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PUBMED FOR HANDHELDS

Journal Abstract Search


156 related items for PubMed ID: 15072950

  • 21.
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  • 22. Rescue of expression and function of long QT syndrome-causing mutant hERG channels by enhancing channel stability in the plasma membrane.
    Davis J, Cornwell JD, Campagna N, Guo J, Li W, Yang T, Wang T, Zhang S.
    J Biol Chem; 2024 Aug; 300(8):107526. PubMed ID: 38960041
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  • 24. The G604S-hERG mutation alters the biophysical properties and exerts a dominant-negative effect on expression of hERG channels in HEK293 cells.
    Huo J, Zhang Y, Huang N, Liu P, Huang C, Guo X, Jiang W, Zhou N, Grace A, Huang CL, Ma A.
    Pflugers Arch; 2008 Aug; 456(5):917-28. PubMed ID: 18386051
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  • 25. Most LQT2 mutations reduce Kv11.1 (hERG) current by a class 2 (trafficking-deficient) mechanism.
    Anderson CL, Delisle BP, Anson BD, Kilby JA, Will ML, Tester DJ, Gong Q, Zhou Z, Ackerman MJ, January CT.
    Circulation; 2006 Jan 24; 113(3):365-73. PubMed ID: 16432067
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  • 28. Identification and functional characterization of the human ether-a-go-go-related gene Q738X mutant associated with hereditary long QT syndrome type 2.
    Han SN, Yang SH, Zhang Y, Sun XY, Duan YY, Hu XJ, Fan TL, Huang CZ, Yang G, Zhang Z, Zhang L.
    Int J Mol Med; 2014 Sep 24; 34(3):810-5. PubMed ID: 24993425
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  • 29. Mutant MiRP1 subunits modulate HERG K+ channel gating: a mechanism for pro-arrhythmia in long QT syndrome type 6.
    Lu Y, Mahaut-Smith MP, Huang CL, Vandenberg JI.
    J Physiol; 2003 Aug 15; 551(Pt 1):253-62. PubMed ID: 12923204
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  • 30.
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  • 31. A splice site mutation in hERG leads to cryptic splicing in human long QT syndrome.
    Gong Q, Zhang L, Moss AJ, Vincent GM, Ackerman MJ, Robinson JC, Jones MA, Tester DJ, Zhou Z.
    J Mol Cell Cardiol; 2008 Mar 15; 44(3):502-9. PubMed ID: 18272172
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  • 32. Characterization of a novel missense mutation in the pore of HERG in a patient with long QT syndrome.
    Yoshida H, Horie M, Otani H, Takano M, Tsuji K, Kubota T, Fukunami M, Sasayama S.
    J Cardiovasc Electrophysiol; 1999 Sep 15; 10(9):1262-70. PubMed ID: 10517660
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  • 35. A common antitussive drug, clobutinol, precipitates the long QT syndrome 2.
    Bellocq C, Wilders R, Schott JJ, Louérat-Oriou B, Boisseau P, Le Marec H, Escande D, Baró I.
    Mol Pharmacol; 2004 Nov 15; 66(5):1093-102. PubMed ID: 15280442
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  • 36. Pharmacological correction of long QT-linked mutations in KCNH2 (hERG) increases the trafficking of Kv11.1 channels stored in the transitional endoplasmic reticulum.
    Smith JL, Reloj AR, Nataraj PS, Bartos DC, Schroder EA, Moss AJ, Ohno S, Horie M, Anderson CL, January CT, Delisle BP.
    Am J Physiol Cell Physiol; 2013 Nov 01; 305(9):C919-30. PubMed ID: 23864605
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  • 37.
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  • 38. Identification and functional characterization of a novel KCNE2 (MiRP1) mutation that alters HERG channel kinetics.
    Isbrandt D, Friederich P, Solth A, Haverkamp W, Ebneth A, Borggrefe M, Funke H, Sauter K, Breithardt G, Pongs O, Schulze-Bahr E.
    J Mol Med (Berl); 2002 Aug 01; 80(8):524-32. PubMed ID: 12185453
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