메뉴 건너뛰기




Volumn 110, Issue 1, 2006, Pages 1-13

Gene-specific therapy for inherited arrhythmogenic diseases

Author keywords

Cardiac arrhythmias; Gene specific therapy; Genetic; Genotype phenotype correlation; Sudden death

Indexed keywords

1 [2 (6 METHYL 2 PYRIDYL)ETHYL] 4 (4 METHYLSULFONYLAMINOBENZOYL)PIPERIDINE; 4 [3 (4 BENZYL 1 PIPERIDINYL)PROPIONYL] 2,3,4,5 TETRAHYDRO 7 METHOXY 1,4 BENZOTHIAZEPINE; ASTEMIZOLE; BETA ADRENERGIC RECEPTOR BLOCKING AGENT; CALCIUM CHANNEL BLOCKING AGENT; CILOSTAZOL; CISAPRIDE; DILTIAZEM; FEXOFENADINE; FLECAINIDE; LIDOCAINE; MEXILETINE; QUINIDINE; RYANODINE RECEPTOR; TEDISAMIL; TERFENADINE; THAPSIGARGIN;

EID: 32644478038     PISSN: 01637258     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pharmthera.2005.08.003     Document Type: Review
Times cited : (26)

References (86)
  • 1
    • 0033574273 scopus 로고    scopus 로고
    • MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia
    • G.W. Abbott, F. Sesti, I. Splawski, M.E. Buck, M.H. Lehmann, and K.W. Timothy MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia Cell 97 1999 175 187
    • (1999) Cell , vol.97 , pp. 175-187
    • Abbott, G.W.1    Sesti, F.2    Splawski, I.3    Buck, M.E.4    Lehmann, M.H.5    Timothy, K.W.6
  • 2
    • 0034702931 scopus 로고    scopus 로고
    • Molecular pharmacology of the sodium channel mutation D1790G linked to the long-QT syndrome
    • H. Abriel, X.H. Wehrens, J. Benhorin, B. Kerem, and R.S. Kass Molecular pharmacology of the sodium channel mutation D1790G linked to the long-QT syndrome Circulation 102 2000 921 925
    • (2000) Circulation , vol.102 , pp. 921-925
    • Abriel, H.1    Wehrens, X.H.2    Benhorin, J.3    Kerem, B.4    Kass, R.S.5
  • 3
    • 0035853405 scopus 로고    scopus 로고
    • Novel arrhythmogenic mechanism revealed by a long-QT syndrome mutation in the cardiac Na(+) channel
    • H. Abriel, C. Cabo, X.H. Wehrens, I. Rivolta, H.K. Motoike, and M. Memmi Novel arrhythmogenic mechanism revealed by a long-QT syndrome mutation in the cardiac Na(+) channel Circ Res 88 2001 740 745
    • (2001) Circ Res , vol.88 , pp. 740-745
    • Abriel, H.1    Cabo, C.2    Wehrens, X.H.3    Rivolta, I.4    Motoike, H.K.5    Memmi, M.6
  • 4
    • 0032572594 scopus 로고    scopus 로고
    • Novel LQT-3 mutation affects Na+ channel activity through interactions between alpha- and beta1-subunits
    • R.H. An, X.L. Wang, B. Kerem, J. Benhorin, A. Medina, and M. Goldmit Novel LQT-3 mutation affects Na+ channel activity through interactions between alpha- and beta1-subunits Circ Res 83 1998 141 146
    • (1998) Circ Res , vol.83 , pp. 141-146
    • An, R.H.1    Wang, X.L.2    Kerem, B.3    Benhorin, J.4    Medina, A.5    Goldmit, M.6
  • 5
    • 0015124692 scopus 로고
    • Intermittent muscular weakness, extrasystoles, and multiple developmental anomalies. a new syndrome?
