Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia
about
Rab11b 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.Binding of serum response factor to cystic fibrosis transmembrane conductance regulator CArG-like elements, as a new potential CFTR transcriptional regulation pathway.Membrane insertion, processing, and topology of cystic fibrosis transmembrane conductance regulator (CFTR) in microsomal membranesRegulation of CFTR chloride channels by syntaxin and Munc18 isoformsLung infections associated with cystic fibrosis.Enteric bacterial toxins: mechanisms of action and linkage to intestinal secretion.Impact 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 conductanImmunolocalization and regulation of cystic fibrosis transmembrane conductance regulator in the adult rat epididymis.Tissue and cellular expression patterns of porcine CFTR: similarities to and differences from human CFTRExpression of cystic fibrosis transmembrane conductance regulator in paracervical ganglia.The cystic fibrosis transmembrane conductance regulator (CFTR) is expressed in maturation stage ameloblasts, odontoblasts and bone cellsDeltaF508 CFTR protein expression in tissues from patients with cystic fibrosis.A PDZ-interacting domain in CFTR is an apical membrane polarization signal.Regulated Cl transport, K and Cl permeability, and exocytosis in T84 cells.Use of kinase inhibitors to correct ΔF508-CFTR function.Uroguanylin: structure and activity of a second endogenous peptide that stimulates intestinal guanylate cyclase.Syntaxin 3 is necessary for cAMP- and cGMP-regulated exocytosis of CFTR: implications for enterotoxigenic diarrhea.Molecular analysis of the ovine cystic fibrosis transmembrane conductance regulator gene.Insulin-like growth factor 1 (IGF-1) enhances the protein expression of CFTR.Role of mutant CFTR in hypersusceptibility of cystic fibrosis patients to lung infections.Transfer of a constitutive viral promoter-cystic fibrosis transmembrane conductance regulator cDNA to human epithelial cells conveys resistance to down-regulation of cAMP-regulated Cl- secretion in the presence of inflammatory stimuli.CFTR!CFTR and differentiation markers expression in non-CF and delta F 508 homozygous CF nasal epithelium.Defective regulatory volume decrease in human cystic fibrosis tracheal cells because of altered regulation of intermediate conductance Ca2+-dependent potassium channelsEndocytic trafficking of CFTR in health and disease.CFTR mediates bicarbonate-dependent activation of miR-125b in preimplantation embryo development.In vivo analysis of DNase I hypersensitive sites in the human CFTR gene.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 membraneAbnormal localization of cystic fibrosis transmembrane conductance regulator in primary cultures of cystic fibrosis airway epitheliaProtein phosphatase 2C dephosphorylates and inactivates cystic fibrosis transmembrane conductance regulatorCystic Fibrosis Transmembrane Conductance Regulator in Sarcoplasmic Reticulum of Airway Smooth Muscle. Implications for Airway ContractilityDisruption of the CFTR gene produces a model of cystic fibrosis in newborn pigs.Three-dimensional reconstruction of human cystic fibrosis transmembrane conductance regulator chloride channel revealed an ellipsoidal structure with orifices beneath the putative transmembrane domainExtracellular nucleotides inhibit oxalate transport by human intestinal Caco-2-BBe cells through PKC-δ activation.Expression of Cystic Fibrosis Transmembrane Conductance Regulator in Ganglia of Human Gastrointestinal TractPathogenesis of human enterovirulent bacteria: lessons from cultured, fully differentiated human colon cancer cell linesLiddle's syndrome mutations disrupt cAMP-mediated translocation of the epithelial Na(+) channel to the cell surfaceStructural cues involved in endoplasmic reticulum degradation of G85E and G91R mutant cystic fibrosis transmembrane conductance regulator.Vasoactive intestinal peptide, forskolin, and genistein increase apical CFTR trafficking in the rectal gland of the spiny dogfish, Squalus acanthias. Acute regulation of CFTR trafficking in an intact epithelium.
P2860
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P2860
Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
Localization of cystic fibrosi ...... n chloride secretory epithelia
@ast
Localization of cystic fibrosi ...... n chloride secretory epithelia
@en
type
label
Localization of cystic fibrosi ...... n chloride secretory epithelia
@ast
Localization of cystic fibrosi ...... n chloride secretory epithelia
@en
prefLabel
Localization of cystic fibrosi ...... n chloride secretory epithelia
@ast
Localization of cystic fibrosi ...... n chloride secretory epithelia
@en
P2093
P2860
P356
P1476
Localization of cystic fibrosi ...... n chloride secretory epithelia
@en
P2093
G M Denning
L S Ostedgaard
P2860
P304
P356
10.1172/JCI115582
P407
P577
1992-01-01T00:00:00Z