Degradation of CFTR by the ubiquitin-proteasome pathwayCristina L. Ward(Stanford University), Satoshi ŌMURA(Kitasato Institute Hospital), Ron R. Kopito(Stanford University)CellOctober 1, 199510.1016/0092-8674(95)90240-6Cited by 1,307Open AccessFull TextSaveCiteExport RISWatch citationsAbstractRelated PapersIdentification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNAJohn R. Riordan, Johanna M. Rommens, Bat-Sheva Kerem et al.|Science|1989|7.4kInhibitors of the proteasome block the degradation of most cell proteins and the generation of peptides presented on MHC class I moleculesKenneth L. Rock, Colette F. Gramm, Lisa Rothstein et al.|Cell|1994|2.5kDefective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosisSeng H. Cheng, Richard J. Gregory, John Marshall et al.|Cell|1990|1.8kCrystal Structure of the 20 <i>S</i> Proteasome from the Archaeon <i>T. acidophilum</i> at 3.4 Å ResolutionJan Löwe, Daniela Stock, Bing K. Jap et al.|Science|1995|1.5kMolecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosisMichael J. Welsh, Alan E. Smith|Cell|1993|1.5k