    • E.D. Andersen, P.A. Krasilnikoff, and H. Overvad Intermittent muscular weakness, extrasystoles, and multiple developmental anomalies. A new syndrome? Acta Paediatr Scand 60 1971 559 564
    • (1971) Acta Paediatr Scand , vol.60 , pp. 559-564
    • Andersen, E.D.1    Krasilnikoff, P.A.2    Overvad, H.3
  • 6
    • 0035112566 scopus 로고    scopus 로고
    • The Brugada syndrome: Ionic basis and arrhythmia mechanisms
    • C. Antzelevitch The Brugada syndrome: ionic basis and arrhythmia mechanisms J Cardiovasc Electrophysiol 12 2001 268 272
    • (2001) J Cardiovasc Electrophysiol , vol.12 , pp. 268-272
    • Antzelevitch, C.1
  • 7
    • 0029952101 scopus 로고    scopus 로고
    • K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current
    • J. Barhanin, F. Lesage, E. Guillemare, M. Fink, M. Lazdunski, and G. Romey K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current Nature 384 1996 78 80
    • (1996) Nature , vol.384 , pp. 78-80
    • Barhanin, J.1    Lesage, F.2    Guillemare, E.3    Fink, M.4    Lazdunski, M.5    Romey, G.6
  • 8
    • 0035933766 scopus 로고    scopus 로고
    • Novel mechanism for Brugada syndrome: Defective surface localization of an SCN5A mutant (R1432G)
    • G. Baroudi, V. Pouliot, I. Denjoy, P. Guicheney, A. Shrier, and M. Chahine Novel mechanism for Brugada syndrome: defective surface localization of an SCN5A mutant (R1432G) Circ Res 88 2001 E78 E83
    • (2001) Circ Res , vol.88
    • Baroudi, G.1    Pouliot, V.2    Denjoy, I.3    Guicheney, P.4    Shrier, A.5    Chahine, M.6
  • 9
    • 0032869692 scopus 로고    scopus 로고
    • Effects of electrophysiologic-guided therapy with Class IA antiarrhythmic drugs on the long-term outcome of patients with idiopathic ventricular fibrillation with or without the Brugada syndrome
    • B. Belhassen, S. Viskin, R. Fish, A. Glick, I. Setbon, and M. Eldar Effects of electrophysiologic-guided therapy with Class IA antiarrhythmic drugs on the long-term outcome of patients with idiopathic ventricular fibrillation with or without the Brugada syndrome J Cardiovasc Electrophysiol 10 1999 1301 1312
    • (1999) J Cardiovasc Electrophysiol , vol.10 , pp. 1301-1312
    • Belhassen, B.1    Viskin, S.2    Fish, R.3    Glick, A.4    Setbon, I.5    Eldar, M.6
  • 10
    • 4644298458 scopus 로고    scopus 로고
    • Efficacy of quinidine in high-risk patients with Brugada syndrome
    • B. Belhassen, A. Glick, and S. Viskin Efficacy of quinidine in high-risk patients with Brugada syndrome Circulation 110 2004 1731 1737
    • (2004) Circulation , vol.110 , pp. 1731-1737
    • Belhassen, B.1    Glick, A.2    Viskin, S.3
  • 12
    • 0029097799 scopus 로고
    • Molecular mechanism for an inherited cardiac arrhythmia
    • P.B. Bennett, K. Yazawa, N. Makita, and A.L. George Jr. Molecular mechanism for an inherited cardiac arrhythmia Nature 376 1995 683 685
    • (1995) Nature , vol.376 , pp. 683-685
    • Bennett, P.B.1    Yazawa, K.2    Makita, N.3    George Jr., A.L.4
  • 13
    • 20344369318 scopus 로고    scopus 로고
    • Short QT syndrome: Mechanisms, diagnosis and treatment
    • P. Bjerregaard, and I. Gussak Short QT syndrome: mechanisms, diagnosis and treatment Nat Clin Pract 2 2 2005 84 87
    • (2005) Nat Clin Pract , vol.2 , Issue.2 , pp. 84-87
    • Bjerregaard, P.1    Gussak, I.2
  • 14
    • 0026466921 scopus 로고
    • Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome. a multicenter report
    • P. Brugada, and J. Brugada Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome. A multicenter report J Am Coll Cardiol 20 1992 1391 1396
    • (1992) J Am Coll Cardiol , vol.20 , pp. 1391-1396
    • Brugada, P.1    Brugada, J.2
  • 16
    • 20344400985 scopus 로고    scopus 로고
    • Bidirectional ventricular tachycardia and fibrillation elicited in a knock-in mouse model carrier of a mutation in the cardiac ryanodine receptor (RyR2)
    • M. Cerrone, B. Colombi, M. Santoro, M. Raffale di Barletta, M. Scelsi, and L. Villani Bidirectional ventricular tachycardia and fibrillation elicited in a knock-in mouse model carrier of a mutation in the cardiac ryanodine receptor (RyR2) Circ Res 96 2005 e77 e82
