Expression of delta F508 cystic fibrosis transmembrane conductance regulator protein and related chloride transport properties in the gallbladder epithelium from cystic fibrosis patients (Q50154478)

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scientific article published in June 1999

Language	Label	Description	Also known as
English	Expression of delta F508 cystic fibrosis transmembrane conductance regulator protein and related chloride transport properties in the gallbladder epithelium from cystic fibrosis patients	scientific article published in June 1999

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/10347100

Expression of delta F508 cystic fibrosis transmembrane conductance regulator protein and related chloride transport properties in the gallbladder epithelium from cystic fibrosis patients (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/10347100

transmembrane transport

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transmembrane protein

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cystic fibrosis

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author name string

Dray-Charier N

1

1 reference

Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/10347100

Paul A

2

1 reference

Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/10347100

Scoazec JY

3

1 reference

Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/10347100

Veissière D

4

1 reference

Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/10347100

Mergey M

5

1 reference

Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/10347100

Capeau J

6

1 reference

Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/10347100

Soubrane O

7

1 reference

Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/10347100

Housset C

8

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Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/10347100

language of work or name

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publication date

1 June 1999

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Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/10347100

1 reference

Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/10347100

29

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Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/10347100

6

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Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/10347100

1624-1634

1 reference

Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/10347100

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

1 reference

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Bile-duct destruction and collagen deposition: a prominent ultrastructural feature of the liver in cystic fibrosis

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

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Immunocytochemical analysis reveals differences between the subcellular localization of normal and delta Phe508 recombinant cystic fibrosis transmembrane conductance regulator

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Regulation of electrogenic anion secretion in normal and cystic fibrosis gallbladder mucosa.

1 reference

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The amino-terminal portion of CFTR forms a regulated Cl- channel.

1 reference

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CFTR protein expression in primary and cultured epithelia

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CFTR and differentiation markers expression in non-CF and delta F 508 homozygous CF nasal epithelium

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Turnover of the cystic fibrosis transmembrane conductance regulator (CFTR): slow degradation of wild-type and delta F508 CFTR in surface membrane preparations of immortalized airway epithelial cells

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Glycerol reverses the misfolding phenotype of the most common cystic fibrosis mutation.

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Identification of revertants for the cystic fibrosis delta F508 mutation using STE6-CFTR chimeras in yeast

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Chloride Conductance Expressed by ΔF508 and Other Mutant CFTRs In Xenopus Oocytes

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Cystic fibrosis transmembrane conductance regulator mediates the cyclic adenosine monophosphate-induced fluid secretion but not the inhibition of resorption in mouse gallbladder epithelium

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ATP-activated chloride permeability in biliary epithelial cells is regulated by calmodulin-dependent protein kinase II.

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Purinoceptor P2U identification and function in human intrahepatic biliary epithelial cell lines.

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Normalization of raised sodium absorption and raised calcium-mediated chloride secretion by adenovirus-mediated expression of cystic fibrosis transmembrane conductance regulator in primary human cystic fibrosis airway epithelial cells

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21 January 2018

The cystic fibrosis transmembrane conductance regulator attenuates the endogenous Ca2+ activated Cl- conductance of Xenopus oocytes

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21 January 2018

Determinants of mild clinical symptoms in cystic fibrosis patients. Residual chloride secretion measured in rectal biopsies in relation to the genotype

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Biliary physiology in rats with bile ductular cell hyperplasia. Evidence for a secretory function of proliferated bile ductules

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

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Clinical denouement and mutation analysis of patients with cystic fibrosis undergoing liver transplantation for biliary cirrhosis

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Morphological findings in the liver of children with cystic fibrosis: a light and electron microscopical study

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Hepatic changes in young infants with cystic fibrosis: Possible relation to focal biliary cirrhosis

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The plasma membrane polarity of human biliary epithelial cells: in situ immunohistochemical analysis and functional implications

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The early stages of absorption of injected horseradish peroxidase in the proximal tubules of mouse kidney: ultrastructural cytochemistry by a new technique

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Mislocalization of ΔF508 CFTR in cystic fibrosis sweat gland

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Differential localization of the cystic fibrosis transmembrane conductance regulator in normal and cystic fibrosis airway epithelium

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X-ray microanalysis of cell elements in normal and cystic fibrosis jejunum: evidence for chloride secretion in villi

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Identifiers

10.1002/HEP.510290634

1 reference

Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/10347100

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 February 2018

http://europepmc.org/abstract/MED/10347100

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