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Journal Abstract Search

377 related items for PubMed ID: 19293460

  • 21. Efficient transduction of hematopoietic stem cells and its potential for gene correction of hematopoietic diseases.
    Thomas D, Mostoslavsky G.
    Methods Mol Biol; 2014; 1114():441-50. PubMed ID: 24557921
    [Abstract] [Full Text] [Related]

  • 22. Fetal hematopoietic stem cell transplantation: a challenge for the twenty-first century.
    Shields LE, Lindton B, Andrews RG, Westgren M.
    J Hematother Stem Cell Res; 2002 Aug; 11(4):617-31. PubMed ID: 12201950
    [Abstract] [Full Text] [Related]

  • 23. Reprogramming based gene therapy for inherited red blood cell disorders.
    Xu X, Qu J, Suzuki K, Li M, Zhang W, Liu GH, Izpisua Belmonte JC.
    Cell Res; 2012 Jun; 22(6):941-4. PubMed ID: 22473006
    [No Abstract] [Full Text] [Related]

  • 24. Gene therapy of Fanconi anemia: preclinical efficacy using lentiviral vectors.
    Galimi F, Noll M, Kanazawa Y, Lax T, Chen C, Grompe M, Verma IM.
    Blood; 2002 Oct 15; 100(8):2732-6. PubMed ID: 12351379
    [Abstract] [Full Text] [Related]

  • 25. Clinical gene therapy in hematology: past and future.
    Richter J, Karlsson S.
    Int J Hematol; 2001 Feb 15; 73(2):162-9. PubMed ID: 11372727
    [Abstract] [Full Text] [Related]

  • 26. New perspectives in gene therapy for inherited disorders.
    Cicalese MP, Aiuti A.
    Pediatr Allergy Immunol; 2020 Feb 15; 31 Suppl 24():5-7. PubMed ID: 32017225
    [Abstract] [Full Text] [Related]

  • 27. Large animal models for foamy virus vector gene therapy.
    Trobridge GD, Horn PA, Beard BC, Kiem HP.
    Viruses; 2012 Dec 07; 4(12):3572-88. PubMed ID: 23223198
    [Abstract] [Full Text] [Related]

  • 28. Contemporary Animal Models For Human Gene Therapy Applications.
    Gopinath C, Nathar TJ, Ghosh A, Hickstein DD, Nelson EJR.
    Curr Gene Ther; 2015 Dec 07; 15(6):531-40. PubMed ID: 26415576
    [Abstract] [Full Text] [Related]

  • 29. Advances in the gene therapy of monogenic blood cell diseases.
    Bueren JA, Quintana-Bustamante O, Almarza E, Navarro S, Río P, Segovia JC, Guenechea G.
    Clin Genet; 2020 Jan 07; 97(1):89-102. PubMed ID: 31231794
    [Abstract] [Full Text] [Related]

  • 30. Gene therapy for canine leukocyte adhesion deficiency with lentiviral vectors using the murine stem cell virus and human phosphoglycerate kinase promoters.
    Hunter MJ, Zhao H, Tuschong LM, Bauer TR, Burkholder TH, Persons DA, Hickstein DD.
    Hum Gene Ther; 2011 Jun 07; 22(6):689-96. PubMed ID: 21275758
    [Abstract] [Full Text] [Related]

  • 31. Protein replacement therapy and gene transfer in canine models of hemophilia A, hemophilia B, von willebrand disease, and factor VII deficiency.
    Nichols TC, Dillow AM, Franck HW, Merricks EP, Raymer RA, Bellinger DA, Arruda VR, High KA.
    ILAR J; 2009 Jun 07; 50(2):144-67. PubMed ID: 19293459
    [Abstract] [Full Text] [Related]

  • 32. Gene therapy in large animal models of muscular dystrophy.
    Wang Z, Chamberlain JS, Tapscott SJ, Storb R.
    ILAR J; 2009 Jun 07; 50(2):187-98. PubMed ID: 19293461
    [Abstract] [Full Text] [Related]

  • 33. Treatment of canine leukocyte adhesion deficiency by foamy virus vectors expressing CD18 from a PGK promoter.
    Bauer TR, Olson EM, Huo Y, Tuschong LM, Allen JM, Li Y, Burkholder TH, Russell DW.
    Gene Ther; 2011 Jun 07; 18(6):553-9. PubMed ID: 21228879
    [Abstract] [Full Text] [Related]

  • 34. Animal models for target diseases in gene therapy--using DNA and siRNA delivery strategies.
    Blagbrough IS, Zara C.
    Pharm Res; 2009 Jan 07; 26(1):1-18. PubMed ID: 18841450
    [Abstract] [Full Text] [Related]

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  • 37. In-Vivo Gene Therapy with Foamy Virus Vectors.
    Rajawat YS, Humbert O, Kiem HP.
    Viruses; 2019 Nov 23; 11(12):. PubMed ID: 31771194
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