An Isoform of Nedd4-2 Plays a Pivotal Role in Electrophysiological Cardiac Abnormalities.

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An Isoform of Nedd4-2 Plays a Pivotal Role in Electrophysiological Cardiac Abnormalities.

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2017 nî lūn-bûn

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2017年論文

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2017年論文

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An Isoform of Nedd4-2 Plays a Pivotal Role in Electrophysiological Cardiac Abnormalities.

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An Isoform of Nedd4-2 Plays a Pivotal Role in Electrophysiological Cardiac Abnormalities.

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An Isoform of Nedd4-2 Plays a Pivotal Role in Electrophysiological Cardiac Abnormalities.

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P1476

An Isoform of Nedd4-2 Plays a Pivotal Role in Electrophysiological Cardiac Abnormalities

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P2093

Hiromichi Wakui

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Hiroshi Doi

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Hisho Kawamura

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Kouichi Tamura

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Lin Chen

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Rie Nakashima-Sasaki

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Shintaro Minegishi

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Tabito Kino

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Tomoaki Ishigami

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Yumi Chiba

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P2860

Cardiac conduction defects associate with mutations in SCN5A

Cell surface expression of human ether-a-go-go-related gene (hERG) channels is regulated by caveolin-3 protein via the ubiquitin ligase Nedd4-2

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

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

Identification of a PY motif in the epithelial Na channel subunits as a target sequence for mutations causing channel activation found in Liddle syndrome

Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

Molecular mechanisms of human hypertension.

The long QT syndrome family of cardiac ion channelopathies: a HuGE review.

P31

scholarly article

P356

10.3390/IJMS18061268

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P407

English

P433

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P478

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P50

Kengo Azushima

P577

2017-06-14T00:00:00Z

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P698

28613240

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P932

5486090

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