Distribution of Misfolded Prion Protein Seeding Activity Alone Does Not Predict Regions of Neurodegeneration

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Alzheimer's and Parkinson's diseases: The prion concept in relation to assembled A , tau, and  -synuclein

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Prion Protein-Specific Antibodies that Detect Multiple TSE Agents with High Sensitivity

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Absence of CD14 Delays Progression of Prion Diseases Accompanied by Increased Microglial Activation

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Comparative Analysis of Gene Expression Profiles Between Cortex and Thalamus in Chinese Fatal Familial Insomnia Patients

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Early Increase and Late Decrease of Purkinje Cell Dendritic Spine Density in Prion-Infected Organotypic Mouse Cerebellar Cultures

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Prion Seeding Activities of Mouse Scrapie Strains with Divergent PrPSc Protease Sensitivities and Amyloid Plaque Content Using RT-QuIC and eQuIC

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Pathogenic protein seeding in alzheimer disease and other neurodegenerative disorders

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Mechanism of PrP-Amyloid Formation in Mice Without Transmissible Spongiform Encephalopathy

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Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion

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Microglial activation and chronic neurodegeneration

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(2009) Athanasios Theocharidis et al.   Nature Protocols

Protein Misfolding and Neurodegeneration

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Comprehensive transcriptional profiling of prion infection in mouse models reveals networks of responsive genes

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Application of a Translational Profiling Approach for the Comparative Analysis of CNS Cell Types

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Role of Erk1/2 activation in prion disease pathogenesis: Absence of CCR1 leads to increased Erk1/2 activation and accelerated disease progression

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Accelerated Prion Replication in, but Prolonged Survival Times of, Prion-Infected CXCR3-/- Mice

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