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Journal Abstract Search

105 related items for PubMed ID: 15975851

  • 1. Promoter dependence of plasmid-pluronics targeted alpha galactosidase A expression in skeletal muscle of Fabry mice.
    Lavigne MD, Pohlschmidt M, Novo JF, Higgins B, Alakhov V, Lochmuller H, Sakuraba H, Goldspink G, MacDermot K, Górecki DC.
    Mol Ther; 2005 Nov; 12(5):985-90. PubMed ID: 15975851
    [No Abstract] [Full Text] [Related]

  • 2. Partial correction of the alpha-galactosidase A deficiency and reduction of glycolipid storage in Fabry mice using synthetic vectors.
    Przybylska M, Wu IH, Zhao H, Ziegler RJ, Tousignant JD, Desnick RJ, Scheule RK, Cheng SH, Yew NS.
    J Gene Med; 2004 Jan; 6(1):85-92. PubMed ID: 14716680
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  • 3. Transient siRNA-mediated attenuation of liver expression from an alpha-galactosidase A plasmid reduces subsequent humoral immune responses to the transgene product in mice.
    Chu Q, Joseph M, Przybylska M, Yew NS, Scheule RK.
    Mol Ther; 2005 Aug; 12(2):264-73. PubMed ID: 15946902
    [Abstract] [Full Text] [Related]

  • 4. Long-term systemic therapy of Fabry disease in a knockout mouse by adeno-associated virus-mediated muscle-directed gene transfer.
    Takahashi H, Hirai Y, Migita M, Seino Y, Fukuda Y, Sakuraba H, Kase R, Kobayashi T, Hashimoto Y, Shimada T.
    Proc Natl Acad Sci U S A; 2002 Oct 15; 99(21):13777-82. PubMed ID: 12370426
    [Abstract] [Full Text] [Related]

  • 5. Promoter-specific lentivectors for long-term, cardiac-directed therapy of Fabry disease.
    Lee CJ, Fan X, Guo X, Medin JA.
    J Cardiol; 2011 Jan 15; 57(1):115-22. PubMed ID: 20846825
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  • 7. Efficient correction of Fabry mice and patient cells mediated by lentiviral transduction of hematopoietic stem/progenitor cells.
    Yoshimitsu M, Higuchi K, Ramsubir S, Nonaka T, Rasaiah VI, Siatskas C, Liang SB, Murray GJ, Brady RO, Medin JA.
    Gene Ther; 2007 Feb 15; 14(3):256-65. PubMed ID: 16929352
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  • 9. 4-Phenylbutyrate rescues trafficking incompetent mutant alpha-galactosidase A without restoring its functionality.
    Yam GH, Roth J, Zuber C.
    Biochem Biophys Res Commun; 2007 Aug 24; 360(2):375-80. PubMed ID: 17592721
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  • 10. AAV2 vector harboring a liver-restricted promoter facilitates sustained expression of therapeutic levels of alpha-galactosidase A and the induction of immune tolerance in Fabry mice.
    Ziegler RJ, Lonning SM, Armentano D, Li C, Souza DW, Cherry M, Ford C, Barbon CM, Desnick RJ, Gao G, Wilson JM, Peluso R, Godwin S, Carter BJ, Gregory RJ, Wadsworth SC, Cheng SH.
    Mol Ther; 2004 Feb 24; 9(2):231-40. PubMed ID: 14759807
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  • 15. [Fabry disease].
    Jakubowska E, Ryba M, Hruby Z.
    Przegl Lek; 2006 Feb 24; 63(4):218-9. PubMed ID: 17080745
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  • 19. Fabry disease: clinical features and recent advances in enzyme replacement therapy.
    Desnick RJ, Wasserstein MP.
    Adv Nephrol Necker Hosp; 2001 Feb 24; 31():317-39. PubMed ID: 11692469
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  • 20. Promoter- and strain-selective enhancement of gene expression in a mouse skeletal muscle by a polymer excipient Pluronic P85.
    Yang Z, Zhu J, Sriadibhatla S, Gebhart C, Alakhov V, Kabanov A.
    J Control Release; 2005 Nov 28; 108(2-3):496-512. PubMed ID: 16154658
    [Abstract] [Full Text] [Related]

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