A unifying role for prions in neurodegenerative diseases

Science

Volumn 336, Issue 6088, 2012, Pages 1511-1513

  Prusiner, Stanley B ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA SYNUCLEIN; AMYLOID; AMYLOID BETA PROTEIN; CHAPERONE; COPPER ZINC SUPEROXIDE DISMUTASE; CYTOPLASMIC POLYADENYLATION ELEMENT BINDING PROTEIN; HUNTINGTIN; MEMBRANE PROTEIN; MITOCHONDRIAL ANTIVIRAL SIGNALING PROTEIN; PRION PROTEIN; T CELL RESTRICTED INTRACELLULAR ANTIGEN 1; T LYMPHOCYTE ANTIGEN; TAU PROTEIN; UNCLASSIFIED DRUG; FUNGAL PROTEIN;

ETIOLOGY; NERVOUS SYSTEM DISORDER; NEUROLOGY;

AMYLOID PLAQUE; AMYOTROPHIC LATERAL SCLEROSIS; CELL FUNCTION; DEGENERATIVE DISEASE; DNA MODIFICATION; FRONTOTEMPORAL DEMENTIA; HAPLOINSUFFICIENCY; HUMAN; HUNTINGTON CHOREA; INNATE IMMUNITY; LEWY BODY; NEUROFIBRILLARY TANGLE; NONHUMAN; PARKINSON DISEASE; POSTTRAUMATIC STRESS DISORDER; PRIORITY JOURNAL; PROTEIN AGGREGATION; PROTEIN CONFORMATION; PROTEIN DEGRADATION; PROTEIN MODIFICATION; PROTEIN STRUCTURE; PROTEIN SYNTHESIS; SHORT SURVEY; SOMATIC MUTATION; TAUOPATHY; ANIMAL; ARTICLE; CHEMISTRY; METABOLISM; PATHOGENICITY; PRION; PRION DISEASE;

ANIMALS; FUNGAL PROTEINS; HUMANS; NEURODEGENERATIVE DISEASES; PRION DISEASES; PRIONS; PROTEIN CONFORMATION;

EID: 84862620376     PISSN: 00368075     EISSN: 10959203     Source Type: Journal    
DOI: 10.1126/science.1222951     Document Type: Short Survey

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