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Factors affecting oogenesis in the South African clawed frog (Xenopus laevis). , Green SL ., Comp Med. August 1, 2002; 52 (4): 307-12.
Kinetics of tethering quaternary ammonium compounds to K(+) channels. , Blaustein RO., J Gen Physiol. August 1, 2002; 120 (2): 203-16.
Calcium/calmodulin-dependent protein kinase II phosphorylates and regulates the Drosophila eag potassium channel. , Wang Z, Wilson GF, Griffith LC., J Biol Chem. July 5, 2002; 277 (27): 24022-9.
Open channel block by KCB-328 [1-(2-amino-4-methanesulfonamidophenoxy)-2-[N-(3,4-dimethoxyphenethyl)-N-methylamino]ethane hydrochloride] of the heterologously expressed human ether-a- go-go-related gene K+ channels. , Park JB , Choe H, Lee YK , Ha KC, Rhee KS, Ko JK, Joo CU, Chae SW, Kwak YG., J Pharmacol Exp Ther. July 1, 2002; 302 (1): 314-9.
Molecular determinants of voltage-dependent human ether-a- go-go related gene ( HERG) K+ channel block. , Sánchez-Chapula JA, Navarro-Polanco RA, Culberson C, Chen J , Sanguinetti MC., J Biol Chem. June 28, 2002; 277 (26): 23587-95.
Interactions between S4-S5 linker and S6 transmembrane domain modulate gating of HERG K+ channels. , Tristani-Firouzi M, Chen J , Sanguinetti MC., J Biol Chem. May 24, 2002; 277 (21): 18994-9000.
The antidepressant drug fluoxetine is an inhibitor of human ether-a- go-go-related gene ( HERG) potassium channels. , Thomas D, Gut B, Wendt-Nordahl G, Kiehn J., J Pharmacol Exp Ther. February 1, 2002; 300 (2): 543-8.
Inhibition of cardiac potassium currents by pentobarbital. , Bachmann A, Mueller S, Kopp K, Brueggemann A, Suessbrich H, Gerlach U, Busch AE., Naunyn Schmiedebergs Arch Pharmacol. January 1, 2002; 365 (1): 29-37.
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., Mol Pharmacol. December 1, 2001; 60 (6): 1343-8.
Identification of a nonmammalian Golf subtype: functional role in olfactory signaling of airborne odorants in Xenopus laevis. , Mezler M, Fleischer J, Conzelmann S, Korchi A, Widmayer P, Breer H, Boekhoff I., J Comp Neurol. October 29, 2001; 439 (4): 400-10.
Developmental biology. Organs await blood vessels'' go signal. , Seydel C., Science. September 28, 2001; 293 (5539): 2365.
The S4-S5 linker couples voltage sensing and activation of pacemaker channels. , Chen J , Mitcheson JS, Tristani-Firouzi M, Lin M, Sanguinetti MC., Proc Natl Acad Sci U S A. September 25, 2001; 98 (20): 11277-82.
Functional characterization of the C-terminus of the human ether-à- go-go-related gene K(+) channel ( HERG). , Aydar E, Palmer C., J Physiol. July 1, 2001; 534 (Pt 1): 1-14.
Molecular cloning and expression of cERG, the ether à go-go-related gene from canine myocardium. , Zehelein J, Zhang W, Koenen M, Graf M, Heinemann SH, Katus HA., Pflugers Arch. May 1, 2001; 442 (2): 188-91.
High-affinity blockade of human ether-a- go-go-related gene human cardiac potassium channels by the novel antiarrhythmic drug BRL-32872. , Thomas D, Wendt-Nordahl G, Röckl K, Ficker E, Brown AM, Kiehn J., J Pharmacol Exp Ther. May 1, 2001; 297 (2): 753-61.
Inhibitory effects of berberine on IK1, IK, and HERG channels of cardiac myocytes. , Li BX, Yang BF, Zhou J, Xu CQ, Li YR., Acta Pharmacol Sin. February 1, 2001; 22 (2): 125-31.
Antiarrhythmic drug carvedilol inhibits HERG potassium channels. , Karle CA, Kreye VA, Thomas D, Röckl K, Kathöfer S, Zhang W, Kiehn J., Cardiovasc Res. February 1, 2001; 49 (2): 361-70.