    • (2005) Circ Res , vol.96
    • Cerrone, M.1    Colombi, B.2    Santoro, M.3    Raffale Di Barletta, M.4    Scelsi, M.5    Villani, L.6
  • 17
    • 0032546384 scopus 로고    scopus 로고
    • Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
    • Q. Chen, G.E. Kirsch, D. Zhang, R. Brugada, J. Brugada, and P. Brugada Genetic basis and molecular mechanism for idiopathic ventricular fibrillation Nature 392 1998 293 296
    • (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
  • 18
    • 0037428218 scopus 로고    scopus 로고
    • KCNQ1 gain-of-function mutation in familial atrial fibrillation
    • Y.H. Chen, S.J. Xu, S. Bendahhou, X.L. Wang, Y. Wang, and W.Y. Xu KCNQ1 gain-of-function mutation in familial atrial fibrillation Science 299 2003 251 254
    • (2003) Science , vol.299 , pp. 251-254
    • Chen, Y.H.1    Xu, S.J.2    Bendahhou, S.3    Wang, X.L.4    Wang, Y.5    Xu, W.Y.6
  • 19
    • 0029831629 scopus 로고    scopus 로고
    • Genetically defined therapy of inherited long-QT syndrome. Correction of abnormal repolarization by potassium
    • S.J. Compton, R.L. Lux, M.R. Ramsey, K.R. Strelich, M.C. Sanguinetti, and L.S. Green Genetically defined therapy of inherited long-QT syndrome. Correction of abnormal repolarization by potassium Circulation 94 1996 1018 1022
    • (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
  • 20
    • 0001276591 scopus 로고
    • Catecholaminergic-induced severe ventricular arrhythmias with Adams-Stokes syndrome in children: Report of four cases
    • P. Coumel, J. Fidelle, V. Lucet, P. Attuel, and Y. Bouvrain Catecholaminergic-induced severe ventricular arrhythmias with Adams-Stokes syndrome in children: report of four cases Br Heart J 40 1978 28 37
    • (1978) Br Heart J , vol.40 , pp. 28-37
    • Coumel, P.1    Fidelle, J.2    Lucet, V.3    Attuel, P.4    Bouvrain, Y.5
  • 22
    • 2442682788 scopus 로고    scopus 로고
    • Andersen-Tawil syndrome: A model of clinical variability, pleiotropy, and genetic heterogeneity
    • M.R. Donaldson, G. Yoon, Y.H. Fu, and L.J. Ptacek Andersen-Tawil syndrome: a model of clinical variability, pleiotropy, and genetic heterogeneity Ann Med 36 Suppl. 1, 92-7 2004 92 97
    • (2004) Ann Med , vol.36 , Issue.92-97 SUPPL. 1 , pp. 92-97
    • Donaldson, M.R.1    Yoon, G.2    Fu, Y.H.3    Ptacek, L.J.4
  • 23
    • 0036667608 scopus 로고    scopus 로고
    • Body surface area of ST elevation and the presence of late potentials correlate to the inducibility of ventricular tachyarrhythmias in Brugada syndrome
    • L. Eckardt, H.J. Bruns, M. Paul, P. Kirchhof, E. Schulze-Bahr, and T. Wichter Body surface area of ST elevation and the presence of late potentials correlate to the inducibility of ventricular tachyarrhythmias in Brugada syndrome J Cardiovasc Electrophysiol 13 2002 742 749
    • (2002) J Cardiovasc Electrophysiol , vol.13 , pp. 742-749
    • Eckardt, L.1    Bruns, H.J.2    Paul, M.3    Kirchhof, P.4    Schulze-Bahr, E.5    Wichter, T.6
  • 24
    • 3242694238 scopus 로고    scopus 로고
    • Loss-of-function mutations of the K(+) channel gene KCNJ2 constitute a rare cause of long QT syndrome
    • H. Fodstad, H. Swan, M. Auberson, I. Gautschi, J. Loffing, and L. Schild Loss-of-function mutations of the K(+) channel gene KCNJ2 constitute a rare cause of long QT syndrome J Mol Cell Cardiol 37 2004 593 602
    • (2004) J Mol Cell Cardiol , vol.37 , pp. 593-602
    • Fodstad, H.1    Swan, H.2    Auberson, M.3    Gautschi, I.4    Loffing, J.5    Schild, L.6
  • 28
    • 2942577638 scopus 로고    scopus 로고
    • New KCNQ1 mutations leading to haploinsufficiency in a general population; Defective trafficking of a KvLQT1 mutant
    • L. Gouas, C. Bellocq, M. Berthet, F. Potet, S. Demolombe, and A. Forhan New KCNQ1 mutations leading to haploinsufficiency in a general population; defective trafficking of a KvLQT1 mutant Cardiovasc Res 63 2004 60 68
    • (2004) Cardiovasc Res , vol.63 , pp. 60-68
    • Gouas, L.1    Bellocq, C.2    Berthet, M.3    Potet, F.4    Demolombe, S.5    Forhan, A.6
  • 31
    • 0037047646 scopus 로고    scopus 로고
