Activation of CFTR by genistein in human airway epithelial cell lines
- 29 July 2003
- journal article
- Published by Elsevier BV in Biochemical and Biophysical Research Communications
- Vol. 308 (3), 518-522
- https://doi.org/10.1016/s0006-291x(03)01436-0
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- The human DnaJ homologue (Hdj)-1/heat-shock protein (Hsp) 40 co-chaperone is required for the in vivo stabilization of the cystic fibrosis transmembrane conductance regulator by Hsp70Biochemical Journal, 2002
- The Hsc70 co-chaperone CHIP targets immature CFTR for proteasomal degradationNature, 2000
- Cystic Fibrosis F508del Patients Have Apically Localized CFTR in a Reduced Number of Airway CellsLaboratory Investigation, 2000
- ΔF508 CFTR protein expression in tissues from patients with cystic fibrosisJCI Insight, 1999
- The Hdj-2/Hsc70 chaperone pair facilitates early steps in CFTR biogenesisThe EMBO Journal, 1999
- The Molecular Chaperone Hsc70 Assists the in VitroFolding of the N-terminal Nucleotide-binding Domain of the Cystic Fibrosis Transmembrane Conductance RegulatorPublished by Elsevier BV ,1997
- Degradation of CFTR by the ubiquitin-proteasome pathwayCell, 1995
- The common variant of cystic fibrosis transmembrane conductance regulator is recognized by hsp70 and degraded in a pre-Golgi nonlysosomal compartment.Proceedings of the National Academy of Sciences of the United States of America, 1993
- Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosisCell, 1990
- Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNAScience, 1989