(Q54039989)

24 May 2018

title

CFTR, MDR1, and MRP1 immunolocalization in normal human nasal respiratory mucosa. (English)

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24 May 2018

author name string

M A Wioland

1

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24 May 2018

J Fleury-Feith

2

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24 May 2018

P Corlieu

3

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24 May 2018

F Commo

4

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24 May 2018

G Monceaux

5

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24 May 2018

J Lacau-St-Guily

6

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24 May 2018

J F Bernaudin

7

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24 May 2018

publication date

1 September 2000

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24 May 2018

Journal of Histochemistry and Cytochemistry

published in

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24 May 2018

volume

48

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24 May 2018

issue

9

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24 May 2018

page(s)

1215-1222

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24 May 2018

Azithromycin, the multidrug-resistant protein, and cystic fibrosis.

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1 reference

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Different pattern of MRP localization in ciliated and basal cells from human bronchial epithelium

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Decreased expression of the cystic fibrosis transmembrane conductance regulator protein in remodeled airway epithelium from lung transplanted patients

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ATP depletion induces a loss of respiratory epithelium functional integrity and down-regulates CFTR (cystic fibrosis transmembrane conductance regulator) expression

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Abnormal expression of the cystic fibrosis transmembrane regulator in chronic sinusitis in cystic fibrosis and non-cystic fibrosis patients

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Immunocytochemical localization of the cystic fibrosis gene product CFTR

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

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

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A controlled study of adenoviral-vector-mediated gene transfer in the nasal epithelium of patients with cystic fibrosis

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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CFTR is a conductance regulator as well as a chloride channel.

21 January 2018

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21 January 2018

Identifiers

DOI

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24 May 2018

PubMed ID

10950878

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24 May 2018