BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

96 related articles for article (PubMed ID: 12208786)

  • 1. Block of voltage-operated sodium channels by 2,6-dimethylphenol, a structural analogue of lidocaine's aromatic tail.
    Haeseler G; Bufler J; Merken S; Dengler R; Aronson J; Leuwer M
    Br J Pharmacol; 2002 Sep; 137(2):285-93. PubMed ID: 12208786
    [TBL] [Abstract][Full Text] [Related]  

  • 2. High-affinity blockade of voltage-operated skeletal muscle sodium channels by 2,6-dimethyl-4-chlorophenol.
    Haeseler G; Gudehus S; Bufler J; Dengler R; Leuwer M
    Eur J Anaesthesiol; 2006 Mar; 23(3):190-6. PubMed ID: 16430789
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An improved model for the binding of lidocaine and structurally related local anaesthetics to fast-inactivated voltage-operated sodium channels, showing evidence of cooperativity.
    Leuwer M; Haeseler G; Hecker H; Bufler J; Dengler R; Aronson JK
    Br J Pharmacol; 2004 Jan; 141(1):47-54. PubMed ID: 14662728
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Blockade of voltage-operated neuronal and skeletal muscle sodium channels by S(+)- and R(-)-ketamine.
    Haeseler G; Tetzlaff D; Bufler J; Dengler R; Münte S; Hecker H; Leuwer M
    Anesth Analg; 2003 Apr; 96(4):1019-1026. PubMed ID: 12651652
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Structural requirements for voltage-dependent block of muscle sodium channels by phenol derivatives.
    Haeseler G; Piepenbrink A; Bufler J; Dengler R; Aronson JK; Piepenbrock S; Leuwer M
    Br J Pharmacol; 2001 Apr; 132(8):1916-24. PubMed ID: 11309264
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Differential block of sensory neuronal voltage-gated sodium channels by lacosamide [(2R)-2-(acetylamino)-N-benzyl-3-methoxypropanamide], lidocaine, and carbamazepine.
    Sheets PL; Heers C; Stoehr T; Cummins TR
    J Pharmacol Exp Ther; 2008 Jul; 326(1):89-99. PubMed ID: 18378801
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Use-dependent block by lidocaine but not amitriptyline is more pronounced in tetrodotoxin (TTX)-Resistant Nav1.8 than in TTX-sensitive Na+ channels.
    Leffler A; Reiprich A; Mohapatra DP; Nau C
    J Pharmacol Exp Ther; 2007 Jan; 320(1):354-64. PubMed ID: 17005919
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Tramadol, fentanyl and sufentanil but not morphine block voltage-operated sodium channels.
    Haeseler G; Foadi N; Ahrens J; Dengler R; Hecker H; Leuwer M
    Pain; 2006 Dec; 126(1-3):234-44. PubMed ID: 16949748
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Voltage-dependent block of neuronal and skeletal muscle sodium channels by thymol and menthol.
    Haeseler G; Maue D; Grosskreutz J; Bufler J; Nentwig B; Piepenbrock S; Dengler R; Leuwer M
    Eur J Anaesthesiol; 2002 Aug; 19(8):571-9. PubMed ID: 12200946
    [TBL] [Abstract][Full Text] [Related]  

  • 10. High-affinity blockade of voltage-operated skeletal muscle and neuronal sodium channels by halogenated propofol analogues.
    Haeseler G; Karst M; Foadi N; Gudehus S; Roeder A; Hecker H; Dengler R; Leuwer M
    Br J Pharmacol; 2008 Sep; 155(2):265-75. PubMed ID: 18574460
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Dissecting lidocaine action: diethylamide and phenol mimic separate modes of lidocaine block of sodium channels from heart and skeletal muscle.
    Zamponi GW; French RJ
    Biophys J; 1993 Dec; 65(6):2335-47. PubMed ID: 8312473
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Coexpression of beta 1 with cardiac sodium channel alpha subunits in oocytes decreases lidocaine block.
    Makielski JC; Limberis JT; Chang SY; Fan Z; Kyle JW
    Mol Pharmacol; 1996 Jan; 49(1):30-9. PubMed ID: 8569709
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Lithium increases potency of lidocaine-induced block of voltage-gated Na+ currents in rat sensory neurons in vitro.
    Gold MS; Thut PD
    J Pharmacol Exp Ther; 2001 Nov; 299(2):705-11. PubMed ID: 11602684
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Frequency and voltage-dependent inhibition of type IIA Na+ channels, expressed in a mammalian cell line, by local anesthetic, antiarrhythmic, and anticonvulsant drugs.
    Ragsdale DS; Scheuer T; Catterall WA
    Mol Pharmacol; 1991 Nov; 40(5):756-65. PubMed ID: 1658608
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Distinct local anesthetic affinities in Na+ channel subtypes.
    Wang DW; Nie L; George AL; Bennett PB
    Biophys J; 1996 Apr; 70(4):1700-8. PubMed ID: 8785328
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Propofol blocks human skeletal muscle sodium channels in a voltage-dependent manner.
    Haeseler G; Störmer M; Bufler J; Dengler R; Hecker H; Piepenbrock S; Leuwer M
    Anesth Analg; 2001 May; 92(5):1192-8. PubMed ID: 11323345
    [TBL] [Abstract][Full Text] [Related]  

  • 17. High-affinity block of voltage-operated rat IIA neuronal sodium channels by 2,6 di-tert-butylphenol, a propofol analogue.
    Haeseler G; Leuwer M
    Eur J Anaesthesiol; 2003 Mar; 20(3):220-4. PubMed ID: 12650493
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Vinpocetine is a potent blocker of rat NaV1.8 tetrodotoxin-resistant sodium channels.
    Zhou X; Dong XW; Crona J; Maguire M; Priestley T
    J Pharmacol Exp Ther; 2003 Aug; 306(2):498-504. PubMed ID: 12730276
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Setting up for the block: the mechanism underlying lidocaine's use-dependent inhibition of sodium channels.
    Cummins TR
    J Physiol; 2007 Jul; 582(Pt 1):11. PubMed ID: 17525109
    [No Abstract]   [Full Text] [Related]  

  • 20. Class Ic antiarrhythmics block human skeletal muscle Na channel during myotonia-like stimulation.
    Aoike F; Takahashi MP; Sakoda S
    Eur J Pharmacol; 2006 Feb; 532(1-2):24-31. PubMed ID: 16473348
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.