BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 10933978)

  • 1. Introduction of a xenogeneic gene via hematopoietic stem cells leads to specific tolerance in a rhesus monkey model.
    Heim DA; Hanazono Y; Giri N; Wu T; Childs R; Sellers SE; Muul L; Agricola BA; Metzger ME; Donahue RE; Tisdale JF; Dunbar CE
    Mol Ther; 2000 Jun; 1(6):533-44. PubMed ID: 10933978
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Persistent low-level engraftment of rhesus peripheral blood progenitor cells transduced with the fanconi anemia C gene after conditioning with low-dose irradiation.
    Kang EM; Hanazano Y; Frare P; Vanin EF; De Witte M; Metzger M; Liu JM; Tisdale JF
    Mol Ther; 2001 Jun; 3(6):911-9. PubMed ID: 11407905
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Introduction of the green fluorescent protein gene into hematopoietic stem cells results in prolonged discrepancy of in vivo transduction levels between bone marrow progenitors and peripheral blood cells in nonhuman primates.
    Hanazono Y; Terao K; Shibata H; Nagashima T; Ageyama N; Asano T; Ueda Y; Kato I; Kume A; Hasegawa M; Ozawa K
    J Gene Med; 2002; 4(5):470-7. PubMed ID: 12221639
    [TBL] [Abstract][Full Text] [Related]  

  • 4. In vivo persistence of retrovirally transduced murine long-term repopulating cells is not limited by expression of foreign gene products in the fully or minimally myeloablated setting.
    Kang E; Giri N; Wu T; Sellers S; Kirby M; Hanazono Y; Tisdale J; Dunbar CE
    Hum Gene Ther; 2001 Sep; 12(13):1663-72. PubMed ID: 11535169
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Comparison of five retrovirus vectors containing the human IL-2 receptor gamma chain gene for their ability to restore T and B lymphocytes in the X-linked severe combined immunodeficiency mouse model.
    Avilés Mendoza GJ; Seidel NE; Otsu M; Anderson SM; Simon-Stoos K; Herrera A; Hoogstraten-Miller S; Malech HL; Candotti F; Puck JM; Bodine DM
    Mol Ther; 2001 Apr; 3(4):565-73. PubMed ID: 11319919
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Gene transfer into nonhuman primate hematopoietic stem cells: implications for gene therapy.
    Hanazono Y; Terao K; Ozawa K
    Stem Cells; 2001; 19(1):12-23. PubMed ID: 11209087
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Inhibition of simian/human immunodeficiency virus replication in CD4+ T cells derived from lentiviral-transduced CD34+ hematopoietic cells.
    Braun SE; Wong FE; Connole M; Qiu G; Lee L; Gillis J; Lu X; Humeau L; Slepushkin V; Binder GK; Dropulic B; Johnson RP
    Mol Ther; 2005 Dec; 12(6):1157-67. PubMed ID: 16168713
    [TBL] [Abstract][Full Text] [Related]  

  • 8. In vivo gene marking of rhesus macaque long-term repopulating hematopoietic cells using a VSV-G pseudotyped versus amphotropic oncoretroviral vector.
    Shi PA; De Angioletti M; Donahue RE; Notaro R; Luzzatto L; Dunbar CE
    J Gene Med; 2004 Apr; 6(4):367-73. PubMed ID: 15079811
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Efficient engraftment of in utero transplanted mice with retrovirally transduced hematopoietic stem cells.
    Rio P; Martinez-Palacio J; Ramirez A; Bueren JA; Segovia JC
    Gene Ther; 2005 Feb; 12(4):358-63. PubMed ID: 15550924
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Inhibition of CD26 peptidase activity significantly improves engraftment of retrovirally transduced hematopoietic progenitors.
    Tian C; Bagley J; Forman D; Iacomini J
    Gene Ther; 2006 Apr; 13(7):652-8. PubMed ID: 16341058
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Adeno-associated virus 2-mediated transduction and erythroid lineage-restricted long-term expression of the human beta-globin gene in hematopoietic cells from homozygous beta-thalassemic mice.
    Tan M; Qing K; Zhou S; Yoder MC; Srivastava A
    Mol Ther; 2001 Jun; 3(6):940-6. PubMed ID: 11407908
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sustained transgene expression by human cord blood derived CD34+ cells transduced with simian immunodeficiency virus agmTYO1-based vectors carrying the human coagulation factor VIII gene in NOD/SCID mice.
    Kikuchi J; Mimuro J; Ogata K; Tabata T; Ueda Y; Ishiwata A; Kimura K; Takano K; Madoiwa S; Mizukami H; Hanazono Y; Kume A; Hasegawa M; Ozawa K; Sakata Y
    J Gene Med; 2004 Oct; 6(10):1049-60. PubMed ID: 15386735
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Influence of multiplicity of infection and protein stability on retroviral vector-mediated gene expression in hematopoietic cells.
    Wahlers A; Schwieger M; Li Z; Meier-Tackmann D; Lindemann C; Eckert HG; von Laer D; Baum C
    Gene Ther; 2001 Mar; 8(6):477-86. PubMed ID: 11313827
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Long-term follow-up of gene-marked CD34+ cells after autologous stem cell transplantation for multiple myeloma.
    Alici E; Björkstrand B; Treschow A; Aints A; Smith CI; Gahrton G; Dilber MS
    Cancer Gene Ther; 2007 Mar; 14(3):227-32. PubMed ID: 17082794
    [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. Highly efficient gene transfer into preterm CD34 hematopoietic progenitor cells.
    Shields LE; Kiem HP; Andrews RG
    Am J Obstet Gynecol; 2000 Sep; 183(3):732-7. PubMed ID: 10992201
    [TBL] [Abstract][Full Text] [Related]  

  • 17. In vivo selective expansion of gene-modified hematopoietic cells in a nonhuman primate model.
    Hanazono Y; Nagashima T; Takatoku M; Shibata H; Ageyama N; Asano T; Ueda Y; Dunbar CE; Kume A; Terao K; Hasegawa M; Ozawa K
    Gene Ther; 2002 Aug; 9(16):1055-64. PubMed ID: 12140733
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Deficiency of oncoretrovirally transduced hematopoietic stem cells and correction through ex vivo expansion.
    Bryder D; Björgvinsdóttir H; Sasaki Y; Jacobsen SE
    J Gene Med; 2005 Feb; 7(2):137-44. PubMed ID: 15538726
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Drug-selected co-expression of P-glycoprotein and gp91 in vivo from an MDR1-bicistronic retrovirus vector Ha-MDR-IRES-gp91.
    Sugimoto Y; Tsukahara S; Sato S; Suzuki M; Nunoi H; Malech HL; Gottesman MM; Tsuruo T
    J Gene Med; 2003 May; 5(5):366-76. PubMed ID: 12731085
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Immunity to islet grafts transduced with adenovirus vectors does not inhibit long-term islet function.
    Cheng J; Sun J; Sung RS
    Transpl Immunol; 2009 May; 21(1):33-42. PubMed ID: 19224710
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.