Novel gene hKCNE4 slows the activation of the KCNQ1 channel.

Standard

Novel gene hKCNE4 slows the activation of the KCNQ1 channel. / Teng, Siyong; Ma, Lijuan; Zhen, Yisong; Lin, ChunXia; Bähring, Robert; Vardanyan, Vitya; Pongs, Olaf; Hui, Rutai.

in: BIOCHEM BIOPH RES CO, Jahrgang 303, Nr. 3, 3, 2003, S. 808-813.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Teng, S, Ma, L, Zhen, Y, Lin, C, Bähring, R, Vardanyan, V, Pongs, O & Hui, R 2003, 'Novel gene hKCNE4 slows the activation of the KCNQ1 channel.', BIOCHEM BIOPH RES CO, Jg. 303, Nr. 3, 3, S. 808-813. <http://www.ncbi.nlm.nih.gov/pubmed/12670483?dopt=Citation>

APA

Teng, S., Ma, L., Zhen, Y., Lin, C., Bähring, R., Vardanyan, V., Pongs, O., & Hui, R. (2003). Novel gene hKCNE4 slows the activation of the KCNQ1 channel. BIOCHEM BIOPH RES CO, 303(3), 808-813. [3]. http://www.ncbi.nlm.nih.gov/pubmed/12670483?dopt=Citation

Vancouver

Teng S, Ma L, Zhen Y, Lin C, Bähring R, Vardanyan V et al. Novel gene hKCNE4 slows the activation of the KCNQ1 channel. BIOCHEM BIOPH RES CO. 2003;303(3):808-813. 3.

Bibtex

@article{425de497595b4811b5ce9bbbe6e5a4f6,
title = "Novel gene hKCNE4 slows the activation of the KCNQ1 channel.",
abstract = "The KCNE genes encode small, single transmembrane domain peptides that associate with pore-forming potassium channel subunits to form mixed complexes with unique characteristics. We have identified a novel member of the human KCNE gene family, hKCNE4. The hKCNE4 gene encodes 170 amino acid protein and is localized to chromosome 2q35-36. The protein sequence shows 90% homology to mouse KCNE4 and 38% identity to human KCNE1. Northern blot analysis revealed that hKCNE4 is expressed strongly in heart, skeletal muscle, and kidney, less in placenta, lung, and liver, and weakly in brain and blood cells. Electrophysiological study showed that hKCNE4 modulates the activation of the KCNQ1 channel.",
author = "Siyong Teng and Lijuan Ma and Yisong Zhen and ChunXia Lin and Robert B{\"a}hring and Vitya Vardanyan and Olaf Pongs and Rutai Hui",
year = "2003",
language = "Deutsch",
volume = "303",
pages = "808--813",
journal = "BIOCHEM BIOPH RES CO",
issn = "0006-291X",
publisher = "Academic Press Inc.",
number = "3",

}

RIS

TY - JOUR

T1 - Novel gene hKCNE4 slows the activation of the KCNQ1 channel.

AU - Teng, Siyong

AU - Ma, Lijuan

AU - Zhen, Yisong

AU - Lin, ChunXia

AU - Bähring, Robert

AU - Vardanyan, Vitya

AU - Pongs, Olaf

AU - Hui, Rutai

PY - 2003

Y1 - 2003

N2 - The KCNE genes encode small, single transmembrane domain peptides that associate with pore-forming potassium channel subunits to form mixed complexes with unique characteristics. We have identified a novel member of the human KCNE gene family, hKCNE4. The hKCNE4 gene encodes 170 amino acid protein and is localized to chromosome 2q35-36. The protein sequence shows 90% homology to mouse KCNE4 and 38% identity to human KCNE1. Northern blot analysis revealed that hKCNE4 is expressed strongly in heart, skeletal muscle, and kidney, less in placenta, lung, and liver, and weakly in brain and blood cells. Electrophysiological study showed that hKCNE4 modulates the activation of the KCNQ1 channel.

AB - The KCNE genes encode small, single transmembrane domain peptides that associate with pore-forming potassium channel subunits to form mixed complexes with unique characteristics. We have identified a novel member of the human KCNE gene family, hKCNE4. The hKCNE4 gene encodes 170 amino acid protein and is localized to chromosome 2q35-36. The protein sequence shows 90% homology to mouse KCNE4 and 38% identity to human KCNE1. Northern blot analysis revealed that hKCNE4 is expressed strongly in heart, skeletal muscle, and kidney, less in placenta, lung, and liver, and weakly in brain and blood cells. Electrophysiological study showed that hKCNE4 modulates the activation of the KCNQ1 channel.

M3 - SCORING: Zeitschriftenaufsatz

VL - 303

SP - 808

EP - 813

JO - BIOCHEM BIOPH RES CO

JF - BIOCHEM BIOPH RES CO

SN - 0006-291X

IS - 3

M1 - 3

ER -