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886 related items for PubMed ID: 8900283

  • 1. Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel.
    Sanguinetti MC, Curran ME, Zou A, Shen J, Spector PS, Atkinson DL, Keating MT.
    Nature; 1996 Nov 07; 384(6604):80-3. PubMed ID: 8900283
    [Abstract] [Full Text] [Related]

  • 2. K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current.
    Barhanin J, Lesage F, Guillemare E, Fink M, Lazdunski M, Romey G.
    Nature; 1996 Nov 07; 384(6604):78-80. PubMed ID: 8900282
    [Abstract] [Full Text] [Related]

  • 3. Stereoselective interactions of the enantiomers of chromanol 293B with human voltage-gated potassium channels.
    Yang IC, Scherz MW, Bahinski A, Bennett PB, Murray KT.
    J Pharmacol Exp Ther; 2000 Sep 07; 294(3):955-62. PubMed ID: 10945846
    [Abstract] [Full Text] [Related]

  • 4. Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias.
    Chouabe C, Neyroud N, Guicheney P, Lazdunski M, Romey G, Barhanin J.
    EMBO J; 1997 Sep 01; 16(17):5472-9. PubMed ID: 9312006
    [Abstract] [Full Text] [Related]

  • 5. Molecular basis for differential sensitivity of KCNQ and I(Ks) channels to the cognitive enhancer XE991.
    Wang HS, Brown BS, McKinnon D, Cohen IS.
    Mol Pharmacol; 2000 Jun 01; 57(6):1218-23. PubMed ID: 10825393
    [Abstract] [Full Text] [Related]

  • 6. A constitutively open potassium channel formed by KCNQ1 and KCNE3.
    Schroeder BC, Waldegger S, Fehr S, Bleich M, Warth R, Greger R, Jentsch TJ.
    Nature; 2000 Jan 13; 403(6766):196-9. PubMed ID: 10646604
    [Abstract] [Full Text] [Related]

  • 7. Clinical and electrophysiological characterization of a novel mutation (F193L) in the KCNQ1 gene associated with long QT syndrome.
    Yamaguchi M, Shimizu M, Ino H, Terai H, Hayashi K, Mabuchi H, Hoshi N, Higashida H.
    Clin Sci (Lond); 2003 Apr 13; 104(4):377-82. PubMed ID: 12653681
    [Abstract] [Full Text] [Related]

  • 8. Gating of I(sK) channels expressed in Xenopus oocytes.
    Tzounopoulos T, Maylie J, Adelman JP.
    Biophys J; 1998 May 13; 74(5):2299-305. PubMed ID: 9591657
    [Abstract] [Full Text] [Related]

  • 9. A truncated splice variant of KCNQ1 cloned from rat heart.
    Yamada Y, Chen X, Kobayashi T, Kamada Y, Nagashima M, Tsutsuura M, Seki S, Yamakage M, Namiki A, Tohse N.
    Biochem Biophys Res Commun; 2002 Jun 07; 294(2):199-204. PubMed ID: 12051693
    [Abstract] [Full Text] [Related]

  • 10. Molecular determinants of KCNQ1 channel block by a benzodiazepine.
    Seebohm G, Chen J, Strutz N, Culberson C, Lerche C, Sanguinetti MC.
    Mol Pharmacol; 2003 Jul 07; 64(1):70-7. PubMed ID: 12815162
    [Abstract] [Full Text] [Related]

  • 11. MinK-KvLQT1 fusion proteins, evidence for multiple stoichiometries of the assembled IsK channel.
    Wang W, Xia J, Kass RS.
    J Biol Chem; 1998 Dec 18; 273(51):34069-74. PubMed ID: 9852064
    [Abstract] [Full Text] [Related]

  • 12. Mutations in the hminK gene cause long QT syndrome and suppress IKs function.
    Splawski I, Tristani-Firouzi M, Lehmann MH, Sanguinetti MC, Keating MT.
    Nat Genet; 1997 Nov 18; 17(3):338-40. PubMed ID: 9354802
    [Abstract] [Full Text] [Related]

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  • 15. Isoproterenol exacerbates a long QT phenotype in Kcnq1-deficient neonatal mice: possible roles for human-like Kcnq1 isoform 1 and slow delayed rectifier K+ current.
    Knollmann BC, Casimiro MC, Katchman AN, Sirenko SG, Schober T, Rong Q, Pfeifer K, Ebert SN.
    J Pharmacol Exp Ther; 2004 Jul 18; 310(1):311-8. PubMed ID: 15004216
    [Abstract] [Full Text] [Related]

  • 16. Dependence of I(Ks) biophysical properties on the expression system.
    Seebohm G, Lerche C, Busch AE, Bachmann A.
    Pflugers Arch; 2001 Sep 18; 442(6):891-5. PubMed ID: 11680622
    [Abstract] [Full Text] [Related]

  • 17. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias.
    Wang Q, Curran ME, Splawski I, Burn TC, Millholland JM, VanRaay TJ, Shen J, Timothy KW, Vincent GM, de Jager T, Schwartz PJ, Toubin JA, Moss AJ, Atkinson DL, Landes GM, Connors TD, Keating MT.
    Nat Genet; 1996 Jan 18; 12(1):17-23. PubMed ID: 8528244
    [Abstract] [Full Text] [Related]

  • 18. Inhibition of cardiac delayed rectifier K+ currents by an antisense oligodeoxynucleotide against IsK (minK) and over-expression of IsK mutant D77N in neonatal mouse hearts.
    Ohyama H, Kajita H, Omori K, Takumi T, Hiramoto N, Iwasaka T, Matsuda H.
    Pflugers Arch; 2001 Jun 18; 442(3):329-35. PubMed ID: 11484762
    [Abstract] [Full Text] [Related]

  • 19. Action potential clamp and mefloquine sensitivity of recombinant 'I KS' channels incorporating the V307L KCNQ1 mutation.
    El Harchi A, McPate MJ, Zhang YH, Zhang H, Hancox JC.
    J Physiol Pharmacol; 2010 Apr 18; 61(2):123-31. PubMed ID: 20436212
    [Abstract] [Full Text] [Related]

  • 20. Long QT syndrome-associated mutations in the S4-S5 linker of KvLQT1 potassium channels modify gating and interaction with minK subunits.
    Franqueza L, Lin M, Shen J, Splawski I, Keating MT, Sanguinetti MC.
    J Biol Chem; 1999 Jul 23; 274(30):21063-70. PubMed ID: 10409658
    [Abstract] [Full Text] [Related]

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