Prion protein with an E200K mutation displays properties similar to those of the cellular isoform PrPC

Journal of Neurochemistry

Volumn 76, Issue 6, 2001, Pages 1654-1662

  Rosenmann, H ^a   Talmor, G ^a   Halimi, M ^a   Yanai, A ^a   Gabizon, R ^a   Meiner, Z ^a  

^a HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

Author keywords

Creutzfeldt Jakob disease; E200K; Neuroblastoma cells; Prion; Transgenic mice

Indexed keywords

CELL PROTEIN; PRION PROTEIN; PROTEIN PRP C; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CELL LINE; CHO CELL; CONTROLLED STUDY; CREUTZFELDT JAKOB DISEASE; FIBROBLAST; GENE MUTATION; HUMAN; HUMAN CELL; MOUSE; NEUROBLASTOMA CELL; NONHUMAN; PRION DISEASE; PRIORITY JOURNAL; TRANSGENIC MOUSE;

AMINO ACID SUBSTITUTION; ANIMALS; BRAIN; CELLS, CULTURED; CHO CELLS; CREUTZFELDT-JAKOB SYNDROME; CRICETINAE; FIBROBLASTS; HETEROZYGOTE; HOMOZYGOTE; HUMANS; ISRAEL; JEWS; LIBYA; MICE; MICE, TRANSGENIC; MUTATION, MISSENSE; PRIONS; PRPC PROTEINS; PRPSC PROTEINS; SKIN; TRANSFECTION;

ANIMALIA; CRICETINAE; CRICETULUS GRISEUS; MUS MUSCULUS;

EID: 0035100183     PISSN: 00223042     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1471-4159.2001.00195.x     Document Type: Article

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