-
1
-
-
84904142492
-
Gap junction distribution and regulation in the heart
-
In: Zipes DP, Jalife J, eds Philadelphia, PA Saunders
-
Saffitz JE, Lerner DL, Yamada KA. Gap junction distribution and regulation in the heart. In: Zipes DP, Jalife J, eds. Cardiac Electrophysiology: From Cell to Bedside. Philadelphia, PA: Saunders; 2004:181-191
-
(2004)
Cardiac Electrophysiology: From Cell to Bedside
, pp. 181-191
-
-
Saffitz, J.E.1
Lerner, D.L.2
Yamada, K.A.3
-
2
-
-
79952419481
-
The cardiac conduction system
-
Park DS, Fishman GI. The cardiac conduction system. Circulation. 2011; 123:904-915
-
(2011)
Circulation
, vol.123
, pp. 904-915
-
-
Park, D.S.1
Fishman, G.I.2
-
3
-
-
67649547603
-
Sodium channel mutations and arrhythmias
-
Ruan Y, Liu N, Priori SG. Sodium channel mutations and arrhythmias. Nat Rev Cardiol. 2009;6:337-348
-
(2009)
Nat Rev Cardiol
, vol.6
, pp. 337-348
-
-
Ruan, Y.1
Liu, N.2
Priori, S.G.3
-
4
-
-
16644398147
-
Association of human connexin40 gene polymorphisms with atrial vulnerability as a risk factor for idiopathic atrial fibrillation
-
Firouzi M, Ramanna H, Kok B, Jongsma HJ, Koeleman BPC, Doevendans PA, Groenewegen WA, Hauer RNW. Association of human connexin40 gene polymorphisms with atrial vulnerability as a risk factor for idiopathic atrial fibrillation. Circ Res. 2004;95:e29-e33
-
(2004)
Circ Res
, vol.95
-
-
Firouzi, M.1
Ramanna, H.2
Kok, B.3
Jongsma, H.J.4
Koeleman, B.P.C.5
Doevendans, P.A.6
Groenewegen, W.A.7
Hauer, R.N.W.8
-
5
-
-
33745246602
-
Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation
-
Gollob MH, Jones DL, Krahn AD, Danis L, Gong X-Q, Shao Q, Liu X, Veinot JP, Tang ASL, Stewart AFR, Tesson F, Klein GJ, Yee R, Skanes AC, Guiraudon GM, Ebihara L, Bai D. Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation. N Engl J Med. 2006;354:2677-2688
-
(2006)
N Engl J Med
, vol.354
, pp. 2677-2688
-
-
Gollob, M.H.1
Jones, D.L.2
Krahn, A.D.3
Danis, L.4
Gong, X-.Q.5
Shao, Q.6
Liu, X.7
Veinot, J.P.8
Tang, A.S.L.9
Stewart, A.F.R.10
Tesson, F.11
Klein, G.J.12
Yee, R.13
Skanes, A.C.14
Guiraudon, G.M.15
Ebihara, L.16
Bai, D.17
-
6
-
-
0001487687
-
Etiology and pathology of bilateral bundle branch block in relation to complete heart block
-
Lenégre J. Etiology and pathology of bilateral bundle branch block in relation to complete heart block. Prog Cardiovasc Dis. 1964;6:409-444
-
(1964)
Prog Cardiovasc Dis
, vol.6
, pp. 409-444
-
-
Lenégre, J.1
-
7
-
-
0014847026
-
The pathogenesis of atrioventricular block in coronary disease
-
Lev M, Kinare SG, Pick A. The pathogenesis of atrioventricular block in coronary disease. Circulation. 1970;42:409-425
-
(1970)
Circulation
, vol.42
, pp. 409-425
-
-
Lev, M.1
Kinare, S.G.2
Pick, A.3
-
8
-
-
0037454049
-
Haploinsufficiency in combination with aging causes SCN5A-linked hereditary lenegre disease
-
DOI 10.1016/S0735-1097(02)02864-4
-
