Regulation of the cystic fibrosis transmembrane conductance regulator anion channel by tyrosine phosphorylation
Author:
Publisher
Wiley
Subject
Genetics,Molecular Biology,Biochemistry,Biotechnology
Reference49 articles.
1. The First Nucleotide Binding Domain of Cystic Fibrosis Transmembrane Conductance Regulator Is a Site of Stable Nucleotide Interaction, whereas the Second Is a Site of Rapid Turnover
2. Prolonged Nonhydrolytic Interaction of Nucleotide with CFTR's NH2-terminal Nucleotide Binding Domain and its Role in Channel Gating
3. Regulatory R region of the CFTR chloride channel is a dynamic integrator of phospho-dependent intra- and intermolecular interactions
4. Regulation of Channel Gating by AMP-activated Protein Kinase Modulates Cystic Fibrosis Transmembrane Conductance Regulator Activity in Lung Submucosal Cells
5. LMTK2-mediated Phosphorylation Regulates CFTR Endocytosis in Human Airway Epithelial Cells
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3. Cross‐talk between CFTR and sphingolipids in cystic fibrosis;FEBS Open Bio;2023-06-22
4. Revisiting CFTR Interactions: Old Partners and New Players;International Journal of Molecular Sciences;2021-12-07
5. Cystic Fibrosis: Systems Biology Analysis from Homozygous p.Phe508del Variant Patients’ Samples Reveals Perturbations in Tissue-Specific Pathways;BioMed Research International;2021-12-02
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