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202 related items for PubMed ID: 12388192

  • 1. A common Dubin-Johnson syndrome mutation impairs protein maturation and transport activity of MRP2 (ABCC2).
    Keitel V, Nies AT, Brom M, Hummel-Eisenbeiss J, Spring H, Keppler D.
    Am J Physiol Gastrointest Liver Physiol; 2003 Jan; 284(1):G165-74. PubMed ID: 12388192
    [Abstract] [Full Text] [Related]

  • 2. Impaired protein maturation of the conjugate export pump multidrug resistance protein 2 as a consequence of a deletion mutation in Dubin-Johnson syndrome.
    Keitel V, Kartenbeck J, Nies AT, Spring H, Brom M, Keppler D.
    Hepatology; 2000 Dec; 32(6):1317-28. PubMed ID: 11093739
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  • 3. Trafficking and functional defects by mutations of the ATP-binding domains in MRP2 in patients with Dubin-Johnson syndrome.
    Hashimoto K, Uchiumi T, Konno T, Ebihara T, Nakamura T, Wada M, Sakisaka S, Maniwa F, Amachi T, Ueda K, Kuwano M.
    Hepatology; 2002 Nov; 36(5):1236-45. PubMed ID: 12395335
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  • 4. Exon-intron organization of the human multidrug-resistance protein 2 (MRP2) gene mutated in Dubin-Johnson syndrome.
    Tsujii H, König J, Rost D, Stöckel B, Leuschner U, Keppler D.
    Gastroenterology; 1999 Sep; 117(3):653-60. PubMed ID: 10464142
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  • 5. Identification and functional analysis of two novel mutations in the multidrug resistance protein 2 gene in Israeli patients with Dubin-Johnson syndrome.
    Mor-Cohen R, Zivelin A, Rosenberg N, Shani M, Muallem S, Seligsohn U.
    J Biol Chem; 2001 Oct 05; 276(40):36923-30. PubMed ID: 11477083
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  • 6. A recurrent ABCC2 p.G693R mutation resulting in loss of function of MRP2 and hyperbilirubinemia in Dubin-Johnson syndrome in China.
    Wu L, Li Y, Song Y, Zhou D, Jia S, Xu A, Zhang W, You H, Jia J, Huang J, Ou X.
    Orphanet J Rare Dis; 2020 Mar 18; 15(1):74. PubMed ID: 32183854
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  • 7. Dual hereditary jaundice: simultaneous occurrence of mutations causing Gilbert's and Dubin-Johnson syndrome.
    Cebecauerova D, Jirasek T, Budisova L, Mandys V, Volf V, Novotna Z, Subhanova I, Hrebicek M, Elleder M, Jirsa M.
    Gastroenterology; 2005 Jul 18; 129(1):315-20. PubMed ID: 16012956
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  • 9. Novel mutations in the Dubin-Johnson syndrome gene ABCC2/MRP2 and associated biochemical changes.
    Devgun MS, El-Nujumi AM, O'Dowd GJ, Barbu V, Poupon R.
    Ann Clin Biochem; 2012 Nov 18; 49(Pt 6):609-12. PubMed ID: 23065530
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  • 10. Drug resistance and ATP-dependent conjugate transport mediated by the apical multidrug resistance protein, MRP2, permanently expressed in human and canine cells.
    Cui Y, König J, Buchholz JK, Spring H, Leier I, Keppler D.
    Mol Pharmacol; 1999 May 18; 55(5):929-37. PubMed ID: 10220572
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  • 12. Hepatic secretion of conjugated drugs and endogenous substances.
    Keppler D, König J.
    Semin Liver Dis; 2000 May 18; 20(3):265-72. PubMed ID: 11076395
    [Abstract] [Full Text] [Related]

  • 13. Inhibition of transport across the hepatocyte canalicular membrane by the antibiotic fusidate.
    Bode KA, Donner MG, Leier I, Keppler D.
    Biochem Pharmacol; 2002 Jul 01; 64(1):151-8. PubMed ID: 12106615
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  • 14. Identification of a novel 974C-->G nonsense mutation of the MRP2/ABCC2 gene in a patient with Dubin-Johnson syndrome and analysis of the effects of rifampicin and ursodeoxycholic acid on serum bilirubin and bile acids.
    Corpechot C, Ping C, Wendum D, Matsuda F, Barbu V, Poupon R.
    Am J Gastroenterol; 2006 Oct 01; 101(10):2427-32. PubMed ID: 16952291
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  • 18. Neonatal Dubin-Johnson syndrome: long-term follow-up and MRP2 mutations study.
    Lee JH, Chen HL, Chen HL, Ni YH, Hsu HY, Chang MH.
    Pediatr Res; 2006 Apr 01; 59(4 Pt 1):584-9. PubMed ID: 16549534
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  • 19. Conjugate export pumps of the multidrug resistance protein (MRP) family: localization, substrate specificity, and MRP2-mediated drug resistance.
    König J, Nies AT, Cui Y, Leier I, Keppler D.
    Biochim Biophys Acta; 1999 Dec 06; 1461(2):377-94. PubMed ID: 10581368
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