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Journal Abstract Search

133 related items for PubMed ID: 11896454

  • 1.
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  • 2. Initial isolation and analysis of the human Kv1.7 (KCNA7) gene, a member of the voltage-gated potassium channel gene family.
    Kashuba VI, Kvasha SM, Protopopov AI, Gizatullin RZ, Rynditch AV, Wahlestedt C, Wasserman WW, Zabarovsky ER.
    Gene; 2001 May 02; 268(1-2):115-22. PubMed ID: 11368907
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  • 4. Cloning and developmental expression of Shaker potassium channels in the cochlea of the chicken.
    Duzhyy DE, Sakai Y, Sokolowski BH.
    Brain Res Mol Brain Res; 2004 Feb 05; 121(1-2):70-85. PubMed ID: 14969738
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  • 6. Accessory Kvbeta1 subunits differentially modulate the functional expression of voltage-gated K+ channels in mouse ventricular myocytes.
    Aimond F, Kwak SP, Rhodes KJ, Nerbonne JM.
    Circ Res; 2005 Mar 04; 96(4):451-8. PubMed ID: 15662035
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  • 7. Genomic localization of the human gene for KCNA10, a cGMP-activated K channel.
    Orias M, Bray-Ward P, Curran ME, Keating MT, Desir GV.
    Genomics; 1997 May 15; 42(1):33-7. PubMed ID: 9177773
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  • 8. The KVLQT1 gene is not a common target for mutations in patients with various heart pathologies.
    Moric E, Herbert E, Mazurek U, Samelska J, Cholewa K, Trusz-Gluza M, Wilczok T.
    J Appl Genet; 2002 May 15; 43(2):245-54. PubMed ID: 12080180
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  • 9. Characterization of the outer pore region of the apamin-sensitive Ca2+-activated K+ channel rSK2.
    Jäger H, Grissmer S.
    Toxicon; 2004 Jun 15; 43(8):951-60. PubMed ID: 15208028
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  • 10. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].
    Zhang DL, Ji L, Li YD.
    Yi Chuan Xue Bao; 2004 May 15; 31(5):431-43. PubMed ID: 15478601
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  • 13. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 15; 56(3):105-52. PubMed ID: 19728970
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  • 14. 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
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  • 15. Localization of two potassium channel beta subunit genes, KCNA1B and KCNA2B.
    Schultz D, Litt M, Smith L, Thayer M, McCormack K.
    Genomics; 1996 Feb 01; 31(3):389-91. PubMed ID: 8838324
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  • 16. Voltage-gated potassium channel genes are clustered in paralogous regions of the mouse genome.
    Lock LF, Gilbert DJ, Street VA, Migeon MB, Jenkins NA, Copeland NG, Tempel BL.
    Genomics; 1994 Apr 01; 20(3):354-62. PubMed ID: 8034307
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  • 17. Expression of Shaker-type voltage-gated potassium channel genes in the guinea-pig.
    Manabe I, Tsuboi M, Ahmmed GU, Sasaki N, Ohtahara A, Yamamoto Y, Hiroe K, Yoshida A, Hisatome I, Shigemasa C.
    Res Commun Mol Pathol Pharmacol; 1998 Jan 01; 99(1):33-40. PubMed ID: 9523353
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  • 18. 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 01; 104(4):377-82. PubMed ID: 12653681
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  • 19. The Kv2.2 alpha subunit contributes to delayed rectifier K(+) currents in myocytes from rabbit corpus cavernosum.
    Malysz J, Farrugia G, Ou Y, Szurszewski JH, Nehra A, Gibbons SJ.
    J Androl; 2002 Apr 01; 23(6):899-910. PubMed ID: 12399537
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  • 20. Complete loss of the cytoplasmic carboxyl terminus of the KCNQ2 potassium channel: a novel mutation in a large Czech pedigree with benign neonatal convulsions or other epileptic phenotypes.
    Pereira S, Roll P, Krizova J, Genton P, Brazdil M, Kuba R, Cau P, Rektor I, Szepetowski P.
    Epilepsia; 2004 Apr 01; 45(4):384-90. PubMed ID: 15030501
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