-
1
-
-
72149097863
-
Guide to Receptors and Channels (GRAC), 4th edn
-
Alexander SPH, Mathie A, Peters JA (2009). Guide to Receptors and Channels (GRAC), 4th edn. Br J Pharmacol 158 (Suppl. 1): S1-S254.
-
(2009)
Br J Pharmacol
, vol.158
, Issue.SUPPL. 1
-
-
Alexander, S.P.H.1
Mathie, A.2
Peters, J.A.3
-
2
-
-
34748858527
-
Kvbeta1.3 reduces the degree of stereoselective bupivacaine block of Kv1.5 channels
-
Arias C, Guizy M, David M, Marzian S, Gonzalez T, Decher N et al. (2007). Kvbeta1.3 reduces the degree of stereoselective bupivacaine block of Kv1.5 channels. Anesthesiology 107: 641-651.
-
(2007)
Anesthesiology
, vol.107
, pp. 641-651
-
-
Arias, C.1
Guizy, M.2
David, M.3
Marzian, S.4
Gonzalez, T.5
Decher, N.6
-
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 (2002). 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 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
-
-
0345791517
-
Molecular basis for Kv1.5 channel block - conservation of drug binding sites among voltage-gated K+ channels
-
Decher N, Pirard B, Bundis F, Peukert S, Baringhaus KH, Busch AE et al. (2004). Molecular basis for Kv1.5 channel block - conservation of drug binding sites among voltage-gated K+ channels. J Biol Chem 279: 394-400.
-
(2004)
J Biol Chem
, vol.279
, pp. 394-400
-
-
Decher, N.1
Pirard, B.2
Bundis, F.3
Peukert, S.4
Baringhaus, K.H.5
Busch, A.E.6
-
5
-
-
25144456184
-
Structural basis for competition between drug binding and Kvbeta 1.3 accessory subunit-induced N-type inactivation of Kv1.5 channels
-
Decher N, Kumar P, Gonzalez T, Renigunta V, Sanguinetti MC (2005). Structural basis for competition between drug binding and Kvbeta 1.3 accessory subunit-induced N-type inactivation of Kv1.5 channels. Mol Pharmacol 68: 995-1005.
-
(2005)
Mol Pharmacol
, vol.68
, pp. 995-1005
-
-
Decher, N.1
Kumar, P.2
Gonzalez, T.3
Renigunta, V.4
Sanguinetti, M.C.5
-
6
-
-
33748945382
-
Binding site of a novel Kv1.5 blocker: a 'foot in the door' against atrial fibrillation
-
Decher N, Kumar P, Gonzalez T, Pirard B, Sanguinetti MC (2006). Binding site of a novel Kv1.5 blocker: a 'foot in the door' against atrial fibrillation. Mol Pharmacol 70: 1204-1211.
-
(2006)
Mol Pharmacol
, vol.70
, pp. 1204-1211
-
-
Decher, N.1
Kumar, P.2
Gonzalez, T.3
Pirard, B.4
Sanguinetti, M.C.5
-
7
-
-
66149127646
-
Novel approaches for pharmacological management of atrial fibrillation
-
Ehrlich JR, Nattel S (2009). Novel approaches for pharmacological management of atrial fibrillation. Drugs 69: 757-774.
-
(2009)
Drugs
, vol.69
, pp. 757-774
-
-
Ehrlich, J.R.1
Nattel, S.2
-
8
-
-
33747437950
-
ACC/AHA/ESC 2006 Guidelines for the Management of Patients with Atrial Fibrillation: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines and the European Society of Cardiology Committee for Practice Guidelines (Writing Committee to Revise the 2001 Guidelines for the Management of Patients with Atrial Fibrillation)
-
Developed in Collaboration with the European Heart Rhythm Association and the Heart Rhythm Society
-
Fuster V, Ryden LE, Cannom DS, Crijns HJ, Curtis AB, Ellenbogen KA et al. (2006). ACC/AHA/ESC 2006 Guidelines for the Management of Patients with Atrial Fibrillation: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines and the European Society of Cardiology Committee for Practice Guidelines (Writing Committee to Revise the 2001 Guidelines for the Management of Patients with Atrial Fibrillation): Developed in Collaboration with the European Heart Rhythm Association and the Heart Rhythm Society. Circulation 114: e257-e354.
