KCNQ4 channels expressed in mammalian cells: functional characteristics and pharmacology (Q33937609)

30 July 2017

KCNQ4 channels expressed in mammalian cells: functional characteristics and pharmacology (English)

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30 July 2017

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Søgaard R

1

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30 July 2017

Ljungstrøm T

2

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30 July 2017

Pedersen KA

3

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30 July 2017

Olesen SP

4

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30 July 2017

Jensen BS

5

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30 July 2017

1 April 2001

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American Journal of Physiology - Cell Physiology

30 July 2017

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30 July 2017

280

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30 July 2017

4

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30 July 2017

C859-66

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Reduction of spike frequency adaptation and blockade of M-current in rat CA1 pyramidal neurones by linopirdine (DuP 996), a neurotransmitter release enhancer

30 July 2017

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https://api.crossref.org/works/10.1152%2FAJPCELL.2001.280.4.C859

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPCELL.2001.280.4.C859

A potassium channel mutation in neonatal human epilepsy

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPCELL.2001.280.4.C859

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/10.1152%2FAJPCELL.2001.280.4.C859

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/10.1152%2FAJPCELL.2001.280.4.C859

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/10.1152%2FAJPCELL.2001.280.4.C859

KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.2001.280.4.C859

Small-conductance, calcium-activated potassium channels from mammalian brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.2001.280.4.C859

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/10.1152%2FAJPCELL.2001.280.4.C859

Selective reduction of one mode of M-channel gating by muscarine in sympathetic neurons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.2001.280.4.C859

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.2001.280.4.C859

Modulation of M-current by intracellular Ca2+.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.2001.280.4.C859

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.2001.280.4.C859

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/10.1152%2FAJPCELL.2001.280.4.C859

Inhibition of M-type K+ current by linopirdine, a neurotransmitter-release enhancer, in NG108-15 neuronal cells and rat cerebral neurons in culture.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.2001.280.4.C859

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/10.1152%2FAJPCELL.2001.280.4.C859

A constitutively open potassium channel formed by KCNQ1 and KCNE3

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.2001.280.4.C859

Modulation of the Ca(2+)-dependent K+ channel, hslo, by the substituted diphenylurea NS 1608, paxilline and internal Ca2+.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.2001.280.4.C859

Pharmacological characterization of small-conductance Ca(2+)-activated K(+) channels stably expressed in HEK 293 cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.2001.280.4.C859

Effects of barium, lanthanum and gadolinium on endogenous chloride and potassium currents in Xenopus oocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.2001.280.4.C859

HERG, a human inward rectifier in the voltage-gated potassium channel family

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.2001.280.4.C859

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.2001.280.4.C859

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.2001.280.4.C859

Properties of HERG channels stably expressed in HEK 293 cells studied at physiological temperature

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPCELL.2001.280.4.C859

10.1152/AJPCELL.2001.280.4.C859

21 January 2018

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