-
2
-
-
33645317063
-
HERG potassium channels and cardiac arrhythmia
-
Sanguinetti MC, Tristani-Firouzi M,: hERG potassium channels and cardiac arrhythmia. Nature 2006; 440: 463-469.
-
(2006)
Nature
, vol.440
, pp. 463-469
-
-
Sanguinetti, M.C.1
Tristani-Firouzi, M.2
-
3
-
-
0029007356
-
HERG, a human inward rectifier in the voltage-gated potassium channel family
-
Trudeau MC, Warmke JW, Ganetzky B, Robertson GA,: HERG, a human inward rectifier in the voltage-gated potassium channel family. Science 1995; 269: 92-95.
-
(1995)
Science
, vol.269
, pp. 92-95
-
-
Trudeau, M.C.1
Warmke, J.W.2
Ganetzky, B.3
Robertson, G.A.4
-
4
-
-
0028292927
-
A family of potassium channel genes related to eag in Drosophila and mammals
-
Warmke JW, Ganetzky B,: A family of potassium channel genes related to eag in Drosophila and mammals. Proc Natl Acad Sci USA 1994; 91: 3438-3442.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 3438-3442
-
-
Warmke, J.W.1
Ganetzky, B.2
-
5
-
-
52949142183
-
Role of potassium currents in cardiac arrhythmias
-
Ravens U, Cerbai E,: Role of potassium currents in cardiac arrhythmias. Europace 2008; 10: 1133-1137.
-
(2008)
Europace
, vol.10
, pp. 1133-1137
-
-
Ravens, U.1
Cerbai, E.2
-
6
-
-
0035936798
-
Molecular and cellular mechanisms of cardiac arrhythmias
-
Keating MT, Sanguinetti MC,: Molecular and cellular mechanisms of cardiac arrhythmias. Cell 2001; 104: 569-580.
-
(2001)
Cell
, vol.104
, pp. 569-580
-
-
Keating, M.T.1
Sanguinetti, M.C.2
-
7
-
-
0034609531
-
Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2
-
Splawski I, Shen J, Timothy KW, Lehmann MH, Priori S, Robinson JL, Moss AJ, Schwartz PJ, Towbin JA, Vincent GM, Keating MT,: Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2. Circulation 2000; 102: 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
Moss, A.J.7
Schwartz, P.J.8
Towbin, J.A.9
Vincent, G.M.10
Keating, M.T.11
-
8
-
-
0025884056
-
Efficient selection for high-expression transfectants with a novel eukaryotic vector
-
Niwa H, Yamamura K, Miyazaki J,: Efficient selection for high-expression transfectants with a novel eukaryotic vector. Gene 1991; 108: 193-199.
-
(1991)
Gene
, vol.108
, pp. 193-199
-
-
Niwa, H.1
Yamamura, K.2
Miyazaki, J.3
-
9
-
-
3042802307
-
The common SCN5A mutation R1193Q causes LQTS-type electrophysiological alterations of the cardiac sodium channel
-
Wang Q, Chen S, Chen Q, Wan X, Shen J, Hoeltge GA, Timur AA, Keating MT, Kirsch GE,: The common SCN5A mutation R1193Q causes LQTS-type electrophysiological alterations of the cardiac sodium channel. J Med Genet 2004; 41: e66.
-
(2004)
J Med Genet
, vol.41
-
-
Wang, Q.1
Chen, S.2
Chen, Q.3
Wan, X.4
Shen, J.5
Hoeltge, G.A.6
Timur, A.A.7
Keating, M.T.8
Kirsch, G.E.9
-
11
-
-
7744243863
-
Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: Implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing
-
Ackerman MJ, Splawski I, Makielski JC, Tester DJ, Will ML, Timothy KW, Keating MT, Jones G, Chadha M, Burrow CR, Stephens JC, Xu C, Judson R, Curran ME,: Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: Implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing. Heart Rhythm 2004; 1: 600-607.
-
(2004)
Heart Rhythm
, vol.1
, pp. 600-607
-
-
Ackerman, M.J.1
Splawski, I.2
Makielski, J.C.3
Tester, D.J.4
Will, M.L.5
Timothy, K.W.6
Keating, M.T.7
Jones, G.8
Chadha, M.9
Burrow, C.R.10
Stephens, J.C.11
Xu, C.12
Judson, R.13
Curran, M.E.14
-
12
-
-
22244447116
-
Genetic polymorphisms and haplotypes of the human cardiac sodium channel alpha subunit gene (SCN5A) in Japanese and their association with arrhythmia
-
Maekawa K, Saito Y, Ozawa S, Adachi-Akahane S, Kawamoto M, Komamura K, Shimizu W, Ueno K, Kamakura S, Kamatani N, Kitakaze M, Sawada J,: Genetic polymorphisms and haplotypes of the human cardiac sodium channel alpha subunit gene (SCN5A) in Japanese and their association with arrhythmia. Ann Hum Genet 2005; 69: 413-428.