-
(2006)
Circulation
, vol.114
-
-
Fuster, V.1
Ryden, L.E.2
Cannom, D.S.3
Crijns, H.J.4
Curtis, A.B.5
Ellenbogen, K.A.6
-
9
-
-
33645310407
-
Uptake of cardiovascular drugs into the human heart: expression, regulation, and function of the carnitine transporter OCTN2 (SLC22A5)
-
Grube M, Meyer zu Schwabedissen HE, Prager D, Haney J, Moritz KU, Meissner K et al. (2006). Uptake of cardiovascular drugs into the human heart: expression, regulation, and function of the carnitine transporter OCTN2 (SLC22A5). Circulation 113: 1114-1122.
-
(2006)
Circulation
, vol.113
, pp. 1114-1122
-
-
Grube, M.1
Meyer zu Schwabedissen, H.E.2
Prager, D.3
Haney, J.4
Moritz, K.U.5
Meissner, K.6
-
10
-
-
63849344988
-
Enhanced corneal absorption of erythromycin by modulating p-glycoprotein and MRP mediated efflux with corticosteroids
-
Hariharan S, Gunda S, Mishra GP, Pal D, Mitra AK (2009). Enhanced corneal absorption of erythromycin by modulating p-glycoprotein and MRP mediated efflux with corticosteroids. Pharm Res 26: 1270-1282.
-
(2009)
Pharm Res
, vol.26
, pp. 1270-1282
-
-
Hariharan, S.1
Gunda, S.2
Mishra, G.P.3
Pal, D.4
Mitra, A.K.5
-
11
-
-
0035909047
-
Clinical predictors of prolonged delay in return of the international normalized ratio to within the therapeutic range after excessive anticoagulation with warfarin
-
Hylek EM, Regan S, Go AS, Hughes RA, Singer DE, Skates SJ (2001). Clinical predictors of prolonged delay in return of the international normalized ratio to within the therapeutic range after excessive anticoagulation with warfarin. Ann Intern Med 135: 393-400.
-
(2001)
Ann Intern Med
, vol.135
, pp. 393-400
-
-
Hylek, E.M.1
Regan, S.2
Go, A.S.3
Hughes, R.A.4
Singer, D.E.5
Skates, S.J.6
-
12
-
-
48849091224
-
Involvement of carnitine/organic cation transporter OCTN2 (SLC22A5) in distribution of its substrate carnitine to the heart
-
Iwata D, Kato Y, Wakayama T, Sai Y, Kubo Y, Iseki S et al. (2008). Involvement of carnitine/organic cation transporter OCTN2 (SLC22A5) in distribution of its substrate carnitine to the heart. Drug Metab Pharmacokinet 23: 207-215.
-
(2008)
Drug Metab Pharmacokinet
, vol.23
, pp. 207-215
-
-
Iwata, D.1
Kato, Y.2
Wakayama, T.3
Sai, Y.4
Kubo, Y.5
Iseki, S.6
-
13
-
-
77958518386
-
Overlapping sites for Kv1.5 drug-binding and the receptor site for the Kv beta 1.3 inactivation ball
-
Khumar P, Gonzalez T, Steinmeyer K, Sanguinetti MC (2004). Overlapping sites for Kv1.5 drug-binding and the receptor site for the Kv beta 1.3 inactivation ball. Biophys J 86: 132A-133A.
-
(2004)
Biophys J
, vol.86
-
-
Khumar, P.1
Gonzalez, T.2
Steinmeyer, K.3
Sanguinetti, M.C.4
-
14
-
-
0036229852
-
Drugs as P-glycoprotein substrates, inhibitors, and inducers
-
Kim RB (2002). Drugs as P-glycoprotein substrates, inhibitors, and inducers. Drug Metab Rev 34: 47-54.
-
(2002)
Drug Metab Rev
, vol.34
, pp. 47-54
-
-
Kim, R.B.1
-
15
-
-
33644684769
-
Transporters and drug discovery: why, when, and how
-
Kim RB (2006). Transporters and drug discovery: why, when, and how. Mol Pharm 3: 26-32.
-
(2006)
Mol Pharm
, vol.3
, pp. 26-32
-
-
Kim, R.B.1
-
16
-
-
1342344851
-
Transporters and renal drug elimination
-
Lee W, Kim RB (2004). Transporters and renal drug elimination. Annu Rev Pharmacol Toxicol 44: 137-166.