    • Enhanced basal activity of a cardiac Ca2+ release channel (ryanodine receptor) mutant associated with ventricular tachycardia and sudden death
    • D. Jiang, B. Xiao, L. Zhang, and S.R. Chen Enhanced basal activity of a cardiac Ca2+ release channel (ryanodine receptor) mutant associated with ventricular tachycardia and sudden death Circ Res 91 2002 218 225
    • (2002) Circ Res , vol.91 , pp. 218-225
    • Jiang, D.1    Xiao, B.2    Zhang, L.3    Chen, S.R.4
  • 32
    • 0030945710 scopus 로고    scopus 로고
    • Perioperative considerations in a newly described subtype of congenital long QT syndrome
    • A.M. Joseph-Reynolds, S.M. Auden, and W.L. Sobczyzk Perioperative considerations in a newly described subtype of congenital long QT syndrome Paediatr Anaesth 7 1997 237 241
    • (1997) Paediatr Anaesth , vol.7 , pp. 237-241
    • Joseph-Reynolds, A.M.1    Auden, S.M.2    Sobczyzk, W.L.3
  • 33
    • 4644325716 scopus 로고    scopus 로고
    • Images in cardiovascular medicine. Life-threatening neonatal arrhythmia: Successful treatment and confirmation of clinically suspected extreme long QT-syndrome-3
    • H.G. Kehl, W. Haverkamp, G. Rellensmann, T.M. Yelbuz, T. Krasemann, and J. Vogt Images in cardiovascular medicine. Life-threatening neonatal arrhythmia: successful treatment and confirmation of clinically suspected extreme long QT-syndrome-3 Circulation 109 2004 e205 e206
    • (2004) Circulation , vol.109
    • Kehl, H.G.1    Haverkamp, W.2    Rellensmann, G.3    Yelbuz, T.M.4    Krasemann, T.5    Vogt, J.6
  • 34
    • 0032563712 scopus 로고    scopus 로고
    • Modulation of cardiac Na+ current phenotype by beta1-subunit expression
    • S. Kupershmidt, T. Yang, and D.M. Roden Modulation of cardiac Na+ current phenotype by beta1-subunit expression Circ Res 83 1998 441 447
    • (1998) Circ Res , vol.83 , pp. 441-447
    • Kupershmidt, S.1    Yang, T.2    Roden, D.M.3
  • 35
    • 0028957403 scopus 로고
    • Catecholaminergic polymorphic ventricular tachycardia in children. a 7-year follow-up of 21 patients
    • A. Leenhardt, V. Lucet, I. Denjoy, F. Grau, D.D. Ngoc, and P. Coumel Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients Circulation 91 1995 1512 1519
    • (1995) Circulation , vol.91 , pp. 1512-1519
    • Leenhardt, A.1    Lucet, V.2    Denjoy, I.3    Grau, F.4    Ngoc, D.D.5    Coumel, P.6
  • 36
    • 4444367635 scopus 로고    scopus 로고
    • Calstabin deficiency, ryanodine receptors, and sudden cardiac death
    • S.E. Lehnart, X.H. Wehrens, and A.R. Marks Calstabin deficiency, ryanodine receptors, and sudden cardiac death Biochem Biophys Res Commun 322 2004 1267 1279
    • (2004) Biochem Biophys Res Commun , vol.322 , pp. 1267-1279
    • Lehnart, S.E.1    Wehrens, X.H.2    Marks, A.R.3
  • 37
    • 4444298467 scopus 로고    scopus 로고
    • Sudden death in familial polymorphic ventricular tachycardia associated with calcium release channel (ryanodine receptor) leak
    • S.E. Lehnart, X.H.T. Wehrens, P.J. Laitinen, S.R. Reiken, S.X. Deng, and Z. Cheng Sudden death in familial polymorphic ventricular tachycardia associated with calcium release channel (ryanodine receptor) leak Circulation 109 2004 3208 3214
    • (2004) Circulation , vol.109 , pp. 3208-3214
    • Lehnart, S.E.1    Wehrens, X.H.T.2    Laitinen, P.J.3    Reiken, S.R.4    Deng, S.X.5    Cheng, Z.6
  • 38
    • 0029790830 scopus 로고    scopus 로고
    • Long QT syndrome associated with syndactyly in a female
    • S.E. Levin Long QT syndrome associated with syndactyly in a female Am J Cardiol 78 1996 380
    • (1996) Am J Cardiol , vol.78 , pp. 380
    • Levin, S.E.1
  • 39
    • 0029089136 scopus 로고
    • Long QT syndrome associated with syndactyly identified in females
    • M.L. Marks, D.L. Trippel, and M.T. Keating Long QT syndrome associated with syndactyly identified in females Am J Cardiol 76 1995 744 745
    • (1995) Am J Cardiol , vol.76 , pp. 744-745
    • Marks, M.L.1    Trippel, D.L.2    Keating, M.T.3
  • 41
    • 0036132550 scopus 로고    scopus 로고
    • Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia
