BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

227 related articles for article (PubMed ID: 34376370)

  • 21. [Recurrent intrahepatic cholestasis of pregnancy and chain-like choledocholithiasis in a female patient with stop codon in the ABDC4-gene of the hepatobiliary phospholipid transporter].
    Muehlenberg K; Wiedmann K; Keppeler H; Sauerbruch T; Lammert F
    Z Gastroenterol; 2008 Jan; 46(1):48-53. PubMed ID: 18188816
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The role of genetic mutations in intrahepatic cholestasis of pregnancy.
    Aydın GA; Özgen G; Görükmez O
    Taiwan J Obstet Gynecol; 2020 Sep; 59(5):706-710. PubMed ID: 32917322
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Cryptogenic cholestasis in young and adults: ATP8B1, ABCB11, ABCB4, and TJP2 gene variants analysis by high-throughput sequencing.
    Vitale G; Gitto S; Raimondi F; Mattiaccio A; Mantovani V; Vukotic R; D'Errico A; Seri M; Russell RB; Andreone P
    J Gastroenterol; 2018 Aug; 53(8):945-958. PubMed ID: 29238877
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The spectrum of liver diseases related to ABCB4 gene mutations: pathophysiology and clinical aspects.
    Davit-Spraul A; Gonzales E; Baussan C; Jacquemin E
    Semin Liver Dis; 2010 May; 30(2):134-46. PubMed ID: 20422496
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Evaluation of a Novel Missense Mutation in
    Saleem K; Cui Q; Zaib T; Zhu S; Qin Q; Wang Y; Dam J; Ji W; Liu P; Jia X; Wu J; Bai J; Fu S; Sun W
    Dis Markers; 2020; 2020():6292818. PubMed ID: 32626542
    [TBL] [Abstract][Full Text] [Related]  

  • 26. ABCB4 Mutations in Adults Cause a Spectrum Cholestatic Disorder Histologically Distinct from Other Biliary Disease.
    Sinha A; Bhuva M; Grant C; Gimson AE; Thompson E; Duckworth A; Davies SE; Aithal G; Griffiths WJ
    Dig Dis Sci; 2022 Dec; 67(12):5551-5561. PubMed ID: 35288833
    [TBL] [Abstract][Full Text] [Related]  

  • 27. ABCB4 gene mutation-associated cholelithiasis in adults.
    Rosmorduc O; Hermelin B; Boelle PY; Parc R; Taboury J; Poupon R
    Gastroenterology; 2003 Aug; 125(2):452-9. PubMed ID: 12891548
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Mutations and polymorphisms in the bile salt export pump and the multidrug resistance protein 3 associated with drug-induced liver injury.
    Lang C; Meier Y; Stieger B; Beuers U; Lang T; Kerb R; Kullak-Ublick GA; Meier PJ; Pauli-Magnus C
    Pharmacogenet Genomics; 2007 Jan; 17(1):47-60. PubMed ID: 17264802
    [TBL] [Abstract][Full Text] [Related]  

