Prion infection.

Prion permissive pathways: extracellular matrix genes control susceptibility to prion infection.

Prion amplification and hierarchical Bayesian modeling refine detection of prion infection.

Prion diseases: risks, characteristics, and infection control considerations in dentistry.

Prion infection impairs cholesterol metabolism in neuronal cells.

Genetics of response to slow virus (prion) infection.

A cell-biased effect of estrogen in prion infection.

Scrapie-associated prion protein accumulates in astrocytes during scrapie infection.

Distinct patterns of spread of prion infection in brains of mice expressing anchorless or anchored forms of prion protein.

Classifying prion and prion-like phenomena.

Prion and prion-like diseases in animals.

Prion diseases.

Prion diseases.

Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type.

Treatment of Prion Disease with Heterologous Prion Proteins.

Prion Diseases.

Prion disease.

Prion protein scrapie and the normal cellular prion protein.

Emergence and evolution of yeast prion and prion-like proteins.

Characteristic CSF prion seeding efficiency in humans with prion diseases.

Human prion diseases: surgical lessons learned from iatrogenic prion transmission.

Sporadic Creutzfeldt-Jakob Disease: Prion Pathology in Medulla Oblongata-Possible Routes of Infection and Host Susceptibility.

Prion protein participates in the protection of mice from lipopolysaccharide infection by regulating the inflammatory process.

Role of the goat K222-PrP(C) polymorphic variant in prion infection resistance.

$Human tonsil-derived follicular dendritic-like cells are refractory to human prion infection in vitro and traffic disease-associated prion protein to lysosomes.$
Human tonsil-derived follicular dendritic-like cells are refractory to human prion infection in vitro and traffic disease-associated prion protein to lysosomes.

Suggest Documents

Prion permissive pathways: extracellular matrix genes control susceptibility to prion infection.

Prion amplification and hierarchical Bayesian modeling refine detection of prion infection.

Prion diseases: risks, characteristics, and infection control considerations in dentistry.

Prion infection impairs cholesterol metabolism in neuronal cells.

Genetics of response to slow virus (prion) infection.

A cell-biased effect of estrogen in prion infection.

Scrapie-associated prion protein accumulates in astrocytes during scrapie infection.

Distinct patterns of spread of prion infection in brains of mice expressing anchorless or anchored forms of prion protein.

Classifying prion and prion-like phenomena.

Prion and prion-like diseases in animals.

Prion diseases.

Prion diseases.

Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type.

Treatment of Prion Disease with Heterologous Prion Proteins.

Prion Diseases.

Prion disease.

Prion protein scrapie and the normal cellular prion protein.

Emergence and evolution of yeast prion and prion-like proteins.

Characteristic CSF prion seeding efficiency in humans with prion diseases.

Human prion diseases: surgical lessons learned from iatrogenic prion transmission.

Sporadic Creutzfeldt-Jakob Disease: Prion Pathology in Medulla Oblongata-Possible Routes of Infection and Host Susceptibility.

Prion protein participates in the protection of mice from lipopolysaccharide infection by regulating the inflammatory process.

Role of the goat K222-PrP(C) polymorphic variant in prion infection resistance.

Human tonsil-derived follicular dendritic-like cells are refractory to human prion infection in vitro and traffic disease-associated prion protein to lysosomes.

Prion infection.

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