    • A.R. Marks, S. Priori, M. Memmi, K. Kontula, and P.J. Laitinen Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia J Cell Physiol 190 2002 1 6
    • (2002) J Cell Physiol , vol.190 , pp. 1-6
    • Marks, A.R.1    Priori, S.2    Memmi, M.3    Kontula, K.4    Laitinen, P.J.5
  • 42
    • 0033044699 scopus 로고    scopus 로고
    • The circadian pattern of the development of ventricular fibrillation in patients with Brugada syndrome
    • K. Matsuo, T. Kurita, M. Inagaki, M. Kakishita, N. Aihara, and W. Shimizu The circadian pattern of the development of ventricular fibrillation in patients with Brugada syndrome Eur Heart J 20 1999 465 470
    • (1999) Eur Heart J , vol.20 , pp. 465-470
    • Matsuo, K.1    Kurita, T.2    Inagaki, M.3    Kakishita, M.4    Aihara, N.5    Shimizu, W.6
  • 43
    • 0028861892 scopus 로고
    • ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome
    • A.J. Moss, W. Zareba, J. Benhorin, E.H. Locati, W.J. Hall, and J.L. Robinson ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome Circulation 92 1995 2929 2934
    • (1995) Circulation , vol.92 , pp. 2929-2934
    • Moss, A.J.1    Zareba, W.2    Benhorin, J.3    Locati, E.H.4    Hall, W.J.5    Robinson, J.L.6
  • 44
    • 32644468136 scopus 로고    scopus 로고
    • Prolongation of QT interval and syndactyly: Characterization of a novel variant of the long QT syndrome
    • C. Napolitano, R. Bloise, M. Lunati, M. Gasparini, C. Cavalli, and E. Cerini Prolongation of QT interval and syndactyly: characterization of a novel variant of the long QT syndrome Circulation 104 Suppl II 2001 365 (abstract)
    • (2001) Circulation , vol.104 , Issue.2 SUPPL. , pp. 365
    • Napolitano, C.1    Bloise, R.2    Lunati, M.3    Gasparini, M.4    Cavalli, C.5    Cerini, E.6
  • 45
    • 0035907032 scopus 로고    scopus 로고
    • Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome
    • N.M. Plaster, R. Tawil, M. Tristani-Firouzi, S. Canun, S. Bendahhou, and A. Tsunoda Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome Cell 105 2001 511 519
    • (2001) Cell , vol.105 , pp. 511-519
    • Plaster, N.M.1    Tawil, R.2    Tristani-Firouzi, M.3    Canun, S.4    Bendahhou, S.5    Tsunoda, A.6
  • 46
    • 0029887380 scopus 로고    scopus 로고
    • Differential response to Na+ channel blockade, beta-adrenergic stimulation, and rapid pacing in a cellular model mimicking the SCN5A and HERG defects present in the long-QT syndrome
    • S.G. Priori, C. Napolitano, F. Cantu, A.M. Brown, and P.J. Schwartz Differential response to Na+ channel blockade, beta-adrenergic stimulation, and rapid pacing in a cellular model mimicking the SCN5A and HERG defects present in the long-QT syndrome Circ Res 78 1996 1009 1015
    • (1996) Circ Res , vol.78 , pp. 1009-1015
    • Priori, S.G.1    Napolitano, C.2    Cantu, F.3    Brown, A.M.4    Schwartz, P.J.5
  • 47
    • 0033514263 scopus 로고    scopus 로고
    • Low penetrance in the long-QT syndrome: Clinical impact
    • S.G. Priori, C. Napolitano, and P.J. Schwartz Low penetrance in the long-QT syndrome: clinical impact Circulation 99 1999 529 533
    • (1999) Circulation , vol.99 , pp. 529-533
    • Priori, S.G.1    Napolitano, C.2    Schwartz, P.J.3
  • 49
    • 0035895322 scopus 로고    scopus 로고
    • Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia
    • S.G. Priori, C. Napolitano, N. Tiso, M. Memmi, G. Vignati, and R. Bloise Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia Circulation 103 2001 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
  • 50
    • 0036645605 scopus 로고    scopus 로고
    • Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia
    • S.G. Priori, C. Napolitano, M. Memmi, B. Colombi, F. Drago, and M. Gasparini Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia Circulation 106 2002 69 74
    • (2002) Circulation , vol.106 , pp. 69-74
    • Priori, S.G.1    Napolitano, C.2    Memmi, M.3    Colombi, B.4    Drago, F.5    Gasparini, M.6
  • 51
    • 84904140984 scopus 로고    scopus 로고
    • Genetics of long QT, Brugada and other channellopathies
    • D.P. Zipes J. Jalife 4th ed Elsevier Philadelphia