-
(2005)
Ann Hum Genet
, vol.69
, pp. 413-428
-
-
Maekawa, K.1
Saito, Y.2
Ozawa, S.3
Adachi-Akahane, S.4
Kawamoto, M.5
Komamura, K.6
Shimizu, W.7
Ueno, K.8
Kamakura, S.9
Kamatani, N.10
Kitakaze, M.11
Sawada, J.12
-
13
-
-
0345690174
-
Ethnic differences in cardiac potassium channel variants: Implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome
-
Ackerman MJ, Tester DJ, Jones GS, Will ML, Burrow CR, Curran ME,: Ethnic differences in cardiac potassium channel variants: Implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome. Mayo Clin Proc 2003; 78: 1479-1487.
-
(2003)
Mayo Clin Proc
, vol.78
, pp. 1479-1487
-
-
Ackerman, M.J.1
Tester, D.J.2
Jones, G.S.3
Will, M.L.4
Burrow, C.R.5
Curran, M.E.6
-
14
-
-
0034200837
-
Survey of the coding region of the HERG gene in long QT syndrome reveals six novel mutations and an amino acid polymorphism with possible phenotypic effects
-
Laitinen P, Fodstad H, Piippo K, Swan H, Toivonen L, Viitasalo M, Kaprio J, Kontula K,: Survey of the coding region of the HERG gene in long QT syndrome reveals six novel mutations and an amino acid polymorphism with possible phenotypic effects. Hum Mutat 2000; 15: 580-581.
-
(2000)
Hum Mutat
, vol.15
, pp. 580-581
-
-
Laitinen, P.1
Fodstad, H.2
Piippo, K.3
Swan, H.4
Toivonen, L.5
Viitasalo, M.6
Kaprio, J.7
Kontula, K.8
-
15
-
-
0034911966
-
Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: Implications for acquired and congenital long Q-T syndrome
-
Larsen LA, Andersen PS, Kanters J, Svendsen IH, Jacobsen JR, Vuust J, Wettrell G, Tranebjaerg L, Bathen J, Christiansen M,: Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: Implications for acquired and congenital long Q-T syndrome. Clin Chem 2001; 47: 1390-1395.
-
(2001)
Clin Chem
, vol.47
, pp. 1390-1395
-
-
Larsen, L.A.1
Andersen, P.S.2
Kanters, J.3
Svendsen, I.H.4
Jacobsen, J.R.5
Vuust, J.6
Wettrell, G.7
Tranebjaerg, L.8
Bathen, J.9
Christiansen, M.10
-
16
-
-
2542441586
-
Molecular and functional characterization of common polymorphisms in HERG (KCNH2) potassium channels
-
Anson BD, Ackerman MJ, Tester DJ, Will ML, Delisle BP, Anderson CL, January CT,: Molecular and functional characterization of common polymorphisms in HERG (KCNH2) potassium channels. Am J Physiol Heart Circ Physiol 2004; 286: H2434-H2441.
-
(2004)
Am J Physiol Heart Circ Physiol
, vol.286
-
-
Anson, B.D.1
Ackerman, M.J.2
Tester, D.J.3
Will, M.L.4
Delisle, B.P.5
Anderson, C.L.6
January, C.T.7
-
17
-
-
15044363738
-
Single nucleotide polymorphism map of five long-QT genes
-
Aydin A, Bahring S, Dahm S, Guenther UP, Uhlmann R, Busjahn A, Luft FC,: Single nucleotide polymorphism map of five long-QT genes. J Mol Med (Berl) 2005; 83: 159-165.
-
(2005)
J Mol Med (Berl)
, vol.83
, pp. 159-165
-
-
Aydin, A.1
Bahring, S.2
Dahm, S.3
Guenther, U.P.4
Uhlmann, R.5
Busjahn, A.6
Luft, F.C.7
-
18
-
-
33644931118
-
Genetic polymorphisms in KCNQ1, HERG, KCNE1 and KCNE2 genes in the Chinese, Malay and Indian populations of Singapore
-
Koo SH, Ho WF, Lee EJ,: Genetic polymorphisms in KCNQ1, HERG, KCNE1 and KCNE2 genes in the Chinese, Malay and Indian populations of Singapore. Br J Clin Pharmacol 2006; 61: 301-308.
-
(2006)
Br J Clin Pharmacol
, vol.61
, pp. 301-308
-
-
Koo, S.H.1
Ho, W.F.2
Lee, E.J.3
-
19
-
-
74549219313
-
Pharmacological and electrophysiological characterization of nine, single nucleotide polymorphisms of the hERG-encoded potassium channel
-
Mannikko R, Overend G, Perrey C, Gavaghan CL, Valentin JP, Morten J, Armstrong M, Pollard CE,: Pharmacological and electrophysiological characterization of nine, single nucleotide polymorphisms of the hERG-encoded potassium channel. Br J Pharmacol 2010; 159: 102-114.
