Molecular and cellular mechanisms of cardiac arrhythmias

被引：765

作者：

Keating, MT ^{[1
]}

Sanguinetti, MC

机构：

[1] Harvard Univ, Sch Med,Childrens Hosp, Howard Hughes Med Inst, Dept Cell Biol, Boston, MA 02115 USA

[2] Univ Utah, Hlth Sci Ctr, Dept Med,Eccles Program Human Mol Biol & Genet, Div Cardiol, Salt Lake City, UT 84112 USA

来源：

CELL | 2001年 / 104卷 / 04期

关键词：

D O I：

10.1016/S0092-8674(01)00243-4

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

[No abstract available]

引用

页码：569 / 580

页数：12

共 71 条

[61] SCN5A MUTATIONS ASSOCIATED WITH AN INHERITED CARDIAC-ARRHYTHMIA, LONG QT SYNDROME [J].

WANG, Q ;

SHEN, JX ;

SPLAWSKI, I ;

ATKINSON, D ;

LI, ZZ ;

ROBINSON, JL ;

MOSS, AJ ;

TOWBIN, JA ;

KEATING, MT .

CELL, 1995, 80 (05) :805-811

[62] CARDIAC SODIUM-CHANNEL MUTATIONS IN PATIENTS WITH LONG QT SYNDROME, AN INHERITED CARDIAC-ARRHYTHMIA [J].

WANG, Q ;

SHEN, JX ;

LI, ZZ ;

TIMOTHY, K ;

VINCENT, GM ;

PRIORI, SG ;

SCHWARTZ, PJ ;

KEATING, MT .

HUMAN MOLECULAR GENETICS, 1995, 4 (09) :1603-1607

[63] Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias [J].

Wang, Q ;

Curran, ME ;

Splawski, I ;

Burn, TC ;

Millholland, JM ;

VanRaay, TJ ;

Shen, J ;

Timothy, KW ;

Vincent, GM ;

deJager, T ;

Schwartz, PJ ;

Towbin, JA ;

Moss, AJ ;

Atkinson, DL ;

Landes, GM ;

Connors, TD ;

Keating, MT .

NATURE GENETICS, 1996, 12 (01) :17-23

[64] Functional effects of mutations in KvLQT1 that cause long QT syndrome [J].

Wang, Z ;

Tristani-Firouzi, M ;

Xu, Q ;

Lin, M ;

Keating, MT ;

Sanguinetti, MC .

JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 1999, 10 (06) :817-826

[65]

WARD O C, 1964, J Ir Med Assoc, V54, P103

[66] A FAMILY OF POTASSIUM CHANNEL GENES RELATED TO EAG IN DROSOPHILA AND MAMMALS [J].

WARMKE, JW ;

GANETZKY, B .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (08) :3438-3442

[67] CIRCADIAN VARIATION IN THE INCIDENCE OF SUDDEN CARDIAC DEATH IN THE FRAMINGHAM HEART-STUDY POPULATION [J].

WILLICH, SN ;

LEVY, D ;

ROCCO, MB ;

TOFLER, GH ;

STONE, PH ;

MULLER, JE .

AMERICAN JOURNAL OF CARDIOLOGY, 1987, 60 (10) :801-806

[68] Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias [J].

Wollnik, B ;

Schroeder, BC ;

Kubisch, C ;

Esperer, HD ;

Wieacker, P ;

Jentsch, TJ .

HUMAN MOLECULAR GENETICS, 1997, 6 (11) :1943-1949

[69] KvLQT1, a voltage-gated potassium channel responsible for human cardiac arrhythmias [J].

Yang, WP ;

Levesque, PC ;

Little, WA ;

Conder, ML ;

Shalaby, FY ;

Blanar, MA .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (08) :4017-4021

[70] Functional expression of two KvLQT1-related potassium channels responsible for an inherited idiopathic epilepsy [J].

Yang, WP ;

Levesque, PC ;

Little, WA ;

Conder, ML ;

Ramakrishnan, P ;

Neubauer, MG ;

Blanar, MA .

JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (31) :19419-19423

← 1 2 3 4 5 6 7 8 →