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Journal Abstract Search


129 related items for PubMed ID: 1592353

  • 1. Defective biliary excretion of epinephrine metabolites in mutant (TR-) rats: relation to the pathogenesis of black liver in the Dubin-Johnson syndrome and Corriedale sheep with an analogous excretory defect.
    Kitamura T, Alroy J, Gatmaitan Z, Inoue M, Mikami T, Jansen P, Arias IM.
    Hepatology; 1992 Jun; 15(6):1154-9. PubMed ID: 1592353
    [Abstract] [Full Text] [Related]

  • 2. Defective ATP-dependent bile canalicular transport of organic anions in mutant (TR-) rats with conjugated hyperbilirubinemia.
    Kitamura T, Jansen P, Hardenbrook C, Kamimoto Y, Gatmaitan Z, Arias IM.
    Proc Natl Acad Sci U S A; 1990 May; 87(9):3557-61. PubMed ID: 2333302
    [Abstract] [Full Text] [Related]

  • 3. Dubin-Johnson and Rotor syndromes: molecular basis and pathogenesis.
    Zimniak P.
    Semin Liver Dis; 1993 Aug; 13(3):248-60. PubMed ID: 8235715
    [Abstract] [Full Text] [Related]

  • 4. Effect of diethylmaleate on bile secretion and ultrastructural appearance of hepatocytes in normal rats and mutant rats with defective organic anion secretion.
    Dumont M, D'Hont C, Feldmann G, Rogier E, Moreau A, Jansen PL, Erlinger S.
    Liver; 1996 Feb; 16(1):35-41. PubMed ID: 8868076
    [Abstract] [Full Text] [Related]

  • 5. Two distinct mechanisms for bilirubin glucuronide transport by rat bile canalicular membrane vesicles. Demonstration of defective ATP-dependent transport in rats (TR-) with inherited conjugated hyperbilirubinemia.
    Nishida T, Gatmaitan Z, Roy-Chowdhry J, Arias IM.
    J Clin Invest; 1992 Nov; 90(5):2130-5. PubMed ID: 1430236
    [Abstract] [Full Text] [Related]

  • 6. Hepatobiliary excretion of organic anions in double-mutant rats with a combination of defective canalicular transport and uridine 5'-diphosphate-glucuronyltransferase deficiency.
    Jansen PL, Peters WH, Meijer DK.
    Gastroenterology; 1987 Nov; 93(5):1094-103. PubMed ID: 3115859
    [Abstract] [Full Text] [Related]

  • 7. Multiplicity of hepatic excretory mechanisms for organic anions.
    Alpert S, Mosher M, Shanske A, Arias IM.
    J Gen Physiol; 1969 Feb; 53(2):238-47. PubMed ID: 5764745
    [Abstract] [Full Text] [Related]

  • 8. Erythrocyte membrane transport of glutathione conjugates and oxidized glutathione in the Dubin-Johnson syndrome and in rats with hereditary hyperbilirubinemia.
    Board P, Nishida T, Gatmaitan Z, Che M, Arias IM.
    Hepatology; 1992 Apr; 15(4):722-5. PubMed ID: 1551648
    [Abstract] [Full Text] [Related]

  • 9. Dubin-Johnson syndrome.
    Nisa AU, Ahmad Z.
    J Coll Physicians Surg Pak; 2008 Mar; 18(3):188-9. PubMed ID: 18460254
    [Abstract] [Full Text] [Related]

  • 10. A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin-Johnson syndrome.
    Paulusma CC, Kool M, Bosma PJ, Scheffer GL, ter Borg F, Scheper RJ, Tytgat GN, Borst P, Baas F, Oude Elferink RP.
    Hepatology; 1997 Jun; 25(6):1539-42. PubMed ID: 9185779
    [Abstract] [Full Text] [Related]

  • 11. Biliary excretion of sulfobromophthalein compounds in normal and mutant Corriedale sheep. Evidence for a disproportionate transport defect for conjugated sulfobromophthalein.
    Barnhart JL, Gronwall RR, Combes B.
    Hepatology; 1981 Jun; 1(5):441-7. PubMed ID: 7308989
    [Abstract] [Full Text] [Related]

  • 12. The Dubin-Johnson syndrome: electron microscopic observation of hepatic pigment--a case study.
    Baba N, Ruppert RD.
    Am J Clin Pathol; 1972 Mar; 57(3):306-10. PubMed ID: 4111811
    [No Abstract] [Full Text] [Related]

  • 13. On the natural and excretion of the hepatic pigment in the Dubin-Johnson syndrome.
    Swartz HM, Sarna T, Varma RR.
    Gastroenterology; 1979 May; 76(5 Pt 1):958-64. PubMed ID: 220131
    [No Abstract] [Full Text] [Related]

  • 14. Impaired biliary excretion and whole body elimination of methylmercury in rats with congenital defect in biliary glutathione excretion.
    Ballatori N, Gatmaitan Z, Truong AT.
    Hepatology; 1995 Nov; 22(5):1469-73. PubMed ID: 7590665
    [Abstract] [Full Text] [Related]

  • 15. Dubin-Johnson-like syndrome in golden lion tamarins (Leontopithecus rosalia rosalia).
    Schulman FY, Montali RJ, Bush M, Citino SB, Tell LA, Ballou JD, Hutson TL, St Pierre M, Dufour JF, Gatmaitan Z.
    Vet Pathol; 1993 Nov; 30(6):491-8. PubMed ID: 8116141
    [Abstract] [Full Text] [Related]

  • 16. Unconjugated bilirubin transport in normal and mutant Corriedale sheep with Dubin-Johnson syndrome.
    Mia AS, Gronwall RR, Cornelius CE.
    Proc Soc Exp Biol Med; 1970 Oct; 135(1):33-7. PubMed ID: 4920172
    [No Abstract] [Full Text] [Related]

  • 17. Lysosomal changes in liver tissue from patients with the Dubin-Johnson-Sprinz syndrome.
    Seymour CA, Neale G, Peters TJ.
    Clin Sci Mol Med; 1977 Mar; 52(3):241-8. PubMed ID: 14805
    [Abstract] [Full Text] [Related]

  • 18. Hereditary chronic conjugated hyperbilirubinemia in mutant rats caused by defective hepatic anion transport.
    Jansen PL, Peters WH, Lamers WH.
    Hepatology; 1985 Mar; 5(4):573-9. PubMed ID: 4018730
    [Abstract] [Full Text] [Related]

  • 19. Absence of the canalicular isoform of the MRP gene-encoded conjugate export pump from the hepatocytes in Dubin-Johnson syndrome.
    Kartenbeck J, Leuschner U, Mayer R, Keppler D.
    Hepatology; 1996 May; 23(5):1061-6. PubMed ID: 8621134
    [Abstract] [Full Text] [Related]

  • 20. [Clinical pathology of Dubin-Johnson syndrome].
    Luo Z, Zhang L, Li Y.
    Zhonghua Gan Zang Bing Za Zhi; 2000 Feb; 8(1):45-7. PubMed ID: 10712787
    [Abstract] [Full Text] [Related]


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