CFTR and differentiation markers expression in non-CF and delta F 508 homozygous CF nasal epithelium (Q35763514)

10 August 2017

title

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

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10 August 2017

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Dupuit F

1

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10 August 2017

Kälin N

2

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10 August 2017

Brézillon S

3

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10 August 2017

Hinnrasky J

4

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10 August 2017

Tümmler B

5

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10 August 2017

Puchelle E

6

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10 August 2017

language of work or name

English

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publication date

1 September 1995

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Journal of Clinical Investigation

10 August 2017

published in

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10 August 2017

volume

96

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10 August 2017

issue

3

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10 August 2017

page(s)

1601-1611

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Novel Pseudomonas product stimulates interleukin-8 production in airway epithelial cells in vitro

10 August 2017

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2 October 2017

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2 October 2017

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2 October 2017

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2 October 2017

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12 July 2018

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The cystic fibrosis mutation (delta F508) does not influence the chloride channel activity of CFTR.

12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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

12 July 2018

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12 July 2018

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12 July 2018

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

25 September 2018

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Cyclic AMP-dependent protein kinase opens chloride channels in normal but not cystic fibrosis airway epithelium

25 September 2018

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15 November 2018

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Histochemical study on innervation of glands and blood vessels in nasal polyps

15 November 2018

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12 December 2020

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

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12 December 2020

Mislocalization of ΔF508 CFTR in cystic fibrosis sweat gland

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12 December 2020

Cell-specific localization of CFTR mRNA shows developmentally regulated expression in human fetal tissues

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12 December 2020

Protein kinase C mediates down-regulation of cystic fibrosis transmembrane conductance regulator levels in epithelial cells

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12 December 2020

The delta F508 mutation decreases the stability of cystic fibrosis transmembrane conductance regulator in the plasma membrane. Determination of functional half-lives on transfected cells

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12 December 2020

Submucosal glands are the predominant site of CFTR expression in the human bronchus

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12 December 2020

Protease-antiprotease imbalance in the lungs of children with cystic fibrosis

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12 December 2020

Identifiers

DOI

10.1172/JCI118199

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10 August 2017

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10 August 2017

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