Laëtitia Herzog

Biochemistry, Genetics and Molecular Biology · Life Sciences

17h-index1.4kcitations58works1.62yr avg
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Research Topics

Prion Diseases and Protein Misfolding(56), Neurological diseases and metabolism(15), Trace Elements in Health(12), Amino Acid Enzymes and Metabolism(4), Alzheimer's disease research and treatments(3)

Publications58 total

Optimization and evaluation of new decontamination procedures inactivating human prions
Journal of Hospital Infection·2025· 3 citedOpen Access
Species barrier as molecular basis for adaptation of synthetic prions with N‐terminally truncated <scp>PrP</scp>
FEBS Journal·2024· 1 citedOpen Access
Author response for "Species barrier as molecular basis for adaptation of synthetic prions with N‐terminally truncated &lt;scp&gt;PrP&lt;/scp&gt;"
2024
Assessment of the Zoonotic Potential of Atypical Scrapie Prions in Humanized Mice Reveals Rare Phenotypic Convergence but Not Identity With Sporadic Creutzfeldt-Jakob Disease Prions
The Journal of Infectious Diseases·2024· 3 cited
Optimization and Evaluation of New Decontamination Procedures Inactivating Human Prions
SSRN Electronic Journal·2024· 1 citedOpen Access
Characterising structural heterogeneity of prions: Using synthetic protein libraris (Alphareps) for the study of cellular and Scrapie prion conformers
HAL (Le Centre pour la Communication Scientifique Directe)·2023
The Smallest Infectious Substructure Encoding the Prion Strain Structural Determinant Revealed by Spontaneous Dissociation of Misfolded Prion Protein Assemblies
Journal of Molecular Biology·2023· 9 citedOpen Access
Caractérisation de l’hétérogénéité structurale des prions: Utilisation de banques de protéines ligands synthétiques (AlphaReps) pour l’étude de conformères de la protéine prion cellulaire et scrapie
HAL (Le Centre pour la Communication Scientifique Directe)·2023Open Access
The smallest infectious substructure encoding the prion strain structural determinant revealed by spontaneous dissociation of misfolded prion protein assemblies
2023Open Access
Pathogenicity, strain properties and interspecies transmission capacity of pure recombinant prion protein assemblies
2023Open Access
Prion species barriers: studies with atypical scrapie and prions from pure synthetic origin
SPIRE - Sciences Po Institutional REpository·2021
Prion potentiation after life-long dormancy in mice devoid of PrP
Brain Communications·2021· 15 citedOpen Access
Improving the Predictive Value of Prion Inactivation Validation Methods to Minimize the Risks of Iatrogenic Transmission With Medical Instruments
Frontiers in Bioengineering and Biotechnology·2020· 14 citedOpen Access
Host prion protein expression levels impact prion tropism for the spleen
PLoS Pathogens·2020· 17 citedOpen Access
TSE sources transmitted to tg338 mice.
Figshare·2020Open Access
Crossing Species Barriers Relies on Structurally Distinct Prion Assemblies and Their Complementation
Molecular Neurobiology·2020· 14 citedOpen Access
Correlation between Bioassay and Protein Misfolding Cyclic Amplification for Variant Creutzfeldt-Jakob Disease Decontamination Studies
mSphere·2020· 28 citedOpen Access
Host prion protein expression levels impact prion tropism for the spleen
2019Open Access
Complementation between pathological prion protein subassemblies to cross existing species barriers
2019Open Access
Prion strain-dependent tropism is maintained between spleen and granuloma and relies on lymphofollicular structures
Scientific Reports·2019· 8 citedOpen Access
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Frequent Co-authors

Vincent Béringue(48), Fabienne Reine(41), Mohammed Moudjou(23), Human Rézaei(22), Hubert Laude(16), Jérôme Chapuis(13), Angélique Igel‐Egalon(13), Pierre Sibille(12), Human Rezaei(12), Bruno Passet(11), Philippe Tixador(10), Emilie Jaumain(10), Hubert Laude(10), Jean-Luc Vilotte(10), Annick Le Dur(9), Juan María Torres(8), Florent Laferrière(8), Michel Dron(8), Olivier Andréoletti(7), Davy Martin(7)