-
(2004)
Annu Rev Pharmacol Toxicol
, vol.44
, pp. 137-166
-
-
Lee, W.1
Kim, R.B.2
-
17
-
-
0029876330
-
Adrenergic modulation of ultrarapid delayed rectifier K+ current in human atrial myocytes
-
Li GR, Feng J, Wang Z, Fermini B, Nattel S (1996). Adrenergic modulation of ultrarapid delayed rectifier K+ current in human atrial myocytes. Circ Res 78: 903-915.
-
(1996)
Circ Res
, vol.78
, pp. 903-915
-
-
Li, G.R.1
Feng, J.2
Wang, Z.3
Fermini, B.4
Nattel, S.5
-
18
-
-
68249160805
-
The organic cation transporter, OCTN1, expressed in the human heart, potentiates antagonism of the HERG potassium channel
-
McBride BF, Yang T, Liu K, Urban TJ, Giacomini KM, Kim RB et al. (2009a). The organic cation transporter, OCTN1, expressed in the human heart, potentiates antagonism of the HERG potassium channel. J Cardiovasc Pharmacol 54: 63-71.
-
(2009)
J Cardiovasc Pharmacol
, vol.54
, pp. 63-71
-
-
McBride, B.F.1
Yang, T.2
Liu, K.3
Urban, T.J.4
Giacomini, K.M.5
Kim, R.B.6
-
19
-
-
67349225471
-
Influence of the G2677T/C3435T haplotype of MDR1 on P-glycoprotein trafficking and ibutilide-induced block of HERG
-
McBride BF, Yang T, Roden DM (2009b). Influence of the G2677T/C3435T haplotype of MDR1 on P-glycoprotein trafficking and ibutilide-induced block of HERG. Pharmacogenomics J 9: 194-201.
-
(2009)
Pharmacogenomics J
, vol.9
, pp. 194-201
-
-
McBride, B.F.1
Yang, T.2
Roden, D.M.3
-
20
-
-
69549124105
-
Drug-sensitized zebrafish screen identifies multiple genes, including GINS3, as regulators of myocardial repolarization
-
Milan DJ, Kim AM, Winterfield JR, Jones IL, Pfeufer A, Sanna S et al. (2009). Drug-sensitized zebrafish screen identifies multiple genes, including GINS3, as regulators of myocardial repolarization. Circulation 120: 553-559.
-
(2009)
Circulation
, vol.120
, pp. 553-559
-
-
Milan, D.J.1
Kim, A.M.2
Winterfield, J.R.3
Jones, I.L.4
Pfeufer, A.5
Sanna, S.6
-
21
-
-
0034710933
-
A structural basis for drug-induced long QT syndrome
-
Mitcheson JS, Chen J, Lin M, Culberson C, Sanguinetti MC (2000). A structural basis for drug-induced long QT syndrome. Proc Natl Acad Sci U S A 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
-
22
-
-
0033165609
-
Cardiac ultrarapid delayed rectifiers: a novel potassium current family of functional similarity and molecular diversity
-
Nattel S, Yue L, Wang Z (1999). Cardiac ultrarapid delayed rectifiers: a novel potassium current family of functional similarity and molecular diversity. Cell Physiol Biochem 9: 217-226.
-
(1999)
Cell Physiol Biochem
, vol.9
, pp. 217-226
-
-
Nattel, S.1
Yue, L.2
Wang, Z.3
-
23
-
-
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 et al. (2004). Structural determinants of HERG channel block by clofilium and ibutilide. Mol Pharmacol 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
-
24
-
-
0030853695
-
Blockade of the human cardiac K+ channel Kv1.5 by the antibiotic erythromycin
-
Rampe D, Murawsky MK (1997). Blockade of the human cardiac K+ channel Kv1.5 by the antibiotic erythromycin. Naunyn Schmiedebergs Arch Pharmacol 355: 743-750.
-
(1997)
Naunyn Schmiedebergs Arch Pharmacol
, vol.355
, pp. 743-750
-
-
Rampe, D.1
Murawsky, M.K.2
-
25
-
-
0027250430
-
Verapamil blocks a rapidly activating delayed rectifier K+ channel cloned from human heart
-
Rampe D, Wible B, Fedida D, Dage RC, Brown AM (1993). Verapamil blocks a rapidly activating delayed rectifier K+ channel cloned from human heart. Mol Pharmacol 44: 642-648.
