CFTR regulation in human airway epithelial cells requires integrity of the actin cytoskeleton and compartmentalized cAMP and PKA activity.
about
Decoding F508del misfolding in cystic fibrosis.The dual phosphodiesterase 3 and 4 inhibitor RPL554 stimulates CFTR and ciliary beating in primary cultures of bronchial epithelia.Hypertension-linked mutation of α-adducin increases CFTR surface expression and activity in HEK and cultured rat distal convoluted tubule cells.Soluble adenylyl cyclase in health and disease.A soluble adenylyl cyclase form targets to axonemes and rescues beat regulation in soluble adenylyl cyclase knockout micePKA and PDE4D3 anchoring to AKAP9 provides distinct regulation of cAMP signals at the centrosome.Local modulation of cystic fibrosis conductance regulator: cytoskeleton and compartmentalized cAMP signalling.The Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Uses its C-Terminus to Regulate the A2B Adenosine ReceptorAnchored PDE4 regulates chloride conductance in wild-type and ΔF508-CFTR human airway epithelia.Functional Rescue of F508del-CFTR Using Small Molecule CorrectorsStructural changes of CFTR R region upon phosphorylation: a plastic platform for intramolecular and intermolecular interactions.The secret life of CFTR as a calcium-activated chloride channel.Multiple facets of cAMP signalling and physiological impact: cAMP compartmentalization in the lung.Proteome of the porosome complex in human airway epithelia: interaction with the cystic fibrosis transmembrane conductance regulator (CFTR).Repairing the basic defect in cystic fibrosis - one approach is not enough.Current insights into the role of PKA phosphorylation in CFTR channel activity and the pharmacological rescue of cystic fibrosis disease-causing mutants.Pseudomonas aeruginosa reduces the expression of CFTR via post-translational modification of NHERF1.Proteomic and ionomic profiling reveals significant alterations of protein expression and calcium homeostasis in cystic fibrosis cells.Novel role of cystic fibrosis transmembrane conductance regulator in maintaining adult mouse olfactory neuronal homeostasis.Cigarette smoke activates CFTR through ROS-stimulated cAMP signaling in human bronchial epithelial cells.A sequence upstream of canonical PDZ-binding motif within CFTR COOH-terminus enhances NHERF1 interaction.Recent Progress in CFTR Interactome Mapping and Its Importance for Cystic Fibrosis.Gap Junctions Are Involved in the Rescue of CFTR-Dependent Chloride Efflux by Amniotic Mesenchymal Stem Cells in Coculture with Cystic Fibrosis CFBE41o- Cells.The dopamine D1 receptor is expressed and induces CREB phosphorylation and MUC5AC expression in human airway epithelium.
P2860
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P2860
CFTR regulation in human airway epithelial cells requires integrity of the actin cytoskeleton and compartmentalized cAMP and PKA activity.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
CFTR regulation in human airwa ...... talized cAMP and PKA activity.
@ast
CFTR regulation in human airwa ...... talized cAMP and PKA activity.
@en
type
label
CFTR regulation in human airwa ...... talized cAMP and PKA activity.
@ast
CFTR regulation in human airwa ...... talized cAMP and PKA activity.
@en
prefLabel
CFTR regulation in human airwa ...... talized cAMP and PKA activity.
@ast
CFTR regulation in human airwa ...... talized cAMP and PKA activity.
@en
P2093
P2860
P50
P356
P1476
CFTR regulation in human airwa ...... talized cAMP and PKA activity.
@en
P2093
Maria Favia
Rosa A Cardone
Stefania Monterisi
P2860
P304
P356
10.1242/JCS.089086
P407
P577
2012-02-02T00:00:00Z