    • S.G. Priori, I. Rivolta, and C. Napolitano Genetics of long QT, Brugada and other channellopathies D.P. Zipes J. Jalife Cardiac Electrophysiology 4th ed 2003 Elsevier Philadelphia 462 470
    • (2003) Cardiac Electrophysiology , pp. 462-470
    • Priori, S.G.1    Rivolta, I.2    Napolitano, C.3
  • 53
    • 17644420610 scopus 로고    scopus 로고
    • Genetics of cardiac arrhythmias
    • D.P. Zipes P. Libby R.O. Bonow E. Braunwald Elsevier Philadelphia
    • S.G. Priori, C. Napolitano, and P.J. Schwartz Genetics of cardiac arrhythmias D.P. Zipes P. Libby R.O. Bonow E. Braunwald Braunwald's Heart Disease 2004 Elsevier Philadelphia 689 695
    • (2004) Braunwald's Heart Disease , pp. 689-695
    • Priori, S.G.1    Napolitano, C.2    Schwartz, P.J.3
  • 54
    • 4544387969 scopus 로고    scopus 로고
    • Association of long QT syndrome loci and cardiac events among patients treated with beta-blockers
    • S.G. Priori, C. Napolitano, P.J. Schwartz, M. Grillo, R. Bloise, and E. Ronchetti Association of long QT syndrome loci and cardiac events among patients treated with beta-blockers JAMA 292 2004 1341 1344
    • (2004) JAMA , vol.292 , pp. 1341-1344
    • Priori, S.G.1    Napolitano, C.2    Schwartz, P.J.3    Grillo, M.4    Bloise, R.5    Ronchetti, E.6
  • 55
  • 56
  • 57
    • 0037129911 scopus 로고    scopus 로고
    • Pharmacological rescue of human K(+) channel long-QT2 mutations: Human ether-a-go-go-related gene rescue without block
    • S. Rajamani, C.L. Anderson, B.D. Anson, and C.T. January Pharmacological rescue of human K(+) channel long-QT2 mutations: human ether-a-go-go-related gene rescue without block Circulation 105 2002 2830 2835
    • (2002) Circulation , vol.105 , pp. 2830-2835
    • Rajamani, S.1    Anderson, C.L.2    Anson, B.D.3    January, C.T.4
  • 58
    • 0035903135 scopus 로고    scopus 로고
    • Inherited Brugada and LQT-3 syndrome mutations of a single residue of the cardiac sodium channel confer distinct channel and clinical phenotypes
    • I. Rivolta, H. Abriel, M. Tateyama, H. Liu, M. Memmi, and P. Vardas Inherited Brugada and LQT-3 syndrome mutations of a single residue of the cardiac sodium channel confer distinct channel and clinical phenotypes J Biol Chem 276 2001 30623 30630
    • (2001) J Biol Chem , vol.276 , pp. 30623-30630
    • Rivolta, I.1    Abriel, H.2    Tateyama, M.3    Liu, H.4    Memmi, M.5    Vardas, P.6
  • 59
    • 33846121151 scopus 로고    scopus 로고
    • In vitro characterization of the electrophysiological eefects of mexiletine on SCN5A mutants predicts clinical response in LQT3 patients
    • I. Rivolta, E. Giarda, J. Nastoli, E. Ronchetti, C. Napolitano, and S.G. Priori In vitro characterization of the electrophysiological eefects of mexiletine on SCN5A mutants predicts clinical response in LQT3 patients Circulation 110 17 2004 III-230 (abstract)
    • (2004) Circulation , vol.110 , Issue.17 , pp. 230
    • Rivolta, I.1    Giarda, E.2    Nastoli, J.3    Ronchetti, E.4    Napolitano, C.5    Priori, S.G.6
  • 60
    • 0025978588 scopus 로고
    • Delayed rectifier outward K+ current is composed of two currents in guinea pig atrial cells
    • M.C. Sanguinetti, and N.K. Jurkiewicz Delayed rectifier outward K+ current is composed of two currents in guinea pig atrial cells Am J Physiol 260 1991 H393 H399
    • (1991) Am J Physiol , vol.260
    • Sanguinetti, M.C.1    Jurkiewicz, N.K.2
  • 62
    • 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
    • P.J. Schwartz, S.G. Priori, E.H. Locati, C. Napolitano, F. Cantu, and J.A. Towbin 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 92 1995 3381 3386
    • (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
  • 64
    • 0035830365 scopus 로고    scopus 로고
    • Genotype-phenotype correlation in the long-QT syndrome : ggene-specific triggers for life-threatening arrhythmias
    • P.J. Schwartz, S.G. Priori, C. Spazzolini, A.J. Moss, G.M. Vincent, and C. Napolitano Genotype-phenotype correlation in the long-QT syndrome : gene-specific triggers for life-threatening arrhythmias Circulation 103 2001 89 95
    • (2001) Circulation , vol.103 , pp. 89-95
