-
1
-
-
0027429933
-
Use-dependent block and use-dependent unblock of the delayed rectifier K+ current by almokalant in rabbit ventricular myocytes
-
Carmeliet E. Use-dependent block and use-dependent unblock of the delayed rectifier K+ current by almokalant in rabbit ventricular myocytes. Circ Res 1993, 73:857-868.
-
(1993)
Circ Res
, vol.73
, pp. 857-868
-
-
Carmeliet, E.1
-
2
-
-
31044432330
-
Mechanism of action of a novel human ether-a-go-go-related gene channel activator
-
Casis O, Olesen SP, Sanguinetti MC. Mechanism of action of a novel human ether-a-go-go-related gene channel activator. Mol Pharmacol 2006, 69:658-665.
-
(2006)
Mol Pharmacol
, vol.69
, pp. 658-665
-
-
Casis, O.1
Olesen, S.P.2
Sanguinetti, M.C.3
-
3
-
-
0037126062
-
Position of aromatic residues in the S6 domain, not inactivation, dictates cisapride sensitivity of HERG and eag potassium channels
-
Chen J, Seebohm G, Sanguinetti MC. Position of aromatic residues in the S6 domain, not inactivation, dictates cisapride sensitivity of HERG and eag potassium channels. Proc Natl Acad Sci U S A 2002, 99:12461-12466.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 12461-12466
-
-
Chen, J.1
Seebohm, G.2
Sanguinetti, M.C.3
-
4
-
-
0033043040
-
Effects of outer mouth mutations on hERG channel function: a comparison with similar mutations in the Shaker channel
-
Fan JS, Jiang M, Dun W, Mcdonald TV, Tseng GC. Effects of outer mouth mutations on hERG channel function: a comparison with similar mutations in the Shaker channel. Biophys J 1999, 76:3128-3140.
-
(1999)
Biophys J
, vol.76
, pp. 3128-3140
-
-
Fan, J.S.1
Jiang, M.2
Dun, W.3
Mcdonald, T.V.4
Tseng, G.C.5
-
5
-
-
1642370447
-
Physicochemical features of the HERG channel drug binding site
-
Fernandez D, Ghanta A, Kauffman GW, Sanguinetti MC. Physicochemical features of the HERG channel drug binding site. J Biol Chem 2004, 279:10120-10127.
-
(2004)
J Biol Chem
, vol.279
, pp. 10120-10127
-
-
Fernandez, D.1
Ghanta, A.2
Kauffman, G.W.3
Sanguinetti, M.C.4
-
6
-
-
23844545376
-
HERG channel trafficking
-
discussion 70-54, 95-59
-
Ficker E, Dennis A, Kuryshev Y, Wible BA, Brown AM. HERG channel trafficking. Novartis Found Symp 2005, 266:57-69. discussion 70-54, 95-59
-
(2005)
Novartis Found Symp
, vol.266
, pp. 57-69
-
-
Ficker, E.1
Dennis, A.2
Kuryshev, Y.3
Wible, B.A.4
Brown, A.M.5
-
7
-
-
0035213865
-
Molecular determinants of inactivation and dofetilide block in ether a-go-go (EAG) channels and EAG-related K+ channels
-
Ficker E, Jarolimek W, Brown AM. Molecular determinants of inactivation and dofetilide block in ether a-go-go (EAG) channels and EAG-related K+ channels. Mol Pharmacol 2001, 60:1343-1348.
-
(2001)
Mol Pharmacol
, vol.60
, pp. 1343-1348
-
-
Ficker, E.1
Jarolimek, W.2
Brown, A.M.3
-
8
-
-
0032559552
-
Molecular determinants of dofetilide block of HERG K+ channels
-
Ficker E, Jarolimek W, Kiehn J, Baumann A, Brown AM. Molecular determinants of dofetilide block of HERG K+ channels. Circ Res 1998, 82:386-395.
-
(1998)
Circ Res
, vol.82
, pp. 386-395
-
-
Ficker, E.1
Jarolimek, W.2
Kiehn, J.3
Baumann, A.4
Brown, A.M.5
-
9
-
-
73549100431
-
Pharmacological removal of human ether-a-go-go-related gene potassium channel inactivation by 3-nitro-N-(4-phenoxyphenyl) benzamide (ICA-105574)
-
Gerlach AC, Stoehr SJ, Castle NA. Pharmacological removal of human ether-a-go-go-related gene potassium channel inactivation by 3-nitro-N-(4-phenoxyphenyl) benzamide (ICA-105574). Mol Pharmacol 2010, 77:58-68.
-
(2010)
Mol Pharmacol
, vol.77
, pp. 58-68
-
-
Gerlach, A.C.1
Stoehr, S.J.2
Castle, N.A.3
-
10
-
-
77349100802
-
The amiodarone derivative KB130015 activates hERG1 potassium channels via a novel mechanism
-
Gessner G, Macianskiene R, Starkus JG, Schonherr R, Heinemann SH. The amiodarone derivative KB130015 activates hERG1 potassium channels via a novel mechanism. Eur J Pharmacol 2010, 632:52-59.
