Genetics of sick sinus syndrome.
作者信息
Anderson Jeffrey B, Benson D Woodrow
机构信息
Instructor of Pediatrics, The Heart Institute, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, Ohio.
出版信息
Card Electrophysiol Clin. 2010 Dec 1;2(4):499-507. doi: 10.1016/j.ccep.2010.09.001.
Abstract
摘要
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本文引用的文献
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2
Control of heart rate by cAMP sensitivity of HCN channels.通过超极化激活的环核苷酸门控通道（HCN通道）的环磷酸腺苷（cAMP）敏感性来控制心率。
Proc Natl Acad Sci U S A. 2009 Jul 21;106(29):12189-94. doi: 10.1073/pnas.0810332106. Epub 2009 Jul 1.
3
Molecular architecture of the human sinus node: insights into the function of the cardiac pacemaker.人类窦房结的分子结构：对心脏起搏器功能的深入了解
Circulation. 2009 Mar 31;119(12):1562-75. doi: 10.1161/CIRCULATIONAHA.108.804369. Epub 2009 Mar 16.
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Genetic Na+ channelopathies and sinus node dysfunction.遗传性钠离子通道病与窦房结功能障碍。
Prog Biophys Mol Biol. 2008 Oct-Nov;98(2-3):171-8. doi: 10.1016/j.pbiomolbio.2008.10.003. Epub 2008 Nov 5.
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Genesis and regulation of the heart automaticity.心脏自律性的发生与调节。
Physiol Rev. 2008 Jul;88(3):919-82. doi: 10.1152/physrev.00018.2007.
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HCN4 provides a 'depolarization reserve' and is not required for heart rate acceleration in mice.HCN4提供一种“去极化储备”，对小鼠心率加速并非必需。
EMBO J. 2007 Oct 31;26(21):4423-32. doi: 10.1038/sj.emboj.7601868. Epub 2007 Oct 4.
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Point mutation in the HCN4 cardiac ion channel pore affecting synthesis, trafficking, and functional expression is associated with familial asymptomatic sinus bradycardia.影响合成、转运和功能表达的HCN4心脏离子通道孔中的点突变与家族性无症状窦性心动过缓有关。
Circulation. 2007 Jul 31;116(5):463-70. doi: 10.1161/CIRCULATIONAHA.107.706887. Epub 2007 Jul 23.
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