(Q40702111)

22 September 2017

title

S-Nitrosoglutathione induces functional DeltaF508-CFTR in airway epithelial cells (English)

1 reference

22 September 2017

Charlotte Andersson

1

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22 September 2017

Benjamin Gaston

series ordinal

2

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22 September 2017

Godfried M Roomans

series ordinal

3

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22 September 2017

publication date

1 September 2002

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Biochemical and Biophysical Research Communications

22 September 2017

published in

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22 September 2017

volume

297

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22 September 2017

issue

3

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22 September 2017

page(s)

552-557

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Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

22 September 2017

cites work

1 reference

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Conformational maturation of CFTR but not its mutant counterpart (delta F508) occurs in the endoplasmic reticulum and requires ATP

7 January 2021

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Cotranslational ubiquitination of cystic fibrosis transmembrane conductance regulator in vitro

7 January 2021

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Evidence that endoplasmic reticulum (ER)-associated degradation of cystic fibrosis transmembrane conductance regulator is linked to retrograde translocation from the ER membrane

7 January 2021

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The Hdj-2/Hsc70 chaperone pair facilitates early steps in CFTR biogenesis

7 January 2021

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The common variant of cystic fibrosis transmembrane conductance regulator is recognized by hsp70 and degraded in a pre-Golgi nonlysosomal compartment

7 January 2021

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Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

7 January 2021

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Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive

7 January 2021

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Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutation

7 January 2021

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Chemical chaperones correct the mutant phenotype of the delta F508 cystic fibrosis transmembrane conductance regulator protein

7 January 2021

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In vitro pharmacologic restoration of CFTR-mediated chloride transport with sodium 4-phenylbutyrate in cystic fibrosis epithelial cells containing delta F508-CFTR.

7 January 2021

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Functional enhancement of CFTR expression by mitomycin C

7 January 2021

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Increased functional cell surface expression of CFTR and DeltaF508-CFTR by the anthracycline doxorubicin

7 January 2021

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Partial restoration of defective chloride conductance in DeltaF508 CF mice by trimethylamine oxide

7 January 2021

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S-nitrosoglutathione increases cystic fibrosis transmembrane regulator maturation.

7 January 2021

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Decreased levels of nitrosothiols in the lower airways of patients with cystic fibrosis and normal pulmonary function

7 January 2021

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Regulation of ciliary beat frequency by the nitric oxide-cyclic guanosine monophosphate signaling pathway in rat airway epithelial cells

7 January 2021

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Cysteine Nitrosylation Inactivates the HIV-1 Protease

7 January 2021

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Development and biological applications of chloride-sensitive fluorescent indicators

7 January 2021

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Chloride conductive and cotransport mechanisms in cultures of canine tracheal epithelial cells measured by an entrapped fluorescent indicator.

7 January 2021

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Microfluorometric analysis of Cl- permeability and its relation to oscillatory Ca2+ signalling in glucose-stimulated pancreatic beta-cells

7 January 2021

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Cystic fibrosis F508del patients have apically localized CFTR in a reduced number of airway cells.

7 January 2021

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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

7 January 2021

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8-cyclopentyl-1,3-dipropylxanthine and other xanthines differentially bind to the wild-type and delta F508 first nucleotide binding fold (NBF-1) domains of the cystic fibrosis transmembrane conductance regulator

7 January 2021

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Genistein potentiates wild-type and delta F508-CFTR channel activity

7 January 2021

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Actions of genistein on cystic fibrosis transmembrane conductance regulator channel gating. Evidence for two binding sites with opposite effects

7 January 2021

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Direct action of genistein on CFTR.

7 January 2021

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The 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 Hsp70

7 January 2021

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Induction of HSP70 promotes DeltaF508 CFTR trafficking

7 January 2021

1 reference

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Sodium 4-phenylbutyrate downregulates Hsc70: implications for intracellular trafficking of DeltaF508-CFTR

7 January 2021

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Sodium 4-phenylbutyrate downregulates HSC70 expression by facilitating mRNA degradation

7 January 2021

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Systemic deficiency of glutathione in cystic fibrosis

7 January 2021

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Synthetic chloride channel restores glutathione secretion in cystic fibrosis airway epithelia

7 January 2021

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Inducible nitric oxide synthase expression is reduced in cystic fibrosis murine and human airway epithelial cells

7 January 2021

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S-nitrosoglutathione breakdown prevents airway smooth muscle relaxation in the guinea pig.

7 January 2021

1 reference

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Rethinking cystic fibrosis pathology: the critical role of abnormal reduced glutathione (GSH) transport caused by CFTR mutation

7 January 2021

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Bronchodilator S-nitrosothiol deficiency in asthmatic respiratory failure

7 January 2021

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Lack of inducible nitric oxide synthase in bronchial epithelium: a possible mechanism of susceptibility to infection in cystic fibrosis

7 January 2021

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Acute effects of aerosolized S-nitrosoglutathione in cystic fibrosis

7 January 2021

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10.1016/S0006-291X(02)02245-3

7 January 2021

Identifiers

DOI

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22 September 2017

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