A Systematic Survey Identifies Prions and Illuminates Sequence Features of Prionogenic Proteins

2009/04/01 by Simon Alberti, Randal Halfmann, Oliver D. King +3 · 3 citations
Biochemistry, Genetics and Molecular Biology · Neuroscience · Nursing · #Neurological diseases and metabolism #Prion Diseases and Protein Misfolding #Trace Elements in Health

paper · pdf · doi:10.1016/j.cell.2009.02.044

crossref issued 2009/04/01 · crossref published 2009/04/01 · crossref published-print 2009/04/01 · openalex publication_date 2009/04/01 · crossref created 2009/04/03 · crossref deposited 2021/10/03 · openalex created_date 2025/10/10 · crossref indexed 2026/07/17 · openalex updated_date 2026/07/28

Citations

• Dependence and Independence
• A simple method for displaying the hydropathic character of a protein
• Nature of the Scrapie Agent: Self-replication and Scrapie
• Novel Proteinaceous Infectious Particles Cause Scrapie
• Studies on the transformation of intact yeast cells by the LiAc/SS‐DNA/PEG procedure
• Prions as adaptive conduits of memory and inheritance

Cited by

• Long-term memory consolidation: The role of RNA-binding proteins with prion-like domains
• Dynamic Reorganization of Metabolic Enzymes into Intracellular Bodies
• Prion [wikipedia]