Implications of prion adaptation and evolution paradigm for human neurodegenerative diseases

Neurofibrillary tangle-like tau pathology induced by synthetic tau fibrils in primary neurons over-expressing mutant tau

(2013) Jing L. Guo et al.   FEBS LETTERS

Co-existence of Distinct Prion Types Enables Conformational Evolution of Human PrPScby Competitive Selection

(2013) Tracy Haldiman et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

CSF prion protein concentration and cognition in patients with Alzheimer disease

(2013) Christian Schmidt et al.   Prion

Prions, prionoids and pathogenic proteins in Alzheimer disease

(2013) Karen H. Ashe et al.   Prion

Acquisition of Drug Resistance and Dependence by Prions

(2013) Anja M. Oelschlegel et al.   PLoS Pathogens

Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA

(2012) Piero Parchi et al.   ACTA NEUROPATHOLOGICA

The genetics and neuropathology of Alzheimer’s disease

(2012) Gerard D. Schellenberg et al.   ACTA NEUROPATHOLOGICA

Correlation of Alzheimer Disease Neuropathologic Changes With Cognitive Status: A Review of the Literature

(2012) Peter T. Nelson et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

Sporadic human prion diseases: molecular insights and diagnosis

(2012) Gianfranco Puoti et al.   LANCET NEUROLOGY

Molecular pathogenesis of sporadic prion diseases in man

(2012) Jiri G. Safar   Prion

A Unifying Role for Prions in Neurodegenerative Diseases

(2012) S. B. Prusiner   SCIENCE

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

(2012) Chae Kim et al.   PLoS Pathogens

Biomarkers in Alzheimer's disease drug development

(2011) Jeffrey L. Cummings   Alzheimers & Dementia

The diagnosis of dementia due to Alzheimer’s disease: Recommendations from the National Institute on Aging-Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer's disease

(2011) Guy M. McKhann et al.   Alzheimers & Dementia

The Alzheimer’s Disease Neuroimaging Initiative: A review of papers published since its inception

(2011) Michael W. Weiner et al.   Alzheimers & Dementia

Co-Occurrence of Types 1 and 2 PrP res in Sporadic Creutzfeldt-Jakob Disease MM1

(2011) Atsushi Kobayashi et al.   AMERICAN JOURNAL OF PATHOLOGY

Treatable neurological disorders misdiagnosed as Creutzfeldt-Jakob disease

(2011) Numthip Chitravas et al.   ANNALS OF NEUROLOGY

Rapidly Progressive Alzheimer Disease

(2011) Christian Schmidt   ARCHIVES OF NEUROLOGY

Stages of the Pathologic Process in Alzheimer Disease: Age Categories From 1 to 100 Years

(2011) Heiko Braak et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

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

(2011) Chae Kim et al.   PLoS Pathogens

Clinical Features of Rapidly Progressive Alzheimer’s Disease

(2010) Christian Schmidt et al.   DEMENTIA AND GERIATRIC COGNITIVE DISORDERS

Mammalian Prions Generated from Bacterially Expressed Prion Protein in the Absence of Any Mammalian Cofactors

(2010) Jae-Il Kim et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Coinfecting Prion Strains Compete for a Limiting Cellular Resource

(2010) R. A. Shikiya et al.   JOURNAL OF VIROLOGY

Defining sporadic Creutzfeldt-Jakob disease strains and their transmission properties

(2010) M. T. Bishop et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Darwinian Evolution of Prions in Cell Culture

(2010) J. Li et al.   SCIENCE

Generating a Prion with Bacterially Expressed Recombinant Prion Protein

(2010) F. Wang et al.   SCIENCE

Getting a Grip on Prions: Oligomers, Amyloids, and Pathological Membrane Interactions

(2009) Byron Caughey et al.   Annual Review of Biochemistry

Prion Diseases and Their Biochemical Mechanisms†

(2009) Nathan J. Cobb et al.   BIOCHEMISTRY

Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt–Jakob disease: its effect on the phenotype and prion-type characteristics

(2009) Ignazio Cali et al.   BRAIN

Trajectories of cognitive decline in Alzheimer's disease

(2009) Patricia A. Wilkosz et al.   INTERNATIONAL PSYCHOGERIATRICS

Trans-Dominant Inhibition of Prion Propagation In Vitro Is Not Mediated by an Accessory Cofactor

(2009) James C. Geoghegan et al.   PLoS Pathogens

De Novo Generation of Infectious Prions In Vitro Produces a New Disease Phenotype

(2009) Marcelo A. Barria et al.   PLoS Pathogens

Cell-free propagation of prion strains

(2008) Joaquín Castilla et al.   EMBO JOURNAL

Beyond PrPres Type 1/Type 2 Dichotomy in Creutzfeldt-Jakob Disease

(2008) Emmanuelle Uro-Coste et al.   PLoS Pathogens