相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。The Brugada ECG Pattern A Marker of Channelopathy, Structural Heart Disease, or Neither? Toward a Unifying Mechanism of the Brugada Syndrome
Mark G. Hoogendijk et al.
CIRCULATION-ARRHYTHMIA AND ELECTROPHYSIOLOGY (2010)
Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death
Elena Burashnikov et al.
HEART RHYTHM (2010)
Control of the cardiac action potential: The role of repolarization dynamics
Antonio Zaza
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2010)
A novel computational model of the human ventricular action potential and Ca transient
Eleonora Grandi et al.
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2010)
Human embryonic kidney (HEK293) cells express endogenous voltage-gated sodium currents and Nav1.7 sodium channels
Bingjun He et al.
NEUROSCIENCE LETTERS (2010)
A Mutation in the β3 Subunit of the Cardiac Sodium Channel Associated With Brugada ECG Phenotype
Dan Hu et al.
CIRCULATION-CARDIOVASCULAR GENETICS (2009)
Genetic Modulation of Brugada Syndrome by a Common Polymorphism
Eric Lizotte et al.
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY (2009)
Theoretical investigation of action potential duration dependence on extracellular Ca2+ in human cardiomyocytes
Eleonora Grandi et al.
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2009)
Functional Effects of KCNE3 Mutation and Its Role in the Development of Brugada Syndrome
Eva Delpon et al.
CIRCULATION-ARRHYTHMIA AND ELECTROPHYSIOLOGY (2008)
SCN5A channelopathies - An update on mutations and mechanisms
Thomas Zimmer et al.
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY (2008)
Mutation in glycerol-3-phosphate dehydrogenase 1-like gene (GPD1-L) decreases cardiac Na+ current and causes inherited Arrhythmias
Barry London et al.
CIRCULATION (2007)
Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-Segment elevation, short QT intervals, and sudden cardiac death
Charles Antzelevitch et al.
CIRCULATION (2007)
Cardiac sodium channel dysfunction in sudden infant death syndrome
Dao W. Wang et al.
CIRCULATION (2007)
A common polymorphism in SCN5A is associated with lone atrial fibrillation
L. Y. Chen et al.
CLINICAL PHARMACOLOGY & THERAPEUTICS (2007)
Compound heterozygous mutations P336L and I1660V in the human cardiac sodium channel associated with the Brugada syndrome
Jonathan M. Cordeiro et al.
CIRCULATION (2006)
SCN5A polymorphism restores trafficking of a Brugada syndrome mutation on a separate gene
Steven Poelzing et al.
CIRCULATION (2006)
Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population
L Gouas et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2005)
Sodium channels as macromolecular complexes: Implications for inherited arrhythmia syndromes
LS Meadows et al.
CARDIOVASCULAR RESEARCH (2005)
Pathophysiological mechanisms of Brugada syndrome: Depolarization disorder, repolarization disorder, or more?
PG Meregalli et al.
CARDIOVASCULAR RESEARCH (2005)
Brugada syndrome, report of the Second Consensus Conference (vol 2, pg 429, 2005)
C Antzelevitch
HEART RHYTHM (2005)
A common human SCN5A polymorphism modifies expression of an arrhythmia causing mutation
B Ye et al.
PHYSIOLOGICAL GENOMICS (2003)
A common SCN5A polymorphism modulates the biophysical effects of an SCN5A mutation
PC Viswanathan et al.
JOURNAL OF CLINICAL INVESTIGATION (2003)
Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes
P Yang et al.
CIRCULATION (2002)
A single residue differentiates between human cardiac and skeletal muscle Na+ channel slow inactivation
YY Vilin et al.
BIOPHYSICAL JOURNAL (2001)
Inactivation and recovery of sodium currents in cerebellar Purkinje neurons: Evidence for two mechanisms
IM Raman et al.
BIOPHYSICAL JOURNAL (2001)
Two distinct congenital arrhythmias evoked by a multidysfunctional Na+ channel
MW Veldkamp et al.
CIRCULATION RESEARCH (2000)