Author

Fabienne Reine

Université de Versailles Saint-Quentin-en-Yvelines

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Neuroscience· 1 Pathology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Organism:mouse· 1 Assay:protein sequence· 1 Assay:protein structure· 1

Frequent Co-Authors

Human RezaeiiD· 2 shared Laëtitia Herzog· 2 shared Vincent BéringueiD· 2 shared Alba Marín‐MorenoiD· 1 shared Angélique Igel‐EgaloniD· 1 shared Davy MartiniD· 1 shared Florence JaffréziciD· 1 shared Florent LaferrièreiD· 1 shared

Activity by Year

2019-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersPathology

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2 papers

Recent·Most cited

Human PrP E219K as a new and promising substrate for RT-QuIC amplification of human prion strains: a first step towards strain discrimination

Alba Marín‐Moreno, Fabienne Reine, Florence Jaffrézic, Laëtitia Herzog, Human Rezaei, Isabelle Quadrio, Stéphane Haı̈k, Vincent Béringue, Davy Martin

This paper introduces PrP E219K as a new substrate for RT-QuIC that amplifies multiple human prion strains and enables discrimination between sporadic and variant CJD strains.

Microbiology Spectrum · Jul 10, 2025Peer-reviewedPathology

Complementation between pathological prion protein subassemblies to cross existing species barriers

Angélique Igel‐Egalon, Florent Laferrière, Philippe Tixador, Mohammed Moudjou, Laëtitia Herzog, Fabienne Reine, Juan María Torres, Hubert Laude, Human Rézaei, Vincent Béringue

The paper shows that structurally diverse PrPSc assemblies complement each other to cross species barriers, supporting the quasi-species concept in prions.

bioRxiv · Dec 3, 2019 · PreprintNeuroscience