Absence of CFTR is associated with pleiotropic effects on mucins in mouse gallbladder epithelial cells. (Q53612950)

16 May 2018

title

Absence of CFTR is associated with pleiotropic effects on mucins in mouse gallbladder epithelial cells. (English)

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16 May 2018

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Rahul Kuver

1

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16 May 2018

Thomas Wong

series ordinal

2

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16 May 2018

Johanne Henriette Klinkspoor

series ordinal

3

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16 May 2018

Sum P Lee

series ordinal

4

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16 May 2018

publication date

6 July 2006

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16 May 2018

American Journal of Physiology - Gastrointestinal and Liver Physiology

published in

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16 May 2018

volume

291

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issue

6

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16 May 2018

page(s)

G1148-54

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16 May 2018

Abnormal ion content, hydration and granule expansion of the secretory granules from cystic fibrosis airway glandular cells.

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Defective acidification of intracellular organelles in cystic fibrosis

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Regulation of plasma membrane recycling by CFTR.

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Biosynthesis of mucin type O-glycans: lack of correlation between glycosyltransferase and sulfotransferase activities and CFTR expression

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Increased sulfation of glycoconjugates by cultured nasal epithelial cells from patients with cystic fibrosis

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Abnormal surface liquid pH regulation by cultured cystic fibrosis bronchial epithelium

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MUC5AC and MUC5B Mucins Are Decreased in Cystic Fibrosis Airway Secretions

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Electron microprobe analysis of human labial gland secretory granules in cystic fibrosis

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Characteristics of rodent intestinal mucin Muc3 and alterations in a mouse model of human cystic fibrosis

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Constitutive Mucin Secretion Linked to CFTR Expression

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Isolation and long-term culture of gallbladder epithelial cells from wild-type and CF mice.

21 January 2018

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Mucous granule exocytosis and CFTR expression in gallbladder epithelium

21 January 2018

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Calcium binding to biliary mucins is dependent on sodium ion concentration: relevance to cystic fibrosis

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Mucin glycosylation and sulphation in airway epithelial cells is not influenced by cystic fibrosis transmembrane conductance regulator expression

21 January 2018

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Transcriptional activation of mucin by Pseudomonas aeruginosa lipopolysaccharide in the pathogenesis of cystic fibrosis lung disease

21 January 2018

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A Colorimetric Assay for Glycoproteins Based on the Periodic Acid/Schiff Stain

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Cystic fibrosis mice lacking Muc1 have reduced amounts of intestinal mucus

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Reevaluating gel-forming mucins' roles in cystic fibrosis lung disease

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Heterogeneity in gastrointestinal mucins

21 January 2018

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Characterization of gastric mucoproteins isolated by equilibrium density-gradient centrifugation in caesium chloride

21 January 2018

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CFTR as a cAMP-dependent regulator of sodium channels

21 January 2018

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Intestinal mucins from cystic fibrosis mice show increased fucosylation due to an induced Fucalpha1-2 glycosyltransferase

21 January 2018

1 reference

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C-terminal domain of rodent intestinal mucin Muc3 is proteolytically cleaved in the endoplasmic reticulum to generate extracellular and membrane components

21 January 2018

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Genotypic analysis of respiratory mucous sulfation defects in cystic fibrosis.

21 January 2018

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Control of mucus hydration as a Donnan equilibrium process

21 January 2018

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21 January 2018

Identifiers

DOI

10.1152/AJPGI.00547.2005

1 reference

16 May 2018

1 reference

16 May 2018