BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 21638239)

  • 1. Cholestatic liver diseases from child to adult: the diversity of MDR3 disease.
    Kubitz R; Bode J; Erhardt A; Graf D; Kircheis G; Müller-Stöver I; Reinehr R; Reuter S; Richter J; Sagir A; Schmitt M; Donner M
    Z Gastroenterol; 2011 Jun; 49(6):728-36. PubMed ID: 21638239
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Functional analysis of ABCB4 mutations relates clinical outcomes of progressive familial intrahepatic cholestasis type 3 to the degree of MDR3 floppase activity.
    Gordo-Gilart R; Andueza S; Hierro L; Martínez-Fernández P; D'Agostino D; Jara P; Alvarez L
    Gut; 2015 Jan; 64(1):147-55. PubMed ID: 24594635
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Heterozygous ABCB4 mutations in children with cholestatic liver disease.
    Gordo-Gilart R; Hierro L; Andueza S; Muñoz-Bartolo G; López C; Díaz C; Jara P; Álvarez L
    Liver Int; 2016 Feb; 36(2):258-67. PubMed ID: 26153658
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. The histidine-loop is essential for transport activity of human MDR3. A novel mutation of MDR3 in a patient with progressive familial intrahepatic cholestasis type 3.
    Dzagania T; Engelmann G; Häussinger D; Schmitt L; Flechtenmacher C; Rtskhiladze I; Kubitz R
    Gene; 2012 Sep; 506(1):141-5. PubMed ID: 22766396
    [TBL] [Abstract][Full Text] [Related]  

  • 8. ABCB4 mutations in adult patients with cholestatic liver disease: impact and phenotypic expression.
    Degiorgio D; Crosignani A; Colombo C; Bordo D; Zuin M; Vassallo E; Syrén ML; Coviello DA; Battezzati PM
    J Gastroenterol; 2016 Mar; 51(3):271-80. PubMed ID: 26324191
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A mutation in the canalicular phospholipid transporter gene, ABCB4, is associated with cholestasis, ductopenia, and cirrhosis in adults.
    Gotthardt D; Runz H; Keitel V; Fischer C; Flechtenmacher C; Wirtenberger M; Weiss KH; Imparato S; Braun A; Hemminki K; Stremmel W; Rüschendorf F; Stiehl A; Kubitz R; Burwinkel B; Schirmacher P; Knisely AS; Zschocke J; Sauer P
    Hepatology; 2008 Oct; 48(4):1157-66. PubMed ID: 18781607
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Role of multidrug resistance 3 deficiency in pediatric and adult liver disease: one gene for three diseases.
    Jacquemin E
    Semin Liver Dis; 2001 Nov; 21(4):551-62. PubMed ID: 11745043
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Progressive familial intrahepatic cholestasis with high gamma-glutamyltranspeptidase levels in Taiwanese infants: role of MDR3 gene defect?
    Chen HL; Chang PS; Hsu HC; Lee JH; Ni YH; Hsu HY; Jeng YM; Chang MH
    Pediatr Res; 2001 Jul; 50(1):50-5. PubMed ID: 11420418
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Progressive familial intrahepatic cholestasis.
    Cavestro GM; Frulloni L; Cerati E; Ribeiro LA; Corrente V; Sianesi M; Franzè A; Di Mario F
    Acta Biomed; 2002; 73(3-4):53-6. PubMed ID: 12596388
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Genotype-phenotype relationships in the low-phospholipid-associated cholelithiasis syndrome: a study of 156 consecutive patients.
    Poupon R; Rosmorduc O; Boëlle PY; Chrétien Y; Corpechot C; Chazouillères O; Housset C; Barbu V
    Hepatology; 2013 Sep; 58(3):1105-10. PubMed ID: 23533021
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Low phospholipid-associated cholestasis and cholelithiasis.
    Erlinger S
    Clin Res Hepatol Gastroenterol; 2012 Sep; 36 Suppl 1():S36-40. PubMed ID: 23141892
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Prenatal molecular diagnosis of inherited cholestatic diseases.
    Jung C; Driancourt C; Baussan C; Zater M; Hadchouel M; Meunier-Rotival M; Guiochon-Mantel A; Jacquemin E
    J Pediatr Gastroenterol Nutr; 2007 Apr; 44(4):453-8. PubMed ID: 17414143
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. A new splicing site mutation of the ABCB4 gene in intrahepatic cholestasis of pregnancy with raised serum gamma-GT.
    Tavian D; Degiorgio D; Roncaglia N; Vergani P; Cameroni I; Colombo R; Coviello DA
    Dig Liver Dis; 2009 Sep; 41(9):671-5. PubMed ID: 19261551
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.