Mg(2+) modulates voltage-dependent activation in ether-à- go-go potassium channels by binding between transmembrane segments S2 and S3. , Silverman WR, Tang CY , Mock AF, Huh KB, Papazian DM., J Gen Physiol. November 1, 2000; 116 (5): 663-78.
State-dependent barium block of wild-type and inactivation-deficient HERG channels in Xenopus oocytes. , Weerapura M, Nattel S, Courtemanche M, Doern D, Ethier N, Hebert T., J Physiol. July 15, 2000; 526 Pt 2 265-78.
Inhibition of human ether à go-go potassium channels by Ca(2+)/calmodulin. , Schönherr R, Löber K, Heinemann SH., EMBO J. July 3, 2000; 19 (13): 3263-71.
Differential effects of amino-terminal distal and proximal domains in the regulation of human erg K(+) channel gating. , Viloria CG, Barros F, Giráldez T, Gómez-Varela D, de la Peña P., Biophys J. July 1, 2000; 79 (1): 231-46.
Altered gating of HERG potassium channels by cobalt and lanthanum. , Sanchez-Chapula JA, Sanguinetti MC., Pflugers Arch. June 1, 2000; 440 (2): 264-74.
Hex is a transcriptional repressor that contributes to anterior identity and suppresses Spemann organiser function. , Brickman JM , Jones CM , Clements M, Smith JC , Beddington RS., Development. June 1, 2000; 127 (11): 2303-15.
Redox state dependency of HERGS631C channel pharmacology: relation to C-type inactivation. , Ulens C, Tytgat J., FEBS Lett. May 26, 2000; 474 (1): 111-5.
Preclinical pharmacology of desloratadine, a selective and nonsedating histamine H1 receptor antagonist. 2nd communication: lack of central nervous system and cardiovascular effects. , Kreutner W, Hey JA, Chiu P, Barnett A., Arzneimittelforschung. May 1, 2000; 50 (5): 441-8.
Blockade of the HERG human cardiac K(+) channel by the antidepressant drug amitriptyline. , Jo SH, Youm JB, Lee CO , Lee CO , Earm YE, Ho WK., Br J Pharmacol. April 1, 2000; 129 (7): 1474-80.
Extracellular Mg(2+) modulates slow gating transitions and the opening of Drosophila ether-à- Go-Go potassium channels. , Tang CY , Bezanilla F, Papazian DM., J Gen Physiol. March 1, 2000; 115 (3): 319-38.
Purification of an EH domain-binding protein from rat brain that modulates the gating of the rat ether-à- go-go channel. , Piros ET, Shen L, Huang XY ., J Biol Chem. November 19, 1999; 274 (47): 33677-83.
Voltage-shift of the current activation in HERG S4 mutation (R534C) in LQT2. , Nakajima T, Furukawa T, Hirano Y, Tanaka T, Sakurada H, Takahashi T, Nagai R, Itoh T, Katayama Y, Nakamura Y, Hiraoka M., Cardiovasc Res. November 1, 1999; 44 (2): 283-93.
Inactivation of the ERG current in NG108-15 cells. , Meves H., Biochem Biophys Res Commun. September 24, 1999; 263 (2): 510-5.
Fate maps old and new. , Clarke JD, Tickle C., Nat Cell Biol. August 1, 1999; 1 (4): E103-9.
Proton and zinc effects on HERG currents. , Anumonwo JM, Horta J, Delmar M, Taffet SM, Jalife J., Biophys J. July 1, 1999; 77 (1): 282-98.
Blockade of HERG channels expressed in Xenopus oocytes by external H+. , Jo SH, Youm JB, Kim I, Lee CO , Lee CO , Earm YE, Ho WK., Pflugers Arch. June 1, 1999; 438 (1): 23-9.
Opening mechanism of a cyclic nucleotide-gated channel based on analysis of single channels locked in each liganded state. , Ruiz M, Karpen JW., J Gen Physiol. June 1, 1999; 113 (6): 873-95.
Coupling of M2 muscarinic receptors to membrane ion channels via phosphoinositide 3-kinase gamma and atypical protein kinase C. , Wang YX, Dhulipala PD, Li L, Benovic JL, Kotlikoff MI., J Biol Chem. May 14, 1999; 274 (20): 13859-64.