  • 29. ABCB4 heterozygous gene mutations associated with fibrosing cholestatic liver disease in adults.
    Ziol M; Barbu V; Rosmorduc O; Frassati-Biaggi A; Barget N; Hermelin B; Scheffer GL; Bennouna S; Trinchet JC; Beaugrand M; Ganne-Carrié N
    Gastroenterology; 2008 Jul; 135(1):131-41. PubMed ID: 18482588
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Should patients with symptomatic cholelithiasis before 30 years of age be tested for
    Gouveia C; Flor de Lima M; Pereira F; Rosa B; Cotter J; Banhudo A; Duarte M; Ferreira A; Cravo M; Nunes J
    Scand J Gastroenterol; 2020 Aug; 55(8):958-962. PubMed ID: 32650689
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Sequencing of FIC1, BSEP and MDR3 in a large cohort of patients with cholestasis revealed a high number of different genetic variants.
    Dröge C; Bonus M; Baumann U; Klindt C; Lainka E; Kathemann S; Brinkert F; Grabhorn E; Pfister ED; Wenning D; Fichtner A; Gotthardt DN; Weiss KH; McKiernan P; Puri RD; Verma IC; Kluge S; Gohlke H; Schmitt L; Kubitz R; Häussinger D; Keitel V
    J Hepatol; 2017 Dec; 67(6):1253-1264. PubMed ID: 28733223
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Linkage between a new splicing site mutation in the MDR3 alias ABCB4 gene and intrahepatic cholestasis of pregnancy.
    Schneider G; Paus TC; Kullak-Ublick GA; Meier PJ; Wienker TF; Lang T; van de Vondel P; Sauerbruch T; Reichel C
    Hepatology; 2007 Jan; 45(1):150-8. PubMed ID: 17187437
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Clinical phenotype of adult-onset liver disease in patients with variants in ABCB4, ABCB11, and ATP8B1.
    Nayagam JS; Foskett P; Strautnieks S; Agarwal K; Miquel R; Joshi D; Thompson RJ
    Hepatol Commun; 2022 Oct; 6(10):2654-2664. PubMed ID: 35894240
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A female of progressive familial intrahepatic cholestasis type 3 caused by heterozygous mutations of ABCB4 gene and her cirrhosis improved after treatment of ursodeoxycholic acid: a case report.
    Qiao F; Ren F; Lu W; Yang H; Mo G; Wang S; Liu L; Xu X
    BMC Med Genomics; 2023 Jul; 16(1):171. PubMed ID: 37488596
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Familial cholestasis: progressive familial intrahepatic cholestasis, benign recurrent intrahepatic cholestasis and intrahepatic cholestasis of pregnancy.
    van der Woerd WL; van Mil SW; Stapelbroek JM; Klomp LW; van de Graaf SF; Houwen RH
    Best Pract Res Clin Gastroenterol; 2010 Oct; 24(5):541-53. PubMed ID: 20955958
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Liver diseases related to MDR3 (ABCB4) gene deficiency.
    Gonzales E; Davit-Spraul A; Baussan C; Buffet C; Maurice M; Jacquemin E
    Front Biosci (Landmark Ed); 2009 Jan; 14(11):4242-56. PubMed ID: 19273348
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Sequence analysis of bile salt export pump (ABCB11) and multidrug resistance p-glycoprotein 3 (ABCB4, MDR3) in patients with intrahepatic cholestasis of pregnancy.
    Pauli-Magnus C; Lang T; Meier Y; Zodan-Marin T; Jung D; Breymann C; Zimmermann R; Kenngott S; Beuers U; Reichel C; Kerb R; Penger A; Meier PJ; Kullak-Ublick GA
    Pharmacogenetics; 2004 Feb; 14(2):91-102. PubMed ID: 15077010
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Chinese children with chronic intrahepatic cholestasis and high γ-glutamyl transpeptidase: clinical features and association with ABCB4 mutations.
    Fang LJ; Wang XH; Knisely AS; Yu H; Lu Y; Liu LY; Wang JS
    J Pediatr Gastroenterol Nutr; 2012 Aug; 55(2):150-6. PubMed ID: 22343912
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Synthetic human ABCB4 mRNA therapy rescues severe liver disease phenotype in a BALB/c.Abcb4
    Wei G; Cao J; Huang P; An P; Badlani D; Vaid KA; Zhao S; Wang DQ; Zhuo J; Yin L; Frassetto A; Markel A; Presnyak V; Gandham S; Hua S; Lukacs C; Finn PF; Giangrande PH; Martini PGV; Popov YV
    J Hepatol; 2021 Jun; 74(6):1416-1428. PubMed ID: 33340584
    [TBL] [Abstract][Full Text] [Related]  

  • 40. An expanded role for heterozygous mutations of ABCB4, ABCB11, ATP8B1, ABCC2 and TJP2 in intrahepatic cholestasis of pregnancy.
    Dixon PH; Sambrotta M; Chambers J; Taylor-Harris P; Syngelaki A; Nicolaides K; Knisely AS; Thompson RJ; Williamson C
    Sci Rep; 2017 Sep; 7(1):11823. PubMed ID: 28924228
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.