83 related articles for article (PubMed ID: 15737654)
1. Block of inactivation-deficient cardiac Na(+) channels by acetyl-KIFMK-amide.
Wang SY; Wang GK
Biochem Biophys Res Commun; 2005 Apr; 329(2):780-8. PubMed ID: 15737654
[TBL] [Abstract][Full Text] [Related]
2. Time-dependent block and resurgent tail currents induced by mouse beta4(154-167) peptide in cardiac Na+ channels.
Wang GK; Edrich T; Wang SY
J Gen Physiol; 2006 Mar; 127(3):277-89. PubMed ID: 16505148
[TBL] [Abstract][Full Text] [Related]
3. A human muscle Na+ channel mutation in the voltage sensor IV/S4 affects channel block by the pentapeptide KIFMK.
Peter W; Mitrovic N; Schiebe M; Lehmann-Horn F; Lerche H
J Physiol; 1999 Jul; 518(Pt 1):13-22. PubMed ID: 10373685
[TBL] [Abstract][Full Text] [Related]
4. Restoration of inactivation and block of open sodium channels by an inactivation gate peptide.
Eaholtz G; Scheuer T; Catterall WA
Neuron; 1994 May; 12(5):1041-8. PubMed ID: 8185942
[TBL] [Abstract][Full Text] [Related]
5. Block of inactivation-deficient Na+ channels by local anesthetics in stably transfected mammalian cells: evidence for drug binding along the activation pathway.
Wang SY; Mitchell J; Moczydlowski E; Wang GK
J Gen Physiol; 2004 Dec; 124(6):691-701. PubMed ID: 15545401
[TBL] [Abstract][Full Text] [Related]
6. A critical role for transmembrane segment IVS6 of the sodium channel alpha subunit in fast inactivation.
McPhee JC; Ragsdale DS; Scheuer T; Catterall WA
J Biol Chem; 1995 May; 270(20):12025-34. PubMed ID: 7744852
[TBL] [Abstract][Full Text] [Related]
7. Block of brain sodium channels by peptide mimetics of the isoleucine, phenylalanine, and methionine (IFM) motif from the inactivation gate.
Eaholtz G; Colvin A; Leonard D; Taylor C; Catterall WA
J Gen Physiol; 1999 Feb; 113(2):279-94. PubMed ID: 9925825
[TBL] [Abstract][Full Text] [Related]
8. State-dependent block of wild-type and inactivation-deficient Na+ channels by flecainide.
Wang GK; Russell C; Wang SY
J Gen Physiol; 2003 Sep; 122(3):365-74. PubMed ID: 12913091
[TBL] [Abstract][Full Text] [Related]
9. Preferential block of inactivation-deficient Na+ currents by capsaicin reveals a non-TRPV1 receptor within the Na+ channel.
Wang SY; Mitchell J; Wang GK
Pain; 2007 Jan; 127(1-2):73-83. PubMed ID: 16962240
[TBL] [Abstract][Full Text] [Related]
10. Serine-401 as a batrachotoxin- and local anesthetic-sensing residue in the human cardiac Na+ channel.
Wang SY; Tikhonov DB; Zhorov BS; Mitchell J; Wang GK
Pflugers Arch; 2007 May; 454(2):277-87. PubMed ID: 17205354
[TBL] [Abstract][Full Text] [Related]
11. State- and use-dependent block of muscle Nav1.4 and neuronal Nav1.7 voltage-gated Na+ channel isoforms by ranolazine.
Wang GK; Calderon J; Wang SY
Mol Pharmacol; 2008 Mar; 73(3):940-8. PubMed ID: 18079277
[TBL] [Abstract][Full Text] [Related]
12. State-dependent block of voltage-gated Na+ channels by amitriptyline via the local anesthetic receptor and its implication for neuropathic pain.
Wang GK; Russell C; Wang SY
Pain; 2004 Jul; 110(1-2):166-74. PubMed ID: 15275764
[TBL] [Abstract][Full Text] [Related]
13. Veratridine block of rat skeletal muscle Nav1.4 sodium channels in the inner vestibule.
Wang GK; Wang SY
J Physiol; 2003 May; 548(Pt 3):667-75. PubMed ID: 12626674
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 1H-NMR and circular dichroism spectroscopic studies on changes in secondary structures of the sodium channel inactivation gate peptides as caused by the pentapeptide KIFMK.
Kuroda Y; Maeda Y; Miyamoto K; Tanaka K; Kanaori K; Otaka A; Fujii N; Nakagawa T
Biophys J; 1999 Sep; 77(3):1363-73. PubMed ID: 10465748
[TBL] [Abstract][Full Text] [Related]
16. Suppression of insulin signalling by a synthetic peptide KIFMK suggests the cytoplasmic linker between DIII-S6 and DIV-S1 as a local anaesthetic binding site on the sodium channel.
Hirose M; Kuroda Y; Sawa S; Nakagawa T; Hirata M; Sakaguchi M; Tanaka Y
Br J Pharmacol; 2004 May; 142(1):222-8. PubMed ID: 15037518
[TBL] [Abstract][Full Text] [Related]
17. Minimal sodium channel pore consisting of S5-P-S6 segments preserves intracellular pharmacology.
Pincin C; Ferrera L; Moran O
Biochem Biophys Res Commun; 2005 Aug; 334(1):140-4. PubMed ID: 15992775
[TBL] [Abstract][Full Text] [Related]
18. Charge immobilization of the voltage sensor in domain IV is independent of sodium current inactivation.
Sheets MF; Hanck DA
J Physiol; 2005 Feb; 563(Pt 1):83-93. PubMed ID: 15576449
[TBL] [Abstract][Full Text] [Related]
19. A critical role for the S4-S5 intracellular loop in domain IV of the sodium channel alpha-subunit in fast inactivation.
McPhee JC; Ragsdale DS; Scheuer T; Catterall WA
J Biol Chem; 1998 Jan; 273(2):1121-9. PubMed ID: 9422778
[TBL] [Abstract][Full Text] [Related]
20. Identification of the Ca2+ blocking site of acid-sensing ion channel (ASIC) 1: implications for channel gating.
Paukert M; Babini E; Pusch M; Gründer S
J Gen Physiol; 2004 Oct; 124(4):383-94. PubMed ID: 15452199
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
