Transmissible and geneti prion diseases share a common pathway of neurodegeneration

Nature

Volumn 402, Issue 6763, 1999, Pages 822-826

  Hegde, Ramanujan S ^a,c   Tremblay, Patrick ^a,b   Groth, Darlene ^a,b   DeArmond, Stephen J ^a,b   Prusiner, Stanley B ^a,b   Lingappa, Vishwanath R ^a,b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c NATIONAL INSTITUTES OF HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PRION PROTEIN; (CTM)PRP;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; BOVINE SPONGIFORM ENCEPHALOPATHY; CREUTZFELDT JAKOB DISEASE; DOSE RESPONSE; GENE MUTATION; MOUSE; NERVE DEGENERATION; NONHUMAN; PATHOGENESIS; PREDICTION; PRION DISEASE; PRIORITY JOURNAL; ANIMAL; BRAIN; CELL MEMBRANE; DISEASE TRANSMISSION; DOG; ENDOPLASMIC RETICULUM; GENETICS; HAMSTER; METABOLISM; MUTAGENESIS; PATHOLOGY; PRION; SYRIAN HAMSTER; TRANSGENIC MOUSE;

ANIMALS; BRAIN; CELL MEMBRANE; CRICETINAE; DOGS; ENDOPLASMIC RETICULUM; MESOCRICETUS; MICE; MICE, TRANSGENIC; MUTAGENESIS; NERVE DEGENERATION; PRION DISEASES; PRIONS; PRPSC PROTEINS;

EID: 0033576323     PISSN: 00280836     EISSN: None     Source Type: Journal    
DOI: 10.1038/45574     Document Type: Article

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