    • Schwartz, P.J.1    Priori, S.G.2    Spazzolini, C.3    Moss, A.J.4    Vincent, G.M.5    Napolitano, C.6
  • 67
    • 0034609531 scopus 로고    scopus 로고
    • Spectrum of mutations in long-QT syndrome genes: KVLQT1, HERG, SCN5A, KCNE1, and KCNE2
    • I. Splawski, J. Shen, K.W. Timothy, M.H. Lehmann, S. Priori, and J.L. Robinson Spectrum of mutations in long-QT syndrome genes: KVLQT1, HERG, SCN5A, KCNE1, and KCNE2 Circulation 102 2000 1178 1185
    • (2000) Circulation , vol.102 , pp. 1178-1185
    • Splawski, I.1    Shen, J.2    Timothy, K.W.3    Lehmann, M.H.4    Priori, S.5    Robinson, J.L.6
  • 68
    • 5344223383 scopus 로고    scopus 로고
    • Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism
    • I. Splawski, K.W. Timothy, L.M. Sharpe, N. Decher, P. Kumar, and R. Bloise Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism Cell 119 2004 19 31
    • (2004) Cell , vol.119 , pp. 19-31
    • Splawski, I.1    Timothy, K.W.2    Sharpe, L.M.3    Decher, N.4    Kumar, P.5    Bloise, R.6
  • 69
    • 0033405388 scopus 로고    scopus 로고
    • Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts
    • H. Swan, K. Piippo, M. Viitasalo, P. Heikkila, T. Paavonen, and K. Kainulainen Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts J Am Coll Cardiol 34 1999 2035 2042
    • (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
  • 70
    • 0028298042 scopus 로고
    • Andersen's syndrome: Potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features
    • R. Tawil, L.J. Ptacek, S.G. Pavlakis, D.C. DeVivo, A.S. Penn, and C. Ozdemir Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features Ann Neurol 35 1994 326 330
    • (1994) Ann Neurol , vol.35 , pp. 326-330
    • Tawil, R.1    Ptacek, L.J.2    Pavlakis, S.G.3    Devivo, D.C.4    Penn, A.S.5    Ozdemir, C.6
  • 71
    • 17144415220 scopus 로고    scopus 로고
    • Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing
    • D.J. Tester, M.L. Will, C.M. Haglund, and M.J. Ackerman Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing Heart Rhythm 2 2005 507 517
    • (2005) Heart Rhythm , vol.2 , pp. 507-517
    • Tester, D.J.1    Will, M.L.2    Haglund, C.M.3    Ackerman, M.J.4
  • 72
    • 0036324229 scopus 로고    scopus 로고
    • Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)
    • M. Tristani-Firouzi, J.L. Jensen, M.R. Donaldson, V. Sansone, G. Meola, and A. Hahn Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome) J Clin Invest 110 2002 381 388
    • (2002) J Clin Invest , vol.110 , pp. 381-388
    • Tristani-Firouzi, M.1    Jensen, J.L.2    Donaldson, M.R.3    Sansone, V.4    Meola, G.5    Hahn, A.6
  • 73
    • 0035996742 scopus 로고    scopus 로고
    • Prevention of ventricular fibrillation by cilostazol, an oral phosphodiesterase inhibitor, in a patient with Brugada syndrome
    • T. Tsuchiya, K. Ashikaga, T. Honda, and M. Arita Prevention of ventricular fibrillation by cilostazol, an oral phosphodiesterase inhibitor, in a patient with Brugada syndrome J Cardiovasc Electrophysiol 13 2002 698 701
    • (2002) J Cardiovasc Electrophysiol , vol.13 , pp. 698-701
    • Tsuchiya, T.1    Ashikaga, K.2    Honda, T.3    Arita, M.4
  • 74
    • 0036063688 scopus 로고    scopus 로고
    • A novel SCN5A arrhythmia mutation, M1766L, with expression defect rescued by mexiletine
    • C.R. Valdivia, M.J. Ackerman, D.J. Tester, T. Wada, J. McCormack, and B. Ye A novel SCN5A arrhythmia mutation, M1766L, with expression defect rescued by mexiletine Cardiovasc Res 55 2002 279 289
    • (2002) Cardiovasc Res , vol.55 , pp. 279-289
    • Valdivia, C.R.1    Ackerman, M.J.2    Tester, D.J.3    Wada, T.4    McCormack, J.5    Ye, B.6
  • 77
    • 0028905566 scopus 로고
    • SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
    • Q. Wang, J. Shen, I. Splawski, D. Atkinson, Z. Li, and J.L. Robinson SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome Cell 80 1995 805 811
    • (1995) Cell , vol.80 , pp. 805-811
    • Wang, Q.1    Shen, J.2    Splawski, I.3    Atkinson, D.4    Li, Z.5    Robinson, J.L.6
  • 78
    • 0029825614 scopus 로고    scopus 로고
    • Characterization of human cardiac Na+ channel mutations in the congenital long QT syndrome