-
(2010)
Eur J Pharmacol
, vol.632
, pp. 52-59
-
-
Gessner, G.1
Macianskiene, R.2
Starkus, J.G.3
Schonherr, R.4
Heinemann, S.H.5
-
11
-
-
40849140985
-
2-[2-(3,4-Dichloro-phenyl)-2,3-dihydro-1H-isoindol-5-ylamino]-nicotinic acid (PD-307243) causes instantaneous current through human ether-a-go-go-related gene potassium channels
-
Gordon E, Lozinskaya IM, Lin Z, Semus SF, Blaney FE, Willette RN, Xu X. 2-[2-(3,4-Dichloro-phenyl)-2,3-dihydro-1H-isoindol-5-ylamino]-nicotinic acid (PD-307243) causes instantaneous current through human ether-a-go-go-related gene potassium channels. Mol Pharmacol 2008, 73:639-651.
-
(2008)
Mol Pharmacol
, vol.73
, pp. 639-651
-
-
Gordon, E.1
Lozinskaya, I.M.2
Lin, Z.3
Semus, S.F.4
Blaney, F.E.5
Willette, R.N.6
Xu, X.7
-
13
-
-
50249099700
-
The hERG potassium channel and hERG screening for drug-induced torsades de pointes
-
Hancox JC, Mcpate MJ, El Harchi A, Zhang YH. The hERG potassium channel and hERG screening for drug-induced torsades de pointes. Pharmacol Ther 2008, 119:118-132.
-
(2008)
Pharmacol Ther
, vol.119
, pp. 118-132
-
-
Hancox, J.C.1
Mcpate, M.J.2
El Harchi, A.3
Zhang, Y.H.4
-
14
-
-
33748936880
-
Biophysical characterization of the new human ether-a-go-go-related gene channel opener NS3623 [N-(4-bromo-2-(1H-tetrazol-5-yl)-phenyl)-N′-(3′-trifluoromethylphenyl)urea]
-
Hansen RS, Diness TG, Christ T, Wettwer E, Ravens U, Olesen SP, Grunnet M. Biophysical characterization of the new human ether-a-go-go-related gene channel opener NS3623 [N-(4-bromo-2-(1H-tetrazol-5-yl)-phenyl)-N′-(3′-trifluoromethylphenyl)urea]. Mol Pharmacol 2006, 70:1319-1329.
-
(2006)
Mol Pharmacol
, vol.70
, pp. 1319-1329
-
-
Hansen, R.S.1
Diness, T.G.2
Christ, T.3
Wettwer, E.4
Ravens, U.5
Olesen, S.P.6
Grunnet, M.7
-
15
-
-
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
-
16
-
-
0032529096
-
Transfer of rapid inactivation and sensitivity to the class III antiarrhythmic drug E-4031 from HERG to M-eag channels
-
Herzberg IM, Trudeau MC, Robertson GA. Transfer of rapid inactivation and sensitivity to the class III antiarrhythmic drug E-4031 from HERG to M-eag channels. J Physiol 1998, 511:3-14.
-
(1998)
J Physiol
, vol.511
, pp. 3-14
-
-
Herzberg, I.M.1
Trudeau, M.C.2
Robertson, G.A.3
-
17
-
-
53049102635
-
Mutational analysis of block and facilitation of HERG current by a class III anti-arrhythmic agent, nifekalant
-
Hosaka Y, Iwata M, Kamiya N, Yamada M, Kinoshita K, Fukunishi Y, Tsujimae K, Hibino H, Aizawa Y, Inanobe A, Nakamura H, Kurachi Y. Mutational analysis of block and facilitation of HERG current by a class III anti-arrhythmic agent, nifekalant. Channels (Austin) 2007, 1:198-208.
-
(2007)
Channels (Austin)
, vol.1
, pp. 198-208
-
-
Hosaka, Y.1
Iwata, M.2
Kamiya, N.3
Yamada, M.4
Kinoshita, K.5
Fukunishi, Y.6
Tsujimae, K.7
Hibino, H.8
Aizawa, Y.9
Inanobe, A.10
Nakamura, H.11
Kurachi, Y.12
-
18
-
-
64349094193
-
Docking model of drug binding to the human ether-a-go-go potassium channel guided by tandem dimer mutant patch-clamp data: a synergic approach
-
Imai YN, Ryu S, Oiki S. Docking model of drug binding to the human ether-a-go-go potassium channel guided by tandem dimer mutant patch-clamp data: a synergic approach. J Med Chem 2009, 52:1630-1638.
-
(2009)
J Med Chem
, vol.52
, pp. 1630-1638
-
-
Imai, Y.N.1
Ryu, S.2
Oiki, S.3
-
19
-
-
0032746775
-
Use-dependent 'agonist' effect of azimilide on the HERG channel
-
Jiang M, Dun W, Fan JS, Tseng GN. Use-dependent 'agonist' effect of azimilide on the HERG channel. J Pharmacol Exp Ther 1999, 291:1324-1336.
