BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

110 related articles for article (PubMed ID: 20693878)

  • 1. Block of neuronal Na+ channels by antidepressant duloxetine in a state-dependent manner.
    Wang SY; Calderon J; Kuo Wang G
    Anesthesiology; 2010 Sep; 113(3):655-65. PubMed ID: 20693878
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Local anesthetic-like inhibition of voltage-gated Na(+) channels by the partial μ-opioid receptor agonist buprenorphine.
    Leffler A; Frank G; Kistner K; Niedermirtl F; Koppert W; Reeh PW; Nau C
    Anesthesiology; 2012 Jun; 116(6):1335-46. PubMed ID: 22504149
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Block of persistent late Na+ currents by antidepressant sertraline and paroxetine.
    Wang GK; Mitchell J; Wang SY
    J Membr Biol; 2008 Mar; 222(2):79-90. PubMed ID: 18418539
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Mexiletine block of wild-type and inactivation-deficient human skeletal muscle hNav1.4 Na+ channels.
    Wang GK; Russell C; Wang SY
    J Physiol; 2004 Feb; 554(Pt 3):621-33. PubMed ID: 14608007
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The Local and Systemic Actions of Duloxetine in Allodynia and Hyperalgesia Using a Rat Skin Incision Pain Model.
    Wang CF; Russell G; Strichartz GR; Wang GK
    Anesth Analg; 2015 Aug; 121(2):532-44. PubMed ID: 26049779
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Differential inhibition of cardiac and neuronal Na(+) channels by the selective serotonin-norepinephrine reuptake inhibitors duloxetine and venlafaxine.
    Stoetzer C; Papenberg B; Doll T; Völker M; Heineke J; Stoetzer M; Wegner F; Leffler A
    Eur J Pharmacol; 2016 Jul; 783():1-10. PubMed ID: 27130441
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Heterologous expression and functional analysis of rat Nav1.8 (SNS) voltage-gated sodium channels in the dorsal root ganglion neuroblastoma cell line ND7-23.
    John VH; Main MJ; Powell AJ; Gladwell ZM; Hick C; Sidhu HS; Clare JJ; Tate S; Trezise DJ
    Neuropharmacology; 2004 Mar; 46(3):425-38. PubMed ID: 14975698
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Functional and pharmacological properties of human and rat NaV1.8 channels.
    Browne LE; Clare JJ; Wray D
    Neuropharmacology; 2009 Apr; 56(5):905-14. PubMed ID: 19371587
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Preferential block of late sodium current in the LQT3 DeltaKPQ mutant by the class I(C) antiarrhythmic flecainide.
    Nagatomo T; January CT; Makielski JC
    Mol Pharmacol; 2000 Jan; 57(1):101-7. PubMed ID: 10617684
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. State-dependent mibefradil block of Na+ channels.
    McNulty MM; Hanck DA
    Mol Pharmacol; 2004 Dec; 66(6):1652-61. PubMed ID: 15562257
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Lysine point mutations in Na+ channel D4-S6 reduce inactivated channel block by local anesthetics.
    Wright SN; Wang SY; Wang GK
    Mol Pharmacol; 1998 Oct; 54(4):733-9. PubMed ID: 9765517
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Block of human heart hH1 sodium channels by amitriptyline.
    Nau C; Seaver M; Wang SY; Wang GK
    J Pharmacol Exp Ther; 2000 Mar; 292(3):1015-23. PubMed ID: 10688618
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Point mutations at L1280 in Nav1.4 channel D3-S6 modulate binding affinity and stereoselectivity of bupivacaine enantiomers.
    Nau C; Wang SY; Wang GK
    Mol Pharmacol; 2003 Jun; 63(6):1398-406. PubMed ID: 12761351
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The role of inactivation in open-channel block of the sodium channel: studies with inactivation-deficient mutant channels.
    Grant AO; John JE; Nesterenko VV; Starmer CF; Moorman JR
    Mol Pharmacol; 1996 Dec; 50(6):1643-50. PubMed ID: 8967988
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.