(Q44133654)

30 November 2017

No evidence for inhibition of ENaC through CFTR-mediated release of ATP. (English)

1 reference

30 November 2017

4

1 reference

30 November 2017

Jens König

1

1 reference

PubMed ID

12225848

30 November 2017

R Schreiber

series ordinal

2

1 reference

PubMed ID

12225848

30 November 2017

M Mall

series ordinal

3

1 reference

30 November 2017

1 September 2002

1 reference

Biochimica et Biophysica Acta

30 November 2017

1 reference

30 November 2017

1565

1 reference

30 November 2017

1

1 reference

30 November 2017

17-28

1 reference

Cystic fibrosis transmembrane conductance regulator facilitates ATP release by stimulating a separate ATP release channel for autocrine control of cell volume regulation

30 November 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

UTP inhibits Na+ absorption in wild-type and DeltaF508 CFTR-expressing human bronchial epithelia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

Nedd4 mediates control of an epithelial Na+ channel in salivary duct cells by cytosolic Na+

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

Na+ and Cl- conductances are controlled by cytosolic Cl- concentration in the intralobular duct cells of mouse mandibular glands

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

Epithelial sodium channels: function, structure, and regulation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

CFTR-independent ATP release from epithelial cells triggered by mechanical stimuli.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

CFTR channels expressed in CHO cells do not have detectable ATP conductance

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

Mutations in the putative pore-forming domain of CFTR do not change anion selectivity of the cAMP activated Cl- conductance.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

Feedback inhibition of epithelial Na(+) channels in Xenopus oocytes does not require G(0) or G(i2) proteins

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

Cystic fibrosis transmembrane conductance regulator is required for protein kinase A activation of an outwardly rectified anion channel purified from bovine tracheal epithelia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

Two highly homologous members of the ClC chloride channel family in both rat and human kidney

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

Cytosolic Na+ controls and epithelial Na+ channel via the Go guanine nucleotide-binding regulatory protein

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

The cystic fibrosis transmembrane conductance regulator (CFTR) inhibits ENaC through an increase in the intracellular Cl- concentration

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

Mechanisms of the inhibition of epithelial Na(+) channels by CFTR and purinergic stimulation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

Electrolyte transport in the mammalian colon: mechanisms and implications for disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

CFTR, a regulator of channels

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

Mechanisms for the inhibition of amiloride-sensitive Na+ absorption by extracellular nucleotides in mouse trachea

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

Direct demonstration of mechanically induced release of cellular UTP and its implication for uridine nucleotide receptor activation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

Purified cystic fibrosis transmembrane conductance regulator (CFTR) does not function as an ATP channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

The amiloride-inhibitable Na+ conductance is reduced by the cystic fibrosis transmembrane conductance regulator in normal but not in cystic fibrosis airways.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

Inhibition of amiloride-sensitive epithelial Na(+) absorption by extracellular nucleotides in human normal and cystic fibrosis airways

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

Na+ and K+ regulate the phosphorylation state of nucleoside diphosphate kinase in human airway epithelium

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

Regulation of an amiloride-sensitive Na+-permeable channel by a beta2-adrenergic agonist, cytosolic Ca2+ and Cl- in fetal rat alveolar epithelium

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

Nucleoside diphosphate kinase and Cl(-)-sensitive protein phosphorylation in apical membranes from ovine airway epithelium.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

P2Y2 receptor-mediated inhibition of ion transport in distal lung epithelial cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

Failure of the cystic fibrosis transmembrane conductance regulator to conduct ATP.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

CFTR Cl- channel and CFTR-associated ATP channel: distinct pores regulated by common gates.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

Ion transport abnormalities in rectal suction biopsies from children with cystic fibrosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

Cystic fibrosis transmembrane regulator-independent release of ATP. Its implications for the regulation of P2Y2 receptors in airway epithelia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0005-2736%2802%2900502-3

10.1016/S0005-2736(02)00502-3

7 January 2021

Identifiers

DOI

1 reference

30 November 2017

1 reference

PubMed ID

12225848