Transmissible spongiform encephalopathies

2004/01/01 by Steven Collins, Steven J Collins, Victoria Lawson +3 · 1 citation
Biochemistry, Genetics and Molecular Biology · Neuroscience · #Neurological diseases and metabolism #Prion Diseases and Protein Misfolding

paper · doi:10.1016/s0140-6736(03)15171-9

crossref issued 2004/01/01 · crossref published 2004/01/01 · crossref published-print 2004/01/01 · openalex publication_date 2004/01/01 · crossref created 2004/01/02 · crossref deposited 2020/03/28 · openalex created_date 2025/10/10 · crossref indexed 2026/05/06 · openalex updated_date 2026/07/28

Citations

• The cellular prion protein binds copper in vivo
• Descriptive epidemiology of Creutzfeldt‐Jakob disease in six european countries, 1993–1995
• A Transmembrane Form of the Prion Protein in Neurodegenerative Disease
• Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins.
• Prion Protein Conformation in a Patient with Sporadic Fatal Insomnia
• Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD
• Gerstmann–Sträussler–Scheinker syndrome,fatal familial insomnia, and kuru: a review ofthese less common human transmissiblespongiform encephalopathies
• Human spongiform encephalopathy: The national institutes of health series of 300 cases of experimentally transmitted disease
• Balancing Selection at the Prion Protein Gene Consistent with Prehistoric Kurulike Epidemics
• Molecular Features of the Copper Binding Sites in the Octarepeat Domain of the Prion Protein

Cited by

• Prion [wikipedia]