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Article

Tissue and Species Distribution of mRNA for the i<sub>kr</sub>-like K<sup>+</sup>Channel, ERG

1 Feb 1997

Abstract excerpt

The human K+ channel gene, HERG, has been linked to the type 2 form of the autosomal dominant long-QT syndrome and has been suggested to encode the fast component of the delayed rectifier K+ current (IKr) found in heart. To date, the published electrophysiological and pharmacological data on the Xenopus-expressed HERG are very similar but are not identical to those of the endogenous IKr. In an effort to provide a...

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Identifiers

PMID: 9012748
DOI: 10.1161/01.res.80.2.261

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Related research

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Research trail→

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Tissue and Species Distribution of mRNA for the i<sub>kr</sub>-like K<sup>+</sup>Channel, ERGPMID 9012748Read ↗

I(Kr): the hERG channel.Semantic proximity Read ↗

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Expression and functional characterization of the human ether-à-go-go-related gene (HERG) K+ channel cardiac splice variant in Xenopus laevis oocytes.Semantic proximity Read ↗

Functional Analysis of a Mouse Brain Elk-Type K+ChannelSemantic proximity Read ↗

HERG, a human inward rectifier in the voltage-gated potassium channel family.Semantic proximity Read ↗

KCNE2 Protein Is Expressed in Ventricles of Different Species, and Changes in Its Expression Contribute to Electrical Remodeling in Diseased HeartsSemantic proximity Read ↗

Homozygous premature truncation of the HERG protein : the human HERG knockout.Semantic proximity Read ↗

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