Probst V, Kyndt F, Potet F, Trochu JN, Mialet G, Demolombe S, Schott JJ, Baro I, Escande D, Le Marec H. Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenégre disease. J Am Coll Cardiol. 2003;41:643-652 (Pubitemid 36223331)
-
(2003)
Journal of the American College of Cardiology
, vol.41
, Issue.4
, pp. 643-652
-
-
Probst, V.1
Kyndt, F.2
Potet, F.3
Trochu, J.-N.4
Mialet, G.5
Demolombe, S.6
Schott, J.-J.7
Baro, I.8
Escande, D.9
Le Marec, H.10
-
9
-
-
0028962264
-
Gene for progressive familial heart block type I maps to chromosome 19q13
-
Brink PA, Ferreira A, Moolman JC, Weymar HW, van der Merwe P-L, Corfield VA. Gene for progressive familial heart block type I maps to chromosome 19q13. Circulation. 1995;91:1633-1640
-
(1995)
Circulation
, vol.91
, pp. 1633-1640
-
-
Brink, P.A.1
Ferreira, A.2
Moolman, J.C.3
Weymar, H.W.4
Van Der Merwe, P-.L.5
Corfield, V.A.6
-
10
-
-
0029112853
-
An isolated cardiac conduction disease maps to chromosome 19q
-
de Meeus A, Stephan E, Debrus S, Jean M-K, Loiselet J, Weissenbach J, Demaille J, Bouvagnet P. An isolated cardiac conduction disease maps to chromosome 19q. Circ Res. 1995;77:735-740
-
(1995)
Circ Res
, vol.77
, pp. 735-740
-
-
De Meeus, A.1
Stephan, E.2
Debrus, S.3
Jean, M-.K.4
Loiselet, J.5
Weissenbach, J.6
Demaille, J.7
Bouvagnet, P.8
-
11
-
-
70349215874
-
Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type I
-
Kruse M, Schulze-Bahr E, Corfield V, Beckmann A, Stallmeyer B, Kurtbay G, Ohmert I, Schulze-Bahr E, Brink P, Pongs O. Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type I. J Clin Invest. 2009;119:2737-2744
-
(2009)
J Clin Invest
, vol.119
, pp. 2737-2744
-
-
Kruse, M.1
Schulze-Bahr, E.2
Corfield, V.3
Beckmann, A.4
Stallmeyer, B.5
Kurtbay, G.6
Ohmert, I.7
Schulze-Bahr, E.8
Brink, P.9
Pongs, O.10
-
12
-
-
20244376320
-
Mouse model of SCN5A-linked hereditary Lenegre's: Disease age-related conduction slowing and myocardial fibrosis
-
DOI 10.1161/01.CIR.0000160853.19867.61
-
Royer A, van Veen TAB, Le Bouter S, Marionneau C, Griol-Charhbili V, Leoni A-L, Steenman M, van Rijen HVM, Demolombe S, Goddard CA, Richer C, Escoubet B, Jarry-Guichard T, Colledge WH, Gros D, de Bakker JMT, Grace AA, Escande D, Charpentier F. Mouse model of SCN5A-linked hereditary Lenégre's disease. Age-related conduction slowing and myocardial fibrosis. Circulation. 2005;111:1738-1746 (Pubitemid 40525137)
-
(2005)
Circulation
, vol.111
, Issue.14
, pp. 1738-1746
-
-
Royer, A.1
Van Veen, T.A.B.2
Le Bouter, S.3
Marionneau, C.4
Griol-Charhbili, V.5
Leoni, A.-L.6
Steenman, M.7
Van Rijen, H.V.M.8
Demolombe, S.9
Goddard, C.A.10
Richer, C.11
Escoubet, B.12
Jarry-Guichard, T.13
Colledge, W.H.14
Gros, D.15
De Bakker, J.M.T.16
Grace, A.A.17
Escande, D.18
Charpentier, F.19
-
13
-
-
0032820865
-
Cardiac conduction defects associate with mutations in SCN5A [4]
-
DOI 10.1038/12618
-
Schott JJ, Alshinawi C, Kyndt F, Probst V, Hoorntje TM, Hulsbeek M, Wilde AA, Escande D, Mannens MM, Le Marec H. Cardiac conduction defects associate with mutations in SCN5A. Nat Genet. 1999;23:20-21 (Pubitemid 29418782)
