Modulation of mature cystic fibrosis transmembrane regulator protein by the PDZ domain protein CAL
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Computational design of a PDZ domain peptide inhibitor that rescues CFTR activityIsoform-specific regulation and localization of the coxsackie and adenovirus receptor in human airway epitheliaSolution structure of GOPC PDZ domain and its interaction with the C-terminal motif of neuroliginRole of PDZ proteins in regulating trafficking, signaling, and function of GPCRs: means, motif, and opportunityIsoform-specific interaction of golgin-160 with the Golgi-associated protein PISTRegulation of cystic fibrosis transmembrane regulator trafficking and protein expression by a Rho family small GTPase TC10Myotonia congenita mutation enhances the degradation of human CLC-1 chloride channelsCarbachol-induced MUC17 endocytosis is concomitant with NHE3 internalization and CFTR membrane recruitment in enterocytesMechanistic Approaches to Improve Correction of the Most Common Disease-Causing Mutation in Cystic FibrosisCytosolic COOH terminus of the peptide transporter PEPT2 is involved in apical membrane localization of the protein.De novo biosynthetic profiling of high abundance proteins in cystic fibrosis lung epithelial cells.Serum- and glucocorticoid-induced protein kinase 1 (SGK1) increases the cystic fibrosis transmembrane conductance regulator (CFTR) in airway epithelial cells by phosphorylating Shank2E protein.Syntaxin 6 and CAL mediate the degradation of the cystic fibrosis transmembrane conductance regulator.Bacterial Sphingomyelinase is a State-Dependent Inhibitor of the Cystic Fibrosis Transmembrane conductance Regulator (CFTR)Targeting the regulation of CFTR channels.CFTR chloride channel in the apical compartments: spatiotemporal coupling to its interacting partners.Ubiquitination and degradation of CFTR by the E3 ubiquitin ligase MARCH2 through its association with adaptor proteins CAL and STX6The mucus and mucins of the goblet cells and enterocytes provide the first defense line of the gastrointestinal tract and interact with the immune system.Sorting nexin 27 regulates basal and stimulated brush border trafficking of NHE3.Macromolecular interactions and ion transport in cystic fibrosis.Rescuing Trafficking Mutants of the ATP-binding Cassette Protein, ABCA4, with Small Molecule Correctors as a Treatment for Stargardt Eye Disease.PDZ proteins retain and regulate membrane transporters in polarized epithelial cell membranes.Endoproteolytic cleavage of TUG protein regulates GLUT4 glucose transporter translocationNHERF family and NHE3 regulation.The emerging role of PDZ adapter proteins for regulation of intestinal ion transport.Role of Exchange Protein Activated by cAMP 1 in Regulating Rates of Microtubule Formation in Cystic Fibrosis Epithelial Cells.Inorganic phosphate modulates the expression of the NaPi-2a transporter in the trans-Golgi network and the interaction with PIST in the proximal tubule.MAST205 competes with cystic fibrosis transmembrane conductance regulator (CFTR)-associated ligand for binding to CFTR to regulate CFTR-mediated fluid transportMonitoring protein-protein interactions between the mammalian integral membrane transporters and PDZ-interacting partners using a modified split-ubiquitin membrane yeast two-hybrid systemLocalization studies of rare missense mutations in cystic fibrosis transmembrane conductance regulator (CFTR) facilitate interpretation of genotype-phenotype relationships.Autophagy and innate immunity: triggering, targeting and tuningThe cystic fibrosis transmembrane conductance regulator's expanding SNARE interactome.A proteolytic pathway that controls glucose uptake in fat and muscle.Repairing the basic defect in cystic fibrosis - one approach is not enough.From the endoplasmic reticulum to the plasma membrane: mechanisms of CFTR folding and trafficking.Regulation of Transporters and Channels by Membrane-Trafficking Complexes in Epithelial Cells.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.Scaffolding protein GOPC regulates tight junction structure.NHE-RF1 protein rescues DeltaF508-CFTR function.Targeting CAL as a negative regulator of DeltaF508-CFTR cell-surface expression: an RNA interference and structure-based mutagenetic approach.
P2860
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P2860
Modulation of mature cystic fibrosis transmembrane regulator protein by the PDZ domain protein CAL
description
2004 nî lūn-bûn
@nan
2004 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Modulation of mature cystic fi ...... by the PDZ domain protein CAL
@ast
Modulation of mature cystic fi ...... by the PDZ domain protein CAL
@en
Modulation of mature cystic fi ...... by the PDZ domain protein CAL
@nl
type
label
Modulation of mature cystic fi ...... by the PDZ domain protein CAL
@ast
Modulation of mature cystic fi ...... by the PDZ domain protein CAL
@en
Modulation of mature cystic fi ...... by the PDZ domain protein CAL
@nl
prefLabel
Modulation of mature cystic fi ...... by the PDZ domain protein CAL
@ast
Modulation of mature cystic fi ...... by the PDZ domain protein CAL
@en
Modulation of mature cystic fi ...... by the PDZ domain protein CAL
@nl
P2093
P2860
P3181
P356
P1476
Modulation of mature cystic fi ...... by the PDZ domain protein CAL
@en
P2093
William B Guggino
P2860
P304
P3181
P356
10.1074/JBC.M308640200
P407
P577
2004-01-16T00:00:00Z