Types and strains: Their essential role in understanding protein aggregation in neurodegenerative diseases

Frontiers in Aging Neuroscience

Volumn 9, Issue JUN, 2017, Pages

  Wemheuer, Wiebke M ^a,b   Wrede, Arne ^a,c   Schulz Schaeffer, Walter J ^a,c  

^a SAARLAND UNIVERSITY   (Germany)

^b UNIVERSITY OF LUXEMBOURG   (Luxembourg)

^c UNIVERSITY MEDICAL CENTER GÖTTINGEN   (Germany)

Author keywords

Accelerated seeding; Prion; Protein conformation; synuclein; amyloid

Indexed keywords

ALPHA SYNUCLEIN; AMYLOID BETA PROTEIN; PRION PROTEIN; TAU PROTEIN;

AMINO ACID SEQUENCE; CREUTZFELDT JAKOB DISEASE; DEGENERATIVE DISEASE; DIFFUSE LEWY BODY DISEASE; DISEASE PREDISPOSITION; DISEASE TRANSMISSION; HETEROZYGOSITY; HUMAN; INBRED MOUSE STRAIN; INCUBATION TIME; NERVE DEGENERATION; PARKINSON DISEASE; PRION DISEASE; PROTEIN AGGREGATION; PROTEIN CLEAVAGE; PROTEIN CONFORMATION; PROTEIN FUNCTION; PROTEIN MISFOLDING; PROTEIN MOTIF; REVIEW; SCRAPIE; VIRUS STRAIN;

EID: 85020915211     PISSN: None     EISSN: 16634365     Source Type: Journal    
DOI: 10.3389/fnagi.2017.00187     Document Type: Review

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