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Journal Abstract Search


364 related items for PubMed ID: 10531299

  • 1. 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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  • 3. Thapsigargin selectively rescues the trafficking defective LQT2 channels G601S and F805C.
    Delisle BP, Anderson CL, Balijepalli RC, Anson BD, Kamp TJ, January CT.
    J Biol Chem; 2003 Sep 12; 278(37):35749-54. PubMed ID: 12837749
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  • 7. Defective protein trafficking in hERG-associated hereditary long QT syndrome (LQT2): molecular mechanisms and restoration of intracellular protein processing.
    Thomas D, Kiehn J, Katus HA, Karle CA.
    Cardiovasc Res; 2003 Nov 01; 60(2):235-41. PubMed ID: 14613852
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  • 9. 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 01; 279(4):H1748-56. PubMed ID: 11009462
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  • 14. 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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  • 16. A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel.
    Sanguinetti MC, Jiang C, Curran ME, Keating MT.
    Cell; 1995 Apr 21; 81(2):299-307. PubMed ID: 7736582
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  • 17. A mechanism for the proarrhythmic effects of cisapride (Propulsid): high affinity blockade of the human cardiac potassium channel HERG.
    Rampe D, Roy ML, Dennis A, Brown AM.
    FEBS Lett; 1997 Nov 03; 417(1):28-32. PubMed ID: 9395068
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  • 18. HERG channel dysfunction in human long QT syndrome. Intracellular transport and functional defects.
    Zhou Z, Gong Q, Epstein ML, January CT.
    J Biol Chem; 1998 Aug 14; 273(33):21061-6. PubMed ID: 9694858
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  • 19. 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 14; 32(12):2327-37. PubMed ID: 11113008
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  • 20. 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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