Prion disease: A deadly disease for protein misfolding

Current Pharmaceutical Biotechnology

Volumn 6, Issue 2, 2005, Pages 167-177

  Chakraborty, Chiranjib ^b   Nandi, Shyam ^a   Jana, Snehasis ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY DELHI   (India)

^b Glen Mark Laboratories   (India)

Author keywords

[No Author keywords available]

Indexed keywords

PREALBUMIN; PRION PROTEIN; PROTEIN ANTIBODY; PROTEINASE K;

ALPERS DISEASE; AMINO ACID SEQUENCE; CONFORMATIONAL TRANSITION; CREUTZFELDT JAKOB DISEASE; DISEASE CLASSIFICATION; DISEASE PREDISPOSITION; DISEASE TRANSMISSION; ENZYME DEGRADATION; FAMILIAL AMYLOID POLYNEUROPATHY; FATAL FAMILIAL INSOMNIA; GERSTMANN STRAUSSLER SCHEINKER SYNDROME; HUMAN; IN VITRO STUDY; KURU; NONHUMAN; PRION DISEASE; PROTEIN FOLDING; PROTEIN STRUCTURE; PROTEIN SYNTHESIS; REVIEW; SCRAPIE; SPECIES DIFFERENCE;

ANIMALS; BRAIN; HUMANS; PRION DISEASES; PRIONS; PROTEIN FOLDING; STRUCTURE-ACTIVITY RELATIONSHIP;

ANIMALIA; BOVINAE; MAMMALIA; MUSTELA VISON;

EID: 18344363579     PISSN: 13892010     EISSN: None     Source Type: Journal    
DOI: 10.2174/1389201053642321     Document Type: Review

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