Chloride transport in nasal ciliated cells of cystic fibrosis heterozygotes. (Q47849183)

6 February 2018

title

Chloride transport in nasal ciliated cells of cystic fibrosis heterozygotes. (English)

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10

Gérard Lenoir

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Isabelle Sermet-Gaudelus

1

Isabelle Sermet-Gaudelus

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Anne Fajac

4

Anne Fajac

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Aleksander Edelman

11

Aleksander Edelman

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6 February 2018

Thao Nguyen-Khoa

6

Thao Nguyen-Khoa

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author name string

Michèle Déchaux

2

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Benoît Vallée

3

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Emanuelle Girodon

5

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Rémi Marianovski

7

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Ilse Hurbain

8

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Jean Louis Bresson

9

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language of work or name

English

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publication date

11 February 2005

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American Journal of Respiratory and Critical Care Medicine

published in

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volume

171

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issue

9

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page(s)

1026-1031

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Demonstration That CFTR Is a Chloride Channel by Alteration of Its Anion Selectivity

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Expression of the cystic fibrosis transmembrane conductance regulator gene in the respiratory tract of normal individuals and individuals with cystic fibrosis

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Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblings

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Increased airway epithelial Na+ absorption produces cystic fibrosis-like lung disease in mice

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21 January 2018

Identifiers

DOI

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6 February 2018

PubMed ID

15709055

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6 February 2018