Cystic fibrosis transmembrane conductance regulator and the outwardly rectifying chloride channel: a relationship between two chloride channels expressed in epithelial cells (Q34079148)

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English	Cystic fibrosis transmembrane conductance regulator and the outwardly rectifying chloride channel: a relationship between two chloride channels expressed in epithelial cells	scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

1 reference

Europe PubMed Central

Cystic fibrosis transmembrane conductance regulator and the outwardly rectifying chloride channel: a relationship between two chloride channels expressed in epithelial cells (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

cystic fibrosis

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transmembrane protein

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author name string

Hryciw DH

1

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Guggino WB

2

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

publication date

1 November 2000

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Clinical and Experimental Pharmacology and Physiology

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Europe PubMed Central

PubMed publication ID

30 July 2017

27

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

11

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

892-895

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Interaction between cystic fibrosis transmembrane conductance regulator and outwardly rectified chloride channels

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

Identification of the cystic fibrosis gene: chromosome walking and jumping

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

Separate Cl- conductances activated by cAMP and Ca2+ in Cl(-)-secreting epithelial cells

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

Cystic fibrosis: molecular biology and therapeutic implications

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

Immunocytochemical localization of the cystic fibrosis gene product CFTR

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

Regulation by ATP and ADP of CFTR chloride channels that contain mutant nucleotide-binding domains

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

Regulation of the gating of cystic fibrosis transmembrane conductance regulator C1 channels by phosphorylation and ATP hydrolysis

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

Phosphorylation by protein kinase C is required for acute activation of cystic fibrosis transmembrane conductance regulator by protein kinase A.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

The two nucleotide-binding domains of cystic fibrosis transmembrane conductance regulator (CFTR) have distinct functions in controlling channel activity

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

Identification of cystic fibrosis transmembrane conductance regulator channel-lining residues in and flanking the M6 membrane-spanning segment.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

The amino-terminal portion of CFTR forms a regulated Cl- channel.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

The two halves of CFTR form a dual-pore ion channel

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

CFTR as a cAMP-dependent regulator of sodium channels

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

The first-nucleotide binding domain of the cystic-fibrosis transmembrane conductance regulator is important for inhibition of the epithelial Na+ channel.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

Sensitivity of a renal K+ channel (ROMK2) to the inhibitory sulfonylurea compound glibenclamide is enhanced by coexpression with the ATP-binding cassette transporter cystic fibrosis transmembrane regulator

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

Expression and characterization of the cystic fibrosis transmembrane conductance regulator.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

An animal model for cystic fibrosis made by gene targeting

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

Mutations in G protein-linked receptors: novel insights on disease

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

Kinetic interconversion of rat and bovine homologs of the alpha subunit of an amiloride-sensitive Na+ channel by C-terminal truncation of the bovine subunit

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

The CLC chloride channel family

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

Cloning of an epithelial chloride channel from bovine trachea

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

Cloning and expression of a protein kinase C-regulated chloride channel abundantly expressed in rat brain neuronal cells

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

Molecular identification of a volume-regulated chloride channel

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

A serine residue in ClC-3 links phosphorylation-dephosphorylation to chloride channel regulation by cell volume

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

Stable and functional expression of the CIC-3 chloride channel in somatic cell lines

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

Intracellular cyclic AMP inhibits native and recombinant volume-regulated chloride channels from mammalian heart

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1681.2000.03356.X

21 January 2018

Identifiers

10.1046/J.1440-1681.2000.03356.X

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

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