(Q41193043)

28 September 2017

Changes in neutral amino acid efflux and membrane potential associated with the expression of CFTR protein (English)

1 reference

28 September 2017

3

1 reference

28 September 2017

B M Rotoli

1

1 reference

PubMed ID

24178690

28 September 2017

O Bussolati

series ordinal

2

1 reference

PubMed ID

24178690

28 September 2017

G C Gazzola

series ordinal

4

1 reference

28 September 2017

1 June 1996

1 reference

28 September 2017

1 reference

28 September 2017

11

1 reference

28 September 2017

2

1 reference

28 September 2017

247-255

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00813863

28 September 2017

0 references

cites work

External ATP and its analogs activate the cystic fibrosis transmembrane conductance regulator by a cyclic AMP-independent mechanism.

1 reference

12 December 2020

cAMP-independent regulation of CFTR by the actin cytoskeleton

1 reference

12 December 2020

Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

1 reference

12 December 2020

Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive

1 reference

12 December 2020

Defective acidification of intracellular organelles in cystic fibrosis

1 reference

12 December 2020

Dependence of L-arginine accumulation on membrane potential in cultured human fibroblasts

1 reference

12 December 2020

The cystic fibrosis transmembrane conductance regulator is a dual ATP and chloride channel

1 reference

12 December 2020

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

1 reference

12 December 2020

Protein kinase C activates chloride conductance in C127 cells stably expressing the cystic fibrosis gene

1 reference

12 December 2020

The delta F508 mutation decreases the stability of cystic fibrosis transmembrane conductance regulator in the plasma membrane. Determination of functional half-lives on transfected cells

1 reference

12 December 2020

Influx of L-arginine is an indicator of membrane potential in human fibroblasts

1 reference

12 December 2020

Cystic fibrosis: molecular biology and therapeutic implications

1 reference

12 December 2020

CFTR, a channel with the structure of a transporter

1 reference

12 December 2020

CFTR as a cAMP-dependent regulator of sodium channels

1 reference

12 December 2020

ABC Transporters: From Microorganisms to Man

1 reference

12 December 2020

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

1 reference

12 December 2020

CFTR protein is involved in the efflux of neutral amino acids

1 reference

12 December 2020

Bacterial periplasmic transport systems: structure, mechanism, and evolution

1 reference

12 December 2020

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

1 reference

12 December 2020

Multi-ion pore behaviour in the CFTR chloride channel

1 reference

12 December 2020

A Multifunctional Aqueous Channel Formed by CFTR

1 reference

12 December 2020

Separation of drug transport and chloride channel functions of the human multidrug resistance P-glycoprotein

1 reference

12 December 2020

Identification of a defective cAMP-stimulated Cl- channel in cystic fibrosis fibroblasts

1 reference

12 December 2020

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

1 reference

12 December 2020

Dimensions Publication ID

Identifiers

0 references

1 reference

PubMed ID

24178690