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Journal Abstract Search

265 related items for PubMed ID: 12885765

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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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  • 5. Defective human Ether-à-go-go-related gene trafficking linked to an endoplasmic reticulum retention signal in the C terminus.
    Kupershmidt S, Yang T, Chanthaphaychith S, Wang Z, Towbin JA, Roden DM.
    J Biol Chem; 2002 Jul 26; 277(30):27442-8. PubMed ID: 12021266
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  • 6. 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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  • 14. Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome.
    Ficker E, Thomas D, Viswanathan PC, Dennis AT, Priori SG, Napolitano C, Memmi M, Wible BA, Kaufman ES, Iyengar S, Schwartz PJ, Rudy Y, Brown AM.
    Am J Physiol Heart Circ Physiol; 2000 Oct 13; 279(4):H1748-56. PubMed ID: 11009462
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  • 15. 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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  • 16. Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel.
    Moss AJ, Zareba W, Kaufman ES, Gartman E, Peterson DR, Benhorin J, Towbin JA, Keating MT, Priori SG, Schwartz PJ, Vincent GM, Robinson JL, Andrews ML, Feng C, Hall WJ, Medina A, Zhang L, Wang Z.
    Circulation; 2002 Feb 19; 105(7):794-9. PubMed ID: 11854117
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  • 19. Regulation of deactivation by an amino terminal domain in human ether-à-go-go-related gene potassium channels.
    Wang J, Trudeau MC, Zappia AM, Robertson GA.
    J Gen Physiol; 1998 Nov 19; 112(5):637-47. PubMed ID: 9806971
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  • 20. Retention in the endoplasmic reticulum as a mechanism of dominant-negative current suppression in human long QT syndrome.
    Ficker E, Dennis AT, Obejero-Paz CA, Castaldo P, Taglialatela M, Brown AM.
    J Mol Cell Cardiol; 2000 Dec 19; 32(12):2327-37. PubMed ID: 11113008
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