CFTR chloride channel in the apical compartments: spatiotemporal coupling to its interacting partners.
about
An association study on contrasting cystic fibrosis endophenotypes recognizes KRT8 but not KRT18 as a modifier of cystic fibrosis disease severity and CFTR mediated residual chloride secretionEpithelial sodium channels (ENaC) are uniformly distributed on motile cilia in the oviduct and the respiratory airwaysEmerging role of cystic fibrosis transmembrane conductance regulator - an epithelial chloride channel in gastrointestinal cancersCompartmentalized accumulation of cAMP near complexes of multidrug resistance protein 4 (MRP4) and cystic fibrosis transmembrane conductance regulator (CFTR) contributes to drug-induced diarrhea.Structural insights into PDZ-mediated interaction of NHERF2 and LPA2, a cellular event implicated in CFTR channel regulationFunctional regulation of cystic fibrosis transmembrane conductance regulator-containing macromolecular complexes: a small-molecule inhibitor approachCFTR and TNR-CFTR expression and function in the kidney.Stabilizing rescued surface-localized δf508 CFTR by potentiation of its interaction with Na(+)/H(+) exchanger regulatory factor 1.Lumacaftor/ivacaftor combination for cystic fibrosis patients homozygous for Phe508del-CFTR.Targeting the regulation of CFTR channels.Hypertension-linked mutation of α-adducin increases CFTR surface expression and activity in HEK and cultured rat distal convoluted tubule cells.Apical CFTR expression in human nasal epithelium correlates with lung disease in cystic fibrosis.Serum and glucocorticoid-inducible kinase1 increases plasma membrane wt-CFTR in human airway epithelial cells by inhibiting its endocytic retrieval.Analysis of CFTR interactome in the macromolecular complexes.A chemokine receptor CXCR2 macromolecular complex regulates neutrophil functions in inflammatory diseasesCFTR regulation in human airway epithelial cells requires integrity of the actin cytoskeleton and compartmentalized cAMP and PKA activity.Prolactin and dexamethasone regulate second messenger-stimulated cl(-) secretion in mammary epitheliaDrug-induced secretory diarrhea: A role for CFTR.CFTR mutations altering CFTR fragmentation.CXCR2 macromolecular complex in pancreatic cancer: a potential therapeutic target in tumor growthLocal modulation of cystic fibrosis conductance regulator: cytoskeleton and compartmentalized cAMP signalling.MAST205 competes with cystic fibrosis transmembrane conductance regulator (CFTR)-associated ligand for binding to CFTR to regulate CFTR-mediated fluid transportThe adenosine A2B receptor is involved in anion secretion in human pancreatic duct Capan-1 epithelial cells.H2O2 stimulates cystic fibrosis transmembrane conductance regulator through an autocrine prostaglandin pathway, using multidrug-resistant protein-4MARCH2 regulates autophagy by promoting CFTR ubiquitination and degradation and PIK3CA-AKT-MTOR signalingMechanosensitive signalling in fish gill and other ion transporting epithelia.IRBIT: it is everywhere.The cystic fibrosis transmembrane conductance regulator's expanding SNARE interactome.Molecular regulation of lumen morphogenesis.Recent advances and new perspectives in targeting CFTR for therapy of cystic fibrosis and enterotoxin-induced secretory diarrheas.Förster resonance energy transfer - an approach to visualize the spatiotemporal regulation of macromolecular complex formation and compartmentalized cell signalingCongenital diarrhoeal disorders: advances in this evolving web of inherited enteropathies.Altered cGMP dynamics at the plasma membrane contribute to diarrhea in ulcerative colitis.Current insights into the role of PKA phosphorylation in CFTR channel activity and the pharmacological rescue of cystic fibrosis disease-causing mutants.Possible Recovery of Manifestation of Prolactin Receptor and Some of Its Target Proteins in the Liver and Kidney Cells of Female Rats after Relief of Cholestasis Complicated and Not Complicated by Hyperprolactinemia.Pseudohalide anions reveal a novel extracellular site for potentiators to increase CFTR function.Localization of cystic fibrosis transmembrane conductance regulator signaling complexes in human salivary gland striated duct cells.CFTR is a mechanosensitive anion channel: a real stretch?In vitro analysis of PDZ-dependent CFTR macromolecular signaling complexes.CFTR-NHERF2-LPA₂ Complex in the Airway and Gut Epithelia.
P2860
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P2860
CFTR chloride channel in the apical compartments: spatiotemporal coupling to its interacting partners.
description
2010 nî lūn-bûn
@nan
2010 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի մարտին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
CFTR chloride channel in the a ...... g to its interacting partners.
@ast
CFTR chloride channel in the a ...... g to its interacting partners.
@en
CFTR chloride channel in the a ...... g to its interacting partners.
@nl
type
label
CFTR chloride channel in the a ...... g to its interacting partners.
@ast
CFTR chloride channel in the a ...... g to its interacting partners.
@en
CFTR chloride channel in the a ...... g to its interacting partners.
@nl
prefLabel
CFTR chloride channel in the a ...... g to its interacting partners.
@ast
CFTR chloride channel in the a ...... g to its interacting partners.
@en
CFTR chloride channel in the a ...... g to its interacting partners.
@nl
P2860
P356
P1433
P1476
CFTR chloride channel in the a ...... g to its interacting partners.
@en
P2093
Anjaparavanda P Naren
Chunying Li
P2860
P304
P356
10.1039/B924455G
P577
2010-03-05T00:00:00Z