Defining sporadic Creutzfeldt-Jakob disease strains and their transmission properties

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

Volumn 107, Issue 26, 2010, Pages 12005-12010

  Bishop, Matthew T ^a   Will, Robert G ^a   Manson, Jean C ^b  

^a UNIVERSITY OF EDINBURGH   (United Kingdom)

^b UNIVERSITY OF EDINBURGH   (United Kingdom)

Author keywords

Codon 129 genotype; Mouse model; Prion disease; Transmission strains

Indexed keywords

GELATINASE A; INTERSTITIAL COLLAGENASE; MATRIX METALLOPROTEINASE; PRION PROTEIN; PROTEIN MV1; PROTEIN MV2; PROTEIN VV1; PROTEIN VV2; UNCLASSIFIED DRUG;

ARTICLE; CODON; HUMAN; HUMAN TISSUE; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN TRANSPORT; SPORADIC CREUTZFELDT JAKOB DISEASE;

ANIMALS; BRAIN; CODON; CREUTZFELDT-JAKOB SYNDROME; GENETIC VARIATION; GENOTYPE; HUMANS; IMMUNOHISTOCHEMISTRY; MICE; MICE, TRANSGENIC; PHENOTYPE; PRPSC PROTEINS; RECOMBINANT PROTEINS; VACUOLES;

MUS;

EID: 77955344991     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1004688107     Document Type: Article

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