-
(1993)
Mol Pharmacol
, vol.44
, pp. 642-648
-
-
Rampe, D.1
Wible, B.2
Fedida, D.3
Dage, R.C.4
Brown, A.M.5
-
26
-
-
33645120204
-
KN-93 (2-[N-(2-hydroxyethyl)]-N-(4-methoxybenzenesulfonyl)]amino-N-(4-chlorocinn amyl)-N-methylbenzylamine), a calcium/calmodulin-dependent protein kinase II inhibitor, is a direct extracellular blocker of voltage-gated potassium channels
-
Rezazadeh S, Claydon TW, Fedida D (2006). KN-93 (2-[N-(2-hydroxyethyl)]-N-(4-methoxybenzenesulfonyl)]amino-N-(4-chlorocinn amyl)-N-methylbenzylamine), a calcium/calmodulin-dependent protein kinase II inhibitor, is a direct extracellular blocker of voltage-gated potassium channels. J Pharmacol Exp Ther 317: 292-299.
-
(2006)
J Pharmacol Exp Ther
, vol.317
, pp. 292-299
-
-
Rezazadeh, S.1
Claydon, T.W.2
Fedida, D.3
-
27
-
-
70349779184
-
Digoxin and ouabain induce P-glycoprotein by activating calmodulin kinase II and hypoxia-inducible factor-1alpha in human colon cancer cells
-
Riganti C, Campia I, Polimeni M, Pescarmona G, Ghigo D, Bosia A (2009). Digoxin and ouabain induce P-glycoprotein by activating calmodulin kinase II and hypoxia-inducible factor-1alpha in human colon cancer cells. Toxicol Appl Pharmacol 240: 385-392.
-
(2009)
Toxicol Appl Pharmacol
, vol.240
, pp. 385-392
-
-
Riganti, C.1
Campia, I.2
Polimeni, M.3
Pescarmona, G.4
Ghigo, D.5
Bosia, A.6
-
28
-
-
44649145463
-
Anti-arrhythmic drug therapy for atrial fibrillation: current anti-arrhythmic drugs, investigational agents, and innovative approaches
-
Savelieva I, Camm J (2008a). Anti-arrhythmic drug therapy for atrial fibrillation: current anti-arrhythmic drugs, investigational agents, and innovative approaches. Europace 10: 647-665.
-
(2008)
Europace
, vol.10
, pp. 647-665
-
-
Savelieva, I.1
Camm, J.2
-
29
-
-
40049093293
-
Update on atrial fibrillation: part I
-
Savelieva I, Camm J (2008b). Update on atrial fibrillation: part I. Clin Cardiol 31: 55-62.
-
(2008)
Clin Cardiol
, vol.31
, pp. 55-62
-
-
Savelieva, I.1
Camm, J.2
-
30
-
-
0242721858
-
Pharmacological activation of normal and arrhythmia-associated mutant KCNQ1 potassium channels
-
Seebohm G, Pusch M, Chen J, Sanguinetti MC (2003). Pharmacological activation of normal and arrhythmia-associated mutant KCNQ1 potassium channels. Circ Res 93: 941-947.
-
(2003)
Circ Res
, vol.93
, pp. 941-947
-
-
Seebohm, G.1
Pusch, M.2
Chen, J.3
Sanguinetti, M.C.4
-
31
-
-
0033567425
-
Interaction of the P-glycoprotein multidrug transporter (MDR1) with high affinity peptide chemosensitizers in isolated membranes, reconstituted systems, and intact cells
-
Sharom FJ, Yu X, Lu P, Liu R, Chu JW, Szabo K et al. (1999). Interaction of the P-glycoprotein multidrug transporter (MDR1) with high affinity peptide chemosensitizers in isolated membranes, reconstituted systems, and intact cells. Biochem Pharmacol 58: 571-586.
