(Q22254006)

potassium ion transmembrane transport

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

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C Lerche

1

C

Lerche

1 reference

8 February 2023

C R Scherer

2

C R

Scherer

1 reference

8 February 2023

G Seebohm

3

G

Seebohm

1 reference

8 February 2023

C Derst

4

C

Derst

1 reference

8 February 2023

A D Wei

5

A D

Wei

1 reference

8 February 2023

A E Busch

6

A E

Busch

1 reference

8 February 2023

K Steinmeyer

7

K

Journal of Biological Chemistry

Steinmeyer

1 reference

8 February 2023

language of work or name

English

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publication date

21 July 2000

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published in

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volume

275

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page(s)

22395-400

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issue

29

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cites work

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

Cloning of a membrane protein that induces a slow voltage-gated potassium current

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

KvLQT1, a voltage-gated potassium channel responsible for human cardiac arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

Molecular genetic insights into cardiovascular disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

Dysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

KCNE1 mutations cause jervell and Lange-Nielsen syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

A constitutively open potassium channel formed by KCNQ1 and KCNE3

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

A new class of inhibitors of cAMP-mediated Cl- secretion in rabbit colon, acting by the reduction of cAMP-activated K+ conductance

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

A potassium channel mutation in neonatal human epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

Functional expression of two KvLQT1-related potassium channels responsible for an inherited idiopathic epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

The KCNQ2 potassium channel: splice variants, functional and developmental expression. Brain localization and comparison with KCNQ3

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

Inhibition of KCNQ1-4 potassium channels expressed in mammalian cells via M1 muscarinic acetylcholine receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

A recessive C-terminal Jervell and Lange-Nielsen mutation of the KCNQ1 channel impairs subunit assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

Activation and inactivation of homomeric KvLQT1 potassium channels.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

Voltage-dependent inactivation of the human K+ channel KvLQT1 is eliminated by association with minimal K+ channel (minK) subunits

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

Differential tetraethylammonium sensitivity of KCNQ1-4 potassium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

Specific blockade of slowly activating I(sK) channels by chromanols -- impact on the role of I(sK) channels in epithelia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

The role of the IsK protein in the specific pharmacological properties of the IKs channel complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

Separation of M-like current and ERG current in NG108-15 cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (EPM2)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

Juvenile myoclonic epilepsy in chromosome 6p12-p11: locus heterogeneity and recombinations

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

A new wave for heart rhythms

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

Muscarinic suppression of a novel voltage-sensitive K+ current in a vertebrate neurone

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

Mutations affecting TEA blockade and ion permeation in voltage-activated K+ channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

7 January 2021

Isoproterenol antagonizes prolongation of refractory period by the class III antiarrhythmic agent E-4031 in guinea pig myocytes. Mechanism of action

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

7 January 2021

Kainate binding proteins possess functional ion channel domains.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

7 January 2021

Reconstitution of muscarinic modulation of the KCNQ2/KCNQ3 K(+) channels that underlie the neuronal M current

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M002378200

7 January 2021