BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

195 related articles for article (PubMed ID: 26474921)

  • 21. Genetics and Molecular Modeling of New Mutations of Familial Intrahepatic Cholestasis in a Single Italian Center.
    Giovannoni I; Callea F; Bellacchio E; Torre G; De Ville De Goyet J; Francalanci P
    PLoS One; 2015; 10(12):e0145021. PubMed ID: 26678486
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Hepatobiliary phospholipid transporter ABCB4, MDR3 gene variants in a large cohort of Italian women with intrahepatic cholestasis of pregnancy.
    Floreani A; Carderi I; Paternoster D; Soardo G; Azzaroli F; Esposito W; Montagnani M; Marchesoni D; Variola A; Rosa Rizzotto E; Braghin C; Mazzella G
    Dig Liver Dis; 2008 May; 40(5):366-70. PubMed ID: 18083082
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Variations of ABCB4 and ABCB11 genes are associated with primary intrahepatic stones.
    Pan S; Li X; Jiang P; Jiang Y; Shuai L; He Y; Li Z
    Mol Med Rep; 2015 Jan; 11(1):434-46. PubMed ID: 25323205
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Molecular mechanistic explanation for the spectrum of cholestatic disease caused by the S320F variant of ABCB4.
    Andress EJ; Nicolaou M; Romero MR; Naik S; Dixon PH; Williamson C; Linton KJ
    Hepatology; 2014 May; 59(5):1921-31. PubMed ID: 24806754
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. 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]  

  • 28. [Progressive familial intrahepatic cholestasis type 3].
    Lipiński P; Jankowska I
    Dev Period Med; 2018; 22(4):385-389. PubMed ID: 30636238
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Molecular characterization of exons 6, 8 and 9 of ABCB4 gene in children with Progressive Familial Intrahepatic Cholestasis type 3.
    Fathy M; Kamal M; Al-Sharkawy M; Al-Karaksy H; Hassan N
    Biomarkers; 2016 Nov; 21(7):573-7. PubMed ID: 27075526
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Liver disease associated with hereditary defects of hepatobiliary transporters].
    Wendum D
    Ann Pathol; 2010 Dec; 30(6):426-31. PubMed ID: 21167428
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Spectrum of genomic variations in Indian patients with progressive familial intrahepatic cholestasis.
    Sharma A; Poddar U; Agnihotry S; Phadke SR; Yachha SK; Aggarwal R
    BMC Gastroenterol; 2018 Jul; 18(1):107. PubMed ID: 29973134
    [TBL] [Abstract][Full Text] [Related]  

  • 32. MRCK-Alpha and Its Effector Myosin II Regulatory Light Chain Bind ABCB4 and Regulate Its Membrane Expression.
    Bruneau A; Delaunay JL; Durand-Schneider AM; Vauthier V; Ben Saad A; Aoudjehane L; El Mourabit H; Morichon R; Falguières T; Gautheron J; Housset C; Aït-Slimane T
    Cells; 2022 Feb; 11(4):. PubMed ID: 35203270
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Treatment of paediatric cholestasis due to canalicular transport defects: yet another step forward.
    Marin JJ; Houwen RH
    Gut; 2015 Jan; 64(1):6-8. PubMed ID: 24861269
    [No Abstract]   [Full Text] [Related]  

  • 34. Clinical and genetic study of ABCB4 gene-related cholestatic liver disease in China: children and adults.
    Cao L; Ling X; Yan J; Feng D; Dong Y; Xu Z; Wang F; Zhu S; Gao Y; Cao Z; Zhang M
    Orphanet J Rare Dis; 2024 Apr; 19(1):157. PubMed ID: 38610052
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Dietary lecithin protects against cholestatic liver disease in cholic acid-fed Abcb4- deficient mice.
    Lamireau T; Bouchard G; Yousef IM; Clouzeau-Girard H; Rosenbaum J; Desmoulière A; Tuchweber B
    Pediatr Res; 2007 Feb; 61(2):185-90. PubMed ID: 17237720
    [TBL] [Abstract][Full Text] [Related]  

  • 36. ABCB4 missense mutations D243A, K435T, G535D, I490T, R545C, and S978P significantly impair the lipid floppase and likely predispose to secondary pathologies in the human population.
    Andress EJ; Nicolaou M; McGeoghan F; Linton KJ
    Cell Mol Life Sci; 2017 Jul; 74(13):2513-2524. PubMed ID: 28220208
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. 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]  

  • 39. [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]  

  • 40. Novel resequencing chip customized to diagnose mutations in patients with inherited syndromes of intrahepatic cholestasis.
    Liu C; Aronow BJ; Jegga AG; Wang N; Miethke A; Mourya R; Bezerra JA
    Gastroenterology; 2007 Jan; 132(1):119-26. PubMed ID: 17241866
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.