BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

314 related articles for article (PubMed ID: 33256620)

  • 1. Case report: progressive familial intrahepatic cholestasis type 3 with compound heterozygous ABCB4 variants diagnosed 15 years after liver transplantation.
    Goubran M; Aderibigbe A; Jacquemin E; Guettier C; Girgis S; Bain V; Mason AL
    BMC Med Genet; 2020 Nov; 21(1):238. PubMed ID: 33256620
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Autoimmune BSEP disease: disease recurrence after liver transplantation for progressive familial intrahepatic cholestasis.
    Kubitz R; Dröge C; Kluge S; Stross C; Walter N; Keitel V; Häussinger D; Stindt J
    Clin Rev Allergy Immunol; 2015 Jun; 48(2-3):273-84. PubMed ID: 25342496
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Liver-directed gene therapy results in long-term correction of progressive familial intrahepatic cholestasis type 3 in mice.
    Aronson SJ; Bakker RS; Shi X; Duijst S; Ten Bloemendaal L; de Waart DR; Verheij J; Ronzitti G; Oude Elferink RP; Beuers U; Paulusma CC; Bosma PJ
    J Hepatol; 2019 Jul; 71(1):153-162. PubMed ID: 30935993
    [TBL] [Abstract][Full Text] [Related]  

  • 5. ABCB4 disease: Many faces of one gene deficiency.
    Sticova E; Jirsa M
    Ann Hepatol; 2020; 19(2):126-133. PubMed ID: 31759867
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Variants in ABCB4 (MDR3) across the spectrum of cholestatic liver diseases in adults.
    Stättermayer AF; Halilbasic E; Wrba F; Ferenci P; Trauner M
    J Hepatol; 2020 Sep; 73(3):651-663. PubMed ID: 32376413
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel ABCB4 mutation in a Chinese female patient with progressive familial intrahepatic cholestasis type 3: a case report.
    Wu Z; Zhang S; Zhang L; Li M
    Diagn Pathol; 2020 Apr; 15(1):39. PubMed ID: 32321542
    [TBL] [Abstract][Full Text] [Related]  

  • 8. ABCB4 Gene Aberrations in Human Liver Disease: An Evolving Spectrum.
    Reichert MC; Lammert F
    Semin Liver Dis; 2018 Nov; 38(4):299-307. PubMed ID: 30357767
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Reversal of advanced fibrosis after long-term ursodeoxycholic acid therapy in a patient with residual expression of MDR3.
    Frider B; Castillo A; Gordo-Gilart R; Bruno A; Amante M; Alvarez L; Mathet V
    Ann Hepatol; 2015; 14(5):745-51. PubMed ID: 26256905
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ductopenia and cirrhosis in a 32-year-old woman with progressive familial intrahepatic cholestasis type 3: A case report and review of the literature.
    Tan YW; Ji HL; Lu ZH; Ge GH; Sun L; Zhou XB; Sheng JH; Gong YH
    World J Gastroenterol; 2018 Nov; 24(41):4716-4720. PubMed ID: 30416319
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Progressive familial intrahepatic cholestasis.
    Jacquemin E
    Clin Res Hepatol Gastroenterol; 2012 Sep; 36 Suppl 1():S26-35. PubMed ID: 23141890
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. ABCB4 disease mimicking morbus Wilson: A potential diagnostic pitfall.
    Sticova E; Neroldova M; Kotalova R; Subhanova I; Jirsa M
    Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub; 2020 Mar; 164(1):121-125. PubMed ID: 31728073
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Paucity of Interlobular Bile Ducts in Multidrug-Resistant P-Glycoprotein 3 (MDR3) Deficiency.
    Vij M; Valamparampil J; Shanmugum N; Reddy SM; Rajindrajith S; Rela M
    Int J Surg Pathol; 2019 May; 27(3):343-347. PubMed ID: 30222019
    [TBL] [Abstract][Full Text] [Related]  

  • 16. ABCB4/MDR3 in health and disease - at the crossroads of biochemistry and medicine.
    Prescher M; Kroll T; Schmitt L
    Biol Chem; 2019 Sep; 400(10):1245-1259. PubMed ID: 30730833
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel etiologic factor of highly elevated cholestanol levels: progressive familial intrahepatic cholestasis.
    Küçükçongar Yavaş A; Çavdarlı B; Ünal Uzun Ö; Uncuoğlu A; Gündüz M
    J Pediatr Endocrinol Metab; 2020 May; 33(5):665-669. PubMed ID: 32229667
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Case Report: A rare case of young adult progressive familial intrahepatic cholestasis-type 3 with a novel heterozygous pathogenic variant of
    Zhu H; Wang S; Li L; Geng W; Wan X; Hua R; Wang D; Gao P
    Front Pediatr; 2022; 10():1012825. PubMed ID: 36330364
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A missense mutation in ABCB4 gene involved in progressive familial intrahepatic cholestasis type 3 leads to a folding defect that can be rescued by low temperature.
    Delaunay JL; Durand-Schneider AM; Delautier D; Rada A; Gautherot J; Jacquemin E; Aït-Slimane T; Maurice M
    Hepatology; 2009 Apr; 49(4):1218-27. PubMed ID: 19185004
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Progressive familial intrahepatic cholestasis.
    Davit-Spraul A; Gonzales E; Baussan C; Jacquemin E
    Orphanet J Rare Dis; 2009 Jan; 4():1. PubMed ID: 19133130
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.