Participation of the endoplasmic reticulum chaperone calnexin (p88, IP90) in the biogenesis of the cystic fibrosis transmembrane conductance regulator
about
Mechanisms of CFTR Folding at the Endoplasmic ReticulumMolecular Chaperones as Targets to Circumvent the CFTR Defect in Cystic FibrosisMechanisms of pharmacological rescue of trafficking-defective hERG mutant channels in human long QT syndromePerturbation of Hsp90 interaction with nascent CFTR prevents its maturation and accelerates its degradation by the proteasomeThe Hdj-2/Hsc70 chaperone pair facilitates early steps in CFTR biogenesisThe human DnaJ homologue (Hdj)-1/heat-shock protein (Hsp) 40 co-chaperone is required for the in vivo stabilization of the cystic fibrosis transmembrane conductance regulator by Hsp70Interactions between newly synthesized glycoproteins, calnexin and a network of resident chaperones in the endoplasmic reticulumThe PEST sequence does not contribute to the stability of the cystic fibrosis transmembrane conductance regulatorThe delicate balance between secreted protein folding and endoplasmic reticulum-associated degradation in human physiologyTraffic-independent function of the Sar1p/COPII machinery in proteasomal sorting of the cystic fibrosis transmembrane conductance regulatorDistinct roles for the Hsp40 and Hsp90 molecular chaperones during cystic fibrosis transmembrane conductance regulator degradation in yeast.A systematic search for endoplasmic reticulum (ER) membrane-associated RING finger proteins identifies Nixin/ZNRF4 as a regulator of calnexin stability and ER homeostasisBiosynthesis of inositol trisphosphate receptors: selective association with the molecular chaperone calnexinThe endoplasmic reticulum-associated Hsp40 DNAJB12 and Hsc70 cooperate to facilitate RMA1 E3-dependent degradation of nascent CFTRDeltaF508Development of CFTR StructureActivation of chloride transport in CF airway epithelial cell lines and primary CF nasal epithelial cells by S-nitrosoglutathione.Additive effect of multiple pharmacological chaperones on maturation of CFTR processing mutantsNovel pharmacologic therapies for cystic fibrosisSyntaxin 1A inhibits CFTR chloride channels by means of domain-specific protein-protein interactionsEnhancing the Potency of F508del Correction: A Multi-Layer Combinational Approach to Drug Discovery for Cystic Fibrosis.Cystic fibrosis as a disease of misprocessing of the cystic fibrosis transmembrane conductance regulator glycoproteinCD4 glycoprotein degradation induced by human immunodeficiency virus type 1 Vpu protein requires the function of proteasomes and the ubiquitin-conjugating pathwayMost F508del-CFTR is targeted to degradation at an early folding checkpoint and independently of calnexinDeltaF508 CFTR protein expression in tissues from patients with cystic fibrosis.Molecular characterization of neurally expressing genes in the para sodium channel gene cluster of drosophila.Quality control of transmembrane domain assembly in the tetraspanin CD82Cystic fibrosis transmembrane conductance regulator degradation: cross-talk between the ubiquitylation and SUMOylation pathways.HIV-1 protein Nef inhibits activity of ATP-binding cassette transporter A1 by targeting endoplasmic reticulum chaperone calnexinEmergent properties of proteostasis in managing cystic fibrosis.Rescuing protein conformation: prospects for pharmacological therapy in cystic fibrosisERp29 regulates DeltaF508 and wild-type cystic fibrosis transmembrane conductance regulator (CFTR) trafficking to the plasma membrane in cystic fibrosis (CF) and non-CF epithelial cells.4-Phenylbutyrate stimulates Hsp70 expression through the Elp2 component of elongator and STAT-3 in cystic fibrosis epithelial cellsSmall heat-shock proteins select deltaF508-CFTR for endoplasmic reticulum-associated degradation.Selective up-regulation of chemokine IL-8 expression in cystic fibrosis bronchial gland cells in vivo and in vitroDelta F508 CFTR pool in the endoplasmic reticulum is increased by calnexin overexpression.Peptide-based interactions with calnexin target misassembled membrane proteins into endoplasmic reticulum-derived multilamellar bodies.Interaction Between HIV-1 Nef and Calnexin: From Modeling to Small Molecule Inhibitors Reversing HIV-Induced Lipid Accumulation.Assembly of ER-associated protein degradation in vitro: dependence on cytosol, calnexin, and ATP.An endoplasmic reticulum storage disease causing congenital goiter with hypothyroidism.The organization of endoplasmic reticulum export complexes.
P2860
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P2860
Participation of the endoplasmic reticulum chaperone calnexin (p88, IP90) in the biogenesis of the cystic fibrosis transmembrane conductance regulator
description
1994 nî lūn-bûn
@nan
1994 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի ապրիլին 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
Participation of the endoplasm ...... membrane conductance regulator
@ast
Participation of the endoplasm ...... membrane conductance regulator
@en
Participation of the endoplasm ...... membrane conductance regulator
@nl
type
label
Participation of the endoplasm ...... membrane conductance regulator
@ast
Participation of the endoplasm ...... membrane conductance regulator
@en
Participation of the endoplasm ...... membrane conductance regulator
@nl
prefLabel
Participation of the endoplasm ...... membrane conductance regulator
@ast
Participation of the endoplasm ...... membrane conductance regulator
@en
Participation of the endoplasm ...... membrane conductance regulator
@nl
P2093
P921
P1476
Participation of the endoplasm ...... membrane conductance regulator
@en
P2093
P304
P407
P577
1994-04-29T00:00:00Z