Cystic Fibrosis as a Disease of Misprocessing of the Cystic Fibrosis Transmembrane Conductance Regulator Glycoprotein
- 1 June 1999
- journal article
- review article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 64 (6) , 1499-1504
- https://doi.org/10.1086/302429
Abstract
No abstract availableThis publication has 39 references indexed in Scilit:
- From the ER to the Golgi: Insights from the Study of Combined Factors V and VIII DeficiencyAmerican Journal of Human Genetics, 1999
- Aggresomes: A Cellular Response to Misfolded ProteinsThe Journal of cell biology, 1998
- Cargo Selection by the COPII Budding Machinery during Export from the ERThe Journal of cell biology, 1998
- Limited proteolysis as a probe for arrested conformational maturation of ΔF508 CFTRNature Structural & Molecular Biology, 1998
- Association and Stoichiometry of KATP Channel SubunitsPublished by Elsevier ,1997
- Disease-associated Mutations in the Fourth Cytoplasmic Loop of Cystic Fibrosis Transmembrane Conductance Regulator Compromise Biosynthetic Processing and Chloride Channel ActivityPublished by Elsevier ,1996
- Alteration of the Cystic Fibrosis Transmembrane Conductance Regulator Folding PathwayJournal of Biological Chemistry, 1996
- Mislocalization of ΔF508 CFTR in cystic fibrosis sweat glandNature Genetics, 1992
- Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutationNature, 1991
- Chloride Conductance Expressed by ΔF508 and Other Mutant CFTRs In Xenopus OocytesScience, 1991