid fibrillation pathway.The Journal of biological chemistry · 2012
    Article
11. Lack of association between PRNP 1368 polymorphism and Alzheimer's disease or vascular dementia.BMC medical genetics · 2009
    Article
12. Association of sporadic Creutzfeldt-Jakob disease with homozygous genotypes at PRNP codons 129 and 219 in the Korean population.Neurogenetics · 2005
    Article
13. Polymorphisms of the prion protein gene (PRNP) in a Korean population.Journal of human genetics · 2004
    Article
14. Lack of evidence to support the association of the human prion gene with schizophrenia.Molecular psychiatry · 2001
    Article
15. Is the prevalent human prion protein 129M/V mutation a living fossil from a Paleolithic panzootic superprion pandemic?Prion
    Article

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

Authors and funding

2 authors.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

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