202 related articles for article (PubMed ID: 20375276)
1. Ceramide modulates HERG potassium channel gating by translocation into lipid rafts.
Ganapathi SB; Fox TE; Kester M; Elmslie KS
Am J Physiol Cell Physiol; 2010 Jul; 299(1):C74-86. PubMed ID: 20375276
[TBL] [Abstract][Full Text] [Related]
2. Sphingolipid metabolite ceramide causes metabolic perturbation contributing to HERG K+ channel dysfunction.
Bai Y; Wang J; Shan H; Lu Y; Zhang Y; Luo X; Yang B; Wang Z
Cell Physiol Biochem; 2007; 20(5):429-40. PubMed ID: 17762170
[TBL] [Abstract][Full Text] [Related]
3. State-dependent block of HERG potassium channels by R-roscovitine: implications for cancer therapy.
Ganapathi SB; Kester M; Elmslie KS
Am J Physiol Cell Physiol; 2009 Apr; 296(4):C701-10. PubMed ID: 19244476
[TBL] [Abstract][Full Text] [Related]
4. hERG potassium channel gating is mediated by N- and C-terminal region interactions.
Gustina AS; Trudeau MC
J Gen Physiol; 2011 Mar; 137(3):315-25. PubMed ID: 21357734
[TBL] [Abstract][Full Text] [Related]
5. Extracellular K+ is a prerequisite for the function and plasma membrane stability of HERG channels.
Massaeli H; Guo J; Xu J; Zhang S
Circ Res; 2010 Apr; 106(6):1072-82. PubMed ID: 20133899
[TBL] [Abstract][Full Text] [Related]
6. Kv11.1 (ERG1) K+ channels localize in cholesterol and sphingolipid enriched membranes and are modulated by membrane cholesterol.
Balijepalli RC; Delisle BP; Balijepalli SY; Foell JD; Slind JK; Kamp TJ; January CT
Channels (Austin); 2007; 1(4):263-72. PubMed ID: 18708743
[TBL] [Abstract][Full Text] [Related]
7. A novel missense mutation causing a G487R substitution in the S2-S3 loop of human ether-à-go-go-related gene channel.
Kinoshita K; Yamaguchi Y; Nishide K; Kimoto K; Nonobe Y; Fujita A; Asano K; Tabata T; Mori H; Inoue H; Hata Y; Fukurotani K; Nishida N
J Cardiovasc Electrophysiol; 2012 Nov; 23(11):1246-53. PubMed ID: 22764740
[TBL] [Abstract][Full Text] [Related]
8. Proton block of the pore underlies the inhibition of hERG cardiac K+ channels during acidosis.
Van Slyke AC; Cheng YM; Mafi P; Allard CR; Hull CM; Shi YP; Claydon TW
Am J Physiol Cell Physiol; 2012 Jun; 302(12):C1797-806. PubMed ID: 22517356
[TBL] [Abstract][Full Text] [Related]
9. Modulation of hERG potassium currents in HEK-293 cells by protein kinase C. Evidence for direct phosphorylation of pore forming subunits.
Cockerill SL; Tobin AB; Torrecilla I; Willars GB; Standen NB; Mitcheson JS
J Physiol; 2007 Jun; 581(Pt 2):479-93. PubMed ID: 17363390
[TBL] [Abstract][Full Text] [Related]
10. Sequence of gating charge movement and pore gating in HERG activation and deactivation pathways.
Goodchild SJ; Macdonald LC; Fedida D
Biophys J; 2015 Mar; 108(6):1435-1447. PubMed ID: 25809256
[TBL] [Abstract][Full Text] [Related]
11. The cardiac hERG/IKr potassium channel as pharmacological target: structure, function, regulation, and clinical applications.
Thomas D; Karle CA; Kiehn J
Curr Pharm Des; 2006; 12(18):2271-83. PubMed ID: 16787254
[TBL] [Abstract][Full Text] [Related]
12. Downregulation of the HERG (KCNH2) K(+) channel by ceramide: evidence for ubiquitin-mediated lysosomal degradation.
Chapman H; Ramström C; Korhonen L; Laine M; Wann KT; Lindholm D; Pasternack M; Törnquist K
J Cell Sci; 2005 Nov; 118(Pt 22):5325-34. PubMed ID: 16263765
[TBL] [Abstract][Full Text] [Related]
13. The evolutionarily conserved residue A653 plays a key role in HERG channel closing.
Stepanovic SZ; Potet F; Petersen CI; Smith JA; Meiler J; Balser JR; Kupershmidt S
J Physiol; 2009 Jun; 587(Pt 11):2555-66. PubMed ID: 19406877
[TBL] [Abstract][Full Text] [Related]
14. Components of gating charge movement and S4 voltage-sensor exposure during activation of hERG channels.
Wang Z; Dou Y; Goodchild SJ; Es-Salah-Lamoureux Z; Fedida D
J Gen Physiol; 2013 Apr; 141(4):431-43. PubMed ID: 23478995
[TBL] [Abstract][Full Text] [Related]
15. The neutral, hydrophobic isoleucine at position I521 in the extracellular S4 domain of hERG contributes to channel gating equilibrium.
Dou Y; Goodchild SJ; Velde RV; Wu Y; Fedida D
Am J Physiol Cell Physiol; 2013 Aug; 305(4):C468-78. PubMed ID: 23761630
[TBL] [Abstract][Full Text] [Related]
16. Mesoridazine: an open-channel blocker of human ether-a-go-go-related gene K+ channel.
Su Z; Martin R; Cox BF; Gintant G
J Mol Cell Cardiol; 2004 Jan; 36(1):151-60. PubMed ID: 14734057
[TBL] [Abstract][Full Text] [Related]
17. Altered gating of HERG potassium channels by cobalt and lanthanum.
Sanchez-Chapula JA; Sanguinetti MC
Pflugers Arch; 2000 Jun; 440(2):264-74. PubMed ID: 10898527
[TBL] [Abstract][Full Text] [Related]
18. Inhibition of the HERG channel by droperidol depends on channel gating and involves the S6 residue F656.
Luo T; Luo A; Liu M; Liu X
Anesth Analg; 2008 Apr; 106(4):1161-70, table of contents. PubMed ID: 18349188
[TBL] [Abstract][Full Text] [Related]
19. PKA phosphorylation of HERG protein regulates the rate of channel synthesis.
Chen J; Sroubek J; Krishnan Y; Li Y; Bian J; McDonald TV
Am J Physiol Heart Circ Physiol; 2009 May; 296(5):H1244-54. PubMed ID: 19234087
[TBL] [Abstract][Full Text] [Related]
20. Inhibition of the rapid component of the delayed rectifier potassium current in ventricular myocytes by angiotensin II via the AT1 receptor.
Wang YH; Shi CX; Dong F; Sheng JW; Xu YF
Br J Pharmacol; 2008 May; 154(2):429-39. PubMed ID: 18414380
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
