Electrical heart disease: Genetic and molecular basis of cardiac arrhythmias in normal structural hearts.

about

The genetic and clinical features of cardiac channelopathies.

P2860

Q37770572-02FA6676-94E5-4508-877B-01213A04B41F

P2860

Electrical heart disease: Genetic and molecular basis of cardiac arrhythmias in normal structural hearts.

Item

http://www.wikidata.org/entity/Q36898735

description

2007 nî lūn-bûn

@nan

2007年の論文

@ja

2007年論文

@yue

2007年論文

@zh-hant

2007年論文

@zh-hk

2007年論文

@zh-mo

2007年論文

@zh-tw

2007年论文

@wuu

2007年论文

@zh

2007年论文

@zh-cn

name

Electrical heart disease: Gene ...... s in normal structural hearts.

@en

type

Item

label

Electrical heart disease: Gene ...... s in normal structural hearts.

@en

prefLabel

Electrical heart disease: Gene ...... s in normal structural hearts.

@en

P1476

Electrical heart disease: Gene ...... s in normal structural hearts.

@en

P2093

David Farwell

http://www.w3.org/2001/XMLSchema#string

Michael H Gollob

http://www.w3.org/2001/XMLSchema#string

P2860

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

PKA phosphorylation dissociates FKBP12.6 from the calcium release channel (ryanodine receptor): defective regulation in failing hearts

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

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

Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation

Sudden death in familial polymorphic ventricular tachycardia associated with calcium release channel (ryanodine receptor) leak

A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel

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

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

K201 (JTV519) suppresses spontaneous Ca2+ release and [3H]ryanodine binding to RyR2 irrespective of FKBP12.6 association

P304

16A-22A

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1016/S0828-282X(07)71001-2

http://www.w3.org/2001/XMLSchema#string

P478

23 Suppl A

http://www.w3.org/2001/XMLSchema#string

P577

2007-08-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

17668083

http://www.w3.org/2001/XMLSchema#string

P932

2786999

http://www.w3.org/2001/XMLSchema#string

Electrical heart disease: Genetic and molecular basis of cardiac arrhythmias in normal structural hearts.

about

P2860

P2860

Electrical heart disease: Genetic and molecular basis of cardiac arrhythmias in normal structural hearts.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P577

P698

P932