BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 14670130)

  • 1. Lentiviral vector-mediated delivery of short hairpin RNA results in persistent knockdown of gene expression in mouse brain.
    Van den Haute C; Eggermont K; Nuttin B; Debyser Z; Baekelandt V
    Hum Gene Ther; 2003 Dec; 14(18):1799-807. PubMed ID: 14670130
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Stable RNA interference: comparison of U6 and H1 promoters in endothelial cells and in mouse brain.
    Mäkinen PI; Koponen JK; Kärkkäinen AM; Malm TM; Pulkkinen KH; Koistinaho J; Turunen MP; Ylä-Herttuala S
    J Gene Med; 2006 Apr; 8(4):433-41. PubMed ID: 16389634
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Gene transfer into the central nervous system in vivo using a recombinanat lentivirus vector.
    Lai Z; Brady RO
    J Neurosci Res; 2002 Feb; 67(3):363-71. PubMed ID: 11813241
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A lentivirus-based system to functionally silence genes in primary mammalian cells, stem cells and transgenic mice by RNA interference.
    Rubinson DA; Dillon CP; Kwiatkowski AV; Sievers C; Yang L; Kopinja J; Rooney DL; Zhang M; Ihrig MM; McManus MT; Gertler FB; Scott ML; Van Parijs L
    Nat Genet; 2003 Mar; 33(3):401-6. PubMed ID: 12590264
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Silencing of choline acetyltransferase expression by lentivirus-mediated RNA interference in cultured cells and in the adult rodent brain.
    Santamaria J; Khalfallah O; Sauty C; Brunet I; Sibieude M; Mallet J; Berrard S; Lecomte MJ
    J Neurosci Res; 2009 Feb; 87(2):532-44. PubMed ID: 18803282
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Characterization of lentiviral vector-mediated gene transfer in adult mouse brain.
    Baekelandt V; Claeys A; Eggermont K; Lauwers E; De Strooper B; Nuttin B; Debyser Z
    Hum Gene Ther; 2002 May; 13(7):841-53. PubMed ID: 11975850
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Lentivirus-mediated RNA interference therapy for human immunodeficiency virus type 1 infection.
    Morris KV; Rossi JJ
    Hum Gene Ther; 2006 May; 17(5):479-86. PubMed ID: 16716105
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Transgene expression in hypertrophied and aged skeletal muscle in vivo by lentivirus delivery.
    Ouyang J; Alway SE
    J Gene Med; 2004 Mar; 6(3):278-87. PubMed ID: 15026989
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Gene transfer in ovarian cancer cells: a comparison between retroviral and lentiviral vectors.
    Indraccolo S; Habeler W; Tisato V; Stievano L; Piovan E; Tosello V; Esposito G; Wagner R; Uberla K; Chieco-Bianchi L; Amadori A
    Cancer Res; 2002 Nov; 62(21):6099-107. PubMed ID: 12414634
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Lentiviral vector-mediated gene transfer and RNA silencing technology in neuronal dysfunctions.
    Dreyer JL
    Methods Mol Biol; 2010; 614():3-35. PubMed ID: 20225033
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Lentiviral-mediated RNA interference.
    Abbas-Terki T; Blanco-Bose W; Déglon N; Pralong W; Aebischer P
    Hum Gene Ther; 2002 Dec; 13(18):2197-201. PubMed ID: 12542850
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Development of gene therapy for treatment of age-related macular degeneration.
    Askou AL
    Acta Ophthalmol; 2014 Jul; 92 Thesis3():1-38. PubMed ID: 24953666
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Construction of a lentiviral vector for RNA interference of PRL-3 gene and its stable expression in SW480 cells].
    Liu YH; Li JM; Zhou J; Ding YQ
    Nan Fang Yi Ke Da Xue Xue Bao; 2008 Apr; 28(4):509-12. PubMed ID: 18495578
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Construction of simple and efficient DNA vector-based short hairpin RNA expression systems for specific gene silencing in mammalian cells.
    Cheng TL; Chang WT
    Methods Mol Biol; 2007; 408():223-41. PubMed ID: 18314586
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Stable transgene expression in tumors and metastases after transduction with lentiviral vectors based on human immunodeficiency virus type 1.
    Bao L; Jaligam V; Zhang XY; Kutner RH; Kantrow SP; Reiser J
    Hum Gene Ther; 2004 May; 15(5):445-56. PubMed ID: 15144575
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A miR-21 hairpin structure-based gene knockdown vector.
    Yue J; Sheng Y; Ren A; Penmatsa S
    Biochem Biophys Res Commun; 2010 Apr; 394(3):667-72. PubMed ID: 20226761
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A general method for gene knockdown in mice by using lentiviral vectors expressing small interfering RNA.
    Tiscornia G; Singer O; Ikawa M; Verma IM
    Proc Natl Acad Sci U S A; 2003 Feb; 100(4):1844-8. PubMed ID: 12552109
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prostate-tumor targeting of gene expression by lentiviral vectors containing elements of the probasin promoter.
    Yu D; Jia WW; Gleave ME; Nelson CC; Rennie PS
    Prostate; 2004 Jun; 59(4):370-82. PubMed ID: 15065085
    [TBL] [Abstract][Full Text] [Related]  

  • 19. RNAi-inducing lentiviral vectors for anti-HIV-1 gene therapy.
    Liu YP; Westerink JT; ter Brake O; Berkhout B
    Methods Mol Biol; 2011; 721():293-311. PubMed ID: 21431693
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Conditional RNAi Using the Lentiviral GLTR System.
    Pfeiffenberger E; Sigl R; Geley S
    Methods Mol Biol; 2016; 1448():121-38. PubMed ID: 27317178
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.