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Volumn 275, Issue 43, 2000, Pages 33650-33654

Solution structure of the E200K variant of human prion protein. Implications for the mechanism of pathogenesis in familial prion diseases

(5) Zhang, Yongbo a Swietnicki, Wieslaw a Zagorski, Michael G a Surewicz, Witold K a Sönnichsen, Frank D b

a CASE WESTERN RESERVE UNIVERSITY (United States)

b CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHAPERONE; PRION PROTEIN;

ARTICLE; CREUTZFELDT JAKOB DISEASE; FAMILIAL DISEASE; GENE MUTATION; PATHOGENESIS; PRION DISEASE; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; PROTEIN STRUCTURE; PROTEIN TERTIARY STRUCTURE; PROTEIN VARIANT;

BASE SEQUENCE; CREUTZFELDT-JAKOB SYNDROME; HUMANS; MOLECULAR SEQUENCE DATA; MUTATION; PRIONS; PROTEIN FOLDING; PROTEIN STRUCTURE, SECONDARY; SOLUTIONS;

EID: 0034721767 PISSN: 00219258 EISSN: None Source Type: Journal
DOI: 10.1074/jbc.C000483200 Document Type: Article

Times cited : (120)

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