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Volumn 20, Issue 11, 1995, Pages 456-459
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Defective protein folding as a basis of human disease
a a b |
Author keywords
[No Author keywords available]
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Indexed keywords
AMYLOIDOSIS;
AMYOTROPHIC LATERAL SCLEROSIS;
CANCER;
CATARACT;
CYSTIC FIBROSIS;
ENZYME DEFICIENCY;
FAMILIAL HYPERCHOLESTEROLEMIA;
HUMAN;
MARFAN SYNDROME;
MUTATION;
OSTEOGENESIS IMPERFECTA;
PRIORITY JOURNAL;
PROTEIN FOLDING;
PROTEIN MODIFICATION;
RETINITIS PIGMENTOSA;
REVIEW;
SCURVY;
AMINO ACID ISOMERASES;
CARRIER PROTEINS;
CYSTIC FIBROSIS;
CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR;
DISEASE;
HUMAN;
ISOMERASES;
MOLECULAR CHAPERONES;
PEPTIDYLPROLYL ISOMERASE;
PROTEIN DISULFIDE-ISOMERASE;
PROTEIN FOLDING;
PROTEIN STRUCTURE, TERTIARY;
SUPPORT, NON-U.S. GOV'T;
SUPPORT, U.S. GOV'T, P.H.S.;
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EID: 0028856292
PISSN: 09680004
EISSN: None
Source Type: Journal
DOI: 10.1016/S0968-0004(00)89100-8 Document Type: Review |
Times cited : (487)
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References (43)
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