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Results: 1-22 |
Results: 22
Molecular and cellular mechanisms of cardiac arrhythmias
Authors: Keating, MT Sanguinetti, MC
Citation: Mt. Keating et Mc. Sanguinetti, Molecular and cellular mechanisms of cardiac arrhythmias, CELL, 104(4), 2001, pp. 569-580
The S4-S5 linker couples voltage sensing and activation of pacemaker channels
Authors: Chen, J Mitcheson, JS Tristani-Firouzi, M Lin, M Sanguinetti, MC
Citation: J. Chen et al., The S4-S5 linker couples voltage sensing and activation of pacemaker channels, P NAS US, 98(20), 2001, pp. 11277-11282
Open channel block of HERG K+ channels by vesnarinone
Authors: Kamiya, K Mitcheson, JS Yasui, K Kodama, I Sanguinetti, MC
Citation: K. Kamiya et al., Open channel block of HERG K+ channels by vesnarinone, MOLEC PHARM, 60(2), 2001, pp. 244-253
Long-QT syndrome-associated missense mutations in the pore helix of the HERG potassium channel
Authors: Huang, FD Chen, J Lin, M Keating, MT Sanguinetti, MC
Citation: Fd. Huang et al., Long-QT syndrome-associated missense mutations in the pore helix of the HERG potassium channel, CIRCULATION, 104(9), 2001, pp. 1071-1075
Short- and long-term effects of amiodarone on the two components of cardiac delayed rectifier K+ current
Authors: Kamiya, K Nishiyama, A Yasui, K Hojo, M Sanguinetti, MC Kodama, I
Citation: K. Kamiya et al., Short- and long-term effects of amiodarone on the two components of cardiac delayed rectifier K+ current, CIRCULATION, 103(9), 2001, pp. 1317-1324
Molecular biology of K+ channels and their role in cardiac arrhythmias
Authors: Tristani-Firouzi, M Chen, J Mitcheson, JS Sanguinetti, MC
Citation: M. Tristani-firouzi et al., Molecular biology of K+ channels and their role in cardiac arrhythmias, AM J MED, 110(1), 2001, pp. 50-59
The molecular basis of the long QT syndrome
Authors: Tristani-Firouzi, M Sanguinetti, MC
Citation: M. Tristani-firouzi et Mc. Sanguinetti, The molecular basis of the long QT syndrome, POTASSIUM CHANNELS IN CARDIOVASCULAR BIOLOGY, 2001, pp. 753-772
Maximal function of minimal K+ channel subunits
Authors: Sanguinetti, MC
Citation: Mc. Sanguinetti, Maximal function of minimal K+ channel subunits, TRENDS PHAR, 21(6), 2000, pp. 199-201
Long QT syndrome: Ionic basis and arrhythmia mechanism in long QT syndrometype 1
Authors: Sanguinetti, MC
Citation: Mc. Sanguinetti, Long QT syndrome: Ionic basis and arrhythmia mechanism in long QT syndrometype 1, J CARD ELEC, 11(6), 2000, pp. 710-712
Altered gating of HERG potassium channels by cobalt and lanthanum
Authors: Sanchez-Chapula, JA Sanguinetti, MC
Citation: Ja. Sanchez-chapula et Mc. Sanguinetti, Altered gating of HERG potassium channels by cobalt and lanthanum, PFLUG ARCH, 440(2), 2000, pp. 264-274
Functional consequences of chloride channel gene (CLCN1) mutations causingmyotonia congenita
Authors: Zhang, J Bendahhou, S Sanguinetti, MC Ptacek, LJ
Citation: J. Zhang et al., Functional consequences of chloride channel gene (CLCN1) mutations causingmyotonia congenita, NEUROLOGY, 54(4), 2000, pp. 937-942
A structural basis for drug-induced long QT syndrome
Authors: Mitcheson, JS Chen, J Lin, M Culberson, C Sanguinetti, MC
Citation: Js. Mitcheson et al., A structural basis for drug-induced long QT syndrome, P NAS US, 97(22), 2000, pp. 12329-12333
Trapping of a methanesulfonanilide by closure of the HERG potassium channel activation gate
