BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

108 related articles for article (PubMed ID: 8174607)

  • 1. Pharmacological modulation of human cardiac Na+ channels.
    Krafte DS; Davison K; Dugrenier N; Estep K; Josef K; Barchi RL; Kallen RG; Silver PJ; Ezrin AM
    Eur J Pharmacol; 1994 Feb; 266(3):245-54. PubMed ID: 8174607
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Expression of cardiac Na channels with appropriate physiological and pharmacological properties in Xenopus oocytes.
    Krafte DS; Volberg WA; Dillon K; Ezrin AM
    Proc Natl Acad Sci U S A; 1991 May; 88(10):4071-4. PubMed ID: 1709733
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Lidocaine block of human heart sodium channels expressed in Xenopus oocytes.
    Chahine M; Chen LQ; Barchi RL; Kallen RG; Horn R
    J Mol Cell Cardiol; 1992 Nov; 24(11):1231-6. PubMed ID: 1336062
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Human cardiac sodium channels expressed in Xenopus oocytes.
    Tomaselli GF; Feldman AM; Yellen G; Marban E
    Am J Physiol; 1990 Mar; 258(3 Pt 2):H903-6. PubMed ID: 1690519
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Electrophysiological characterization of a TTX-sensitive sodium current in native Xenopus oocytes.
    Bourinet E; Nargeot J; Charnet P
    Proc Biol Sci; 1992 Nov; 250(1328):127-32. PubMed ID: 1361986
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Properties of endogenous voltage-dependent sodium currents in Xenopus laevis oocytes.
    Krafte DS; Volberg WA
    J Neurosci Methods; 1992 Jul; 43(2-3):189-93. PubMed ID: 1383646
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Characterization of the effects of the new inotropic agent BDF 9148 in isolated papillary muscles and myocytes of the guinea-pig heart.
    Ravens U; Wettwer E; Pfeifer T; Himmel H; Armah B
    Br J Pharmacol; 1991 Dec; 104(4):1019-23. PubMed ID: 1667282
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Intrinsic lidocaine affinity for Na channels expressed in Xenopus oocytes depends on alpha (hH1 vs. rSkM1) and beta 1 subunits.
    Makielski JC; Limberis J; Fan Z; Kyle JW
    Cardiovasc Res; 1999 May; 42(2):503-9. PubMed ID: 10533585
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Common molecular determinants of flecainide and lidocaine block of heart Na+ channels: evidence from experiments with neutral and quaternary flecainide analogues.
    Liu H; Atkins J; Kass RS
    J Gen Physiol; 2003 Mar; 121(3):199-214. PubMed ID: 12601084
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The cloned cardiac Na channel alpha-subunit expressed in Xenopus oocytes show gating and blocking properties of native channels.
    Satin J; Kyle JW; Chen M; Rogart RB; Fozzard HA
    J Membr Biol; 1992 Oct; 130(1):11-22. PubMed ID: 1335083
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Responsiveness of cardiac Na+ channels to antiarrhythmic drugs: the role of inactivation.
    Benz I; Kohlhardt M
    J Membr Biol; 1991 Jun; 122(3):267-78. PubMed ID: 1656048
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Local anesthetics as effectors of allosteric gating. Lidocaine effects on inactivation-deficient rat skeletal muscle Na channels.
    Balser JR; Nuss HB; Orias DW; Johns DC; Marban E; Tomaselli GF; Lawrence JH
    J Clin Invest; 1996 Dec; 98(12):2874-86. PubMed ID: 8981936
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Block of tetrodotoxin-sensitive, Na(V)1.7 and tetrodotoxin-resistant, Na(V)1.8, Na+ channels by ranolazine.
    Rajamani S; Shryock JC; Belardinelli L
    Channels (Austin); 2008; 2(6):449-60. PubMed ID: 19077543
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Class I antiarrhythmic drug receptor: biochemical evidence for state-dependent interaction with quinidine and lidocaine.
    Hill RJ; Duff HJ; Sheldon RS
    Mol Pharmacol; 1989 Jul; 36(1):150-9. PubMed ID: 2546048
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Common molecular determinants of local anesthetic, antiarrhythmic, and anticonvulsant block of voltage-gated Na+ channels.
    Ragsdale DS; McPhee JC; Scheuer T; Catterall WA
    Proc Natl Acad Sci U S A; 1996 Aug; 93(17):9270-5. PubMed ID: 8799190
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cardiac sodium channels (hH1) are intrinsically more sensitive to block by lidocaine than are skeletal muscle (mu 1) channels.
    Nuss HB; Tomaselli GF; Marbán E
    J Gen Physiol; 1995 Dec; 106(6):1193-209. PubMed ID: 8786356
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Effects of bisaramil, a novel class I antiarrhythmic agent, on heart, skeletal muscle and brain Na+ channels.
    Pugsley MK; Goldin AL
    Eur J Pharmacol; 1998 Jan; 342(1):93-104. PubMed ID: 9544797
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The effects of class Ic antiarrhythmics on tetrodotoxin-resistant Na+ currents in rat sensory neurons.
    Osawa Y; Oda A; Iida H; Tanahashi S; Dohi S
    Anesth Analg; 2004 Aug; 99(2):464-71, table of contents. PubMed ID: 15271726
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Enhancing effects of salicylate on quinidine-induced block of human wild type and LQT3 related mutant cardiac Na+ channels.
    Urashima T; Kurata Y; Miake J; Kato M; Ogura K; Yano A; Adachi M; Tanaka Y; Yamada K; Hamada T; Mizuta E; Kuwabara M; Kato M; Yamamoto Y; Ogino K; Yoshida A; Shirayoshi Y; Hisatome I
    Biomed Res; 2011 Oct; 32(5):303-12. PubMed ID: 22033299
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.