BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

451 related articles for article (PubMed ID: 11813241)

  • 1. 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]  

  • 2. Intercellular delivery of a herpes simplex virus VP22 fusion protein from cells infected with lentiviral vectors.
    Lai Z; Han I; Zirzow G; Brady RO; Reiser J
    Proc Natl Acad Sci U S A; 2000 Oct; 97(21):11297-302. PubMed ID: 11027330
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Efficient delivery of Cre-recombinase to neurons in vivo and stable transduction of neurons using adeno-associated and lentiviral vectors.
    Ahmed BY; Chakravarthy S; Eggers R; Hermens WT; Zhang JY; Niclou SP; Levelt C; Sablitzky F; Anderson PN; Lieberman AR; Verhaagen J
    BMC Neurosci; 2004 Jan; 5():4. PubMed ID: 15005815
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Adeno-associated virus and lentivirus vectors mediate efficient and sustained transduction of cultured mouse and human dorsal root ganglia sensory neurons.
    Fleming J; Ginn SL; Weinberger RP; Trahair TN; Smythe JA; Alexander IE
    Hum Gene Ther; 2001 Jan; 12(1):77-86. PubMed ID: 11177545
    [TBL] [Abstract][Full Text] [Related]  

  • 6. HSV-1 VP22 augments adenoviral gene transfer to CNS neurons in the retina and striatum in vivo.
    Kretz A; Wybranietz WA; Hermening S; Lauer UM; Isenmann S
    Mol Ther; 2003 May; 7(5 Pt 1):659-69. PubMed ID: 12718909
    [TBL] [Abstract][Full Text] [Related]  

  • 7. HIV-1-based defective lentiviral vectors efficiently transduce human monocytes-derived macrophages and suppress replication of wild-type HIV-1.
    Zeng L; Planelles V; Sui Z; Gartner S; Maggirwar SB; Dewhurst S; Ye L; Nerurkar VR; Yanagihara R; Lu Y
    J Gene Med; 2006 Jan; 8(1):18-28. PubMed ID: 16142830
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Development of multigene and regulated lentivirus vectors.
    Reiser J; Lai Z; Zhang XY; Brady RO
    J Virol; 2000 Nov; 74(22):10589-99. PubMed ID: 11044103
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 173(1):22-30. PubMed ID: 11771936
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Efficient gene transfer to human peripheral blood monocyte-derived dendritic cells using human immunodeficiency virus type 1-based lentiviral vectors.
    Chinnasamy N; Chinnasamy D; Toso JF; Lapointe R; Candotti F; Morgan RA; Hwu P
    Hum Gene Ther; 2000 Sep; 11(13):1901-9. PubMed ID: 10986562
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Neuron-specific gene transfer through retrograde transport of lentiviral vector pseudotyped with a novel type of fusion envelope glycoprotein.
    Kato S; Kuramochi M; Takasumi K; Kobayashi K; Inoue K; Takahara D; Hitoshi S; Ikenaka K; Shimada T; Takada M; Kobayashi K
    Hum Gene Ther; 2011 Dec; 22(12):1511-23. PubMed ID: 21806473
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Transgene expression in the guinea pig cochlea mediated by a lentivirus-derived gene transfer vector.
    Han JJ; Mhatre AN; Wareing M; Pettis R; Gao WQ; Zufferey RN; Trono D; Lalwani AK
    Hum Gene Ther; 1999 Jul; 10(11):1867-73. PubMed ID: 10446926
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Specific transgene expression in human and mouse CD4+ cells using lentiviral vectors with regulatory sequences from the CD4 gene.
    Marodon G; Mouly E; Blair EJ; Frisen C; Lemoine FM; Klatzmann D
    Blood; 2003 May; 101(9):3416-23. PubMed ID: 12511423
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Simian immunodeficiency virus vector pseudotypes differ in transduction efficiency and target cell specificity in brain.
    Liehl B; Hlavaty J; Moldzio R; Tonar Z; Unger H; Salmons B; Günzburg WH; Renner M
    Gene Ther; 2007 Sep; 14(18):1330-43. PubMed ID: 17611586
    [TBL] [Abstract][Full Text] [Related]  

  • 15. High levels of transgene expression following transduction of long-term NOD/SCID-repopulating human cells with a modified lentiviral vector.
    Gao Z; Golob J; Tanavde VM; Civin CI; Hawley RG; Cheng L
    Stem Cells; 2001; 19(3):247-59. PubMed ID: 11359950
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Efficient transduction of neurons using Ross River glycoprotein-pseudotyped lentiviral vectors.
    Jakobsson J; Nielsen TT; Staflin K; Georgievska B; Lundberg C
    Gene Ther; 2006 Jun; 13(12):966-73. PubMed ID: 16511527
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Lentivirus-mediated gene transfer and expression in established human tumor antigen-specific cytotoxic T cells and primary unstimulated T cells.
    Zhou X; Cui Y; Huang X; Yu Z; Thomas AM; Ye Z; Pardoll DM; Jaffee EM; Cheng L
    Hum Gene Ther; 2003 Jul; 14(11):1089-105. PubMed ID: 12885348
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Multiply attenuated, self-inactivating lentiviral vectors efficiently transduce human coronary artery cells in vitro and rat arteries in vivo.
    Céfaï D; Simeoni E; Ludunge KM; Driscoll R; von Segesser LK; Kappenberger L; Vassalli G
    J Mol Cell Cardiol; 2005 Feb; 38(2):333-44. PubMed ID: 15698840
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Tropism, intracerebral distribution, and transduction efficiency of HIV- and SIV-based lentiviral vectors after injection into the mouse brain: a qualitative and quantitative in vivo study.
    Hlavatý J; Tonar Z; Renner M; Panitz S; Petznek H; Schweizer M; Schüle S; Kloke BP; Moldzio R; Witter K
    Histochem Cell Biol; 2017 Sep; 148(3):313-329. PubMed ID: 28397143
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Engineered lentiviral vector targeting astrocytes in vivo.
    Colin A; Faideau M; Dufour N; Auregan G; Hassig R; Andrieu T; Brouillet E; Hantraye P; Bonvento G; Déglon N
    Glia; 2009 Apr; 57(6):667-79. PubMed ID: 18942755
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 23.