(Q34570321)

3 August 2017

Interregulation of proton-gated Na(+) channel 3 and cystic fibrosis transmembrane conductance regulator (English)

1 reference

3 August 2017

0 references

transmembrane protein

0 references

7

Eric J Sorscher

1 reference

3 August 2017

Estelle Cormet-Boyaka

4

object named as

Estelle Cormet-Boyaka

1 reference

3 August 2017

8

Dale J Benos

1 reference

3 August 2017

Xuefeng Su

1

1 reference

3 August 2017

Qingnan Li

2

1 reference

3 August 2017

Kedar Shrestha

3

1 reference

3 August 2017

Lan Chen

5

1 reference

3 August 2017

Peter R Smith

6

1 reference

3 August 2017

Sadis Matalon

9

1 reference

3 August 2017

Hong-Long Ji

10

1 reference

3 August 2017

language of work or name

English

0 references

publication date

29 September 2006

1 reference

Journal of Biological Chemistry

3 August 2017

1 reference

3 August 2017

281

1 reference

3 August 2017

36960-36968

1 reference

3 August 2017

48

1 reference

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

3 August 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Cystic fibrosis transmembrane conductance regulator differentially regulates human and mouse epithelial sodium channels in Xenopus oocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

ENaC is inhibited by an increase in the intracellular Cl(-) concentration mediated through activation of Cl(-) channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

cAMP-dependent activation of CFTR inhibits the epithelial sodium channel (ENaC) without affecting its surface expression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Epithelial sodium channels regulate cystic fibrosis transmembrane conductance regulator chloride channels in Xenopus oocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

The cytosolic termini of the beta- and gamma-ENaC subunits are involved in the functional interactions between cystic fibrosis transmembrane conductance regulator and epithelial sodium channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Cl- transport by cystic fibrosis transmembrane conductance regulator (CFTR) contributes to the inhibition of epithelial Na+ channels (ENaCs) in Xenopus oocytes co-expressing CFTR and ENaC.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Role of CFTR's PDZ1-binding domain, NBF1 and Cl(-) conductance in inhibition of epithelial Na(+) channels in Xenopus oocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Evidence for reduced Cl- and increased Na+ permeability in cystic fibrosis human primary cell cultures.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Downregulation of epithelial sodium channel (ENaC) by CFTR co-expressed in Xenopus oocytes is independent of Cl- conductance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Genistein restores functional interactions between Delta F508-CFTR and ENaC in Xenopus oocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

H(+)-gated cation channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

H(+)-gated cation channels: neuronal acid sensors in the NaC/DEG family of ion channels.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

The ASICs: signaling molecules? Modulators?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Expression of cystic fibrosis transmembrane conductance regulator in rat efferent duct epithelium.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Molecular cloning and functional expression of a novel amiloride-sensitive Na+ channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Abnormal fluid transport by the epididymis as a cause of obstructive azoospermia

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Pancreatic acinar cell dysfunction in CFTR(-/-) mice is associated with impairments in luminal pH and endocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Osmotic water permeabilities of cultured, well-differentiated normal and cystic fibrosis airway epithelia

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Exhaled breath condensate pH and exhaled nitric oxide in allergic asthma and in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Molecular cloning of a non-inactivating proton-gated Na+ channel specific for sensory neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Molecular cloning and regional distribution of a human proton receptor subunit with biphasic functional properties

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Functional properties and pharmacological inhibition of ASIC channels in the human SJ-RH30 skeletal muscle cell line.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Acid-sensing ion channels in malignant gliomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Reactive oxygen nitrogen species decrease cystic fibrosis transmembrane conductance regulator expression and cAMP-mediated Cl- secretion in airway epithelia

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Up-regulation of acid-gated Na(+) channels (ASICs) by cystic fibrosis transmembrane conductance regulator co-expression in Xenopus oocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Chemical gating of gap junction channels; roles of calcium, pH and calmodulin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

A small molecule CFTR inhibitor produces cystic fibrosis-like submucosal gland fluid secretions in normal airways

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Hyposecretion, not hyperabsorption, is the basic defect of cystic fibrosis airway glands.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Regulation of amiloride-sensitive Na(+) transport by basal nitric oxide.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Delta-subunit confers novel biophysical features to alpha beta gamma-human epithelial sodium channel (ENaC) via a physical interaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

pH Dependency and desensitization kinetics of heterologously expressed combinations of acid-sensing ion channel subunits.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Regulation of channel gating by AMP-activated protein kinase modulates cystic fibrosis transmembrane conductance regulator activity in lung submucosal cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Regulation of intracellular pH in Calu-3 human airway cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Endogenous airway acidification. Implications for asthma pathophysiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Degenerin sites mediate proton activation of deltabetagamma-epithelial sodium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Duodenal pH in cystic fibrosis and its relationship to fat malabsorption

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

Na+ and Cl? conductances in airway epithelial cells: increased Na+ conductance in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M608002200

21 January 2018

Identifiers

DOI

10.1074/JBC.M608002200

1 reference

3 August 2017

1 reference