(Q45804174)

16 December 2017

title

Role of HCN4 channel in preventing ventricular arrhythmia (English)

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16 December 2017

author name string

Kazuo Ueda

1

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16 December 2017

Yuji Hirano

2

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16 December 2017

Yasushi Higashiuesato

3

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16 December 2017

Yoshiyasu Aizawa

4

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16 December 2017

Takeharu Hayashi

5

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16 December 2017

Natsuko Inagaki

6

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16 December 2017

Takeshi Tana

7

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16 December 2017

Yusuke Ohya

8

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16 December 2017

Shuichi Takishita

9

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16 December 2017

Hiromi Muratani

10

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16 December 2017

Masayasu Hiraoka

11

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16 December 2017

Akinori Kimura

12

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16 December 2017

publication date

23 January 2009

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16 December 2017

Journal of Human Genetics

published in

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16 December 2017

volume

54

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16 December 2017

page(s)

115-121

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16 December 2017

issue

2

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16 December 2017

https://scigraph.springernature.com/pub.10.1038/jhg.2008.16

exact match

0 references

cites work

Pacemaker channel dysfunction in a patient with sinus node disease

1 reference

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Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)

21 January 2018

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Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

21 January 2018

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Simulation study of cellular electric properties in heart failure.

21 January 2018

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https://api.crossref.org/works/10.1038%2FJHG.2008.16

A dynamic model of the cardiac ventricular action potential. I. Simulations of ionic currents and concentration changes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.16

Functional characterization of a trafficking-defective HCN4 mutation, D553N, associated with cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.16

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.16

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.16

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.16

7 January 2021

Mutations in the hminK gene cause long QT syndrome and suppress IKs function

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.16

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.16

7 January 2021

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism

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7 January 2021

Sudden death associated with short-QT syndrome linked to mutations in HERG.

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https://api.crossref.org/works/10.1038%2FJHG.2008.16

7 January 2021

Mutation in the KCNQ1 gene leading to the short QT-interval syndrome.

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https://api.crossref.org/works/10.1038%2FJHG.2008.16

7 January 2021

KCNQ1 gain-of-function mutation in familial atrial fibrillation

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https://api.crossref.org/works/10.1038%2FJHG.2008.16

7 January 2021

Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation

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https://api.crossref.org/works/10.1038%2FJHG.2008.16

7 January 2021

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

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https://api.crossref.org/works/10.1038%2FJHG.2008.16

7 January 2021

Cardiac conduction defects associate with mutations in SCN5A

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https://api.crossref.org/works/10.1038%2FJHG.2008.16

7 January 2021

Cardiac channelopathies

1 reference

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7 January 2021

Compound mutations: a common cause of severe long-QT syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.16

7 January 2021

Novel missense mutation in cardiac beta myosin heavy chain gene found in a Japanese patient with hypertrophic cardiomyopathy

1 reference

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7 January 2021

Genomic organization of the human SCN5A gene encoding the cardiac sodium channel

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7 January 2021

Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.

1 reference

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7 January 2021

Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome

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https://api.crossref.org/works/10.1038%2FJHG.2008.16

7 January 2021

The S4-S5 linker couples voltage sensing and activation of pacemaker channels.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.16

7 January 2021

A model for human ventricular tissue.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.16

7 January 2021

The Properties of the Pacemaker Current IFin Human Ventricular Myocytes are Modulated by Cardiac Disease

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.16

7 January 2021

Molecular diversity of pacemaker ion channels

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.16

7 January 2021

Prognostic value of electrophysiologic investigations in Brugada syndrome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2008.16

7 January 2021

Identifiers

DOI

10.1038/JHG.2008.16

1 reference

16 December 2017

Dimensions Publication ID

0 references

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16 December 2017