-
(1999)
J Pharmacol Exp Ther
, vol.291
, pp. 1324-1336
-
-
Jiang, M.1
Dun, W.2
Fan, J.S.3
Tseng, G.N.4
-
20
-
-
28244474869
-
Dynamic conformational changes of extracellular S5-P linkers in the hERG channel
-
Jiang M, Zhang M, Maslennikov IV, Liu J, Wu DM, Korolkova YV, Arseniev AS, Grishin EV, Tseng GN. Dynamic conformational changes of extracellular S5-P linkers in the hERG channel. J Physiol 2005, 569:75-89.
-
(2005)
J Physiol
, vol.569
, pp. 75-89
-
-
Jiang, M.1
Zhang, M.2
Maslennikov, I.V.3
Liu, J.4
Wu, D.M.5
Korolkova, Y.V.6
Arseniev, A.S.7
Grishin, E.V.8
Tseng, G.N.9
-
21
-
-
0037198625
-
The open pore conformation of potassium channels
-
Jiang YX, Lee A, Chen JY, Cadene M, Chait BT, Mackinnon R. The open pore conformation of potassium channels. Nature 2002, 417:523-526.
-
(2002)
Nature
, vol.417
, pp. 523-526
-
-
Jiang, Y.X.1
Lee, A.2
Chen, J.Y.3
Cadene, M.4
Chait, B.T.5
Mackinnon, R.6
-
22
-
-
59449093463
-
The pore domain outer helix contributes to both activation and inactivation of the HERG K+ channel
-
Ju P, Pages G, Riek RP, Chen PC, Torres AM, Bansal PS, Kuyucak S, Kuchel PW, Vandenberg JI. The pore domain outer helix contributes to both activation and inactivation of the HERG K+ channel. J Biol Chem 2009, 284:1000-1008.
-
(2009)
J Biol Chem
, vol.284
, pp. 1000-1008
-
-
Ju, P.1
Pages, G.2
Riek, R.P.3
Chen, P.C.4
Torres, A.M.5
Bansal, P.S.6
Kuyucak, S.7
Kuchel, P.W.8
Vandenberg, J.I.9
-
23
-
-
0034914537
-
Open channel block of HERG K+ channels by vesnarinone
-
Kamiya K, Mitcheson JS, Yasui K, Kodama I, Sanguinetti MC. Open channel block of HERG K+ channels by vesnarinone. Mol Pharmacol 2001, 60:244-253.
-
(2001)
Mol Pharmacol
, vol.60
, pp. 244-253
-
-
Kamiya, K.1
Mitcheson, J.S.2
Yasui, K.3
Kodama, I.4
Sanguinetti, M.C.5
-
24
-
-
33645816995
-
Molecular determinants of HERG channel block
-
Kamiya K, Niwa R, Mitcheson JS, Sanguinetti MC. Molecular determinants of HERG channel block. Mol Pharmacol 2006, 69:1709-1716.
-
(2006)
Mol Pharmacol
, vol.69
, pp. 1709-1716
-
-
Kamiya, K.1
Niwa, R.2
Mitcheson, J.S.3
Sanguinetti, M.C.4
-
25
-
-
56649106666
-
Molecular determinants of hERG channel block by terfenadine and cisapride
-
Kamiya K, Niwa R, Morishima M, Honjo H, Sanguinetti MC. Molecular determinants of hERG channel block by terfenadine and cisapride. J Pharmacol Sci 2008, 108:301-307.
-
(2008)
J Pharmacol Sci
, vol.108
, pp. 301-307
-
-
Kamiya, K.1
Niwa, R.2
Morishima, M.3
Honjo, H.4
Sanguinetti, M.C.5
-
26
-
-
20144373180
-
Discovery of a small molecule activator of the human ether-a-go-go-related gene (HERG) cardiac K+ channel
-
Kang J, Chen Xl, Wang H, Ji J, Cheng H, Incardona J, Reynolds W, Viviani F, Tabart M, Rampe D. Discovery of a small molecule activator of the human ether-a-go-go-related gene (HERG) cardiac K+ channel. Mol Pharmacol 2005, 67:827-836.
-
(2005)
Mol Pharmacol
, vol.67
, pp. 827-836
-
-
Kang, J.1
Chen, X.2
Wang, H.3
Ji, J.4
Cheng, H.5
Incardona, J.6
Reynolds, W.7
Viviani, F.8
Tabart, M.9
Rampe, D.10
-
27
-
-
0346118860
-
Gating of shaker-type channels requires the flexibility of S6 caused by prolines
-
Labro AJ, Raes AL, Bellens I, Ottschytsch N, Snyders DJ. Gating of shaker-type channels requires the flexibility of S6 caused by prolines. J Biol Chem 2003, 278:50724-50731.
