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Journal Abstract Search

280 related items for PubMed ID: 17006327

  • 1. Ex vivo lentivirus transduction and immediate transplantation of uncultured hepatocytes for treating hyperbilirubinemic Gunn rat.
    Nguyen TH, Birraux J, Wildhaber B, Myara A, Trivin F, Le Coultre C, Trono D, Chardot C.
    Transplantation; 2006 Sep 27; 82(6):794-803. PubMed ID: 17006327
    [Abstract] [Full Text] [Related]

  • 2. Therapeutic lentivirus-mediated neonatal in vivo gene therapy in hyperbilirubinemic Gunn rats.
    Nguyen TH, Bellodi-Privato M, Aubert D, Pichard V, Myara A, Trono D, Ferry N.
    Mol Ther; 2005 Nov 27; 12(5):852-9. PubMed ID: 16140582
    [Abstract] [Full Text] [Related]

  • 3. Repopulation of rat liver by fetal hepatoblasts and adult hepatocytes transduced ex vivo with lentiviral vectors.
    Oertel M, Rosencrantz R, Chen YQ, Thota PN, Sandhu JS, Dabeva MD, Pacchia AL, Adelson ME, Dougherty JP, Shafritz DA.
    Hepatology; 2003 May 27; 37(5):994-1005. PubMed ID: 12717380
    [Abstract] [Full Text] [Related]

  • 4. A step toward liver gene therapy: efficient correction of the genetic defect of hepatocytes isolated from a patient with Crigler-Najjar syndrome type 1 with lentiviral vectors.
    Birraux J, Menzel O, Wildhaber B, Jond C, Nguyen TH, Chardot C.
    Transplantation; 2009 Apr 15; 87(7):1006-12. PubMed ID: 19352119
    [Abstract] [Full Text] [Related]

  • 5. Complete correction of hyperbilirubinemia in the Gunn rat model of Crigler-Najjar syndrome type I following transient in vivo adenovirus-mediated expression of human bilirubin UDP-glucuronosyltransferase.
    Askari FK, Hitomi Y, Mao M, Wilson JM.
    Gene Ther; 1996 May 15; 3(5):381-8. PubMed ID: 9156798
    [Abstract] [Full Text] [Related]

  • 6. Efficient ex vivo gene transfer into non-human primate hepatocytes using HIV-1 derived lentiviral vectors.
    Parouchev A, Nguyen TH, Dagher I, Mainot S, Groyer-Picard MT, Branger J, Gonin P, Di Santo J, Franco D, Gras G, Weber A.
    J Hepatol; 2006 Jul 15; 45(1):99-107. PubMed ID: 16723167
    [Abstract] [Full Text] [Related]

  • 7. Lentiviral vectors that express UGT1A1 in liver and contain miR-142 target sequences normalize hyperbilirubinemia in Gunn rats.
    Schmitt F, Remy S, Dariel A, Flageul M, Pichard V, Boni S, Usal C, Myara A, Laplanche S, Anegon I, Labrune P, Podevin G, Ferry N, Nguyen TH.
    Gastroenterology; 2010 Sep 15; 139(3):999-1007, 1007.e1-2. PubMed ID: 20546738
    [Abstract] [Full Text] [Related]

  • 8. Successful gene therapy of the Gunn rat by in vivo neonatal hepatic gene transfer using murine oncoretroviral vectors.
    Bellodi-Privato M, Aubert D, Pichard V, Myara A, Trivin F, Ferry N.
    Hepatology; 2005 Aug 15; 42(2):431-8. PubMed ID: 16025517
    [Abstract] [Full Text] [Related]

  • 9. A highly efficient, stable, and rapid approach for ex vivo human liver gene therapy via a FLAP lentiviral vector.
    Giannini C, Morosan S, Tralhao JG, Guidotti JE, Battaglia S, Mollier K, Hannoun L, Kremsdorf D, Gilgenkrantz H, Charneau P.
    Hepatology; 2003 Jul 15; 38(1):114-22. PubMed ID: 12829993
    [Abstract] [Full Text] [Related]