-
(1999)
Nature Genetics
, vol.23
, Issue.1
, pp. 20-21
-
-
Probst, V.1
Hoorntje, T.M.2
Hulsbeek, M.3
Wilde, A.A.M.4
Escande, D.5
Mannens, M.M.A.M.6
Le Marec, H.7
-
14
-
-
45749090058
-
Sodium channel 1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans
-
DOI 10.1172/JCI33891
-
Watanabe H, Koopmann TT, Le Scouarnec S, Yang T, Ingram CR, Schott JJ, Demolombe S, Probst V, Anselme F, Escande D, Wiesfeld AC, Pfeufer A, Kaab S, Wichmann HE, Hasdemir C, Aizawa Y, Wilde AA, Roden DM, Bezzina CR. Sodium channel beta1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans. J Clin Invest. 2008;118:2260-2268 (Pubitemid 351872343)
-
(2008)
Journal of Clinical Investigation
, vol.118
, Issue.6
, pp. 2260-2268
-
-
Watanabe, H.1
Koopmann, T.T.2
Le Scouarnec, S.3
Yang, T.4
Ingram, C.R.5
Schott, J.-J.6
Demolombe, S.7
Probst, V.8
Anselme, F.9
Escande, D.10
Wiesfeld, A.C.P.11
Pfeufer, A.12
Kaab, S.13
Wichmann, H.-E.14
Hasdemir, C.15
Aizawa, Y.16
Wilde, A.A.M.17
Roden, D.M.18
Bezzina, C.R.19
-
15
-
-
5644229494
-
SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia
-
DOI 10.1161/01.CIR.0000144458.58660.BB
-
McNair WP, Ku L, Taylor MRG, Fain PR, Dao D, Wolfel E, Mestroni L; Familial Cardiomyopathy Registry Research Group. SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia. Circulation. 2004;110:2163-2167 (Pubitemid 39372495)
-
(2004)
Circulation
, vol.110
, Issue.15
, pp. 2163-2167
-
-
McNair, W.P.1
Ku, L.2
Taylor, M.R.G.3
Fain, P.R.4
Dao, D.5
Wolfel, E.6
Mestroni, L.7
-
16
-
-
2942612343
-
Architectural and functional asymmetry of the His-Purkinje system of the murine heart
-
DOI 10.1016/j.cardiores.2004.03.007, PII S0008636304001233
-
Miquerol L, Meysen S, Mangoni M, Bois P, van Rijen HVM, Abran P, Jongsma H, Nargeot J, Gros D. Architectural and functional asymmetry of the His-Purkinje system of the murine heart. Cardiovasc Res. 2004; 63:77-86 (Pubitemid 38759812)
-
(2004)
Cardiovascular Research
, vol.63
, Issue.1
, pp. 77-86
-
-
Miquerol, L.1
Meysen, S.2
Mangoni, M.3
Bois, P.4
Van Rijen, H.V.M.5
Abran, P.6
Jongsma, H.7
Nargeot, J.8
Gros, D.9
-
17
-
-
79960867817
-
HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies
-
Ackerman MJ, Priori SG, Willems S, Berul C, Brugada R, Calkins H, Camm AJ, Ellinor PT, Gollob M, Hamilton R, Hershberger RE, Judge DP, Le Marec H, McKenna WJ, Schulze-Bahr E, Semsarian C, Towbin JA, Watkins H, Wilde A, Wolpert C, Zipes DP. HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies. Heart Rhythm. 2011;8:1308-1339
-
(2011)
Heart Rhythm
, vol.8
, pp. 1308-1339
-
-
Ackerman, M.J.1
Priori, S.G.2
Willems, S.3
Berul, C.4
Brugada, R.5
Calkins, H.6
Camm, A.J.7
Ellinor, P.T.8
Gollob, M.9
Hamilton, R.10
Hershberger, R.E.11
Judge, D.P.12
Le Marec, H.13
McKenna, W.J.14
Schulze-Bahr, E.15
Semsarian, C.16
Towbin, J.A.17
Watkins, H.18
Wilde, A.19
Wolpert, C.20
Zipes, D.P.21
more..
