Alba Moreno-Marin

Madrid, MD, Spain

Last Updated: 09/26/2026

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Found 37 publications

Formic acid treatment drastically reduces sporadic Creutzfeldt-Jakob disease and variant Creutzfeldt-Jakob disease infectivity in histological samples as tested in a high-sensitivity mouse bioassay.

Formic acid treatment drastically reduces sporadic Creutzfeldt-Jakob disease and variant Creutzfeldt-Jakob disease infectivity in histological samples as tested in a high-sensitivity mouse bioassay.

Journal: The Journal of general virology

Published: August 10, 2026

Silent Propagation of Classical Scrapie Prions in Homozygous K222 Transgenic Mice.

Silent Propagation of Classical Scrapie Prions in Homozygous K222 Transgenic Mice.

Journal: Emerging infectious diseases

Published: January 06, 2026

Classical BSE emergence from Nor98/atypical scrapie: Unraveling the shift vs. selection dichotomy in the prion field.

Classical BSE emergence from Nor98/atypical scrapie: Unraveling the shift vs. selection dichotomy in the prion field.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: July 15, 2025

Human PrP E219K: a new and promising substrate for robust RT-QuIC amplification of human prions with potential for strain discrimination.

Human PrP E219K: a new and promising substrate for robust RT-QuIC amplification of human prions with potential for strain discrimination.

Journal: Microbiology spectrum

Published: July 10, 2025

Substitution of histidine 95 by tyrosine in the prion protein causes spontaneous neurodegeneration in transgenic mice.

Substitution of histidine 95 by tyrosine in the prion protein causes spontaneous neurodegeneration in transgenic mice.

Journal: PLoS pathogens

Published: January 13, 2025

Strain-Dependent Susceptibility to Prion Infection Encoded by Arg171 and Lys176 Sheep Prion Protein Polymorphic Variants.

Strain-Dependent Susceptibility to Prion Infection Encoded by Arg171 and Lys176 Sheep Prion Protein Polymorphic Variants.

Journal: The Journal of infectious diseases

Published: November 19, 2024

Species barrier as molecular basis for adaptation of synthetic prions with N-terminally truncated PrP.

Species barrier as molecular basis for adaptation of synthetic prions with N-terminally truncated PrP.

Journal: The FEBS journal

Published: February 26, 2024

Classical BSE dismissed as the cause of CWD in Norwegian red deer despite strain similarities between both prion agents.

Classical BSE dismissed as the cause of CWD in Norwegian red deer despite strain similarities between both prion agents.

Journal: Veterinary research

Published: January 26, 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.

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.

Journal: The Journal of infectious diseases

Published: December 13, 2023

Experimental transmission of ovine atypical scrapie to cattle.

Experimental transmission of ovine atypical scrapie to cattle.

Journal: Veterinary research

Published: June 27, 2023

Transgenic Mouse Models for the Study of Neurodegenerative Diseases.

Transgenic Mouse Models for the Study of Neurodegenerative Diseases.

Journal: Frontiers in bioscience (Landmark edition)

Published: December 07, 2022

Classical BSE prions emerge from asymptomatic pigs challenged with atypical/Nor98 scrapie.

Classical BSE prions emerge from asymptomatic pigs challenged with atypical/Nor98 scrapie.

Journal: Scientific reports

Published: May 20, 2021

Showing 1-12 of 37

Last Updated: 09/26/2026