149 related articles for article (PubMed ID: 21306584)
1. Effect of verapamil on the action of methanethiosulfonate reagents on human voltage-gated K(v)1.3 channels: implications for the C-type inactivated state.
Schmid SI; Grissmer S
Br J Pharmacol; 2011 Jun; 163(3):662-74. PubMed ID: 21306584
[TBL] [Abstract][Full Text] [Related]
2. Verapamil- and state-dependent effect of 2-aminoethylmethanethiosulphonate (MTSEA) on hK(v)1.3 channels.
Nikouee A; Janbein M; Grissmer S
Br J Pharmacol; 2012 Nov; 167(6):1378-88. PubMed ID: 22748056
[TBL] [Abstract][Full Text] [Related]
3. Effect of K+ and Rb+ on the action of verapamil on a voltage-gated K+ channel, hKv1.3: implications for a second open state?
Kuras Z; Grissmer S
Br J Pharmacol; 2009 Jul; 157(5):757-68. PubMed ID: 19371328
[TBL] [Abstract][Full Text] [Related]
4. Evidence for a deep pore activation gate in small conductance Ca2+-activated K+ channels.
Bruening-Wright A; Lee WS; Adelman JP; Maylie J
J Gen Physiol; 2007 Dec; 130(6):601-10. PubMed ID: 17998394
[TBL] [Abstract][Full Text] [Related]
5. Cyclic nucleotide-gated channels. Pore topology studied through the accessibility of reporter cysteines.
Becchetti A; Gamel K; Torre V
J Gen Physiol; 1999 Sep; 114(3):377-92. PubMed ID: 10469728
[TBL] [Abstract][Full Text] [Related]
6. Localization of the activation gate for small conductance Ca2+-activated K+ channels.
Bruening-Wright A; Schumacher MA; Adelman JP; Maylie J
J Neurosci; 2002 Aug; 22(15):6499-506. PubMed ID: 12151529
[TBL] [Abstract][Full Text] [Related]
7. Gating dependence of inner pore access in inward rectifier K(+) channels.
Phillips LR; Enkvetchakul D; Nichols CG
Neuron; 2003 Mar; 37(6):953-62. PubMed ID: 12670424
[TBL] [Abstract][Full Text] [Related]
8. Kinetic Aspects of Verapamil Binding (On-Rate) on Wild-Type and Six hKv1.3 Mutant Channels.
Diesch AK; Grissmer S
Cell Physiol Biochem; 2017; 44(1):172-184. PubMed ID: 29131061
[TBL] [Abstract][Full Text] [Related]
9. Structural determinants of the closed KCa3.1 channel pore in relation to channel gating: results from a substituted cysteine accessibility analysis.
Klein H; Garneau L; Banderali U; Simoes M; Parent L; Sauvé R
J Gen Physiol; 2007 Apr; 129(4):299-315. PubMed ID: 17353352
[TBL] [Abstract][Full Text] [Related]
10. Structural and gating changes of the sodium channel induced by mutation of a residue in the upper third of IVS6, creating an external access path for local anesthetics.
Sunami A; Glaaser IW; Fozzard HA
Mol Pharmacol; 2001 Apr; 59(4):684-91. PubMed ID: 11259611
[TBL] [Abstract][Full Text] [Related]
11. Residue-specific effects on slow inactivation at V787 in D2-S6 of Na(v)1.4 sodium channels.
O'Reilly JP; Wang SY; Wang GK
Biophys J; 2001 Oct; 81(4):2100-11. PubMed ID: 11566781
[TBL] [Abstract][Full Text] [Related]
12. Block of the lymphocyte K(+) channel mKv1.3 by the phenylalkylamine verapamil: kinetic aspects of block and disruption of accumulation of block by a single point mutation.
Röbe RJ; Grissmer S
Br J Pharmacol; 2000 Dec; 131(7):1275-84. PubMed ID: 11090098
[TBL] [Abstract][Full Text] [Related]
13. Evidence for a centrally located gate in the pore of a serotonin-gated ion channel.
Panicker S; Cruz H; Arrabit C; Slesinger PA
J Neurosci; 2002 Mar; 22(5):1629-39. PubMed ID: 11880493
[TBL] [Abstract][Full Text] [Related]
14. Substituted cysteine scanning in D1-S6 of the sodium channel hNav1.4 alters kinetics and structural interactions of slow inactivation.
Beard JM; Shockett PE; O'Reilly JP
Biochim Biophys Acta Biomembr; 2020 Feb; 1862(2):183129. PubMed ID: 31738900
[TBL] [Abstract][Full Text] [Related]
15. Cysteine mapping in the ion selectivity and toxin binding region of the cardiac Na+ channel pore.
Chen S; Hartmann HA; Kirsch GE
J Membr Biol; 1997 Jan; 155(1):11-25. PubMed ID: 9002421
[TBL] [Abstract][Full Text] [Related]
16. Role of domain 4 in sodium channel slow inactivation.
Mitrovic N; George AL; Horn R
J Gen Physiol; 2000 Jun; 115(6):707-18. PubMed ID: 10828245
[TBL] [Abstract][Full Text] [Related]
17. Change of pore helix conformational state upon opening of cyclic nucleotide-gated channels.
Liu J; Siegelbaum SA
Neuron; 2000 Dec; 28(3):899-909. PubMed ID: 11163275
[TBL] [Abstract][Full Text] [Related]
18. Accessibility of mid-segment domain IV S6 residues of the voltage-gated Na+ channel to methanethiosulfonate reagents.
Sunami A; Tracey A; Glaaser IW; Lipkind GM; Hanck DA; Fozzard HA
J Physiol; 2004 Dec; 561(Pt 2):403-13. PubMed ID: 15579536
[TBL] [Abstract][Full Text] [Related]
19. Flexibility of the Kir6.2 inward rectifier K(+) channel pore.
Loussouarn G; Phillips LR; Masia R; Rose T; Nichols CG
Proc Natl Acad Sci U S A; 2001 Mar; 98(7):4227-32. PubMed ID: 11274446
[TBL] [Abstract][Full Text] [Related]
20. Cysteine modification of a putative pore residue in ClC-0: implication for the pore stoichiometry of ClC chloride channels.
Lin CW; Chen TY
J Gen Physiol; 2000 Oct; 116(4):535-46. PubMed ID: 11004203
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
