Two Creutzfeldt-Jakob disease agents reproduce prion protein-independent identities in cell cultures

Proceedings of the National Academy of Sciences of the United States of America

Volumn 101, Issue 23, 2004, Pages 8768-8773

  Arjona, Alvaro ^a   Simarro, Laura ^a   Islinger, Florian ^a   Nishida, Noriyuki ^b   Manuelidis, Laura ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b NAGASAKI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

Agent strains; High infectivity; In situ detection; In vitro propagation; Transmissible encephalopathies

Indexed keywords

PRION PROTEIN;

ANIMAL CELL; ARTICLE; CELL CULTURE; CONTROLLED STUDY; CREUTZFELDT JAKOB DISEASE; DEGENERATIVE DISEASE; GENETIC CODE; IMMUNE RESPONSE; IN VITRO STUDY; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN PURIFICATION; RAT; SCRAPIE AGENT; VIRUS INFECTIVITY; VIRUS STRAIN;

ANIMALS; BRAIN; CELL LINE; CREUTZFELDT-JAKOB SYNDROME; GLIAL FIBRILLARY ACIDIC PROTEIN; HUMANS; MICE; PRIONS;

ANIMALIA; MURINAE; OVIS ARIES; RNA VIRUSES; SCRAPIE PRION;

EID: 2942616523     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0400158101     Document Type: Article

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