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Biology and Genetics of Prions Causing Neurodegeneration

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Small Protease Sensitive Oligomers of PrPSc in Distinct Human Prions Determine Conversion Rate of PrPC

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(2011) D. J. Selkoe   Cold Spring Harbor Perspectives in Biology

Protease-Sensitive Conformers in Broad Spectrum of Distinct PrPSc Structures in Sporadic Creutzfeldt-Jakob Disease Are Indicator of Progression Rate

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Distinct Stability States of Disease-Associated Human Prion Protein Identified by Conformation-Dependent Immunoassay

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Presenilin 1 gene mutation (M139I) in a patient with an early-onset Alzheimer’s disease: clinical characteristics and genetic identification

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A New Method for the Characterization of Strain-Specific Conformational Stability of Protease-Sensitive and Protease-Resistant PrPSc

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(2008) Michael D. Geschwind et al.   ANNALS OF NEUROLOGY

Transmission and Detection of Prions in Feces

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Molecular structural basis for polymorphism in Alzheimer's  -amyloid fibrils

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