-
(2010)
Br J Pharmacol
, vol.159
, pp. 102-114
-
-
Mannikko, R.1
Overend, G.2
Perrey, C.3
Gavaghan, C.L.4
Valentin, J.P.5
Morten, J.6
Armstrong, M.7
Pollard, C.E.8
-
20
-
-
3242717751
-
Pharmacological rescue of trafficking defective HERG channels formed by coassembly of wild-type and long QT mutant N470D subunits
-
Gong Q, Anderson CL, January CT, Zhou Z,: Pharmacological rescue of trafficking defective HERG channels formed by coassembly of wild-type and long QT mutant N470D subunits. Am J Physiol Heart Circ Physiol 2004; 287: H652-H658.
-
(2004)
Am J Physiol Heart Circ Physiol
, vol.287
-
-
Gong, Q.1
Anderson, C.L.2
January, C.T.3
Zhou, Z.4
-
21
-
-
77952656180
-
+ channels expressed in neonatal mouse cardiomyocytes
-
+ channels expressed in neonatal mouse cardiomyocytes. Am J Physiol Heart Circ Physiol 2010; 298: H1842-H1849.
-
(2010)
Am J Physiol Heart Circ Physiol
, vol.298
-
-
Lin, E.C.1
Holzem, K.M.2
Anson, B.D.3
Moungey, B.M.4
Balijepalli, S.Y.5
Tester, D.J.6
Ackerman, M.J.7
Delisle, B.P.8
Balijepalli, R.C.9
January, C.T.10
-
22
-
-
0032563717
-
Novel mechanism of HERG current suppression in LQT2: Shift in voltage dependence of HERG inactivation
-
Nakajima T, Furukawa T, Tanaka T, Katayama Y, Nagai R, Nakamura Y, Hiraoka M,: Novel mechanism of HERG current suppression in LQT2: Shift in voltage dependence of HERG inactivation. Circ Res 1998; 83: 415-422.
-
(1998)
Circ Res
, vol.83
, pp. 415-422
-
-
Nakajima, T.1
Furukawa, T.2
Tanaka, T.3
Katayama, Y.4
Nagai, R.5
Nakamura, Y.6
Hiraoka, M.7
-
23
-
-
0032516934
-
HERG channel dysfunction in human long QT syndrome. Intracellular transport and functional defects
-
Zhou Z, Gong Q, Epstein ML, January CT,: HERG channel dysfunction in human long QT syndrome. Intracellular transport and functional defects. J Biol Chem 1998; 273: 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
-
24
-
-
0035254154
-
Bradycardia-induced long QT syndrome caused by a de novo missense mutation in the S2-S3 inner loop of HERG
-
Yoshida H, Horie M, Otani H, Kawashima T, Onishi Y, Sasayama S,: Bradycardia-induced long QT syndrome caused by a de novo missense mutation in the S2-S3 inner loop of HERG. Am J Med Genet 2001; 98: 348-352.
-
(2001)
Am J Med Genet
, vol.98
, pp. 348-352
-
-
Yoshida, H.1
Horie, M.2
Otani, H.3
Kawashima, T.4
Onishi, Y.5
Sasayama, S.6
-
25
-
-
77958604381
-
Novel characteristics of a trafficking-defective G572R-hERG channel linked to hereditary long QT syndrome
-
Lian J, Huang N, Zhou J, Ge S, Huang X, Huo J, Liu L, Xu W, Zhang S, Yang X, Zhou J, Huang C,: Novel characteristics of a trafficking-defective G572R-hERG channel linked to hereditary long QT syndrome. Can J Caridol 2010; 26: 417-422.
-
(2010)
Can J Caridol
, vol.26
, pp. 417-422
-
-
Lian, J.1
Huang, N.2
Zhou, J.3
Ge, S.4
Huang, X.5
Huo, J.6
Liu, L.7
Xu, W.8
Zhang, S.9
Yang, X.10
Zhou, J.11
Huang, C.12
-
27
-
-
36148997249
-
Activation gating of hERG potassium channels: S6 glycines are not required as gating hinges
-
Hardman RM, Stansfeld PJ, Dalibalta S, Sutcliffe MJ, Mitcheson JS,: Activation gating of hERG potassium channels: S6 glycines are not required as gating hinges. J Biol Chem 2007; 282: 31972-31981.
-
(2007)
J Biol Chem
, vol.282
, pp. 31972-31981
-
-
Hardman, R.M.1
Stansfeld, P.J.2
Dalibalta, S.3
Sutcliffe, M.J.4
Mitcheson, J.S.5
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