-
(2003)
J Biol Chem
, vol.278
, pp. 50724-50731
-
-
Labro, A.J.1
Raes, A.L.2
Bellens, I.3
Ottschytsch, N.4
Snyders, D.J.5
-
28
-
-
0033952902
-
Molecular determinant of high-affinity dofetilide binding to HERG1 expressed in Xenopus oocytes: involvement of S6 sites
-
Lees-Miller JP, Duan Y, Teng GQ, Duff HJ. Molecular determinant of high-affinity dofetilide binding to HERG1 expressed in Xenopus oocytes: involvement of S6 sites. Mol Pharmacol 2000, 57:367-374.
-
(2000)
Mol Pharmacol
, vol.57
, pp. 367-374
-
-
Lees-Miller, J.P.1
Duan, Y.2
Teng, G.Q.3
Duff, H.J.4
-
29
-
-
0036845677
-
Structural and functional role of the extracellular S5-P linker in the HERG potassium channel
-
Liu J, Zhang M, Jiang M, Tseng GN. Structural and functional role of the extracellular S5-P linker in the HERG potassium channel. J Gen Physiol 2002, 120:723-737.
-
(2002)
J Gen Physiol
, vol.120
, pp. 723-737
-
-
Liu, J.1
Zhang, M.2
Jiang, M.3
Tseng, G.N.4
-
30
-
-
0038580641
-
Negative charges in the transmembrane domains of the HERG K channel are involved in the activation- and deactivation-gating processes
-
Liu J, Zhang M, Jiang M, Tseng GN. Negative charges in the transmembrane domains of the HERG K channel are involved in the activation- and deactivation-gating processes. J Gen Physiol 2003, 121:599-614.
-
(2003)
J Gen Physiol
, vol.121
, pp. 599-614
-
-
Liu, J.1
Zhang, M.2
Jiang, M.3
Tseng, G.N.4
-
31
-
-
23244456428
-
Crystal structure of a mammalian voltage-dependent Shaker family K+ channel
-
Long SB, Campbell EB, Mackinnon R. Crystal structure of a mammalian voltage-dependent Shaker family K+ channel. Science 2005, 309:897-903.
-
(2005)
Science
, vol.309
, pp. 897-903
-
-
Long, S.B.1
Campbell, E.B.2
Mackinnon, R.3
-
32
-
-
57349159464
-
Pharmacology of the short QT syndrome N588K-hERG K+ channel mutation: differential impact on selected class I and class III antiarrhythmic drugs
-
McPate MJ, Duncan RS, Hancox JC, Witchel HJ. Pharmacology of the short QT syndrome N588K-hERG K+ channel mutation: differential impact on selected class I and class III antiarrhythmic drugs. Br J Pharmacol 2008, 155:957-966.
-
(2008)
Br J Pharmacol
, vol.155
, pp. 957-966
-
-
McPate, M.J.1
Duncan, R.S.2
Hancox, J.C.3
Witchel, H.J.4
-
33
-
-
0038497465
-
Blockade of HERG potassium currents by fluvoxamine: incomplete attenuation by S6 mutations at F656 or Y652
-
Milnes JT, Crociani O, Arcangeli A, Hancox JC, Witchel HJ. Blockade of HERG potassium currents by fluvoxamine: incomplete attenuation by S6 mutations at F656 or Y652. Br J Pharmacol 2003, 139:887-898.
-
(2003)
Br J Pharmacol
, vol.139
, pp. 887-898
-
-
Milnes, J.T.1
Crociani, O.2
Arcangeli, A.3
Hancox, J.C.4
Witchel, H.J.5
-
34
-
-
33750315762
-
HERG K+ channel blockade by the antipsychotic drug thioridazine: An obligatory role for the S6 helix residue F656
-
Milnes JT, Witchel HJ, Leaney JL, Leishman DJ, Hancox JC. hERG K+ channel blockade by the antipsychotic drug thioridazine: An obligatory role for the S6 helix residue F656. Biochem Biophys Res Commun 2006, 351:273-280.
-
(2006)
Biochem Biophys Res Commun
, vol.351
, pp. 273-280
-
-
Milnes, J.T.1
Witchel, H.J.2
Leaney, J.L.3
Leishman, D.J.4
Hancox, J.C.5
-
35
-
-
0034710933
-
A structural basis for drug-induced long QT syndrome
-
Mitcheson JS, Chen J, Lin M, Culberson C, Sanguinetti MC. A structural basis for drug-induced long QT syndrome. Proc Natl Acad Sci U S A 2000a, 97:12329-12333.
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 12329-12333
-
-
Mitcheson, J.S.1
Chen, J.2
Lin, M.3
Culberson, C.4
Sanguinetti, M.C.5
-
36
-
-
0033818157
-
Trapping of a methanesulfonanilide by closure of the HERG potassium channel activation gate
-
Mitcheson JS, Chen J, Sanguinetti MC. Trapping of a methanesulfonanilide by closure of the HERG potassium channel activation gate. J Gen Physiol 2000b, 115:229-240.
