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Volumn 93, Issue 11, 1996, Pages 5610-5614

Two mutant prion proteins expressed in cultured cells acquire biochemical properties reminiscent of the scrapie isoform

Author keywords

Creutzfeldt Jakob disease; genetic; metabolism; neurodegenerative; posttranslational

Indexed keywords

AMINO ACID SUBSTITUTION; ANIMAL CELL; ARTICLE; CHO CELL; CODON; CREUTZFELDT JAKOB DISEASE; GENE EXPRESSION; NERVE DEGENERATION; NONHUMAN; NUCLEOTIDE REPEAT; POINT MUTATION; PRION; PRIORITY JOURNAL; PROTEIN PROCESSING; SCRAPIE AGENT;

EID: 0030006902     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.93.11.5610     Document Type: Article
Times cited : (98)

References (38)
  • 1
    • 0000857618 scopus 로고
    • eds. Fields, B. N. & Knipe, D. M. (Raven, New York), 2nd Ed.
    • Gajdusek, D. C. (1990) in Virology, eds. Fields, B. N. & Knipe, D. M. (Raven, New York), 2nd Ed., pp. 2289-2323.
    • (1990) Virology , pp. 2289-2323
    • Gajdusek, D.C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.