Control of dynamic CFTR selectivity by glutamate and ATP in epithelial cells (Q44475278)

3 December 2017

Control of dynamic CFTR selectivity by glutamate and ATP in epithelial cells (English)

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3 December 2017

Reddy MM

1

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3 December 2017

Quinton PM

series ordinal

2

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3 December 2017

language of work or name

English

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publication date

1 June 2003

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3 December 2017

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3 December 2017

423

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3 December 2017

6941

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3 December 2017

756-760

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https://scigraph.springernature.com/pub.10.1038/nature01694

3 December 2017

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Nucleoside triphosphates are required to open the CFTR chloride channel.

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ATPase activity of the cystic fibrosis transmembrane conductance regulator

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

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Glutamate and GABA activate different receptors and Cl(-) conductances in crab peptide-secretory neurons

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Glutamate antagonists: deadly liaisons with cancer

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Mislocalization of ΔF508 CFTR in cystic fibrosis sweat gland

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

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

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Regulation of mitochondrial glutamine/glutamate metabolism by glutamate transport: studies with (15)N.

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Location and function of the epithelial Na channel in the cochlea.

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Amino acids are compatible osmolytes for volume recovery after hypertonic shrinkage in vascular endothelial cells

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Glutamate signalling in non-neuronal tissues

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Beta-cell mitochondria in the regulation of insulin secretion: a new culprit in type II diabetes

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Ca2+ flux through promiscuous cardiac Na+ channels: slip-mode conductance.

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Molecular physiology of P2X receptors and ATP signalling at synapses

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7 January 2021

Adenosine triphosphate-dependent asymmetry of anion permeation in the cystic fibrosis transmembrane conductance regulator chloride channel

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7 January 2021

Conformational states of CFTR associated with channel gating: the role ATP binding and hydrolysis.

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7 January 2021

Activation of the epithelial Na+ channel (ENaC) requires CFTR Cl- channel function

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7 January 2021

Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

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7 January 2021

Chloride Conductance Expressed by ΔF508 and Other Mutant CFTRs In Xenopus Oocytes

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7 January 2021

Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties.

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7 January 2021

Bicarbonate conductance and pH regulatory capability of cystic fibrosis transmembrane conductance regulator

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7 January 2021

Aberrant CFTR-dependent HCO3- transport in mutations associated with cystic fibrosis

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A molecular mechanism for aberrant CFTR-dependent HCO(3)(-) transport in cystic fibrosis

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7 January 2021

Identifiers

DOI

10.1038/NATURE01694

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Dimensions Publication ID

3 December 2017

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