메뉴 건너뛰기




Volumn 76, Issue 3, 2007, Pages 379-380

Penetrance of monogenetic cardiac conduction diseases. A matter of conduction reserve?

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 43; MESSENGER RNA; SODIUM CHANNEL;

EID: 35548942206     PISSN: 00086363     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cardiores.2007.10.001     Document Type: Editorial
Times cited : (5)

References (24)
  • 1
    • 0037454049 scopus 로고    scopus 로고
    • Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenegre disease
    • Probst V., Kyndt F., Potet F., Trochu J.N., Mialet G., Demolombe S., et al. Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenegre disease. J Am Coll Cardiol 41 (2003) 643-652
    • (2003) J Am Coll Cardiol , vol.41 , pp. 643-652
    • Probst, V.1    Kyndt, F.2    Potet, F.3    Trochu, J.N.4    Mialet, G.5    Demolombe, S.6
  • 3
    • 35548941783 scopus 로고    scopus 로고
    • A novel C-terminal truncation SCN5A mutation from a patient with sick sinus syndrome, conduction disorder and ventricular tachycardia
    • Tan B.H., Iturralde-Torres P., Medeiros-Domingo A., Nava S., Tester D.J., Valdivia C.R., et al. A novel C-terminal truncation SCN5A mutation from a patient with sick sinus syndrome, conduction disorder and ventricular tachycardia. Cardiovasc Res 76 (2007) 409-417
    • (2007) Cardiovasc Res , vol.76 , pp. 409-417
    • Tan, B.H.1    Iturralde-Torres, P.2    Medeiros-Domingo, A.3    Nava, S.4    Tester, D.J.5    Valdivia, C.R.6
  • 4
    • 18844479760 scopus 로고    scopus 로고
    • Basic mechanisms of cardiac impulse propagation and associated arrhythmias
    • Kleber A.G., and Rudy Y. Basic mechanisms of cardiac impulse propagation and associated arrhythmias. Physiol Rev 84 (2004) 431-488
    • (2004) Physiol Rev , vol.84 , pp. 431-488
    • Kleber, A.G.1    Rudy, Y.2
  • 8
    • 0032562189 scopus 로고    scopus 로고
    • Disparate effects of deficient expression of connexin43 on atrial and ventricular conduction: evidence for chamber-specific molecular determinants of conduction
    • Thomas S.A., Schuessler R.B., Berul C.I., Beardslee M.A., Beyer E.C., Mendelsohn M.E., et al. Disparate effects of deficient expression of connexin43 on atrial and ventricular conduction: evidence for chamber-specific molecular determinants of conduction. Circulation 97 (1998) 686-691
    • (1998) Circulation , vol.97 , pp. 686-691
    • Thomas, S.A.1    Schuessler, R.B.2    Berul, C.I.3    Beardslee, M.A.4    Beyer, E.C.5    Mendelsohn, M.E.6
  • 9
    • 0032851539 scopus 로고    scopus 로고
    • Characterization of conduction in the ventricles of normal and heterozygous Cx43 knockout mice using optical mapping
    • Morley G.E., Vaidya D., Samie F.H., Lo C., Delmar M., and Jalife J. Characterization of conduction in the ventricles of normal and heterozygous Cx43 knockout mice using optical mapping. J Cardiovasc Electrophysiol 10 (1999) 1361-1375
    • (1999) J Cardiovasc Electrophysiol , vol.10 , pp. 1361-1375
    • Morley, G.E.1    Vaidya, D.2    Samie, F.H.3    Lo, C.4    Delmar, M.5    Jalife, J.6
  • 10
    • 0347635339 scopus 로고    scopus 로고
    • Functional role of connexin43 gap junction channels in adult mouse heart assessed by inducible gene deletion
    • Eckardt D., Theis M., Degen J., Ott T., van Rijen H.V., Kirchhoff S., et al. Functional role of connexin43 gap junction channels in adult mouse heart assessed by inducible gene deletion. J Mol Cell Cardiol 36 (2004) 101-110
