Genetics, molecular mechanisms and management of long QT syndrome.
about
PAS domains: internal sensors of oxygen, redox potential, and lightTargeted disruption of the Kcnq1 gene produces a mouse model of Jervell and Lange-Nielsen Syndrome.Characterization of the cardiac sodium channel SCN5A mutation, N1325S, in single murine ventricular myocytes.Ion channels and the genetic contribution to epilepsy.Congenital long QT syndromes and Brugada syndrome: the arrhythmogenic ion channel disorders.The dog's role in the preclinical assessment of QT interval prolongation.LQT4 gene: the "missing" ankyrin.Cardiac sodium channel regulator MOG1 regulates cardiac morphogenesis and rhythm.αB-Crystallin Interacts with Nav1.5 and Regulates Ubiquitination and Internalization of Cell Surface Nav1.5.Risk of serious cardiovascular problems with medications for attention-deficit hyperactivity disorder.A recessive C-terminal Jervell and Lange-Nielsen mutation of the KCNQ1 channel impairs subunit assembly.HERG biosynthesis: the positive influence of negative charge.Reentry via high-frequency pacing in a mathematical model for human-ventricular cardiac tissue with a localized fibrotic region.
P2860
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P2860
Genetics, molecular mechanisms and management of long QT syndrome.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
Genetics, molecular mechanisms and management of long QT syndrome.
@en
type
label
Genetics, molecular mechanisms and management of long QT syndrome.
@en
prefLabel
Genetics, molecular mechanisms and management of long QT syndrome.
@en
P2093
P2860
P1433
P1476
Genetics, molecular mechanisms and management of long QT syndrome.
@en
P2093
P2860
P356
10.3109/07853899808999385
P407
P577
1998-02-01T00:00:00Z