(Q24307520)

1

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M E Egan

2

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T H Hwang

3

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S B Fulmer

4

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S S Allen

5

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G R Cutting

Non-invasive liposome-mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant mice

6

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language of work or name

English

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publication date

30 June 1995

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published in

Cell

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volume

81

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issue

7

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page(s)

1063-73

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cites work

1 reference

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7 January 2021

G protein-coupled receptors for ATP and other nucleotides: a new receptor family

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7 January 2021

Mechanism of sodium hyperabsorption in cultured cystic fibrosis nasal epithelium: a patch-clamp study

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7 January 2021

Chloride secretory response to extracellular ATP in human normal and cystic fibrosis nasal epithelia

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7 January 2021

cAMP-activated Cl channels in CFTR-transfected cystic fibrosis pancreatic epithelial cells

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7 January 2021

Defective regulation of outwardly rectifying Cl- channels by protein kinase A corrected by insertion of CFTR

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7 January 2021

CFTR and outward rectifying chloride channels are distinct proteins with a regulatory relationship

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7 January 2021

Extracellular ATP: effects, sources and fate

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7 January 2021

Hyperabsorption of Na+ and raised Ca(2+)-mediated Cl- secretion in nasal epithelia of CF mice.

1 reference

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7 January 2021

Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches

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7 January 2021

Cl- channels in CF: lack of activation by protein kinase C and cAMP-dependent protein kinase

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7 January 2021

Correction of the ion transport defect in cystic fibrosis transgenic mice by gene therapy

1 reference

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7 January 2021

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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7 January 2021

Activation by extracellular nucleotides of chloride secretion in the airway epithelia of patients with cystic fibrosis

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7 January 2021

An Immortalized Cystic Fibrosis Tracheal Epithelial Cell Line Homozygous for the ΔF508 CFTR Mutation

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7 January 2021

Chloride impermeability in cystic fibrosis

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7 January 2021

Control of CFTR chloride conductance by ATP levels through non-hydrolytic binding

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7 January 2021

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

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7 January 2021

Identification of the cystic fibrosis gene: chromosome walking and jumping

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7 January 2021

Both CFTR and outwardly rectifying chloride channels contribute to cAMP-stimulated whole cell chloride currents

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2805%2980011-X

7 January 2021

Heterotrimeric G proteins, vesicle trafficking, and CFTR Cl- channels

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7 January 2021

Inhibition of the cystic fibrosis transmembrane conductance regulator by ATP-sensitive K+ channel regulators

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7 January 2021

Multiple modes of regulation of airway epithelial chloride secretion by extracellular ATP

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7 January 2021

A volume-sensitive chloride conductance in human colonic cell line T84.

1 reference

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7 January 2021

A Cystic Fibrosis Bronchial Epithelial Cell Line: Immortalization by Adeno-12-SV40 Infection

1 reference

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7 January 2021