Three mechanisms underlie KCNQ2/3 heteromeric potassium M-channel potentiation. (Q48810175)

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4 January 2020

title

Three mechanisms underlie KCNQ2/3 heteromeric potassium M-channel potentiation (English)

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4 January 2020

author name string

Ainhoa Etxeberria

1

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4 January 2020

Irene Santana-Castro

2

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4 January 2020

M Paz Regalado

3

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4 January 2020

Paloma Aivar

4

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4 January 2020

Alvaro Villarroel

5

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language of work or name

English

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publication date

1 October 2004

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4 January 2020

published in

Journal of Neuroscience

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4 January 2020

volume

24

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issue

41

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4 January 2020

page(s)

9146-9152

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KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

4 January 2020

cites work

1 reference

12 December 2020

A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions

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12 December 2020

Surface expression and single channel properties of KCNQ2/KCNQ3, M-type K+ channels involved in epilepsy

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12 December 2020

Modulation and genetic identification of the M channel

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A structural basis for drug-induced long QT syndrome

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Ion selectivity filter regulates local anesthetic inhibition of G-protein-gated inwardly rectifying K+ channels

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Neuronal KCNQ potassium channels: physiology and role in disease.

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Identification of specific pore residues mediating KCNQ1 inactivation. A novel mechanism for long QT syndrome

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12 December 2020

Properties of single M-type KCNQ2/KCNQ3 potassium channels expressed in mammalian cells

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12 December 2020

Mechanism of Ba(2+) block of a mouse inwardly rectifying K+ channel: differential contribution by two discrete residues

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12 December 2020

Determinants involved in Kv1 potassium channel folding in the endoplasmic reticulum, glycosylation in the Golgi, and cell surface expression

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12 December 2020

Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channel

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12 December 2020

Identification of a trafficking determinant localized to the Kv1 potassium channel pore

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12 December 2020

The identification and characterization of a noncontinuous calmodulin-binding site in noninactivating voltage-dependent KCNQ potassium channels

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12 December 2020

ER transport signals and trafficking of potassium channels and receptors

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12 December 2020

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12 December 2020

Energetics of pore opening in a voltage-gated K(+) channel

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12 December 2020

A carboxy-terminal domain determines the subunit specificity of KCNQ K+ channel assembly

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12 December 2020

C-terminal interaction of KCNQ2 and KCNQ3 K+ channels

1 reference

12 December 2020

Stoichiometry of expressed KCNQ2/KCNQ3 potassium channels and subunit composition of native ganglionic M channels deduced from block by tetraethylammonium

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12 December 2020

AMPA receptor tetramerization is mediated by Q/R editing

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12 December 2020

The therapeutic potential of neuronal KCNQ channel modulators

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12 December 2020

International Union of Pharmacology. XLI. Compendium of voltage-gated ion channels: potassium channels

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12 December 2020

Ionic permeation and conduction properties of neuronal KCNQ2/KCNQ3 potassium channels.

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12 December 2020

Single-channel analysis of KCNQ K+ channels reveals the mechanism of augmentation by a cysteine-modifying reagent.

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12 December 2020

Mutations affecting internal TEA blockade identify the probable pore-forming region of a K+ channel.

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12 December 2020

Inward rectification of both AMPA and kainate subtype glutamate receptors generated by polyamine-mediated ion channel block

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12 December 2020

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

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12 December 2020

Inhibition of the Kv4 (Shal) family of transient K+ currents by arachidonic acid.

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12 December 2020

Control of channel activity through a unique amino acid residue of a G protein-gated inwardly rectifying K+ channel subunit

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12 December 2020

Signal-mediated sorting of membrane proteins between the endoplasmic reticulum and the golgi apparatus

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12 December 2020

Mutations in the pore region of ROMK enhance Ba2+ block.

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12 December 2020

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

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12 December 2020

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12 December 2020

A potassium channel mutation in neonatal human epilepsy

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12 December 2020

The Structure of the Potassium Channel: Molecular Basis of K + Conduction and Selectivity

1 reference

12 December 2020

KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel

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12 December 2020

Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy

1 reference

12 December 2020

10.1523/JNEUROSCI.3194-04.2004

Identifiers

DOI

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4 January 2020

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PubMed publication ID

15483133

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