메뉴 건너뛰기




Volumn 9, Issue 2, 2002, Pages 206-214

The molecular basis of cardiac arrhythmias

Author keywords

[No Author keywords available]

Indexed keywords

CONTRACTILE PROTEIN; ION CHANNEL; STRUCTURAL PROTEIN;

EID: 0036521076     PISSN: 10713581     EISSN: None     Source Type: Journal    
DOI: 10.1067/mnc.2002.122763     Document Type: Article
Times cited : (1)

References (30)
  • 1
    • 0033514256 scopus 로고    scopus 로고
    • Genetic and molecular basis of cardiac arrhythmias: Impact on clinical management parts I and II
    • Priori SG, Barhanin J, Hauer RN, Haverkamp W, Jongsma HJ, Kleber AG, et al. Genetic and molecular basis of cardiac arrhythmias: impact on clinical management parts I and II. Circulation 1999;99:518-28.
    • (1999) Circulation , vol.99 , pp. 518-528
    • Priori, S.G.1    Barhanin, J.2    Hauer, R.N.3    Haverkamp, W.4    Jongsma, H.J.5    Kleber, A.G.6
  • 3
    • 0001855096 scopus 로고    scopus 로고
    • Ion channels in cardiac muscle
    • Langer GA, editor. 2nd ed. San Diego: Academic Press
    • Weiss JN. Ion channels in cardiac muscle. In: Langer GA, editor. The mammalian myocardium. 2nd ed. San Diego: Academic Press; 1997. p. 101.
    • (1997) The Mammalian Myocardium , pp. 101
    • Weiss, J.N.1
  • 4
    • 0033017643 scopus 로고    scopus 로고
    • Structure and function of cardiac potassium channels
    • Snyders DJ. Structure and function of cardiac potassium channels. Cardiovasc Res 1999;42:377-90.
    • (1999) Cardiovasc. Res , vol.42 , pp. 377-390
    • Snyders, D.J.1
  • 6
    • 0029560263 scopus 로고
    • Increased vulnerability of the subendocardium to ischaemic injury. an electrophysiological explanation
    • Krishnan SC, Shivkumar K, Garan H, Ruskin JN. Increased vulnerability of the subendocardium to ischaemic injury. an electrophysiological explanation. Lancet 1995;346:1612-4.
    • (1995) Lancet , vol.346 , pp. 1612-1614
    • Krishnan, S.C.1    Shivkumar, K.2    Garan, H.3    Ruskin, J.N.4
  • 8
    • 0035313235 scopus 로고    scopus 로고
    • Molecular biology and the prolonged QT syndromes
    • Towbin JA, Vatta M. Molecular biology and the prolonged QT syndromes. Am J Med 2001;110:385-98.
    • (2001) Am. J. Med , vol.110 , pp. 385-398
    • Towbin, J.A.1    Vatta, M.2
  • 9
    • 0028874658 scopus 로고
    • Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy
    • Schwartz PJ, Priori SG, Locati EH, Napolitano C, Cantu F, Towbin JA, et al. Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy. Circulation 1995;92:3381-6.
    • (1995) Circulation , vol.92 , pp. 3381-3386
    • Schwartz, P.J.1    Priori, S.G.2    Locati, E.H.3    Napolitano, C.4    Cantu, F.5    Towbin, J.A.6
  • 10
    • 0029831629 scopus 로고    scopus 로고
    • Genetically defined therapy of inherited long-QT syndrome. Correction of abnormal repolarization by potassium
    • Compton SJ, Lux RL, Ramsey MR, Strelich KR, Sanguinetti MC, Green LS, et al. Genetically defined therapy of inherited long-QT syndrome. Correction of abnormal repolarization by potassium. Circulation 1996;94:1018-22.
    • (1996) Circulation , vol.94 , pp. 1018-1022
    • Compton, S.J.1    Lux, R.L.2    Ramsey, M.R.3    Strelich, K.R.4    Sanguinetti, M.C.5    Green, L.S.6
  • 11
    • 0033530381 scopus 로고    scopus 로고
    • Long QT syndromes and torsade de pointes
    • Viskin S. Long QT syndromes and torsade de pointes. Lancet 1999;354:1625-33.
    • (1999) Lancet , vol.354 , pp. 1625-1633
    • Viskin, S.1
  • 12
    • 0034662689 scopus 로고    scopus 로고
    • Images in cardiovascular medicine. Labile repolarization from "cell to bedside"
    • Shivkumar K. Images in cardiovascular medicine. Labile repolarization from "cell to bedside." Circulation 2000;102:817-8.
    • (2000) Circulation , vol.102 , pp. 817-818
    • Shivkumar, K.1
  • 13
    • 0032546384 scopus 로고    scopus 로고
    • Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
    • Chen Q, Kirsch GE, Zhang D, Brugada R, Brugada J, Brugada P, et al. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation. Nature 1998;392:293-6.
    • (1998) Nature , vol.392 , pp. 293-296
    • Chen, Q.1    Kirsch, G.E.2    Zhang, D.3    Brugada, R.4    Brugada, J.5    Brugada, P.6
  • 15
    • 0033405388 scopus 로고    scopus 로고
    • Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts
    • Swan H, Piippo K, Viitasalo M, Heikkila P, Paavonen T, Kainulainen K, et al. Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts. J Am Coll Cardiol 1999;34:2035-42.
    • (1999) J. Am. Coll. Cardiol , vol.34 , pp. 2035-2042
    • Swan, H.1    Piippo, K.2    Viitasalo, M.3    Heikkila, P.4    Paavonen, T.5    Kainulainen, K.6
  • 16
    • 0035969990 scopus 로고    scopus 로고
    • Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia
