• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Dilated cardiomyopathy due to sodium channel dysfunction: what is the connection?

作者信息

Bezzina Connie R, Remme Carol Ann

出版信息

Circ Arrhythm Electrophysiol. 2008 Jun 1;1(2):80-2. doi: 10.1161/CIRCEP.108.791434.

DOI:10.1161/CIRCEP.108.791434
PMID:19808397
Abstract
摘要

相似文献

1
Dilated cardiomyopathy due to sodium channel dysfunction: what is the connection?钠通道功能障碍所致扩张型心肌病:有何关联?
Circ Arrhythm Electrophysiol. 2008 Jun 1;1(2):80-2. doi: 10.1161/CIRCEP.108.791434.
2
[The cardiac sodium channel gene SCN5A mutation and dilated cardiomyopathy].[心脏钠通道基因SCN5A突变与扩张型心肌病]
Sheng Li Ke Xue Jin Zhan. 2010 Feb;41(1):72-4.
3
Dilated cardiomyopathy is associated with reduced expression of the cardiac sodium channel Scn5a.扩张型心肌病与心脏钠通道Scn5a的表达降低有关。
Cardiovasc Res. 2007 Aug 1;75(3):498-509. doi: 10.1016/j.cardiores.2007.04.009. Epub 2007 Apr 21.
4
SCN5A overlap syndromes: no end to disease complexity?SCN5A重叠综合征:疾病复杂性无尽头?
Europace. 2008 Nov;10(11):1253-5. doi: 10.1093/europace/eun267. Epub 2008 Sep 26.
5
Arrhythmias and dilated cardiomyopathy common pathogenetic pathways?心律失常和扩张型心肌病有共同的发病机制吗?
J Am Coll Cardiol. 2011 May 24;57(21):2169-71. doi: 10.1016/j.jacc.2010.11.061.
6
[Update on cardiac SCN5A gene mutation and dilated cardiomyopathy].[心脏SCN5A基因突变与扩张型心肌病的研究进展]
Zhonghua Xin Xue Guan Bing Za Zhi. 2011 Feb;39(2):182-4.
7
Phenotypical manifestations of mutations in the genes encoding subunits of the cardiac sodium channel.心脏钠离子通道亚单位基因突变的表型表现。
Circ Res. 2011 Apr 1;108(7):884-97. doi: 10.1161/CIRCRESAHA.110.238469.
8
Letter regarding article by McNair et al, "SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia".关于 McNair 等人所著文章《与扩张型心肌病、传导障碍和心律失常相关的 SCN5A 突变》的信函
Circulation. 2005 Jul 5;112(1):e9; author reply e9-10. doi: 10.1161/CIRCULATIONAHA.104.531475.
9
Do cypher gene mutations cause left ventricular noncompaction with subclinical myopathy?Cypher基因突变会导致左心室心肌致密化不全合并亚临床心肌病吗?
J Am Coll Cardiol. 2004 Sep 1;44(5):1139; author reply 1139-40. doi: 10.1016/j.jacc.2004.06.007.
10
SCN5A--a mechanistic link between inherited cardiomyopathies and a predisposition to arrhythmias?
JAMA. 2005 Jan 26;293(4):491-3. doi: 10.1001/jama.293.4.491.

引用本文的文献

1
Hypoxia-responsive zinc finger E-box-binding homeobox 2 (ZEB2) regulates a network of calcium-handling genes in the injured heart.缺氧反应性锌指E盒结合同源盒蛋白2(ZEB2)调控受损心脏中钙处理基因网络。
Cardiovasc Res. 2024 Dec 4;120(15):1869-1883. doi: 10.1093/cvr/cvae163.
2
channelopathy: arrhythmia, cardiomyopathy, epilepsy and beyond.通道病:心律失常、心肌病、癫痫等。
Philos Trans R Soc Lond B Biol Sci. 2023 Jun 19;378(1879):20220164. doi: 10.1098/rstb.2022.0164. Epub 2023 May 1.
3
Late Sodium Current of the Heart: Where Do We Stand and Where Are We Going?
心脏的晚钠电流:我们现状如何,又将走向何方?
Pharmaceuticals (Basel). 2022 Feb 15;15(2):231. doi: 10.3390/ph15020231.
4
Identification of p.C335R Variant in a Large Family with Dilated Cardiomyopathy and Conduction Disease.一个大型扩张型心肌病伴传导疾病家系中 p.C335R 变异的鉴定。
Int J Mol Sci. 2021 Nov 30;22(23):12990. doi: 10.3390/ijms222312990.
5
Genetic basis and molecular biology of cardiac arrhythmias in cardiomyopathies.心肌疾病中心律失常的遗传基础和分子生物学。
Cardiovasc Res. 2020 Jul 15;116(9):1600-1619. doi: 10.1093/cvr/cvaa116.
6
Heritable arrhythmia syndromes associated with abnormal cardiac sodium channel function: ionic and non-ionic mechanisms.遗传性心律失常综合征与心脏钠通道功能异常相关:离子和非离子机制。
Cardiovasc Res. 2020 Jul 15;116(9):1557-1570. doi: 10.1093/cvr/cvaa082.
7
Absence of Functional Na1.8 Channels in Non-diseased Atrial and Ventricular Cardiomyocytes.非病变的心房和心室心肌细胞中功能性 Na1.8 通道的缺失。
Cardiovasc Drugs Ther. 2019 Dec;33(6):649-660. doi: 10.1007/s10557-019-06925-6.
8
Functional Consequences of the -p.Y1977N Mutation within the PY Ubiquitylation Motif: Discrepancy between HEK293 Cells and Transgenic Mice.PY 泛素化基序内 -p.Y1977N 突变的功能后果:HEK293 细胞和转基因小鼠之间的差异。
Int J Mol Sci. 2019 Oct 11;20(20):5033. doi: 10.3390/ijms20205033.
9
Cardiac Sodium Channel Dysfunction and Dilated Cardiomyopathy: A Contemporary Reappraisal of Pathophysiological Concepts.心脏钠通道功能障碍与扩张型心肌病:病理生理概念的当代重新评估
J Clin Med. 2019 Jul 12;8(7):1029. doi: 10.3390/jcm8071029.
10
Disease Modifiers of Inherited Channelopathy.遗传性通道病的疾病修饰因子
Front Cardiovasc Med. 2018 Oct 1;5:137. doi: 10.3389/fcvm.2018.00137. eCollection 2018.