BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 19881259)

  • 1. Novel large-scale deletion (whole exon 7) in the ABCC2 gene in a patient with the Dubin-Johnson syndrome.
    Kanda D; Takagi H; Kawahara Y; Yata Y; Takakusagi T; Hatanaka T; Yoshinaga T; Iesaki K; Kashiwabara K; Higuchi T; Mori M; Hirota T; Higuchi S; Ieiri I
    Drug Metab Pharmacokinet; 2009; 24(5):464-8. PubMed ID: 19881259
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 129(1):315-20. PubMed ID: 16012956
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 77(2):117-21. PubMed ID: 12087194
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. In silico screening and analysis of single-nucleotide polymorphic variants of the ABCC2 gene affecting Dubin-Johnson syndrome.
    Sharma P; Sharma S
    Arab J Gastroenterol; 2022 Aug; 23(3):172-187. PubMed ID: 35477852
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 15(1):74. PubMed ID: 32183854
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 276(40):36923-30. PubMed ID: 11477083
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Homozygous mutation Arg768Trp in the ABC-transporter encoding gene MRP2/cMOAT/ABCC2 causes Dubin-Johnson syndrome in a Caucasian patient.
    Materna V; Lage H
    J Hum Genet; 2003; 48(9):484-486. PubMed ID: 12942343
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 49(Pt 6):609-12. PubMed ID: 23065530
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic contribution of ABCC2 to Dubin-Johnson syndrome and inherited cholestatic disorders.
    Corpechot C; Barbu V; Chazouillères O; Broué P; Girard M; Roquelaure B; Chrétien Y; Dong C; Lascols O; Housset C; Jéru I
    Liver Int; 2020 Jan; 40(1):163-174. PubMed ID: 31544333
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Conjugated hyperbilirubinemia after surgery. A diagnosis of Dubin-Johnson syndrome confirmed by genetic testing.
    Baranguán Castro ML; García Romero R; Miramar Gallart MD
    Rev Esp Enferm Dig; 2017 Nov; 109(11):801-802. PubMed ID: 29032691
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel homozygous frameshift variant in the ABCC2-gene in Dubin-Johnson syndrome may predispose to chronic liver disease.
    Philips CA; Agarwal M; Rajesh S; Ahamed R; Augustine P
    Indian J Gastroenterol; 2021 Feb; 40(1):72-76. PubMed ID: 33428121
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genotype-Phenotype Association in
    Kim JH; Kang MW; Kim S; Han JW; Jang JW; Choi JY; Yoon SK; Sung PS
    Int J Mol Sci; 2022 Dec; 23(24):. PubMed ID: 36555809
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genomic structure of the canalicular multispecific organic anion-transporter gene (MRP2/cMOAT) and mutations in the ATP-binding-cassette region in Dubin-Johnson syndrome.
    Toh S; Wada M; Uchiumi T; Inokuchi A; Makino Y; Horie Y; Adachi Y; Sakisaka S; Kuwano M
    Am J Hum Genet; 1999 Mar; 64(3):739-46. PubMed ID: 10053008
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 24(2):154-158. PubMed ID: 33470920
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Clinical features and ABCC2 genotypic analysis of an infant with Dubin-Johnson syndrome].
    Meng LL; Qiu JW; Lin WX; Song YZ
    Zhongguo Dang Dai Er Ke Za Zhi; 2019 Jan; 21(1):64-70. PubMed ID: 30675866
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 10(1):487. PubMed ID: 28923092
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.