Prion disease.

Treatment of Prion Disease with Heterologous Prion Proteins.

Shedding light on prion disease.

Alzheimer's disease and prion protein.

Transcriptomic responses to prion disease in rats.

The prion hypothesis of Parkinson's disease.

Behavioral and psychiatric symptoms in prion disease.

Prion Disease Induces Alzheimer Disease-Like Neuropathologic Changes.

G-quadruplexes within prion mRNA: the missing link in prion disease?

Prion disease: A newly identified mutation in prion protein is associated with diarrhoea and autonomic neuropathy.

A naturally occurring variant of the human prion protein completely prevents prion disease.

Disease Transmission by Misfolded Prion-Protein Isoforms, Prion-Like Amyloids, Functional Amyloids and the Central Dogma.

Gerstmann-Sträussler-Scheinker disease and "anchorless prion protein" mice share prion conformational properties diverging from sporadic Creutzfeldt-Jakob disease.

Chronic Wasting Disease Prion Strain Emergence and Host Range Expansion.

Genetic human prion disease modelled in PrP transgenic Drosophila.

Uncontrolled SFK-mediated protein trafficking in prion and Alzheimer's disease.

Spontaneous generation of infectious prion disease in transgenic mice.

The prion hypothesis in Parkinson's disease: Braak to the future.

Two alternative pathways for generating transmissible prion disease de novo.

Parkinson's disease as a member of Prion-like disorders.

Descriptive epidemiology of prion disease in Japan: 1999-2012.

Classifying prion and prion-like phenomena.

A new prion disease: relationship with central and peripheral amyloidoses.

Octarepeat region flexibility impacts prion function, endoproteolysis and disease manifestation.

Initial diagnoses of patients ultimately diagnosed with prion disease.

Suggest Documents

Treatment of Prion Disease with Heterologous Prion Proteins.

Shedding light on prion disease.

Alzheimer's disease and prion protein.

Transcriptomic responses to prion disease in rats.

The prion hypothesis of Parkinson's disease.

Behavioral and psychiatric symptoms in prion disease.

Prion Disease Induces Alzheimer Disease-Like Neuropathologic Changes.

G-quadruplexes within prion mRNA: the missing link in prion disease?

Prion disease: A newly identified mutation in prion protein is associated with diarrhoea and autonomic neuropathy.

A naturally occurring variant of the human prion protein completely prevents prion disease.

Disease Transmission by Misfolded Prion-Protein Isoforms, Prion-Like Amyloids, Functional Amyloids and the Central Dogma.

Gerstmann-Sträussler-Scheinker disease and "anchorless prion protein" mice share prion conformational properties diverging from sporadic Creutzfeldt-Jakob disease.

Chronic Wasting Disease Prion Strain Emergence and Host Range Expansion.

Genetic human prion disease modelled in PrP transgenic Drosophila.

Uncontrolled SFK-mediated protein trafficking in prion and Alzheimer's disease.

Spontaneous generation of infectious prion disease in transgenic mice.

The prion hypothesis in Parkinson's disease: Braak to the future.

Two alternative pathways for generating transmissible prion disease de novo.

Parkinson's disease as a member of Prion-like disorders.

Descriptive epidemiology of prion disease in Japan: 1999-2012.

Classifying prion and prion-like phenomena.

A new prion disease: relationship with central and peripheral amyloidoses.

Octarepeat region flexibility impacts prion function, endoproteolysis and disease manifestation.

Initial diagnoses of patients ultimately diagnosed with prion disease.

Prion disease.

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