Authors: Mitcheson, JS Chen, J Sanguinetti, MC
Citation: Js. Mitcheson et al., Trapping of a methanesulfonanilide by closure of the HERG potassium channel activation gate, J GEN PHYSL, 115(3), 2000, pp. 229-239
Functional roles of charged residues in the putative voltage sensor of theHCN2 pacemaker channel
Authors: Chen, J Mitcheson, JS Lin, M Sanguinetti, MC
Citation: J. Chen et al., Functional roles of charged residues in the putative voltage sensor of theHCN2 pacemaker channel, J BIOL CHEM, 275(46), 2000, pp. 36465-36471
Mechanism of inverted activation of ClC-1 channels caused by a novel myotonia congenita mutation
Authors: Zhang, J Sanguinetti, MC Kwiecinski, H Ptacek, LJ
Citation: J. Zhang et al., Mechanism of inverted activation of ClC-1 channels caused by a novel myotonia congenita mutation, J BIOL CHEM, 275(4), 2000, pp. 2999-3005
Functional effects of mutations in KvLQT1 that cause long QT syndrome
Authors: Wang, Z Tristani-Firouzi, M Xu, Q Lin, M Keating, MT Sanguinetti, MC
Citation: Z. Wang et al., Functional effects of mutations in KvLQT1 that cause long QT syndrome, J CARD ELEC, 10(6), 1999, pp. 817-826
Biophysical properties and molecular basis of cardiac rapid and slow delayed rectifier potassium channels
Authors: Mitcheson, JS Sanguinetti, MC
Citation: Js. Mitcheson et Mc. Sanguinetti, Biophysical properties and molecular basis of cardiac rapid and slow delayed rectifier potassium channels, CELL PHYS B, 9(4-5), 1999, pp. 201-216
Peptide toxins isolated from spider venom that modulate gating of voltage-dependent K+ channels
Authors: Garrett, SA Mueller, AL Sanguinetti, MC
Citation: Sa. Garrett et al., Peptide toxins isolated from spider venom that modulate gating of voltage-dependent K+ channels, PERSP DR D, 16, 1999, pp. 71-81
Mutations of the S4-S5 linker alter activation properties of HERG potassium channels expressed in Xenopus oocytes
Authors: Sanguinetti, MC Xu, QP
Citation: Mc. Sanguinetti et Qp. Xu, Mutations of the S4-S5 linker alter activation properties of HERG potassium channels expressed in Xenopus oocytes, J PHYSL LON, 514(3), 1999, pp. 667-675
Long QT syndrome-associated mutations in the S4-S5 linker of KvLQT1 potassium channels modify gating and interaction with minK subunits. (vol 274, pg21063, 1999)
Authors: Franqueza, L Lin, M Shen, JX Keating, MT Sanguinetti, MC
Citation: L. Franqueza et al., Long QT syndrome-associated mutations in the S4-S5 linker of KvLQT1 potassium channels modify gating and interaction with minK subunits. (vol 274, pg21063, 1999), J BIOL CHEM, 274(35), 1999, pp. 25188-25188
Long QT syndrome-associated mutations in the S4-S5 linker of KvLQT1 potassium channels modify gating and interaction with minK subunits
Authors: Franqueza, L Lin, M Splawski, I Keating, MT Sanguinetti, MC
Citation: L. Franqueza et al., Long QT syndrome-associated mutations in the S4-S5 linker of KvLQT1 potassium channels modify gating and interaction with minK subunits, J BIOL CHEM, 274(30), 1999, pp. 21063-21070
Long QT syndrome-associated mutations in the Per-Arnt-Sim (PAS) domain of HERG potassium channels accelerate channel deactivation
Authors: Chen, J Zou, AR Splawski, I Keating, MT Sanguinetti, MC
Citation: J. Chen et al., Long QT syndrome-associated mutations in the Per-Arnt-Sim (PAS) domain of HERG potassium channels accelerate channel deactivation, J BIOL CHEM, 274(15), 1999, pp. 10113-10118
Risultati: 1-22 |