期刊文献+

CDICdb:一个疾病-离子通道关联库

CDICdb:Database of Correlations between Disease and Ion Channel
下载PDF
导出
摘要 离子通道是镶嵌在生物膜上的蛋白质,提供了离子出入膜的生物孔道。它们不但与许多基本的生理功能相关,现有研究发现它们还与许多疾病的发生发展有密切的关系。疾病-离子通道关联库(DataBase of Correlations between Disease and Ion Channel,CDICdb)实现了依据离子通道查询相关的疾病,以及依据疾病查询相关离子通道和离子通道关联的KEGG库中Pathway通路的信息的功能。利用本数据库提供的关联网络,研究人员可以对离子通道病有更全面的认识。CDICdb是一个关系型数据库,现在可以免费地使用,网址为:http://db.cdicdb.com/channel2disease/index.html。 Ion channels are pore-forming proteins that allow the passive diffusion of ions across biological membranes.They are responsible for various fundamental biological functions,and a large quantity of studies have demonstrated their closer associations with many diseases.Here,we developed a manually curated database,termed CDICdb,which provides comprehensive information between diseases and ion channels.Using the database,users can search ion channels according to ion-based classification,and then obtain related diseases.They can also search a disease to get relevant ion channels and their associated pathway information from KEGG.In addition,the database provides researchers a comprehensive and systematic insight into the pathogenesis of ion channel-induced diseases.CDICdb is a relational database between diseases and ion channels,and is freely available at http://db.cdicdb.com/channel2disease/.
作者 胡贵祥 李霞
出处 《医学信息(中旬刊)》 2011年第4期1245-1247,共3页 Medical Information Operations Sciences Fascicule
基金 国家自然基金(批准号:61073136) 国家863项目(批准号:2007AA02Z329)
关键词 数据库 疾病 离子通道 关联 PATHWAY Database Disease Ion channel Correlation Pathway
  • 相关文献

参考文献23

  • 1Giraudat J,Devillers-Thiery A,Auffray C,et al.Identification of a cDNA clone coding for the acetylcholine binding subunit of Torpedo marmorata acetylcholine receptor[J].EMBO J,1982,1(6):713-7.
  • 2Hübner CA,Jentsch TJ.Ion channel diseases[J].Hum Mol Genet,2002,11(20):2435-45.
  • 3Curran ME,Splawski I,Timothy KW,et al.A molecular basis for cardiac arrhythmia:HERG mutations cause long QT syndrome[J].Cell,1995 Mar 10,80(5):795-803.
  • 4Kullmann DM,Hanna MG.Neurological disorders caused by inherited ion-channel mutations.Lancet Neurol,2002 Jul,1(3):157-66.
  • 5Kass RS.The channelopathies:novel insights into molecular and genetic mechanisms of human disease[J].J Clin Invest,2005 Aug,115(8):1986-9.
  • 6Abbott GW,Butler MH,Bendahhou S,et al.MiRP2 forms potassium channels in skeletal muscle with Kv3.4 and is associated with periodic paralysis[J].Cell,2001 Jan 26,104(2):217-31.
  • 7Pouget J.A new type of periodic paralysis:Andersen-Tawil syndrome[J].Bull Acad Natl Med,2008 Nov,192(8):1551-6,discussion 1556-7.
  • 8Ryan DP,da Silva MR,Soong TW,et al.Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis[J].Cell,2010 Jan 8,140(1):88-98.
  • 9Ptácek LJ,Tawil R,Griggs RC,et al.Dihydropyridine receptor mutations cause hypokalemic periodic paralysis[J].Cell,1994 Jun 17,77(6):863-8.
  • 10Sokolov S,Scheuer T,Catterall WA.Gating pore current in an inherited ion channelopathy[J].Nature,2007 Mar 1,446(7131):76-8.

二级参考文献20

  • 1Brugada R, Brugada J, Brugada P. Right bundle branch block, persistent ST segment elevation in leads Ⅴ1 through Ⅴ3.A marker for sudden death in patients without demonstrable structure heart disease. Circulation, 1998, 97:457-460
  • 2Naccarelli GV, Antzelevitch C. The Brugada syndrome:clinical, genetic, cellular and molecular abnormolities. Am J Medicine, 2001, 110(5):573-581
  • 3Splawski I, Shen J, Timothy KW, et al. Genomic structure of three long QT syndrome genes: KVLQT1, HERG and KCNE1. Genomics, 1998, 51:86-97
  • 4Ilhan A, Yuncer C, Komsuoglu SS, et al. Jervell and Lange-Nielsen syndrome: neurologic and cardiologic evaluation. Pediatr Neurol, 1999, 21:809-813
  • 5Schmitt N, Schwarz M, Peretz A, et al. A recessive Cterminal Jervell and Lange-Nielsen mutation of the KCNQ1 channel impairs subunit assembly. Embo J, 2000, 19:332-340
  • 6Tranebjaerg L, Bathen J, Tyson J, et al. Jervell and Lange-Nielsen syndrome: a Norwegian perspective. Am J Med Genet, 1999, 89:137-146
  • 7Wang Z, Li H, Moss A J, et al. Compound heterozygous mutations in KvLQT1 cause Jervell and Lange-Nielsen syndrome. Mol Genet Metab, 2002, 75(4):308-316
  • 8Ning L, Moss AJ, Zareba W, et al. Novel compound heterozygous mutations in the KCNQI gene associated with autosomal recessive long QT syndrome (Jervell and LangeNielsen syndrome). Ann Noninvasive Electrocardiol, 2003,8(3):246-250
  • 9Herbert E, Trusz-Gluza M, Moric E, et al. KCNQ1 gene mutations and the respective genotype-phenotype correlations in the long QT syndrome. Med Sci Monit, 2002, 8(10):RA240-RA248
  • 10Large V, Hellstrom L, Reynisdottir S, et al. Human β2 adrenoceptor gene polymorphisms are highly frequent in obesity and associates with altered adipocyte β2 adrenoceptor function. J Clin Invest, 1997, 100(12):3005-3013

共引文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部