These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

649 related articles for article (PubMed ID: 16688207)

  • 21. Long-term gene transfer to mouse fetuses with recombinant adenovirus and adeno-associated virus (AAV) vectors.
    Mitchell M; Jerebtsova M; Batshaw ML; Newman K; Ye X
    Gene Ther; 2000 Dec; 7(23):1986-92. PubMed ID: 11175309
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Regulation of gene expression in vivo following transduction by two separate rAAV vectors.
    Rendahl KG; Leff SE; Otten GR; Spratt SK; Bohl D; Van Roey M; Donahue BA; Cohen LK; Mandel RJ; Danos O; Snyder RO
    Nat Biotechnol; 1998 Aug; 16(8):757-61. PubMed ID: 9702775
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Enhanced transduction of mouse bone marrow-derived dendritic cells by repetitive infection with self-complementary adeno-associated virus 6 combined with immunostimulatory ligands.
    Aldrich WA; Ren C; White AF; Zhou SZ; Kumar S; Jenkins CB; Shaw DR; Strong TV; Triozzi PL; Ponnazhagan S
    Gene Ther; 2006 Jan; 13(1):29-39. PubMed ID: 16136165
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Enhancing rAAV vector expression in the lung.
    Virella-Lowell I; Zusman B; Foust K; Loiler S; Conlon T; Song S; Chesnut KA; Ferkol T; Flotte TR
    J Gene Med; 2005 Jul; 7(7):842-50. PubMed ID: 15838934
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Theodore E. Woodward Award. AAV-mediated gene transfer for hemophilia.
    High KA
    Trans Am Clin Climatol Assoc; 2003; 114():337-51; discussion 351-2. PubMed ID: 12813929
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Efficient gene transfer in skeletal muscle with AAV-derived bicistronic vector using the FGF-1 IRES.
    Delluc-Clavières A; Le Bec C; Van den Berghe L; Conte C; Allo V; Danos O; Prats AC
    Gene Ther; 2008 Aug; 15(15):1090-8. PubMed ID: 18369321
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Adeno-associated virus vector-mediated gene transfer into dystrophin-deficient skeletal muscles evokes enhanced immune response against the transgene product.
    Yuasa K; Sakamoto M; Miyagoe-Suzuki Y; Tanouchi A; Yamamoto H; Li J; Chamberlain JS; Xiao X; Takeda S
    Gene Ther; 2002 Dec; 9(23):1576-88. PubMed ID: 12424610
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Systemic AAV-9 transduction in mice is influenced by animal age but not by the route of administration.
    Bostick B; Ghosh A; Yue Y; Long C; Duan D
    Gene Ther; 2007 Nov; 14(22):1605-9. PubMed ID: 17898796
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Circulating anti-wild-type adeno-associated virus type 2 (AAV2) antibodies inhibit recombinant AAV2 (rAAV2)-mediated, but not rAAV5-mediated, gene transfer in the brain.
    Peden CS; Burger C; Muzyczka N; Mandel RJ
    J Virol; 2004 Jun; 78(12):6344-59. PubMed ID: 15163728
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Correction of glycogen storage disease type II by an adeno-associated virus vector containing a muscle-specific promoter.
    Sun B; Zhang H; Franco LM; Brown T; Bird A; Schneider A; Koeberl DD
    Mol Ther; 2005 Jun; 11(6):889-98. PubMed ID: 15922959
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Femoral intra-arterial injection: a tool to deliver and assess recombinant AAV constructs in rodents whole hind limb.
    Gonin P; Arandel L; Van Wittenberghe L; Marais T; Perez N; Danos O
    J Gene Med; 2005 Jun; 7(6):782-91. PubMed ID: 15693034
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Adeno-associated virus vectors serotyped with AAV8 capsid are more efficient than AAV-1 or -2 serotypes for widespread gene delivery to the neonatal mouse brain.
    Broekman ML; Comer LA; Hyman BT; Sena-Esteves M
    Neuroscience; 2006; 138(2):501-10. PubMed ID: 16414198
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Persistent expression of canine factor IX in hemophilia B canines.
    Chao H; Samulski R; Bellinger D; Monahan P; Nichols T; Walsh C
    Gene Ther; 1999 Oct; 6(10):1695-704. PubMed ID: 10516718
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Use of helper-dependent adenoviral vectors of alternative serotypes permits repeat vector administration.
    Parks R; Evelegh C; Graham F
    Gene Ther; 1999 Sep; 6(9):1565-73. PubMed ID: 10490766
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Recombinant adeno-associated virus serotype 9 leads to preferential cardiac transduction in vivo.
    Pacak CA; Mah CS; Thattaliyath BD; Conlon TJ; Lewis MA; Cloutier DE; Zolotukhin I; Tarantal AF; Byrne BJ
    Circ Res; 2006 Aug; 99(4):e3-9. PubMed ID: 16873720
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Gene therapy for new bone formation using adeno-associated viral bone morphogenetic protein-2 vectors.
    Chen Y; Luk KD; Cheung KM; Xu R; Lin MC; Lu WW; Leong JC; Kung HF
    Gene Ther; 2003 Aug; 10(16):1345-53. PubMed ID: 12883531
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Comparison of the ability of adeno-associated viral vectors pseudotyped with serotype 2, 5, and 8 capsid proteins to mediate efficient transduction of the liver in murine and nonhuman primate models.
    Davidoff AM; Gray JT; Ng CY; Zhang Y; Zhou J; Spence Y; Bakar Y; Nathwani AC
    Mol Ther; 2005 Jun; 11(6):875-88. PubMed ID: 15922958
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Adeno-associated virus-mediated delivery of IL-4 prevents collagen-induced arthritis.
    Cottard V; Mulleman D; Bouille P; Mezzina M; Boissier MC; Bessis N
    Gene Ther; 2000 Nov; 7(22):1930-9. PubMed ID: 11127581
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Long-term correction of murine glycogen storage disease type Ia by recombinant adeno-associated virus-1-mediated gene transfer.
    Ghosh A; Allamarvdasht M; Pan CJ; Sun MS; Mansfield BC; Byrne BJ; Chou JY
    Gene Ther; 2006 Feb; 13(4):321-9. PubMed ID: 16195703
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Recombinant adeno-associated virus type 2 mediates highly efficient gene transfer in regenerating rat skeletal muscle.
    Abadie J; Blouin V; Guigand L; Wyers M; Cherel Y
    Gene Ther; 2002 Aug; 9(15):1037-43. PubMed ID: 12101435
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 33.