BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

265 related articles for article (PubMed ID: 29272432)

  • 1. Inhibition of antigen presentation during AAV gene therapy using virus peptides.
    Shao W; Chen X; Samulski RJ; Hirsch ML; Li C
    Hum Mol Genet; 2018 Feb; 27(4):601-613. PubMed ID: 29272432
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cytotoxic-T-lymphocyte-mediated elimination of target cells transduced with engineered adeno-associated virus type 2 vector in vivo.
    Li C; Hirsch M; DiPrimio N; Asokan A; Goudy K; Tisch R; Samulski RJ
    J Virol; 2009 Jul; 83(13):6817-24. PubMed ID: 19369348
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Dual AAV Gene Therapy for Duchenne Muscular Dystrophy with a 7-kb Mini-Dystrophin Gene in the Canine Model.
    Kodippili K; Hakim CH; Pan X; Yang HT; Yue Y; Zhang Y; Shin JH; Yang NN; Duan D
    Hum Gene Ther; 2018 Mar; 29(3):299-311. PubMed ID: 28793798
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Sustained AAV-mediated dystrophin expression in a canine model of Duchenne muscular dystrophy with a brief course of immunosuppression.
    Wang Z; Kuhr CS; Allen JM; Blankinship M; Gregorevic P; Chamberlain JS; Tapscott SJ; Storb R
    Mol Ther; 2007 Jun; 15(6):1160-6. PubMed ID: 17426713
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Gene therapy for muscular dystrophy].
    Takeda S
    No To Hattatsu; 2004 Mar; 36(2):117-23. PubMed ID: 15031985
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Triple trans-splicing adeno-associated virus vectors capable of transferring the coding sequence for full-length dystrophin protein into dystrophic mice.
    Koo T; Popplewell L; Athanasopoulos T; Dickson G
    Hum Gene Ther; 2014 Feb; 25(2):98-108. PubMed ID: 24191945
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Full-length dystrophin reconstitution with adeno-associated viral vectors.
    Lostal W; Kodippili K; Yue Y; Duan D
    Hum Gene Ther; 2014 Jun; 25(6):552-62. PubMed ID: 24580018
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The Effect of Immunomodulatory Treatments on Anti-Dystrophin Immune Response After AAV Gene Therapy in Dystrophin Deficient mdx Mice.
    Li N; Parkes JE; Spathis R; Morales M; Mcdonald J; Kendra RM; Ott EM; Brown KJ; Lawlor MW; Nagaraju K
    J Neuromuscul Dis; 2021; 8(s2):S325-S340. PubMed ID: 34569971
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The AAV-mediated and RNA-guided CRISPR/Cas9 system for gene therapy of DMD and BMD.
    Wang JZ; Wu P; Shi ZM; Xu YL; Liu ZJ
    Brain Dev; 2017 Aug; 39(7):547-556. PubMed ID: 28390761
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cytotoxic T lymphocyte responses to transgene product, not adeno-associated viral capsid protein, limit transgene expression in mice.
    Siders WM; Shields J; Kaplan J; Lukason M; Woodworth L; Wadsworth S; Scaria A
    Hum Gene Ther; 2009 Jan; 20(1):11-20. PubMed ID: 18828728
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Effective suppression of class I major histocompatibility complex expression by the US11 or ICP47 genes can be limited by cell type or interferon-gamma exposure.
    Radosevich TJ; Seregina T; Link CJ
    Hum Gene Ther; 2003 Dec; 14(18):1765-75. PubMed ID: 14670127
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A simplified immune suppression scheme leads to persistent micro-dystrophin expression in Duchenne muscular dystrophy dogs.
    Shin JH; Yue Y; Srivastava A; Smith B; Lai Y; Duan D
    Hum Gene Ther; 2012 Feb; 23(2):202-9. PubMed ID: 21967249
    [TBL] [Abstract][Full Text] [Related]  

  • 14. CTLA4Ig delivered by high-capacity adenoviral vector induces stable expression of dystrophin in mdx mouse muscle.
    Jiang Z; Schiedner G; Gilchrist SC; Kochanek S; Clemens PR
    Gene Ther; 2004 Oct; 11(19):1453-61. PubMed ID: 15269713
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Recombinant adeno-associated viral (rAAV) vectors as therapeutic tools for Duchenne muscular dystrophy (DMD).
    Athanasopoulos T; Graham IR; Foster H; Dickson G
    Gene Ther; 2004 Oct; 11 Suppl 1():S109-21. PubMed ID: 15454965
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genomic removal of a therapeutic mini-dystrophin gene from adult mice elicits a Duchenne muscular dystrophy-like phenotype.
    Wasala NB; Lai Y; Shin JH; Zhao J; Yue Y; Duan D
    Hum Mol Genet; 2016 Jul; 25(13):2633-2644. PubMed ID: 27106099
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Expression of herpes simplex virus ICP47 and human cytomegalovirus US11 prevents recognition of transgene products by CD8(+) cytotoxic T lymphocytes.
    Berger C; Xuereb S; Johnson DC; Watanabe KS; Kiem HP; Greenberg PD; Riddell SR
    J Virol; 2000 May; 74(10):4465-73. PubMed ID: 10775582
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Adeno-associated virus vector carrying human minidystrophin genes effectively ameliorates muscular dystrophy in mdx mouse model.
    Wang B; Li J; Xiao X
    Proc Natl Acad Sci U S A; 2000 Dec; 97(25):13714-9. PubMed ID: 11095710
    [TBL] [Abstract][Full Text] [Related]  

  • 19. TAP-inhibiting proteins US6, ICP47 and UL49.5 differentially affect minor and major histocompatibility antigen-specific recognition by cytotoxic T lymphocytes.
    Oosten LE; Koppers-Lalic D; Blokland E; Mulder A; Ressing ME; Mutis T; van Halteren AG; Wiertz EJ; Goulmy E
    Int Immunol; 2007 Sep; 19(9):1115-22. PubMed ID: 17855435
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Microdystrophin gene therapy of cardiomyopathy restores dystrophin-glycoprotein complex and improves sarcolemma integrity in the mdx mouse heart.
    Yue Y; Li Z; Harper SQ; Davisson RL; Chamberlain JS; Duan D
    Circulation; 2003 Sep; 108(13):1626-32. PubMed ID: 12952841
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.