Blockade of HERG channels expressed in Xenopus laevis oocytes by external divalent cations. , Ho WK, Kim I, Lee CO , Lee CO , Youm JB, Lee SH, Earm YE., Biophys J. April 1, 1999; 76 (4): 1959-71.
Mutations of the S4-S5 linker alter activation properties of HERG potassium channels expressed in Xenopus oocytes. , Sanguinetti MC, Xu QP., J Physiol. February 1, 1999; 514 ( Pt 3) 667-75.
Regulation of deactivation by an amino terminal domain in human ether-à- go-go-related gene potassium channels. , Wang J , Trudeau MC, Zappia AM, Robertson GA., J Gen Physiol. November 1, 1998; 112 (5): 637-47.
Shaker and ether-à- go-go K+ channel subunits fail to coassemble in Xenopus oocytes. , Tang CY , Schulteis CT, Jiménez RM, Papazian DM., Biophys J. September 1, 1998; 75 (3): 1263-70.
Modulation of human erg K+ channel gating by activation of a G protein-coupled receptor and protein kinase C. , Barros F, Gomez-Varela D, Viloria CG, Palomero T, Giráldez T, de la Peña P., J Physiol. September 1, 1998; 511 ( Pt 2) 333-46.
Different signaling pathway between sphingosine-1-phosphate and lysophosphatidic acid in Xenopus oocytes: functional coupling of the sphingosine-1-phosphate receptor to PLC-xbeta in Xenopus oocytes. , Noh SJ, Kim MJ , Shim S , Han JK ., J Cell Physiol. August 1, 1998; 176 (2): 412-23.
Agonist-independent inactivation and agonist-induced desensitization of the G protein-activated K+ channel ( GIRK) in Xenopus oocytes. , Vorobiov D, Levin G, Lotan I, Dascal N ., Pflugers Arch. June 1, 1998; 436 (1): 56-68.
A mutation in the pore region of HERG K+ channels expressed in Xenopus oocytes reduces rectification by shifting the voltage dependence of inactivation. , Zou A, Xu QP, Sanguinetti MC., J Physiol. May 15, 1998; 509 ( Pt 1) 129-37.
Assembly of lampbrush chromosomes from sperm chromatin. , Gall JG , Murphy C., Mol Biol Cell. April 1, 1998; 9 (4): 733-47.
Interaction of the K channel beta subunit, Hyperkinetic, with eag family members. , Wilson GF, Wang Z, Chouinard SW, Griffith LC, Ganetzky B., J Biol Chem. March 13, 1998; 273 (11): 6389-94.
herg encodes a K+ current highly conserved in tumors of different histogenesis: a selective advantage for cancer cells? , Bianchi L, Wible B, Arcangeli A, Taglialatela M, Morra F, Castaldo P, Crociani O, Rosati B, Faravelli L, Olivotto M, Wanke E., Cancer Res. February 15, 1998; 58 (4): 815-22.
Two isoforms of the mouse ether-a- go-go-related gene coassemble to form channels with properties similar to the rapidly activating component of the cardiac delayed rectifier K+ current. , London B, Trudeau MC, Newton KP, Beyer AK, Copeland NG, Gilbert DJ, Jenkins NA, Satler CA, Robertson GA., Circ Res. November 1, 1997; 81 (5): 870-8.
Specific block of cloned Herg channels by clofilium and its tertiary analog LY97241. , Suessbrich H, Schönherr R, Heinemann SH, Lang F , Busch AE., FEBS Lett. September 8, 1997; 414 (2): 435-8.
A quantitative analysis of the activation and inactivation kinetics of HERG expressed in Xenopus oocytes. , Wang S, Liu S , Morales MJ, Strauss HC, Rasmusson RL., J Physiol. July 1, 1997; 502 ( Pt 1) 45-60.
The inhibitory effect of the antipsychotic drug haloperidol on HERG potassium channels expressed in Xenopus oocytes. , Suessbrich H, Schönherr R, Heinemann SH, Attali B, Lang F , Busch AE., Br J Pharmacol. March 1, 1997; 120 (5): 968-74.