The cystic fibrosis transmembrane conductance regulator activates aquaporin 3 in airway epithelial cells.
about
Inhibition of cystic fibrosis transmembrane conductance regulator by novel interaction with the metabolic sensor AMP-activated protein kinaseAquaporins in development -- a reviewPulmonary epithelial barrier function: some new players and mechanismsCFTR in cystic fibrosis and cholera: from membrane transport to clinical practiceMolecular identification and physiological roles of parotid acinar cell maxi-K channelsAquaporin-9 is expressed in rat Sertoli cells and interacts with the cystic fibrosis transmembrane conductance regulatorLung infections associated with cystic fibrosis.Osmotic water permeabilities of cultured, well-differentiated normal and cystic fibrosis airway epitheliaAquaporin 3, a glycerol and water transporter, is regulated by p73 of the p53 family.Yet another role for the cystic fibrosis transmembrane conductance regulator.Structure and function of aquaporin water channels.Receptor-mediated glutamate release from volume sensitive channels in astrocytes.Man Is not a rodent: aquaporins in the airways.CFTR chloride channel in the apical compartments: spatiotemporal coupling to its interacting partners.Co action of CFTR and AQP1 increases permeability of peritoneal epithelial cells on estrogen-induced ovarian hyper stimulation syndrome.Electrolyte transport in the mammalian colon: mechanisms and implications for disease.Open chromatin mapping identifies transcriptional networks regulating human epididymis epithelial function.Aquaporins: multiple roles in the central nervous system.Aquaporin water channels--from atomic structure to clinical medicine.Amazing chloride channels: an overview.Gene expression profiling of laser microdissected airway smooth muscle tissue in asthma and atopy.Analysis of CFTR interactome in the macromolecular complexes.Growth deficits in cystic fibrosis mice begin in utero prior to IGF-1 reduction.Local modulation of cystic fibrosis conductance regulator: cytoskeleton and compartmentalized cAMP signalling.Cutaneous manifestations of cystic fibrosis.Role of CFTR in epithelial physiology.In vitro analysis of PDZ-dependent CFTR macromolecular signaling complexes.The water permeability of Arabidopsis plasma membrane is regulated by divalent cations and pH.Expression of cystic fibrosis transmembrane conductance regulator in rat efferent duct epithelium.Visualization of ATP release in pancreatic acini in response to cholinergic stimulus. Use of fluorescent probes and confocal microscopy.Synergistic effects of cystic fibrosis transmembrane conductance regulator and aquaporin-9 in the rat epididymis.Immunohystochemical analysis of CFTR in normal and disrupted spermatogenesis.High prevalence of aquagenic wrinkling of the palms in patients with cystic fibrosis and association with measurable increases in transepidermal water loss.Aquaporin 3 cloned from Xenopus laevis is regulated by the cystic fibrosis transmembrane conductance regulator.Evaluation of MRP1-5 gene expression in cystic fibrosis patients homozygous for the delta F508 mutation.Secretion and cell volume regulation by salivary acinar cells from mice lacking expression of the Clcn3 Cl- channel gene.The Importance of Aquaporin 1 in Pancreatitis and Its Relation to the CFTR Cl Channel
P2860
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P2860
The cystic fibrosis transmembrane conductance regulator activates aquaporin 3 in airway epithelial cells.
description
1999 nî lūn-bûn
@nan
1999 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
The cystic fibrosis transmembr ...... 3 in airway epithelial cells.
@ast
The cystic fibrosis transmembr ...... 3 in airway epithelial cells.
@en
type
label
The cystic fibrosis transmembr ...... 3 in airway epithelial cells.
@ast
The cystic fibrosis transmembr ...... 3 in airway epithelial cells.
@en
prefLabel
The cystic fibrosis transmembr ...... 3 in airway epithelial cells.
@ast
The cystic fibrosis transmembr ...... 3 in airway epithelial cells.
@en
P2093
P2860
P356
P1476
The cystic fibrosis transmembr ...... 3 in airway epithelial cells.
@en
P2093
Kunzelmann K
Nitschke R
Schreiber R
P2860
P304
11811-11816
P356
10.1074/JBC.274.17.11811
P407
P577
1999-04-01T00:00:00Z