  • 10. A new surgical approach to improve gene transfer in liver using lentiviral vectors.
    Dariel A, Nguyen TH, Pichard V, Schmitt F, Aubert D, Ferry N, Podevin G.
    J Pediatr Surg; 2009 Mar 15; 44(3):517-22. PubMed ID: 19302851
    [Abstract] [Full Text] [Related]

  • 11. Critical assessment of lifelong phenotype correction in hyperbilirubinemic Gunn rats after retroviral mediated gene transfer.
    Nguyen TH, Aubert D, Bellodi-Privato M, Flageul M, Pichard V, Jaidane-Abdelghani Z, Myara A, Ferry N.
    Gene Ther; 2007 Sep 15; 14(17):1270-7. PubMed ID: 17611583
    [Abstract] [Full Text] [Related]

  • 12. [Correction of bilirubin glucuronyl transferase in Gunn rats by gene transfer in the liver using retroviral vectors].
    Branchereau S, Ferry N, Myara A, Sato H, Kowai O, Trivin F, Houssin D, Danos O, Heard J.
    Chirurgie; 2007 Sep 15; 119(10):642-8. PubMed ID: 7729182
    [Abstract] [Full Text] [Related]

  • 13. Retrovirus-mediated expression of HUG Br1 in Crigler-Najjar syndrome type I human fibroblasts and correction of the genetic defect in Gunn rat hepatocytes.
    Askari F, Hitomi E, Thiney M, Wilson JM.
    Gene Ther; 1995 May 15; 2(3):203-8. PubMed ID: 7614251
    [Abstract] [Full Text] [Related]

  • 14. Immune response to lentiviral bilirubin UDP-glucuronosyltransferase gene transfer in fetal and neonatal rats.
    Seppen J, van Til NP, van der Rijt R, Hiralall JK, Kunne C, Elferink RP.
    Gene Ther; 2006 Apr 15; 13(8):672-7. PubMed ID: 16267566
    [Abstract] [Full Text] [Related]

  • 15. Shuttle of lentiviral vectors via transplanted cells in vivo.
    Blömer U, Gruh I, Witschel H, Haverich A, Martin U.
    Gene Ther; 2005 Jan 15; 12(1):67-74. PubMed ID: 15385952
    [Abstract] [Full Text] [Related]

  • 16. Ex vivo and in vitro studies of transgene expression in rat astrocytes transduced with lentiviral vectors.
    Ericson C, Wictorin K, Lundberg C.
    Exp Neurol; 2002 Jan 15; 173(1):22-30. PubMed ID: 11771936
    [Abstract] [Full Text] [Related]

  • 17. Conditional immortalization of Gunn rat hepatocytes: an ex vivo model for evaluating methods for bilirubin-UDP-glucuronosyltransferase gene transfer.
    Fox IJ, Chowdhury NR, Gupta S, Kondapalli R, Schilsky ML, Stockert RJ, Chowdhury JR.
    Hepatology; 1995 Mar 15; 21(3):837-46. PubMed ID: 7875682
    [Abstract] [Full Text] [Related]

  • 18. Successful treatment of UGT1A1 deficiency in a rat model of Crigler-Najjar disease by intravenous administration of a liver-specific lentiviral vector.
    van der Wegen P, Louwen R, Imam AM, Buijs-Offerman RM, Sinaasappel M, Grosveld F, Scholte BJ.
    Mol Ther; 2006 Feb 15; 13(2):374-81. PubMed ID: 16337205
    [Abstract] [Full Text] [Related]

  • 19. Human neonatal hepatocyte transplantation induces long-term rescue of unconjugated hyperbilirubinemia in the Gunn rat.
    Tolosa L, López S, Pareja E, Donato MT, Myara A, Nguyen TH, Castell JV, Gómez-Lechón MJ.
    Liver Transpl; 2015 Jun 15; 21(6):801-11. PubMed ID: 25821167
    [Abstract] [Full Text] [Related]

  • 20. Therapeutic effect of transplanting beta(2)m(-)/Thy1(+) bone marrow-derived hepatocyte stem cells transduced with lentiviral-mediated HGF gene into CCl(4)-injured rats.
    Hu JJ, Sun C, Lan L, Chen YW, Li DG.
    J Gene Med; 2010 Mar 15; 12(3):244-54. PubMed ID: 20143305
    [Abstract] [Full Text] [Related]

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