(Q33151337)

22 July 2017

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

1 reference

22 July 2017

0 references

Kazuo Ueda

1

1 reference

22 July 2017

Kazufumi Nakamura

2

1 reference

22 July 2017

Takeharu Hayashi

3

1 reference

22 July 2017

Natsuko Inagaki

4

1 reference

22 July 2017

Megumi Takahashi

5

1 reference

22 July 2017

Takuro Arimura

6

1 reference

22 July 2017

Hiroshi Morita

7

1 reference

22 July 2017

Yasushi Higashiuesato

8

1 reference

22 July 2017

Yuji Hirano

9

1 reference

22 July 2017

Michio Yasunami

10

1 reference

22 July 2017

Shuichi Takishita

11

1 reference

22 July 2017

Akira Yamashina

12

1 reference

22 July 2017

Tohru Ohe

13

1 reference

22 July 2017

Makoto Sunamori

14

1 reference

22 July 2017

Masayasu Hiraoka

15

1 reference

22 July 2017

Akinori Kimura

16

1 reference

22 July 2017

language of work or name

English

0 references

publication date

30 April 2004

1 reference

Journal of Biological Chemistry

22 July 2017

5

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

22 July 2017

279

1 reference

22 July 2017

27194-27198

1 reference

22 July 2017

26

1 reference

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

22 July 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

The long QT syndrome. Prospective longitudinal study of 328 families

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

21 January 2018

Cardiac channelopathies

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

Pacemaker channel dysfunction in a patient with sinus node disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

Two pacemaker channels from human heart with profoundly different activation kinetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

Molecular characterization of a slowly gating human hyperpolarization-activated channel predominantly expressed in thalamus, heart, and testis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

Molecular mechanism of cAMP modulation of HCN pacemaker channels.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

Cardiac HCN channels: structure, function, and modulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

The hyperpolarization-activated channel HCN4 is required for the generation of pacemaker action potentials in the embryonic heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

Absence epilepsy and sinus dysrhythmia in mice lacking the pacemaker channel HCN2

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

Molecular characterization of the hyperpolarization-activated cation channel in rabbit heart sinoatrial node

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

Selective knockout of mouse ERG1 B potassium channel eliminates I(Kr) in adult ventricular myocytes and elicits episodes of abrupt sinus bradycardia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

HERG channel dysfunction in human long QT syndrome. Intracellular transport and functional defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

Cellular dysfunction of LQT5-minK mutants: abnormalities of IKs, IKr and trafficking in long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

Pacemaker mechanisms in cardiac tissue.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

Current-dependent block of rabbit sino-atrial node I(f) channels by ivabradine

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

Bradycardia-dependent triggered activity: relevance to drug-induced multiform ventricular tachycardia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

Action potential prolongation and induction of abnormal automaticity by low quinidine concentrations in canine Purkinje fibers. Relationship to potassium and cycle length.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

Bradycardia-induced abnormal QT prolongation in patients with complete atrioventricular block with torsades de pointes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311953200

21 January 2018

Identifiers

DOI

10.1074/JBC.M311953200

1 reference

22 July 2017

1 reference