-
(2000)
J Gen Physiol
, vol.115
, pp. 229-240
-
-
Mitcheson, J.S.1
Chen, J.2
Sanguinetti, M.C.3
-
37
-
-
44249086160
-
Topological mapping of the asymmetric drug binding to the human ether-a-go-go-related gene product (HERG) potassium channel by use of tandem dimers
-
Myokai T, Ryu S, Shimizu H, Oiki S. Topological mapping of the asymmetric drug binding to the human ether-a-go-go-related gene product (HERG) potassium channel by use of tandem dimers. Mol Pharmacol 2008, 73:1643-1651.
-
(2008)
Mol Pharmacol
, vol.73
, pp. 1643-1651
-
-
Myokai, T.1
Ryu, S.2
Shimizu, H.3
Oiki, S.4
-
38
-
-
54349123564
-
Drug binding to the inactivated state is necessary but not sufficient for high-affinity binding to human ether-a-go-go-related gene channels
-
Perrin MJ, Kuchel PW, Campbell TJ, Vandenberg JI. Drug binding to the inactivated state is necessary but not sufficient for high-affinity binding to human ether-a-go-go-related gene channels. Mol Pharmacol 2008, 74:1443-1452.
-
(2008)
Mol Pharmacol
, vol.74
, pp. 1443-1452
-
-
Perrin, M.J.1
Kuchel, P.W.2
Campbell, T.J.3
Vandenberg, J.I.4
-
39
-
-
3342988006
-
Structural determinants of HERG channel block by clofilium and ibutilide
-
Perry M, De Groot MJ, Helliwell R, Leishman D, Tristani-Firouzi M, Sanguinetti MC, Mitcheson J. Structural determinants of HERG channel block by clofilium and ibutilide. Mol Pharmacol 2004, 66:240-249.
-
(2004)
Mol Pharmacol
, vol.66
, pp. 240-249
-
-
Perry, M.1
De Groot, M.J.2
Helliwell, R.3
Leishman, D.4
Tristani-Firouzi, M.5
Sanguinetti, M.C.6
Mitcheson, J.7
-
40
-
-
73949151507
-
PD-118057 contacts the pore helix of hERG1 channels to attenuate inactivation and enhance K+ conductance
-
Perry M, Sachse FB, Abbruzzese J, Sanguinetti MC. PD-118057 contacts the pore helix of hERG1 channels to attenuate inactivation and enhance K+ conductance. Proc Natl Acad Sci U S A 2009, 106:20075-20080.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 20075-20080
-
-
Perry, M.1
Sachse, F.B.2
Abbruzzese, J.3
Sanguinetti, M.C.4
-
41
-
-
35348824829
-
Structural basis of action for a human ether-a-go-go-related gene 1 potassium channel activator
-
Perry M, Sachse FB, Sanguinetti MC. Structural basis of action for a human ether-a-go-go-related gene 1 potassium channel activator. Proc Natl Acad Sci U S A 2007, 104:13827-13832.
-
(2007)
Proc Natl Acad Sci U S A
, vol.104
, pp. 13827-13832
-
-
Perry, M.1
Sachse, F.B.2
Sanguinetti, M.C.3
-
42
-
-
31044447745
-
Drug binding interactions in the inner cavity of HERG channels: molecular insights from structure-activity relationships of clofilium and ibutilide analogs
-
Perry M, Stansfeld PJ, Leaney J, Wood C, De Groot MJ, Leishman D, Sutcliffe MJ, Mitcheson JS. Drug binding interactions in the inner cavity of HERG channels: molecular insights from structure-activity relationships of clofilium and ibutilide analogs. Mol Pharmacol 2006, 69:509-519.
-
(2006)
Mol Pharmacol
, vol.69
, pp. 509-519
-
-
Perry, M.1
Stansfeld, P.J.2
Leaney, J.3
Wood, C.4
De Groot, M.J.5
Leishman, D.6
Sutcliffe, M.J.7
Mitcheson, J.S.8
-
43
-
-
0041836223
-
Gating currents associated with intramembrane charge displacement in HERG potassium channels
-
Piper DR, Varghese A, Sanguinetti MC, Tristani-Firouzi M. Gating currents associated with intramembrane charge displacement in HERG potassium channels. Proc Natl Acad Sci U S A 2003, 100:10534-10539.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 10534-10539
-
-
Piper, D.R.1
Varghese, A.2
Sanguinetti, M.C.3
Tristani-Firouzi, M.4
-
44
-
-
14844318017
-
Regional specificity of hERG channel activation and inactivation gating
-
Piper DR, Hinz WA, Tallurri CK, Sanguinetti MC, Tristani-Firouzi M. Regional specificity of hERG channel activation and inactivation gating. J Biol Chem 2005, 280:7206-7217.
