Cystic fibrosis: premature degradation of mutant proteins as a molecular disease mechanism.

Methods in molecular biology (Clifton, N.J.)

Volumn 232, Issue , 2003, Pages 27-37

  Gelman, Marina S ^a   Kopito, Ron R ^a  

^a STANFORD UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CFTR PROTEIN, HUMAN; CYSTEINE PROTEINASE; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR DELTA F508; MULTIENZYME COMPLEX; PROTEASOME; TRANSMEMBRANE CONDUCTANCE REGULATOR; UBIQUITIN;

CYSTIC FIBROSIS; GENETICS; HUMAN; METABOLISM; MUTATION; PROTEIN FOLDING; REVIEW;

CYSTEINE ENDOPEPTIDASES; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; HUMANS; MULTIENZYME COMPLEXES; MUTATION; PROTEASOME ENDOPEPTIDASE COMPLEX; PROTEIN FOLDING; UBIQUITIN;

EID: 1542675960     PISSN: 10643745     EISSN: None     Source Type: Journal    
DOI: 10.1385/1-59259-394-1:27     Document Type: Review

References (55)