-
18
-
-
3042777256
-
Loss of electrical communication, but not plaque formation, after mutations in the cytoplasmic loop of connexin43
-
DOI 10.1016/j.hrthm.2004.03.066, PII S1547527104000967
-
Seki A, Coombs W, Taffet SM, Delmar M. Loss of electrical communication, but not plaque formation, after mutations in the cytoplasmic loop of connexin43. Heart Rhythm. 2004;1:227-233 (Pubitemid 38878243)
-
(2004)
Heart Rhythm
, vol.1
, Issue.2
, pp. 227-233
-
-
Seki, A.1
Coombs, W.2
Taffet, S.M.3
Delmar, M.4
-
19
-
-
0035853435
-
The carboxyl terminal domain regulates the unitary conductance and voltage dependence of connexin40 Gap junction channels
-
Anumonwo JMB, Taffet SM, Gu H, Chanson M, Moreno AP, Delmar M. The carboxyl terminal domain regulates the unitary conductance and voltage dependence of connexin40 gap junction channels. Circ Res 2001;88:666-673 (Pubitemid 32378135)
-
(2001)
Circulation Research
, vol.88
, Issue.7
, pp. 666-673
-
-
Anumonwo, J.M.B.1
Taffet, S.M.2
Gu, H.3
Chanson, M.4
Moreno, A.P.5
Delmar, M.6
-
20
-
-
34047240645
-
Translational efficiency of EMCV IRES in bicistronic vectors is dependent upon IRES sequence and gene location
-
Bochkov YA, Palmenberg AC. Translational efficiency of EMCV IRES in bicistronic vectors is dependent upon IRES sequence and gene location. Biotechniques. 2006;41:283-284
-
(2006)
Biotechniques
, vol.41
, pp. 283-284
-
-
Bochkov, Y.A.1
Palmenberg, A.C.2
-
21
-
-
75749122164
-
Several common variants modulate heart rate, PR interval and QRS duration
-
Holm H, Gudbjartsson DF, Arnar DO, Thorleifsson G, Thorgeirsson G, Stefansdottir H, Gudjonsson SA, Jonasdottir A, Mathiesen EB, Njolstad I, Nyrnes A, Wilsgaard T, Hald EM, Hveem K, Stoltenberg C, Lochen M-L, Kong A, Thorsteinsdottir U, Stefansson K. Several common variants modulate heart rate, PR interval and QRS duration. Nat Genet 2010;42:117-122
-
(2010)
Nat Genet
, vol.42
, pp. 117-122
-
-
Holm, H.1
Gudbjartsson, D.F.2
Arnar, D.O.3
Thorleifsson, G.4
Thorgeirsson, G.5
Stefansdottir, H.6
Gudjonsson, S.A.7
Jonasdottir, A.8
Mathiesen, E.B.9
Njolstad, I.10
Nyrnes, A.11
Wilsgaard, T.12
Hald, E.M.13
Hveem, K.14
Stoltenberg, C.15
Lochen, M-.L.16
Kong, A.17
Thorsteinsdottir, U.18
Stefansson, K.19
-
22
-
-
75749097235
-
Genome-wide association study of PR interval
-