-
(2005)
J Biol Chem
, vol.280
, pp. 7206-7217
-
-
Piper, D.R.1
Hinz, W.A.2
Tallurri, C.K.3
Sanguinetti, M.C.4
Tristani-Firouzi, M.5
-
45
-
-
33750480200
-
Drug-induced long QT syndrome: hERG K+ channel block and disruption of protein trafficking by fluoxetine and norfluoxetine
-
Rajamani S, Eckhardt LL, Valdivia CR, Klemens CA, Gillman BM, Anderson CL, Holzem KM, Delisle BP, Anson BD, Makielski JC, January CT. Drug-induced long QT syndrome: hERG K+ channel block and disruption of protein trafficking by fluoxetine and norfluoxetine. Br J Pharmacol 2006, 149:481-489.
-
(2006)
Br J Pharmacol
, vol.149
, pp. 481-489
-
-
Rajamani, S.1
Eckhardt, L.L.2
Valdivia, C.R.3
Klemens, C.A.4
Gillman, B.M.5
Anderson, C.L.6
Holzem, K.M.7
Delisle, B.P.8
Anson, B.D.9
Makielski, J.C.10
January, C.T.11
-
46
-
-
14544268139
-
QT prolongation through hERG K+ channel blockade: current knowledge and strategies for the early prediction during drug development
-
Recanatini M, Poluzzi E, Masetti M, Cavalli A, De Ponti F. QT prolongation through hERG K+ channel blockade: current knowledge and strategies for the early prediction during drug development. Med Res Rev 2005, 25:133-166.
-
(2005)
Med Res Rev
, vol.25
, pp. 133-166
-
-
Recanatini, M.1
Poluzzi, E.2
Masetti, M.3
Cavalli, A.4
De Ponti, F.5
-
47
-
-
0344492207
-
Relationships between preclinical cardiac electrophysiology, clinical QT interval prolongation and torsade de pointes for a broad range of drugs: evidence for a provisional safety margin in drug development
-
Redfern WS, Carlsson L, Davis AS, Lynch WG, Mackenzie I, Palethorpe S, Siegl PK, Strang I, Sullivan AT, Wallis R, Camm AJ, Hammond TG. Relationships between preclinical cardiac electrophysiology, clinical QT interval prolongation and torsade de pointes for a broad range of drugs: evidence for a provisional safety margin in drug development. Cardiovasc Res 2003, 58:32-45.
-
(2003)
Cardiovasc Res
, vol.58
, pp. 32-45
-
-
Redfern, W.S.1
Carlsson, L.2
Davis, A.S.3
Lynch, W.G.4
Mackenzie, I.5
Palethorpe, S.6
Siegl, P.K.7
Strang, I.8
Sullivan, A.T.9
Wallis, R.10
Camm, A.J.11
Hammond, T.G.12
-
48
-
-
2342575536
-
Lidoflazine is a high affinity blocker of the HERG K+ channel
-
Ridley JM, Dooley PC, Milnes JT, Witchel HJ, Hancox JC. Lidoflazine is a high affinity blocker of the HERG K+ channel. J Mol Cell Cardiol 2004, 36:701-705.
-
(2004)
J Mol Cell Cardiol
, vol.36
, pp. 701-705
-
-
Ridley, J.M.1
Dooley, P.C.2
Milnes, J.T.3
Witchel, H.J.4
Hancox, J.C.5
-
49
-
-
0032552038
-
Mechanisms and management of proarrhythmia
-
Roden DM. Mechanisms and management of proarrhythmia. Am J Cardiol 1998, 82:49I-57I.
-
(1998)
Am J Cardiol
, vol.82
-
-
Roden, D.M.1
-
50
-
-
0038407463
-
Voltage-dependent profile of human ether-a-go-go-related gene channel block is influenced by a single residue in the S6 transmembrane domain
-
Sanchez-Chapula JA, Ferrer T, Navarro-Polanco RA, Sanguinetti MC. Voltage-dependent profile of human ether-a-go-go-related gene channel block is influenced by a single residue in the S6 transmembrane domain. Mol Pharmacol 2003, 63:1051-1058.
-
(2003)
Mol Pharmacol
, vol.63
, pp. 1051-1058
-
-
Sanchez-Chapula, J.A.1
Ferrer, T.2
Navarro-Polanco, R.A.3
Sanguinetti, M.C.4
-
51
-
-
0037189588
-
Molecular determinants of voltage-dependent human ether-a-go-go related gene (HERG) K+ channel block
-
Sanchez-Chapula JA, Navarro-Polanco RA, Culberson C, Chen J, Sanguinetti MC. Molecular determinants of voltage-dependent human ether-a-go-go related gene (HERG) K+ channel block. J Biol Chem 2002, 277:23587-23595.
