340 related articles for article (PubMed ID: 10220559)
1. Differential sensitivity of voltage-gated potassium channels Kv1.5 and Kv1.2 to acidic pH and molecular identification of pH sensor.
Steidl JV; Yool AJ
Mol Pharmacol; 1999 May; 55(5):812-20. PubMed ID: 10220559
[TBL] [Abstract][Full Text] [Related]
2. Differential sensitivity of Kv1.4, Kv1.2, and their tandem channel to acidic pH: involvement of a histidine residue in high sensitivity to acidic pH.
Ishii K; Nunoki K; Yamagishi T; Okada H; Taira N
J Pharmacol Exp Ther; 2001 Feb; 296(2):405-11. PubMed ID: 11160624
[TBL] [Abstract][Full Text] [Related]
3. Tityustoxin-K(alpha) blockade of the voltage-gated potassium channel Kv1.3.
Rodrigues AR; Arantes EC; Monje F; Stühmer W; Varanda WA
Br J Pharmacol; 2003 Jul; 139(6):1180-6. PubMed ID: 12871837
[TBL] [Abstract][Full Text] [Related]
4. A set of homology models of pore loop domain of six eukaryotic voltage-gated potassium channels Kv1.1-Kv1.6.
Liu HL; Lin JC
Proteins; 2004 May; 55(3):558-67. PubMed ID: 15103620
[TBL] [Abstract][Full Text] [Related]
5. Synergistic inhibition of the maximum conductance of Kv1.5 channels by extracellular K+ reduction and acidification.
Fedida D; Zhang S; Kwan DC; Eduljee C; Kehl SJ
Cell Biochem Biophys; 2005; 43(2):231-42. PubMed ID: 16049348
[TBL] [Abstract][Full Text] [Related]
6. Molecular determinants of KCNQ1 channel block by a benzodiazepine.
Seebohm G; Chen J; Strutz N; Culberson C; Lerche C; Sanguinetti MC
Mol Pharmacol; 2003 Jul; 64(1):70-7. PubMed ID: 12815162
[TBL] [Abstract][Full Text] [Related]
7. The 'functional' dyad of scorpion toxin Pi1 is not itself a prerequisite for toxin binding to the voltage-gated Kv1.2 potassium channels.
Mouhat S; Mosbah A; Visan V; Wulff H; Delepierre M; Darbon H; Grissmer S; De Waard M; Sabatier JM
Biochem J; 2004 Jan; 377(Pt 1):25-36. PubMed ID: 12962541
[TBL] [Abstract][Full Text] [Related]
8. Cumulative inactivation and the pore domain in the Kv1 channels.
Shimizu Y; Kubo T; Furukawa Y
Pflugers Arch; 2002 Mar; 443(5-6):720-30. PubMed ID: 11889569
[TBL] [Abstract][Full Text] [Related]
9. Characterization of the outer pore region of the apamin-sensitive Ca2+-activated K+ channel rSK2.
Jäger H; Grissmer S
Toxicon; 2004 Jun; 43(8):951-60. PubMed ID: 15208028
[TBL] [Abstract][Full Text] [Related]
10. 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
Mol Pharmacol; 2005 Oct; 68(4):995-1005. PubMed ID: 16024663
[TBL] [Abstract][Full Text] [Related]
11. Constitutive inactivation of the hKv1.5 mutant channel, H463G, in K+-free solutions at physiological pH.
Zhang S; Eduljee C; Kwan DC; Kehl SJ; Fedida D
Cell Biochem Biophys; 2005; 43(2):221-30. PubMed ID: 16049347
[TBL] [Abstract][Full Text] [Related]
12. A single residue in the S6 transmembrane domain governs the differential flecainide sensitivity of voltage-gated potassium channels.
Herrera D; Mamarbachi A; Simoes M; Parent L; Sauvé R; Wang Z; Nattel S
Mol Pharmacol; 2005 Aug; 68(2):305-16. PubMed ID: 15883204
[TBL] [Abstract][Full Text] [Related]
13. Accessory Kvbeta1 subunits differentially modulate the functional expression of voltage-gated K+ channels in mouse ventricular myocytes.
Aimond F; Kwak SP; Rhodes KJ; Nerbonne JM
Circ Res; 2005 Mar; 96(4):451-8. PubMed ID: 15662035
[TBL] [Abstract][Full Text] [Related]
14. Effect of external pH on activation of the Kv1.5 potassium channel.
Trapani JG; Korn SJ
Biophys J; 2003 Jan; 84(1):195-204. PubMed ID: 12524275
[TBL] [Abstract][Full Text] [Related]
15. NH2-terminal inactivation peptide binding to C-type-inactivated Kv channels.
Kurata HT; Wang Z; Fedida D
J Gen Physiol; 2004 May; 123(5):505-20. PubMed ID: 15078918
[TBL] [Abstract][Full Text] [Related]
16. Mutations in the P-region of a mammalian potassium channel (RCK1): a comparison with the Shaker potassium channel.
Tytgat J
Biochem Biophys Res Commun; 1994 Aug; 203(1):513-8. PubMed ID: 8074696
[TBL] [Abstract][Full Text] [Related]
17. K+ activation of kir3.1/kir3.4 and kv1.4 K+ channels is regulated by extracellular charges.
Claydon TW; Makary SY; Dibb KM; Boyett MR
Biophys J; 2004 Oct; 87(4):2407-18. PubMed ID: 15454439
[TBL] [Abstract][Full Text] [Related]
18. Quercetin activates human Kv1.5 channels by a residue I502 in the S6 segment.
Yang L; Ma JH; Zhang PH; Zou AR; Tu DN
Clin Exp Pharmacol Physiol; 2009 Feb; 36(2):154-61. PubMed ID: 18986330
[TBL] [Abstract][Full Text] [Related]
19. Inhibition of the K+ channel kv1.4 by acidosis: protonation of an extracellular histidine slows the recovery from N-type inactivation.
Claydon TW; Boyett MR; Sivaprasadarao A; Ishii K; Owen JM; O'Beirne HA; Leach R; Komukai K; Orchard CH
J Physiol; 2000 Jul; 526 Pt 2(Pt 2):253-64. PubMed ID: 10896716
[TBL] [Abstract][Full Text] [Related]
20. The glycosylation state of Kv1.2 potassium channels affects trafficking, gating, and simulated action potentials.
Watanabe I; Zhu J; Sutachan JJ; Gottschalk A; Recio-Pinto E; Thornhill WB
Brain Res; 2007 May; 1144():1-18. PubMed ID: 17324383
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
