Cystic fibrosis: How do CFTR mutations cause cystic fibrosis? (Q41072064)

26 September 2017

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title

Cystic fibrosis: How do CFTR mutations cause cystic fibrosis? (English)

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26 September 2017

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Wine JJ

1

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PubMed ID

8749384

26 September 2017

language of work or name

English

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publication date

1 December 1995

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26 September 2017

3

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inferred from page(s)

published in

Current Biology

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26 September 2017

5

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26 September 2017

1357-1359

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26 September 2017

12

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Abnormal Ion Permeation Through Cystic Fibrosis Respiratory Epithelium

26 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900269-7

7 January 2021

Chloride impermeability in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900269-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900269-7

7 January 2021

Cystic fibrosis transmembrane conductance regulator: a chloride channel with novel regulation

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900269-7

7 January 2021

Volume-regulated chloride channels associated with the human multidrug-resistance P-glycoprotein

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900269-7

7 January 2021

Selection for MDR1/P-glycoprotein enhances swelling-activated K+ and Cl- currents in NIH/3T3 cells

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900269-7

7 January 2021

CFTR as a cAMP-dependent regulator of sodium channels

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900269-7

7 January 2021

The basic defect in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900269-7

7 January 2021

CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900269-7

7 January 2021

Pharmacologic treatment of abnormal ion transport in the airway epithelium in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900269-7

7 January 2021

An animal model for cystic fibrosis made by gene targeting

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900269-7

7 January 2021

Relationship of a non-cystic fibrosis transmembrane conductance regulator-mediated chloride conductance to organ-level disease in Cftr(-/-) mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900269-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900269-7

7 January 2021

Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2895%2900269-7

7 January 2021

10.1016/S0960-9822(95)00269-7

Identifiers

DOI

1 reference

26 September 2017

1 reference

PubMed ID

8749384