-
(2002)
J Biol Chem
, vol.277
, pp. 23587-23595
-
-
Sanchez-Chapula, J.A.1
Navarro-Polanco, R.A.2
Culberson, C.3
Chen, J.4
Sanguinetti, M.C.5
-
52
-
-
0029002969
-
A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel
-
Sanguinetti MC, Jiang C, Curran ME, Keating MT. A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel. Cell 1995, 81:299-307.
-
(1995)
Cell
, vol.81
, pp. 299-307
-
-
Sanguinetti, M.C.1
Jiang, C.2
Curran, M.E.3
Keating, M.T.4
-
53
-
-
0030054878
-
Molecular determinants for activation and inactivation of HERG, a human inward rectifier potassium channel
-
Schonherr R, Heinemann SH. Molecular determinants for activation and inactivation of HERG, a human inward rectifier potassium channel. J Physiol 1996, 493:635-642.
-
(1996)
J Physiol
, vol.493
, pp. 635-642
-
-
Schonherr, R.1
Heinemann, S.H.2
-
54
-
-
0030025308
-
The inward rectification mechanism of the HERG cardiac potassium channel
-
Smith PL, Baukrowitz T, Yellen G. The inward rectification mechanism of the HERG cardiac potassium channel. Nature 1996, 379:833-836.
-
(1996)
Nature
, vol.379
, pp. 833-836
-
-
Smith, P.L.1
Baukrowitz, T.2
Yellen, G.3
-
55
-
-
0036097030
-
Fast and slow voltage sensor movements in HERG potassium channels
-
Smith PL, Yellen G. Fast and slow voltage sensor movements in HERG potassium channels. J Gen Physiol 2002, 119:275-293.
-
(2002)
J Gen Physiol
, vol.119
, pp. 275-293
-
-
Smith, P.L.1
Yellen, G.2
-
56
-
-
0030058762
-
Class III antiarrhythmic drugs block HERG, a human cardiac delayed rectifier K+ channel. Open-channel block by methanesulfonanilides
-
Spector PS, Curran ME, Keating MT, Sanguinetti MC. Class III antiarrhythmic drugs block HERG, a human cardiac delayed rectifier K+ channel. Open-channel block by methanesulfonanilides. Circ Res 1996a, 78:499-503.
-
(1996)
Circ Res
, vol.78
, pp. 499-503
-
-
Spector, P.S.1
Curran, M.E.2
Keating, M.T.3
Sanguinetti, M.C.4
-
57
-
-
0029926887
-
Fast inactivation causes rectification of the IKr channel
-
Spector PS, Curran ME, Zou A, Keating MT, Sanguinetti MC. Fast inactivation causes rectification of the IKr channel. J Gen Physiol 1996b, 107:611-619.
-
(1996)
J Gen Physiol
, vol.107
, pp. 611-619
-
-
Spector, P.S.1
Curran, M.E.2
Zou, A.3
Keating, M.T.4
Sanguinetti, M.C.5
-
58
-
-
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
-
59
-
-
47249121368
-
Insight into the mechanism of inactivation and pH sensitivity in potassium channels from molecular dynamics simulations
-
Stansfeld PJ, Grottesi A, Sands ZA, Sansom MS, Gedeck P, Gosling M, Cox B, Stanfield PR, Mitcheson JS, Sutcliffe MJ. Insight into the mechanism of inactivation and pH sensitivity in potassium channels from molecular dynamics simulations. Biochemistry 2008, 47:7414-7422.
-
(2008)
Biochemistry
, vol.47
, pp. 7414-7422
-
-
Stansfeld, P.J.1
Grottesi, A.2
Sands, Z.A.3
Sansom, M.S.4
Gedeck, P.5
Gosling, M.6
Cox, B.7
Stanfield, P.R.8
Mitcheson, J.S.9
Sutcliffe, M.J.10
-
60
-
-
34547902408
-
State dependent dissociation of HERG channel inhibitors
-
Stork D, Timin EN, Berjukow S, Huber C, Hohaus A, Auer M, Hering S. State dependent dissociation of HERG channel inhibitors. Br J Pharmacol 2007, 151:1368-1376.
-
(2007)
Br J Pharmacol
, vol.151
, pp. 1368-1376
-
-
Stork, D.1
Timin, E.N.2
Berjukow, S.3
Huber, C.4
Hohaus, A.5
Auer, M.6
Hering, S.7
-
61
-
-
4344686915
-
Molecular basis of slow activation of the human ether-á-go-go related gene potassium channel
-
Subbiah RN, Clarke CE, Smith DJ, Zhao J, Campbell TJ, Vandenberg JI. Molecular basis of slow activation of the human ether-á-go-go related gene potassium channel. J Physiol 2004, 558:417-431.
-
(2004)
J Physiol
, vol.558
, pp. 417-431
-
-
Subbiah, R.N.1
Clarke, C.E.2
Smith, D.J.3
Zhao, J.4
Campbell, T.J.5
Vandenberg, J.I.6
-
62
-
-
29244451869
-
Tryptophan scanning mutagenesis of the HERG K+ channel: the S4 domain is loosely packed and likely to be lipid exposed
-
Subbiah RN, Kondo M, Campbell TJ, Vandenberg JI. Tryptophan scanning mutagenesis of the HERG K+ channel: the S4 domain is loosely packed and likely to be lipid exposed. J Physiol 2005, 569:367-379.
