Rapid endocytosis of the cystic fibrosis transmembrane conductance regulator chloride channel.
about
Ca2+-calmodulin-dependent myosin light chain kinase is essential for activation of TRPC5 channels expressed in HEK293 cellsMyosin VI regulates endocytosis of the cystic fibrosis transmembrane conductance regulatorRab11b regulates the apical recycling of the cystic fibrosis transmembrane conductance regulator in polarized intestinal epithelial cellsCFTR chloride channels are regulated by a SNAP-23/syntaxin 1A complex.Chemotoxicity of doxorubicin and surface expression of P-glycoprotein (MDR1) is regulated by the Pseudomonas aeruginosa toxin CifGlycosylation and the cystic fibrosis transmembrane conductance regulatorInvolvement of the Cdc42 pathway in CFTR post-translational turnover and in its plasma membrane stability in airway epithelial cellsImpact of heterogeneity within cultured cells on bacterial invasion: analysis of Pseudomonas aeruginosa and Salmonella enterica serovar typhi entry into MDCK cells by using a green fluorescent protein-labelled cystic fibrosis transmembrane conductanQuantitation of plasma membrane expression of a fusion protein of Na/H exchanger NHE3 and green fluorescence protein (GFP) in living PS120 fibroblasts.Cystic fibrosis as a disease of misprocessing of the cystic fibrosis transmembrane conductance regulator glycoproteinCystic fibrosis: exploiting its genetic basis in the hunt for new therapiesModulation of endocytic trafficking and apical stability of CFTR in primary human airway epithelial culturesRole for the ubiquitin-proteasome system in the vacuolar degradation of Ste6p, the a-factor transporter in Saccharomyces cerevisiaeDeltaF508 CFTR protein expression in tissues from patients with cystic fibrosis.Endocytic trafficking routes of wild type and DeltaF508 cystic fibrosis transmembrane conductance regulatorSyntaxin 3 is necessary for cAMP- and cGMP-regulated exocytosis of CFTR: implications for enterotoxigenic diarrhea.Biophysical characterisation of calumenin as a charged F508del-CFTR folding modulatorA stable human-cell system overexpressing cystic fibrosis transmembrane conductance regulator recombinant protein at the cell surfaceDirect interaction with filamins modulates the stability and plasma membrane expression of CFTR.Ammonia inhibits cAMP-regulated intestinal Cl- transport. Asymmetric effects of apical and basolateral exposure and implications for epithelial barrier function.Cystic fibrosis mice carrying the missense mutation G551D replicate human genotype-phenotype correlations.Endocytic trafficking of CFTR in health and disease.Comparative processing and function of human and ferret cystic fibrosis transmembrane conductance regulator.COOH-terminal truncations promote proteasome-dependent degradation of mature cystic fibrosis transmembrane conductance regulator from post-Golgi compartments.CFTR: covalent modification of cysteine-substituted channels expressed in Xenopus oocytes shows that activation is due to the opening of channels resident in the plasma membraneRegulated recycling of mutant CFTR is partially restored by pharmacological treatment.Role of Fyn and PI3K in H2O2-induced inhibition of apical Cl-/OH- exchange activity in human intestinal epithelial cellsCystic fibrosis transmembrane conductance regulator activation stimulates endosome fusion in vivoA delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo.Expression and distribution of cystic fibrosis transmembrane conductance regulator in neurons of the human brain.Cystic fibrosis transmembrane conductance regulator-mediated corneal epithelial cell ingestion of Pseudomonas aeruginosa is a key component in the pathogenesis of experimental murine keratitisVIP-dependent increase in F508del-CFTR membrane localization is mediated by PKCε.Effect of Annexin A5 on CFTR: regulated traffic or scaffolding?Role of calpain in the regulation of CFTR (cystic fibrosis transmembrane conductance regulator) turnover.Homeostatic regulation of Kv1.2 potassium channel trafficking by cyclic AMP.Nitric oxide inhibits cAMP-dependent CFTR trafficking in intestinal epithelial cells.Molecular assembly of cystic fibrosis transmembrane conductance regulator in plasma membrane.Normalization of intracellular Ca(2+) induces a glucose-responsive state in glucose-unresponsive beta-cells.Molecular cloning and characterization of an intracellular chloride channel in the proximal tubule cell line, LLC-PK1.Cystic fibrosis F508del patients have apically localized CFTR in a reduced number of airway cells.
P2860
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P2860
Rapid endocytosis of the cystic fibrosis transmembrane conductance regulator chloride channel.
description
1994 nî lūn-bûn
@nan
1994 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
Rapid endocytosis of the cysti ...... ce regulator chloride channel.
@ast
Rapid endocytosis of the cysti ...... ce regulator chloride channel.
@en
type
label
Rapid endocytosis of the cysti ...... ce regulator chloride channel.
@ast
Rapid endocytosis of the cysti ...... ce regulator chloride channel.
@en
prefLabel
Rapid endocytosis of the cysti ...... ce regulator chloride channel.
@ast
Rapid endocytosis of the cysti ...... ce regulator chloride channel.
@en
P2093
P2860
P356
P1476
Rapid endocytosis of the cysti ...... ce regulator chloride channel.
@en
P2093
Marchase RB
Workman RB Jr
P2860
P304
P356
10.1073/PNAS.91.11.5192
P407
P577
1994-05-01T00:00:00Z