Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis
- 1 July 1993
- Vol. 73 (7) , 1251-1254
- https://doi.org/10.1016/0092-8674(93)90353-r
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- The cystic fibrosis mutation (ΔF508) does not influence the chloride channel activity of CFTRNature Genetics, 1993
- Identification of revertants for the cystic fibrosis ΔF508 mutation using STE6-CFTR chimeras in yeastCell, 1993
- Regulation by ATP and ADP of CFTR Chloride Channels That Contain Mutant Nucleotide-Binding DomainsScience, 1992
- Abnormal localization of cystic fibrosis transmembrane conductance regulator in primary cultures of cystic fibrosis airway epithelia.The Journal of cell biology, 1992
- Cystic fibrosis transmembrane conductance regulator: A chloride channel with novel regulationNeuron, 1992
- Mutations and sequence variations detected in the cystic fibrosis transmembrane conductance regulator (CFTR) gene: A report from the cystic fibrosis genetic analysis consortiumHuman Mutation, 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
- Defective acidification of intracellular organelles in cystic fibrosisNature, 1991
- Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNAScience, 1989