-
(2005)
J Physiol
, vol.569
, pp. 367-379
-
-
Subbiah, R.N.1
Kondo, M.2
Campbell, T.J.3
Vandenberg, J.I.4
-
63
-
-
62549106559
-
Electrophysiologic characterization of a novel hERG channel activator
-
Su Z, Limberis J, Souers A, Kym P, Mikhail A, Houseman K, Diaz G, Liu X, Martin RL, Cox BF, Gintant GA. Electrophysiologic characterization of a novel hERG channel activator. Biochem Pharmacol 2009, 77:1383-1390.
-
(2009)
Biochem Pharmacol
, vol.77
, pp. 1383-1390
-
-
Su, Z.1
Limberis, J.2
Souers, A.3
Kym, P.4
Mikhail, A.5
Houseman, K.6
Diaz, G.7
Liu, X.8
Martin, R.L.9
Cox, B.F.10
Gintant, G.A.11
-
64
-
-
9944226711
-
Towards a structural view of gating in potassium channels
-
Swartz KJ. Towards a structural view of gating in potassium channels. Nat Rev Neurosci 2004, 5:905-916.
-
(2004)
Nat Rev Neurosci
, vol.5
, pp. 905-916
-
-
Swartz, K.J.1
-
65
-
-
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
-
66
-
-
1942467020
-
Intracellular gate opening in Shaker K+ channels defined by high-affinity metal bridges
-
Webster SM, Del Camino D, Dekker JP, Yellen G. Intracellular gate opening in Shaker K+ channels defined by high-affinity metal bridges. Nature 2004, 428:864-868.
-
(2004)
Nature
, vol.428
, pp. 864-868
-
-
Webster, S.M.1
Del Camino, D.2
Dekker, J.P.3
Yellen, G.4
-
67
-
-
44249098289
-
Probing the binding sites and mechanisms of action of two human ether-a-go-go-related gene channel activators, 1,3-bis-(2-hydroxy-5-trifluoromethyl-phenyl)-urea (NS1643) and 2-[2-(3,4-dichloro-phenyl)-2,3-dihydro-1H-isoindol-5-ylamino]-nicotinic acid (PD307243)
-
Xu X, Recanatini M, Roberti M, Tseng GN. Probing the binding sites and mechanisms of action of two human ether-a-go-go-related gene channel activators, 1,3-bis-(2-hydroxy-5-trifluoromethyl-phenyl)-urea (NS1643) and 2-[2-(3,4-dichloro-phenyl)-2,3-dihydro-1H-isoindol-5-ylamino]-nicotinic acid (PD307243). Mol Pharmacol 2008, 73:1709-1721.
-
(2008)
Mol Pharmacol
, vol.73
, pp. 1709-1721
-
-
Xu, X.1
Recanatini, M.2
Roberti, M.3
Tseng, G.N.4
-
68
-
-
33751168514
-
Mallotoxin is a novel human ether-a-go-go-related gene (hERG) potassium channel activator
-
Zeng H, Lozinskaya IM, Lin Z, Willette RN, Brooks DP, Xu X. Mallotoxin is a novel human ether-a-go-go-related gene (hERG) potassium channel activator. J Pharmacol Exp Ther 2006, 319:957-962.
-
(2006)
J Pharmacol Exp Ther
, vol.319
, pp. 957-962
-
-
Zeng, H.1
Lozinskaya, I.M.2
Lin, Z.3
Willette, R.N.4
Brooks, D.P.5
Xu, X.6
-
69
-
-
10344246598
-
Gating charges in the activation and inactivation processes of the HERG channel
-
Zhang M, Liu J, Tseng GN. Gating charges in the activation and inactivation processes of the HERG channel. J Gen Physiol 2004, 124:703-718.
-
(2004)
J Gen Physiol
, vol.124
, pp. 703-718
-
-
Zhang, M.1
Liu, J.2
Tseng, G.N.3
-
70
-
-
23944441185
-
Novel potent human ether-a-go-go-related gene (hERG) potassium channel enhancers and their in vitro antiarrhythmic activity
-
Zhou J, Augelli-Szafran CE, Bradley JA, Chen X, Koci BJ, Volberg WA, Sun Z, Cordes JS. Novel potent human ether-a-go-go-related gene (hERG) potassium channel enhancers and their in vitro antiarrhythmic activity. Mol Pharmacol 2005, 68:876-884.
-
(2005)
Mol Pharmacol
, vol.68
, pp. 876-884
-
-
Zhou, J.1
Augelli-Szafran, C.E.2
Bradley, J.A.3
Chen, X.4
Koci, B.J.5
Volberg, W.A.6
Sun, Z.7
Cordes, J.S.8
|