Intracellular calcium handling dysfunction and arrhythmogenesis - A new challenge for the electrophysiologist

被引：20

作者：

Priori, SG

Napolitano, C

机构：

[1] Univ Pavia, Maugeri Fdn, IRCCS, I-27100 Pavia, Italy

[2] Univ Pavia, Dept Cardiol, I-27100 Pavia, Italy

来源：

CIRCULATION RESEARCH | 2005年 / 97卷 / 11期

关键词：

sudden death; arrhythmias; genetics;

D O I：

10.1161/01.RES.0000194556.41865.e2

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：1077 / 1079

页数：3

共 24 条

[1] Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system [J].

Bezzina, CR ;

Rook, MB ;

Groenewegen, WA ;

Herfst, LJ ;

van der Wal, AC ;

Lam, J ;

Jongsma, HJ ;

Wilde, AAM ;

Mannens, MMAM .

CIRCULATION RESEARCH, 2003, 92 (02) :159-168

[2] Bidirectional ventricular tachycardia and fibrillation elicited in a knock-in mouse model carrier of a mutation in the cardiac ryanodine receptor [J].

Cerrone, M ;

Colombi, B ;

Santoro, M ;

di Barletta, MR ;

Scelsi, M ;

Villani, L ;

Napolitano, C ;

Priori, SG .

CIRCULATION RESEARCH, 2005, 96 (10) :E77-E82

[3]

Coumel P., 1978, BRIT HEART J, V40, P28

[4] Ryanodine receptor mutations associated with stress-induced ventricular tachycardia mediate increased calcium release in stimulated cardiomyocytes [J].

George, CH ;

Higgs, GV ;

Lai, FA .

CIRCULATION RESEARCH, 2003, 93 (06) :531-540

[5] RyR2 mutations linked to ventricular tachycardia and sudden death reduce the threshold for store-overload-induced Ca2+ release (SOICR) [J].

Jiang, DW ;

Xiao, BL ;

Yang, DM ;

Wang, RW ;

Choi, P ;

Zhang, L ;

Cheng, HP ;

Chen, SRW .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (35) :13062-13067

[6] Enhanced basal activity of a cardiac Ca2+ release channel (Ryanodine receptor) mutant associated with ventricular tachycardia and sudden death [J].

Jiang, DW ;

Xiao, BL ;

Zhang, L ;

Chen, SRW .

CIRCULATION RESEARCH, 2002, 91 (03) :218-225

[7] Enhanced store overload-induced Ca2+ release and channel sensitivity to luminal Ca2+ activation are common defects of RyR2 mutations linked to ventricular tachycardia and sudden death [J].

Jiang, DW ;

Wang, RW ;

Xiao, BL ;

Kong, HH ;

Hunt, DJ ;

Choi, P ;

Zhang, L ;

Chen, SRW .

CIRCULATION RESEARCH, 2005, 97 (11) :1173-1181

[8] Cellular mechanism of calcium-mediated triggered activity in the heart [J].

Katra, RP ;

Laurita, KR .

CIRCULATION RESEARCH, 2005, 96 (05) :535-542

[9] A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel [J].

Lahat, H ;

Pras, E ;

Olender, T ;

Avidan, N ;

Ben-Asher, E ;

Man, O ;

Levy-Nissenbaum, E ;

Khoury, A ;

Lorber, A ;

Goldman, B ;

Lancet, D ;

Eldar, M .

AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (06) :1378-1384

[10] Calstabin deficiency, ryanodine receptors, and sudden cardiac death [J].

Lehnart, SE ;

Wehrens, XHT ;

Marks, AR .

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 322 (04) :1267-1279

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