Constitutive internalization of cystic fibrosis transmembrane conductance regulator occurs via clathrin-dependent endocytosis and is regulated by protein phosphorylation.
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Myosin VI regulates endocytosis of the cystic fibrosis transmembrane conductance regulatorMyosin Vb is required for trafficking of the cystic fibrosis transmembrane conductance regulator in Rab11a-specific apical recycling endosomes in polarized human airway epithelial cellsChemotoxicity of doxorubicin and surface expression of P-glycoprotein (MDR1) is regulated by the Pseudomonas aeruginosa toxin CifThe subcellular localization of an aquaporin-2 tetramer depends on the stoichiometry of phosphorylated and nonphosphorylated monomers.Modulation of mature cystic fibrosis transmembrane regulator protein by the PDZ domain protein CALcAMP-dependent protein kinase A and the dynamics of epithelial cell surface domains: moving membranes to keep in shapeRegulation of cystic fibrosis transmembrane regulator trafficking and protein expression by a Rho family small GTPase TC10Multiple endocytic signals in the C-terminal tail of the cystic fibrosis transmembrane conductance regulatorPseudomonas aeruginosa inhibits endocytic recycling of CFTR in polarized human airway epithelial cellsSTa and cGMP stimulate CFTR translocation to the surface of villus enterocytes in rat jejunum and is regulated by protein kinase GUnconventional EGF-induced ERK1/2-mediated Kv1.3 endocytosisLMTK2-mediated phosphorylation regulates CFTR endocytosis in human airway epithelial cells.Dynamin2, clathrin, and lipid rafts mediate endocytosis of the apical Na/K/2Cl cotransporter NKCC2 in thick ascending limbs.Membrane lateral diffusion and capture of CFTR within transient confinement zones.Monomeric CFTR in plasma membranes in live cells revealed by single molecule fluorescence imaging.Modulation of endocytic trafficking and apical stability of CFTR in primary human airway epithelial culturesSerum- and glucocorticoid-induced protein kinase 1 (SGK1) increases the cystic fibrosis transmembrane conductance regulator (CFTR) in airway epithelial cells by phosphorylating Shank2E protein.Bacterial Sphingomyelinase is a State-Dependent Inhibitor of the Cystic Fibrosis Transmembrane conductance Regulator (CFTR)Endocytic trafficking routes of wild type and DeltaF508 cystic fibrosis transmembrane conductance regulatorListeria monocytogenes exploits cystic fibrosis transmembrane conductance regulator (CFTR) to escape the phagosome.Adaptor and clathrin exchange at the plasma membrane and trans-Golgi network.Direct interaction with filamins modulates the stability and plasma membrane expression of CFTR.Disabled-2 protein facilitates assembly polypeptide-2-independent recruitment of cystic fibrosis transmembrane conductance regulator to endocytic vesicles in polarized human airway epithelial cellsEndocytic trafficking of CFTR in health and disease.COOH-terminal truncations promote proteasome-dependent degradation of mature cystic fibrosis transmembrane conductance regulator from post-Golgi compartments.Tissue-specific control of CFTR endocytosis by Dab2: Cargo recruitment as a therapeutic target.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 membranec-Cbl reduces stability of rescued ∆F508-CFTR in human airway epithelial cells: Implications for cystic fibrosis treatment.Local modulation of cystic fibrosis conductance regulator: cytoskeleton and compartmentalized cAMP signalling.Regulated recycling of mutant CFTR is partially restored by pharmacological treatment.Imaging CFTR in its native environment.Moderate intensity exercise mediates comparable increases in exhaled chloride as albuterol in individuals with cystic fibrosis.Rescue of DeltaF508-CFTR by the SGK1/Nedd4-2 signaling pathwayExhaled breath condensate detects baseline reductions in chloride and increases in response to albuterol in cystic fibrosis patients.Repairing the basic defect in cystic fibrosis - one approach is not enough.Trafficking and function of the cystic fibrosis transmembrane conductance regulator: a complex network of posttranslational modifications.CFTR Folding Consortium: methods available for studies of CFTR folding and correctionVIP-dependent increase in F508del-CFTR membrane localization is mediated by PKCε.The short apical membrane half-life of rescued {Delta}F508-cystic fibrosis transmembrane conductance regulator (CFTR) results from accelerated endocytosis of {Delta}F508-CFTR in polarized human airway epithelial cells.Internalization of swine vesicular disease virus into cultured cells: a comparative study with foot-and-mouth disease virus.
P2860
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P2860
Constitutive internalization of cystic fibrosis transmembrane conductance regulator occurs via clathrin-dependent endocytosis and is regulated by protein phosphorylation.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
Constitutive internalization o ...... ed by protein phosphorylation.
@en
type
label
Constitutive internalization o ...... ed by protein phosphorylation.
@en
prefLabel
Constitutive internalization o ...... ed by protein phosphorylation.
@en
P2093
P2860
P921
P356
P1433
P1476
Constitutive internalization o ...... ed by protein phosphorylation.
@en
P2093
P2860
P304
P356
10.1042/BJ3280353
P407
P478
328 ( Pt 2)
P577
1997-12-01T00:00:00Z