-
(1999)
Biochem Pharmacol
, vol.58
, pp. 571-586
-
-
Sharom, F.J.1
Yu, X.2
Lu, P.3
Liu, R.4
Chu, J.W.5
Szabo, K.6
-
32
-
-
16644374851
-
Cotransport of macrolide and fluoroquinolones, a beneficial interaction reversing P-glycoprotein efflux
-
Sikri V, Pal D, Jain R, Kalyani D, Mitra AK (2004). Cotransport of macrolide and fluoroquinolones, a beneficial interaction reversing P-glycoprotein efflux. Am J Ther 11: 433-442.
-
(2004)
Am J Ther
, vol.11
, pp. 433-442
-
-
Sikri, V.1
Pal, D.2
Jain, R.3
Kalyani, D.4
Mitra, A.K.5
-
33
-
-
0027321972
-
A rapidly activating and slowly inactivating potassium channel cloned from human heart. Functional analysis after stable mammalian cell culture expression
-
Snyders DJ, Tamkun MM, Bennett PB (1993). A rapidly activating and slowly inactivating potassium channel cloned from human heart. Functional analysis after stable mammalian cell culture expression. J Gen Physiol 101: 513-543.
-
(1993)
J Gen Physiol
, vol.101
, pp. 513-543
-
-
Snyders, D.J.1
Tamkun, M.M.2
Bennett, P.B.3
-
34
-
-
35848947983
-
Comparison of potent Kv1.5 potassium channel inhibitors reveals the molecular basis for blocking kinetics and binding mode
-
Strutz-Seebohm N, Gutcher I, Decher N, Steinmeyer K, Lang F, Seebohm G (2007). Comparison of potent Kv1.5 potassium channel inhibitors reveals the molecular basis for blocking kinetics and binding mode. Cell Physiol Biochem 20: 791-800.
-
(2007)
Cell Physiol Biochem
, vol.20
, pp. 791-800
-
-
Strutz-Seebohm, N.1
Gutcher, I.2
Decher, N.3
Steinmeyer, K.4
Lang, F.5
Seebohm, G.6
-
35
-
-
33644849222
-
Heart Disease and Stroke Statistics - 2006 Update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee
-
Thom T, Haase N, Rosamond W, Howard VJ, Rumsfeld J, Manolio T et al. (2006). Heart Disease and Stroke Statistics - 2006 Update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee. Circulation 113: e85-151.
-
(2006)
Circulation
, vol.113
-
-
Thom, T.1
Haase, N.2
Rosamond, W.3
Howard, V.J.4
Rumsfeld, J.5
Manolio, T.6
-
36
-
-
0027376226
-
Sustained depolarization-induced outward current in human atrial myocytes. Evidence for a novel delayed rectifier K+ current similar to Kv1.5 cloned channel currents
-
Wang Z, Fermini B, Nattel S (1993). Sustained depolarization-induced outward current in human atrial myocytes. Evidence for a novel delayed rectifier K+ current similar to Kv1.5 cloned channel currents. Circ Res 73: 1061-1076.
-
(1993)
Circ Res
, vol.73
, pp. 1061-1076
-
-
Wang, Z.1
Fermini, B.2
Nattel, S.3
-
37
-
-
0032935034
-
Novel membrane transporter OCTN1 mediates multispecific, bidirectional, and PH-dependent transport of organic cations
-
Yabuuchi H, Tamai I, Nezu J, Sakamoto K, Oku A, Shimane M et al. (1999). Novel membrane transporter OCTN1 mediates multispecific, bidirectional, and PH-dependent transport of organic cations. J Pharmacol Exp Ther 289: 768-773.
-
(1999)
J Pharmacol Exp Ther
, vol.289
, pp. 768-773
-
-
Yabuuchi, H.1
Tamai, I.2
Nezu, J.3
Sakamoto, K.4
Oku, A.5
Shimane, M.6
-
38
-
-
0029976743
-
Molecular analysis of a binding site for quinidine in a human cardiac delayed rectifier K+ channel. Role of S6 in antiarrhythmic drug binding
-
Yeola SW, Rich TC, Uebele VN, Tamkun MM, Snyders DJ (1996). Molecular analysis of a binding site for quinidine in a human cardiac delayed rectifier K+ channel. Role of S6 in antiarrhythmic drug binding. Circ Res 78: 1105-1114.
-
(1996)
Circ Res
, vol.78
, pp. 1105-1114
-
-
Yeola, S.W.1
Rich, T.C.2
Uebele, V.N.3
Tamkun, M.M.4
Snyders, D.J.5
|