Keeping hyperactive voltage-gated sodium channels in silent mode.
作者信息
Bendahhou Saïd
机构信息
CNRS - LP2M, Université de Nice Sophia Antipolis, Faculté des Science Parc Valrose, Nice, France.
出版信息
J Physiol. 2012 Jun 1;590(11):2543-4. doi: 10.1113/jphysiol.2012.229310.
Abstract
摘要
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本文引用的文献
1
Biophysical characterization of M1476I, a sodium channel founder mutation associated with cold-induced myotonia in French Canadians.M1476I 钠离子通道致病变异的生物物理特性研究，该突变与法裔加拿大人的低温诱发肌强直相关。
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2
Skeletal muscle na channel disorders.骨骼肌钠离子通道病。
Front Pharmacol. 2011 Oct 14;2:63. doi: 10.3389/fphar.2011.00063. eCollection 2011.
3
Mechanisms underlying a life-threatening skeletal muscle Na+ channel disorder.危及生命的骨骼肌钠离子通道病的发病机制。
J Physiol. 2011 Jul 1;589(Pt 13):3115-24. doi: 10.1113/jphysiol.2011.207977. Epub 2011 Apr 26.
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Severe neonatal episodic laryngospasm due to de novo SCN4A mutations: a new treatable disorder.严重新生儿发作性喉痉挛与 SCN4A 基因突变有关：一种新的可治疗疾病。
Neurology. 2010 Aug 17;75(7):641-5. doi: 10.1212/WNL.0b013e3181ed9e96.
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A novel founder SCN4A mutation causes painful cold-induced myotonia in French-Canadians.一种新的始祖SCN4A突变导致法裔加拿大人出现疼痛性冷诱导性肌强直。
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Mexiletine block of wild-type and inactivation-deficient human skeletal muscle hNav1.4 Na+ channels.美西律对野生型和失活缺陷型人骨骼肌hNav1.4钠通道的阻断作用。
J Physiol. 2004 Feb 1;554(Pt 3):621-33. doi: 10.1113/jphysiol.2003.054973. Epub 2003 Nov 7.
7
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8
Impaired slow inactivation in mutant sodium channels.突变钠通道中缓慢失活受损。
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9
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Biophys J. 1994 Feb;66(2 Pt 1):542. doi: 10.1016/s0006-3495(94)80807-0.
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