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265 related items for PubMed ID: 12354768

  • 1. A novel mutation (T65P) in the PAS domain of the human potassium channel HERG results in the long QT syndrome by trafficking deficiency.
    Paulussen A, Raes A, Matthijs G, Snyders DJ, Cohen N, Aerssens J.
    J Biol Chem; 2002 Dec 13; 277(50):48610-6. PubMed ID: 12354768
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  • 3. The binding site for channel blockers that rescue misprocessed human long QT syndrome type 2 ether-a-gogo-related gene (HERG) mutations.
    Ficker E, Obejero-Paz CA, Zhao S, Brown AM.
    J Biol Chem; 2002 Feb 15; 277(7):4989-98. PubMed ID: 11741928
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  • 6. Correction of defective protein trafficking of a mutant HERG potassium channel in human long QT syndrome. Pharmacological and temperature effects.
    Zhou Z, Gong Q, January CT.
    J Biol Chem; 1999 Oct 29; 274(44):31123-6. PubMed ID: 10531299
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  • 8. Novel KCNQ1 and HERG missense mutations in Dutch long-QT families.
    Jongbloed RJ, Wilde AA, Geelen JL, Doevendans P, Schaap C, Van Langen I, van Tintelen JP, Cobben JM, Beaufort-Krol GC, Geraedts JP, Smeets HJ.
    Hum Mutat; 1999 Oct 29; 13(4):301-10. PubMed ID: 10220144
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  • 18. Bradycardia-induced long QT syndrome caused by a de novo missense mutation in the S2-S3 inner loop of HERG.
    Yoshida H, Horie M, Otani H, Kawashima T, Onishi Y, Sasayama S.
    Am J Med Genet; 2001 Feb 01; 98(4):348-52. PubMed ID: 11170080
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  • 19. Is restoration of intracellular trafficking clinically feasible in the long QT syndrome?: The example of HERG mutations.
    Kaufman ES, Ficker E.
    J Cardiovasc Electrophysiol; 2003 Mar 01; 14(3):320-2. PubMed ID: 12716119
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