BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

197 related articles for article (PubMed ID: 14608006)

  • 1. Inactivation and recovery in Kv1.4 K+ channels: lipophilic interactions at the intracellular mouth of the pore.
    Bett GC; Rasmusson RL
    J Physiol; 2004 Apr; 556(Pt 1):109-20. PubMed ID: 14608006
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Regulation of N- and C-type inactivation of Kv1.4 by pHo and K+: evidence for transmembrane communication.
    Li X; Bett GC; Jiang X; Bondarenko VE; Morales MJ; Rasmusson RL
    Am J Physiol Heart Circ Physiol; 2003 Jan; 284(1):H71-80. PubMed ID: 12388308
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Kv1.4 channel block by quinidine: evidence for a drug-induced allosteric effect.
    Wang S; Morales MJ; Qu YJ; Bett GC; Strauss HC; Rasmusson RL
    J Physiol; 2003 Jan; 546(Pt 2):387-401. PubMed ID: 12527726
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Differential effects of S6 mutations on binding of quinidine and 4-aminopyridine to rat isoform of Kv1.4: common site but different factors in determining blockers' binding affinity.
    Zhang H; Zhu B; Yao JA; Tseng GN
    J Pharmacol Exp Ther; 1998 Oct; 287(1):332-43. PubMed ID: 9765354
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Regulation of transient Na+ conductance by intra- and extracellular K+ in the human delayed rectifier K+ channel Kv1.5.
    Wang Z; Zhang X; Fedida D
    J Physiol; 2000 Mar; 523 Pt 3(Pt 3):575-91. PubMed ID: 10718739
    [TBL] [Abstract][Full Text] [Related]  

  • 6. C-type inactivation involves a significant decrease in the intracellular aqueous pore volume of Kv1.4 K+ channels expressed in Xenopus oocytes.
    Jiang X; Bett GC; Li X; Bondarenko VE; Rasmusson RL
    J Physiol; 2003 Jun; 549(Pt 3):683-95. PubMed ID: 12730347
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular basis involved in the blocking effect of antidepressant metergoline on C-type inactivation of Kv1.4 channel.
    Bai HW; Eom S; Yeom HD; Nguyen KVA; Lee J; Sohn SO; Lee JH
    Neuropharmacology; 2019 Mar; 146():65-73. PubMed ID: 30465811
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. The N-terminal domain of a K+ channel beta subunit increases the rate of C-type inactivation from the cytoplasmic side of the channel.
    Morales MJ; Wee JO; Wang S; Strauss HC; Rasmusson RL
    Proc Natl Acad Sci U S A; 1996 Dec; 93(26):15119-23. PubMed ID: 9005448
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular determinant of high-affinity dofetilide binding to HERG1 expressed in Xenopus oocytes: involvement of S6 sites.
    Lees-Miller JP; Duan Y; Teng GQ; Duff HJ
    Mol Pharmacol; 2000 Feb; 57(2):367-74. PubMed ID: 10648647
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Two pore residues mediate acidosis-induced enhancement of C-type inactivation of the Kv1.4 K(+) channel.
    Claydon TW; Boyett MR; Sivaprasadarao A; Orchard CH
    Am J Physiol Cell Physiol; 2002 Oct; 283(4):C1114-21. PubMed ID: 12225975
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Regulation of mammalian Shaker-related K+ channels: evidence for non-conducting closed and non-conducting inactivated states.
    Jäger H; Rauer H; Nguyen AN; Aiyar J; Chandy KG; Grissmer S
    J Physiol; 1998 Jan; 506 ( Pt 2)(Pt 2):291-301. PubMed ID: 9490854
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Modulation of slow inactivation in human cardiac Kv1.5 channels by extra- and intracellular permeant cations.
    Fedida D; Maruoka ND; Lin S
    J Physiol; 1999 Mar; 515 ( Pt 2)(Pt 2):315-29. PubMed ID: 10050000
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Voltage-gated K+ channels contain multiple intersubunit association sites.
    Tu L; Santarelli V; Sheng Z; Skach W; Pain D; Deutsch C
    J Biol Chem; 1996 Aug; 271(31):18904-11. PubMed ID: 8702552
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. N-Terminal deletions of rKv1.4 channels affect the voltage dependence of channel availability.
    Höllerer-Beitz G; Schönherr R; Koenen M; Heinemann SH
    Pflugers Arch; 1999 Jul; 438(2):141-6. PubMed ID: 10370099
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular basis for Kv1.5 channel block: conservation of drug binding sites among voltage-gated K+ channels.
    Decher N; Pirard B; Bundis F; Peukert S; Baringhaus KH; Busch AE; Steinmeyer K; Sanguinetti MC
    J Biol Chem; 2004 Jan; 279(1):394-400. PubMed ID: 14578345
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Inverted allosteric coupling between activation and inactivation gates in K
    Labro AJ; Cortes DM; Tilegenova C; Cuello LG
    Proc Natl Acad Sci U S A; 2018 May; 115(21):5426-5431. PubMed ID: 29735651
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.