Molecular basis for defective glycosylation and Pseudomonas pathogenesis in cystic fibrosis lung (Q33950252)

30 July 2017

title

Molecular basis for defective glycosylation and Pseudomonas pathogenesis in cystic fibrosis lung (English)

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30 July 2017

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J F Poschet

1

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30 July 2017

J C Boucher

2

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30 July 2017

L Tatterson

3

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30 July 2017

J Skidmore

4

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30 July 2017

R W Van Dyke

5

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30 July 2017

V Deretic

6

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30 July 2017

language of work or name

English

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publication date

1 November 2001

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Proceedings of the National Academy of Sciences of the United States of America

30 July 2017

published in

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30 July 2017

volume

98

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30 July 2017

issue

24

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30 July 2017

page(s)

13972-13977

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Conversion to mucoidy in Pseudomonas aeruginosa infecting cystic fibrosis patients

30 July 2017

cites work

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5 July 2018

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Lack of adherence of clinical isolates of Pseudomonas aeruginosa to asialo-GM(1) on epithelial cells

5 July 2018

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Terminal sialylation is altered in airway cells with impaired CFTR-mediated chloride transport

5 July 2018

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Evidence against the acidification hypothesis in cystic fibrosis

5 July 2018

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Role of the cystic fibrosis transmembrane conductance regulator in innate immunity to Pseudomonas aeruginosa infections

5 July 2018

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Innate lung defenses and compromised Pseudomonas aeruginosa clearance in the malnourished mouse model of respiratory infections in cystic fibrosis

5 July 2018

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Activation of the epithelial Na channel (ENaC) requires CFTR Cl- channel function

5 July 2018

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Airway epithelial tight junctions and binding and cytotoxicity of Pseudomonas aeruginosa.

5 July 2018

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The first-nucleotide binding domain of the cystic-fibrosis transmembrane conductance regulator is important for inhibition of the epithelial Na channel.

5 July 2018

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Cystic fibrosis and the salt controversy

5 July 2018

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Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways disease

5 July 2018

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

5 July 2018

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Overproduction of the CFTR R domain leads to increased levels of asialoGM1 and increased Pseudomonas aeruginosa binding by epithelial cells

5 July 2018

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Visualizing secretion and synaptic transmission with pH-sensitive green fluorescent proteins

5 July 2018

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Glycosylation differences between a cystic fibrosis and rescued airway cell line are not CFTR dependent

5 July 2018

1 reference

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Ion composition of airway surface liquid of patients with cystic fibrosis as compared with normal and disease-control subjects

5 July 2018

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Cystic fibrosis transmembrane conductance regulator is an epithelial cell receptor for clearance of Pseudomonas aeruginosa from the lung.

5 July 2018

1 reference

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Cystic fibrosis transmembrane conductance regulator inverts protein kinase A-mediated regulation of epithelial sodium channel single channel kinetics

5 July 2018

1 reference

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Human beta-defensin-1 is a salt-sensitive antibiotic in lung that is inactivated in cystic fibrosis

5 July 2018

1 reference

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Two naturally occurring alpha2,6-sialyltransferase forms with a single amino acid change in the catalytic domain differ in their catalytic activity and proteolytic processing

5 July 2018

1 reference

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Microbial pathogenesis in cystic fibrosis: mucoid Pseudomonas aeruginosa and Burkholderia cepacia

5 July 2018

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Evidence against defective trans-Golgi acidification in cystic fibrosis

5 July 2018

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Regulation of epithelial sodium channels by the cystic fibrosis transmembrane conductance regulator

5 July 2018

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Cystic fibrosis airway epithelia fail to kill bacteria because of abnormal airway surface fluid.

5 July 2018

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Role of mutant CFTR in hypersusceptibility of cystic fibrosis patients to lung infections.

5 July 2018

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Cystic fibrosis epithelial cells have a receptor for pathogenic bacteria on their apical surface

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=61151

CFTR as a cAMP-dependent regulator of sodium channels

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=61151

CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP

5 July 2018

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Heterologous expression of delta F508 CFTR results in decreased sialylation of membrane glycoconjugates

5 July 2018

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Many pulmonary pathogenic bacteria bind specifically to the carbohydrate sequence GalNAc beta 1-4Gal found in some glycolipids

5 July 2018

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A Cystic Fibrosis Bronchial Epithelial Cell Line: Immortalization by Adeno-12-SV40 Infection

5 July 2018

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Defective acidification of intracellular organelles in cystic fibrosis

5 July 2018

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Second messengers regulate endosomal acidification in Swiss 3T3 fibroblasts

5 July 2018

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Defective regulation of outwardly rectifying Cl- channels by protein kinase A corrected by insertion of CFTR

5 July 2018

1 reference

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Correction of the apical membrane chloride permeability defect in polarized cystic fibrosis airway epithelia following retroviral-mediated gene transfer

5 July 2018

1 reference

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CFTR is a conductance regulator as well as a chloride channel

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=61151

Ganglioside biosynthesis in rat liver. Characterization of three sialyltransferases

29 October 2018

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12 December 2020

Binding of Pseudomonas aeruginosa to respiratory epithelial cells from patients with various mutations in the cystic fibrosis transmembrane regulator

1 reference

12 December 2020

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

1 reference

12 December 2020

Pathophysiology of the ciliary motility syndromes

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12 December 2020

Identifiers

DOI

10.1073/PNAS.241182598

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30 July 2017

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30 July 2017

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