Pfeufer A, van Noord C, Marciante KD, Arking DE, Larson MG, Smith AV, Tarasov KV, Muller M, Sotoodehnia N, Sinner MF, Verwoert GC, Li M, Kao WHL, Kottgen A, Coresh J, Bis JC, Psaty BM, Rice K, Rotter JI, Rivadeneira F, Hofman A, Kors JA, Stricker BHC, Uitterlinden AG, van Duijn CM, Beckmann BM, Sauter W, Gieger C, Lubitz SA, Newton-Cheh C, Wang TJ, Magnani JW, Schnabel RB, Chung MK, Barnard J, Smith JD, Van Wagoner DR, Vasan RS, Aspelund T, Eiriksdottir G, Harris TB, Launer LJ, Najjar SS, Lakatta E, Schlessinger D, Uda M, Abecasis GR, Muller-Myhsok B, Ehret GB, Boerwinkle E, Chakravarti A, Soliman EZ, Lunetta KL, Perz S, Wichmann HE, Meitinger T, Levy D, Gudnason V, Ellinor PT, Sanna S, Kaab S, Witteman JCM, Alonso A, Benjamin EJ, Heckbert SR. Genome-wide association study of PR interval. Nat Genet. 2010;42:153-159
-
(2010)
Nat Genet
, vol.42
, pp. 153-159
-
-
Pfeufer, A.1
Van Noord, C.2
Marciante, K.D.3
Arking, D.E.4
Larson, M.G.5
Smith, A.V.6
Tarasov, K.V.7
Muller, M.8
Sotoodehnia, N.9
Sinner, M.F.10
Verwoert, G.C.11
Li, M.12
Kao, W.H.L.13
Kottgen, A.14
Coresh, J.15
Bis, J.C.16
Psaty, B.M.17
Rice, K.18
Rotter, J.I.19
Rivadeneira, F.20
Hofman, A.21
Kors, J.A.22
Stricker, B.H.C.23
Uitterlinden, A.G.24
Van Duijn, C.M.25
Beckmann, B.M.26
Sauter, W.27
Gieger, C.28
Lubitz, S.A.29
Newton-Cheh, C.30
Wang, T.J.31
Magnani, J.W.32
Schnabel, R.B.33
Chung, M.K.34
Barnard, J.35
Smith, J.D.36
Van Wagoner, D.R.37
Vasan, R.S.38
Aspelund, T.39
Eiriksdottir, G.40
Harris, T.B.41
Launer, L.J.42
Najjar, S.S.43
Lakatta, E.44
Schlessinger, D.45
Uda, M.46
Abecasis, G.R.47
Muller-Myhsok, B.48
Ehret, G.B.49
Boerwinkle, E.50
Chakravarti, A.51
Soliman, E.Z.52
Lunetta, K.L.53
Perz, S.54
Wichmann, H.E.55
Meitinger, T.56
Levy, D.57
Gudnason, V.58
Ellinor, P.T.59
Sanna, S.60
Kaab, S.61
Witteman, J.C.M.62
Alonso, A.63
Benjamin, E.J.64
Heckbert, S.R.65
more..
-
23
-
-
77954954398
-
Paradigm of genetic mosaicism and lone atrial fibrillation: Physiological characterization of a connexin 43-deletion mutant identified from atrial tissue
-
Thibodeau IL, Xu J, Li Q, Liu G, Lam K, Veinot JP, Birnie DH, Jones DL, Krahn AD, Lemery R, Nicholson BJ, Gollob MH. Paradigm of genetic mosaicism and lone atrial fibrillation: Physiological characterization of a connexin 43-deletion mutant identified from atrial tissue. Circulation. 2010;122:236-244
-
(2010)
Circulation
, vol.122
, pp. 236-244
-
-
Thibodeau, I.L.1
Xu, J.2
Li, Q.3
Liu, G.4
Lam, K.5
Veinot, J.P.6
Birnie, D.H.7
Jones, D.L.8
Krahn, A.D.9
Lemery, R.10
Nicholson, B.J.11
Gollob, M.H.12
-
24
-
-
20444397355
-
Structural organization of gap junction channels
-
DOI 10.1016/j.bbamem.2005.04.001, PII S0005273605000878
-
Sosinsky GE, Nicholson BJ. Structural organization of gap junction channels. Biochim Biophys Acta. 2005;1711:99-125. (Pubitemid 40799287)
-
(2005)
Biochimica et Biophysica Acta - Biomembranes
, vol.1711
, Issue.SPEC. ISS.
, pp. 99-125
-
-
Sosinsky, G.E.1
Nicholson, B.J.2
|