Protein folding, unfolding and misfolding: Role played by intermediate states

Mini-Reviews in Medicinal Chemistry

Volumn 8, Issue 1, 2008, Pages 57-62

  Santucci, R ^a   Sinibaldi, F ^a   Fiorucci, L ^a  

^a UNIVERSITY OF ROME TOR VERGATA   (Italy)

Author keywords

Alzheimer; Cell apoptosis; Genetic diseases; Intermediate conformers; Protein folding and misfolding

Indexed keywords

ALPHA 1 ANTITRYPSIN; ALPHA LACTALBUMIN; AMYLOID; AMYLOID BETA PROTEIN; APOLIPOPROTEIN E4; APOPTOTIC PROTEASE ACTIVATING FACTOR 1; CYTOCHROME C; LEUKOCYTE ELASTASE; OLEIC ACID; PRION PROTEIN; TRANSMEMBRANE CONDUCTANCE REGULATOR;

ALPHA 1 ANTITRYPSIN DEFICIENCY; ALZHEIMER DISEASE; AMYLOIDOSIS; APOPTOSIS; CREUTZFELDT JAKOB DISEASE; CYSTIC FIBROSIS; DEGENERATIVE DISEASE; DISEASE ASSOCIATION; GENE DELETION; HUMAN; HYDROPHOBICITY; LIVER DISEASE; LUNG DISEASE; MITOCHONDRION; MOLECULAR MECHANICS; PARKINSON DISEASE; PATHOPHYSIOLOGY; POINT MUTATION; PROTEIN AGGREGATION; PROTEIN CONFORMATION; PROTEIN FOLDING; PROTEIN FUNCTION; PROTEIN SECRETION; PROTEIN STABILITY; PROTEIN STRUCTURE; REVIEW;

ALZHEIMER DISEASE; HUMANS; KINETICS; NEOPLASMS; PARKINSON DISEASE; PROTEIN FOLDING; PROTEIN STRUCTURE, SECONDARY; PROTEINS;

EID: 40049100326     PISSN: 13895575     EISSN: None     Source Type: Journal    
DOI: 10.2174/138955708783331522     Document Type: Review

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