    • (2004) J Mol Cell Cardiol , vol.36 , pp. 101-110
    • Eckardt, D.1    Theis, M.2    Degen, J.3    Ott, T.4    van Rijen, H.V.5    Kirchhoff, S.6
  • 11
    • 1442359119 scopus 로고    scopus 로고
    • Slow conduction and enhanced anisotropy increase the propensity for ventricular tachyarrhythmias in adult mice with induced deletion of connexin43
    • van Rijen H.V.M., Eckardt D., Degen J., Theis M., Ott T., Willecke K., et al. Slow conduction and enhanced anisotropy increase the propensity for ventricular tachyarrhythmias in adult mice with induced deletion of connexin43. Circulation 109 (2004) 1048-1055
    • (2004) Circulation , vol.109 , pp. 1048-1055
    • van Rijen, H.V.M.1    Eckardt, D.2    Degen, J.3    Theis, M.4    Ott, T.5    Willecke, K.6
  • 13
    • 0033990686 scopus 로고    scopus 로고
    • Mouse electrocardiography: an interval of thirty years
    • Wehrens X.H., Kirchhoff S., and Doevendans P.A. Mouse electrocardiography: an interval of thirty years. Cardiovasc Res 45 (2000) 231-237
    • (2000) Cardiovasc Res , vol.45 , pp. 231-237
    • Wehrens, X.H.1    Kirchhoff, S.2    Doevendans, P.A.3
  • 14
    • 18344362987 scopus 로고    scopus 로고
    • Slowed conduction and ventricular tachycardia after targeted disruption of the cardiac sodium channel gene Scn5a
    • Papadatos G.A., Wallerstein P.M., Head C.E., Ratcliff R., Brady P.A., Benndorf K., et al. Slowed conduction and ventricular tachycardia after targeted disruption of the cardiac sodium channel gene Scn5a. Proc Natl Acad Sci U S A 99 (2002) 6210-6215
    • (2002) Proc Natl Acad Sci U S A , vol.99 , pp. 6210-6215
    • Papadatos, G.A.1    Wallerstein, P.M.2    Head, C.E.3    Ratcliff, R.4    Brady, P.A.5    Benndorf, K.6
  • 15
    • 33751562042 scopus 로고    scopus 로고
    • Mice carrying the SCN5A mutation 1798insD, equivalent to human 1795insD, display bradycardia, conduction delay and QT-prolongation
    • Remme C.A., Veldkamp M.W., van Ginneken A.C., Verkerk A.O., van Brunschot S., Belterman C.N., et al. Mice carrying the SCN5A mutation 1798insD, equivalent to human 1795insD, display bradycardia, conduction delay and QT-prolongation. Circulation 112 (2005) SII-220
    • (2005) Circulation , vol.112
    • Remme, C.A.1    Veldkamp, M.W.2    van Ginneken, A.C.3    Verkerk, A.O.4    van Brunschot, S.5    Belterman, C.N.6
  • 16
    • 20244376320 scopus 로고    scopus 로고
    • Mouse model of SCN5A-linked hereditary Lenegre's disease: age-related conduction slowing and myocardial fibrosis
    • Royer A., van Veen T.A., Le Bouter S., Marionneau C., Griol-Charhbili V., Leoni A.L., et al. Mouse model of SCN5A-linked hereditary Lenegre's disease: age-related conduction slowing and myocardial fibrosis. Circulation 111 (2005) 1738-1746
    • (2005) Circulation , vol.111 , pp. 1738-1746
    • Royer, A.1    van Veen, T.A.2    Le Bouter, S.3    Marionneau, C.4    Griol-Charhbili, V.5    Leoni, A.L.6
  • 17
    • 25444509189 scopus 로고    scopus 로고
    • Impaired impulse propagation in Scn5a-knockout mice. Combined contribution of excitability, connexin expression, and tissue architecture in relation to aging
    • van Veen T.A., Stein M., Royer A., Le Quang K., Charpentier F., Colledge W.H., et al. Impaired impulse propagation in Scn5a-knockout mice. Combined contribution of excitability, connexin expression, and tissue architecture in relation to aging. Circulation 112 (2005) 1927-1935