    • Laitinen PJ, Brown KM, Piippo K, Swan H, Devaney JM, Brahmbhatt B, et al. Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia. Circulation 2001;103:485-90.
    • (2001) Circulation , vol.103 , pp. 485-490
    • Laitinen, P.J.1    Brown, K.M.2    Piippo, K.3    Swan, H.4    Devaney, J.M.5    Brahmbhatt, B.6
  • 17
    • 0035895322 scopus 로고    scopus 로고
    • Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia
    • Priori SG, Napolitano C, Tiso N, Memmi M, Vignati G, Bloise R, et al. Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia. Circulation 2001;103:196-200.
    • (2001) Circulation , vol.103 , pp. 196-200
    • Priori, S.G.1    Napolitano, C.2    Tiso, N.3    Memmi, M.4    Vignati, G.5    Bloise, R.6
  • 18
    • 17944398302 scopus 로고
    • Calcium-induced release of calcium from the cardiac sarcoplasmic reticulum
    • Fabiato A. Calcium-induced release of calcium from the cardiac sarcoplasmic reticulum. Am J Physiol 1983;245:C1-14.
    • (1983) Am. J. Physiol , vol.245 , pp. C1-C14
    • Fabiato, A.1
  • 19
    • 0032526065 scopus 로고    scopus 로고
    • Right ventricular outflow tract tachycardia due to a somatic cell mutation in G protein subunitalphai2
    • Lerman BB, Dong B, Stein KM, Markowitz SM, Linden J, Catanzaro DF. Right ventricular outflow tract tachycardia due to a somatic cell mutation in G protein subunitalphai2. J Clin Invest 1998;101:2862-8.
    • (1998) J. Clin. Invest , vol.101 , pp. 2862-2868
    • Lerman, B.B.1    Dong, B.2    Stein, K.M.3    Markowitz, S.M.4    Linden, J.5    Catanzaro, D.F.6
  • 22
    • 0032568477 scopus 로고    scopus 로고
    • Gene for arrhythmogenic right ventricular cardiomyopathy with diffuse nonepidermolytic palmoplantar keratoderma and woolly hair (Naxos disease) maps to 17q21
    • Coonar AS, Protonotarios N, Tsatsopoulou A, Needham EW, Houlston RS, Cliff S, et al. Gene for arrhythmogenic right ventricular cardiomyopathy with diffuse nonepidermolytic palmoplantar keratoderma and woolly hair (Naxos disease) maps to 17q21. Circulation 1998;97:2049-58.
    • (1998) Circulation , vol.97 , pp. 2049-2058
    • Coonar, A.S.1    Protonotarios, N.2    Tsatsopoulou, A.3    Needham, E.W.4    Houlston, R.S.5    Cliff, S.6
  • 24
    • 0027193330 scopus 로고
    • X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus
    • Towbin JA, Hejtmancik JF, Brink P, Gelb B, Zhu XM, Chamberlain JS, et al. X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus. Circulation 1993;87:1854-65.
    • (1993) Circulation , vol.87 , pp. 1854-1865
    • Towbin, J.A.1    Hejtmancik, J.F.2    Brink, P.3    Gelb, B.4    Zhu, X.M.5    Chamberlain, J.S.6
  • 25
    • 0032076955 scopus 로고    scopus 로고
    • Actin mutations in dilated cardiomyopathy, a heritable form of heart failure
    • Olson TM, Michels VV, Thibodeau SN, Tai YS, Keating MT. Actin mutations in dilated cardiomyopathy, a heritable form of heart failure. Science 1998;280:750-2.
    • (1998) Science , vol.280 , pp. 750-752
    • Olson, T.M.1    Michels, V.V.2    Thibodeau, S.N.3    Tai, Y.S.4    Keating, M.T.5
  • 26
    • 0030031004 scopus 로고    scopus 로고
    • Mapping a cardiomyopathy locus to chromosome 3p22-p25
    • Olson TM, Keating MT. Mapping a cardiomyopathy locus to chromosome 3p22-p25. J Clin Invest 1996;97:528-32.
    • (1996) J. Clin. Invest , vol.97 , pp. 528-532
    • Olson, T.M.1    Keating, M.T.2
  • 27
    • 0017685220 scopus 로고
    • Progressive familial heart block-two types
    • Brink AJ, Torrington M. Progressive familial heart block-two types. S Afr Med J 1977;52:53-9.
    • (1977) S. Afr. Med. J , vol.52 , pp. 53-59
    • Brink, A.J.1    Torrington, M.2
  • 29
    • 0034264850 scopus 로고    scopus 로고
    • A novel genetic pathway for sudden cardiac death via defects in the transition between ventricular and conduction system cell lineages
    • Nguyen-Tran VT, Kubalak SW, Minamisawa S, Fiset C, Wollert KC, Brown AB, et al. A novel genetic pathway for sudden cardiac death via defects in the transition between ventricular and conduction system cell lineages. Cell 2000;102:671-82.
    • (2000) Cell , vol.102 , pp. 671-682
    • Nguyen-Tran, V.T.1    Kubalak, S.W.2    Minamisawa, S.3    Fiset, C.4    Wollert, K.C.5    Brown, A.B.6
  • 30
    • 12644276397 scopus 로고    scopus 로고
    • Mutations affecting the formation and function of the cardiovascular system in the zebrafish embryo
    • Stainier DY, Fouquet B, Chen JN, Warren KS, Weinstein BM, Meiler SE, et al. Mutations affecting the formation and function of the cardiovascular system in the zebrafish embryo. Development 1996;123:285-92.
    • (1996) Development , vol.123 , pp. 285-292
    • Stainier, D.Y.1    Fouquet, B.2    Chen, J.N.3    Warren, K.S.4    Weinstein, B.M.5    Meiler, S.E.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.