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Journal Abstract Search

164 related items for PubMed ID: 23065530

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  • 3. Neonatal Dubin-Johnson syndrome: novel compound heterozygous mutation in the ABCC2 gene.
    Okada H, Kusaka T, Fuke N, Kunikata J, Kondo S, Iwase T, Nan W, Hirota T, Ieiri I, Itoh S.
    Pediatr Int; 2014 Oct; 56(5):e62-4. PubMed ID: 25336012
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  • 4. Genetic and biochemical study of dual hereditary jaundice: Dubin-Johnson and Gilbert's syndromes. Haplotyping and founder effect of deletion in ABCC2.
    Slachtova L, Seda O, Behunova J, Mistrik M, Martasek P.
    Eur J Hum Genet; 2016 May; 24(5):704-9. PubMed ID: 26350512
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  • 5. 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
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  • 6. 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; 101(10):2427-32. PubMed ID: 16952291
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  • 10. Dubin-Johnson syndrome and intrahepatic cholestasis of pregnancy in a Sri Lankan family: a case report.
    Kularatnam GAM, Warawitage D, Vidanapathirana DM, Jayasena S, Jasinge E, de Silva N, Liyanarachchi KLAMS, Wickramasinghe P, Devgun MS, Barbu V, Lascols O.
    BMC Res Notes; 2017 Sep 18; 10(1):487. PubMed ID: 28923092
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  • 11. 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 18; 117(3):653-60. PubMed ID: 10464142
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  • 12. 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 18; 59(4 Pt 1):584-9. PubMed ID: 16549534
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  • 13. A new mutation of the ATP-binding cassette, sub-family C, member 2 (ABCC2) gene in a Japanese patient with Dubin-Johnson syndrome.
    Tate G, Li M, Suzuki T, Mitsuya T.
    Genes Genet Syst; 2002 Apr 18; 77(2):117-21. PubMed ID: 12087194
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  • 15. Dubin-Johnson syndrome.
    Nisa AU, Ahmad Z.
    J Coll Physicians Surg Pak; 2008 Mar 18; 18(3):188-9. PubMed ID: 18460254
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  • 16. A Case of Dubin-Johnson Syndrome Presenting as Neonatal Cholestasis With Paucity of Interlobular Bile Ducts.
    Chan KL, Varughese N, Jones PM, Zwick DL, Rajaram V, Lee M, Ramirez CM.
    Pediatr Dev Pathol; 2021 Mar 18; 24(2):154-158. PubMed ID: 33470920
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