    • D.W. Wang, K. Yazawa, A.L. George Jr., and P.B. Bennett Characterization of human cardiac Na+ channel mutations in the congenital long QT syndrome Proc Natl Acad Sci U S A 93 1996 13200 13205
    • (1996) Proc Natl Acad Sci U S a , vol.93 , pp. 13200-13205
    • Wang, D.W.1    Yazawa, K.2    George Jr., A.L.3    Bennett, P.B.4
  • 79
    • 0037708928 scopus 로고    scopus 로고
    • FKBP12.6 deficiency and defective calcium release channel (ryanodine receptor) function linked to exercise-induced sudden cardiac death
    • X.H. Wehrens, S.E. Lehnart, F. Huang, J.A. Vest, S.R. Reiken, and P.J. Mohler FKBP12.6 deficiency and defective calcium release channel (ryanodine receptor) function linked to exercise-induced sudden cardiac death Cell 113 2003 829 840
    • (2003) Cell , vol.113 , pp. 829-840
    • Wehrens, X.H.1    Lehnart, S.E.2    Huang, F.3    Vest, J.A.4    Reiken, S.R.5    Mohler, P.J.6
  • 80
    • 1842482414 scopus 로고    scopus 로고
    • Protection from cardiac arrhythmia through ryanodine receptor-stabilizing protein calstabin2
    • X.H. Wehrens, S.E. Lehnart, S.R. Reiken, S.X. Deng, J.A. Vest, and D. Cervantes Protection from cardiac arrhythmia through ryanodine receptor-stabilizing protein calstabin2 Science 304 2004 292 296
    • (2004) Science , vol.304 , pp. 292-296
    • Wehrens, X.H.1    Lehnart, S.E.2    Reiken, S.R.3    Deng, S.X.4    Vest, J.A.5    Cervantes, D.6
  • 81
    • 0000297776 scopus 로고
    • Familial auricular fibrillation
    • L. Wolff Familial auricular fibrillation N Engl J Med 229 1943 396 397
    • (1943) N Engl J Med , vol.229 , pp. 396-397
    • Wolff, L.1
  • 82
    • 0032879716 scopus 로고    scopus 로고
    • Cellular basis for the Brugada syndrome and other mechanisms of arrhythmogenesis associated with ST-segment elevation
    • G.X. Yan, and C. Antzelevitch Cellular basis for the Brugada syndrome and other mechanisms of arrhythmogenesis associated with ST-segment elevation Circulation 100 1999 1660 1666
    • (1999) Circulation , vol.100 , pp. 1660-1666
    • Yan, G.X.1    Antzelevitch, C.2
  • 83
    • 6344292572 scopus 로고    scopus 로고
    • Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation
    • G. Yang, M. Xia, Q. Jin, S. Benedahhou, J. Shi, and J. Chen Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation Am J Hum Genet 75 2004 899 905
    • (2004) Am J Hum Genet , vol.75 , pp. 899-905
    • Yang, G.1    Xia, M.2    Jin, Q.3    Benedahhou, S.4    Shi, J.5    Chen, J.6
  • 84
    • 0037469180 scopus 로고    scopus 로고
    • FKBP12.6-mediated stabilization of calcium-release channel (ryanodine receptor) as a novel therapeutic strategy against heart failure
    • M. Yano, S. Kobayashi, M. Kohno, M. Doi, T. Tokuhisa, and S. Okuda FKBP12.6-mediated stabilization of calcium-release channel (ryanodine receptor) as a novel therapeutic strategy against heart failure Circulation 107 2003 477 484
    • (2003) Circulation , vol.107 , pp. 477-484
    • Yano, M.1    Kobayashi, S.2    Kohno, M.3    Doi, M.4    Tokuhisa, T.5    Okuda, S.6
  • 85
    • 0032516934 scopus 로고    scopus 로고
    • HERG channel dysfunction in human long QT syndrome. Intracellular transport and functional defects
    • Z. Zhou, Q. Gong, M.L. Epstein, and C.T. January HERG channel dysfunction in human long QT syndrome. Intracellular transport and functional defects J Biol Chem 273 1998 21061 21066
    • (1998) J Biol Chem , vol.273 , pp. 21061-21066
    • Zhou, Z.1    Gong, Q.2    Epstein, M.L.3    January, C.T.4
  • 86
    • 0033615646 scopus 로고    scopus 로고
    • Correction of defective protein trafficking of a mutant HERG potassium channel in human long QT syndrome. Pharmacological and temperature effects
    • Z. Zhou, Q. Gong, and C.T. January Correction of defective protein trafficking of a mutant HERG potassium channel in human long QT syndrome. Pharmacological and temperature effects J Biol Chem 274 1999 31123 31126
    • (1999) J Biol Chem , vol.274 , pp. 31123-31126
    • Zhou, Z.1    Gong, Q.2    January, C.T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.