    • (2005) Circulation , vol.112 , pp. 1927-1935
    • van Veen, T.A.1    Stein, M.2    Royer, A.3    Le Quang, K.4    Charpentier, F.5    Colledge, W.H.6
  • 18
    • 14844353942 scopus 로고    scopus 로고
    • Hypoxia, electrical uncoupling, and conduction slowing: role of conduction reserve
    • van Rijen H.V., de Bakker J.M., and van Veen T.A. Hypoxia, electrical uncoupling, and conduction slowing: role of conduction reserve. Cardiovasc Res 66 (2005) 9-11
    • (2005) Cardiovasc Res , vol.66 , pp. 9-11
    • van Rijen, H.V.1    de Bakker, J.M.2    van Veen, T.A.3
  • 19
    • 0026466921 scopus 로고
    • Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome. A multicenter report
    • Brugada P., and Brugada J. 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
  • 20
    • 27844591399 scopus 로고    scopus 로고
    • Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiological, genetic, histopathologic, and computational study
    • Coronel R., Casini S., Koopmann T.T., Wilms-Schopman F.J., Verkerk A.O., de Groot J.R., et al. Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiological, genetic, histopathologic, and computational study. Circulation 112 (2005) 2769-2777
    • (2005) Circulation , vol.112 , pp. 2769-2777
    • Coronel, R.1    Casini, S.2    Koopmann, T.T.3    Wilms-Schopman, F.J.4    Verkerk, A.O.5    de Groot, J.R.6
  • 21
    • 0037423552 scopus 로고    scopus 로고
    • Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system
    • Bezzina C.R., Rook M.B., Groenewegen W.A., Herfst L.J., van der Wal A.C., Lam J., et al. Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system. Circ Res 92 (2003) 159-168
    • (2003) Circ Res , vol.92 , pp. 159-168
    • Bezzina, C.R.1    Rook, M.B.2    Groenewegen, W.A.3    Herfst, L.J.4    van der Wal, A.C.5    Lam, J.6
  • 22
    • 12544257550 scopus 로고    scopus 로고
    • Sodium channel mutations and susceptibility to heart failure and atrial fibrillation
    • Olson T.M., Michels V.V., Ballew J.D., Reyna S.P., Karst M.L., Herron K.J., et al. Sodium channel mutations and susceptibility to heart failure and atrial fibrillation. Jama 293 (2005) 447-454
    • (2005) Jama , vol.293 , pp. 447-454
    • Olson, T.M.1    Michels, V.V.2    Ballew, J.D.3    Reyna, S.P.4    Karst, M.L.5    Herron, K.J.6
  • 23
    • 0242330187 scopus 로고    scopus 로고
    • A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channels
    • Makielski J.C., Ye B., Valdivia C.R., Pagel M.D., Pu J., Tester D.J., et al. A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channels. Circ Res 93 (2003) 821-828
    • (2003) Circ Res , vol.93 , pp. 821-828
    • Makielski, J.C.1    Ye, B.2    Valdivia, C.R.3    Pagel, M.D.4    Pu, J.5    Tester, D.J.6
  • 24
    • 21344433631 scopus 로고    scopus 로고
    • Common human SCN5A polymorphisms have altered electrophysiology when expressed in Q1077 splice variants
    • Tan B.H., Valdivia C.R., Rok B.A., Ye B., Ruwaldt K.M., Tester D.J., et al. Common human SCN5A polymorphisms have altered electrophysiology when expressed in Q1077 splice variants. Heart Rhythm 2 (2005) 741-747
    • (2005) Heart Rhythm , vol.2 , pp. 741-747
    • Tan, B.H.1    Valdivia, C.R.2    Rok, B.A.3    Ye, B.4    Ruwaldt, K.M.5    Tester, D.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.