BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

337 related articles for article (PubMed ID: 16433450)

  • 21. Progress and prospects: gene therapy for inherited immunodeficiencies.
    Qasim W; Gaspar HB; Thrasher AJ
    Gene Ther; 2009 Nov; 16(11):1285-91. PubMed ID: 19776764
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genetic modification of hematopoietic cells using retroviral and lentiviral vectors: safety considerations for vector design and delivery into target cells.
    Dropulic B
    Curr Hematol Rep; 2005 Jul; 4(4):300-4. PubMed ID: 16009045
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Gene therapy for adenosine deaminase deficiency].
    Sakiyama Y
    Hokkaido Igaku Zasshi; 1996 Jan; 71(1):27-32. PubMed ID: 8727372
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Gene therapy using hematopoietic stem cells.
    Kohn DB
    Curr Opin Mol Ther; 1999 Aug; 1(4):437-42. PubMed ID: 11713757
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Gene therapy for hematopoietic and immune disorders.
    Kohn DB
    Bone Marrow Transplant; 1996 Dec; 18 Suppl 3():S55-8. PubMed ID: 8971410
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Induced pluripotent stem cells and severe combined immunodeficiency: merely disease modeling or potentially a novel cure?
    Mikkers H; Pike-Overzet K; Staal FJ
    Pediatr Res; 2012 Apr; 71(4 Pt 2):427-32. PubMed ID: 22430378
    [TBL] [Abstract][Full Text] [Related]  

  • 27. In vivo correction of ZAP-70 immunodeficiency by intrathymic gene transfer.
    Adjali O; Marodon G; Steinberg M; Mongellaz C; Thomas-Vaslin V; Jacquet C; Taylor N; Klatzmann D
    J Clin Invest; 2005 Aug; 115(8):2287-95. PubMed ID: 16075064
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Retroviral transduction of IL-7Ralpha into IL-7Ralpha-/- bone marrow progenitors: correction of lymphoid deficiency and induction of neutrophilia.
    Jiang Q; Li WQ; Aiello FB; Klarmann KD; Keller JR; Durum SK
    Gene Ther; 2005 Dec; 12(24):1761-8. PubMed ID: 16208423
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Update on gene therapy for hereditary hematological disorders.
    Herzog RW; Arruda VR
    Expert Rev Cardiovasc Ther; 2003 Jul; 1(2):215-32. PubMed ID: 15030282
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Is it going to be SIN?: a European Society of Gene Therapy commentary. Phasing-out the clinical use of non self-inactivating murine leukemia virus vectors: initiative on hold.
    Buchholz CJ; Cichutek K
    J Gene Med; 2006 Oct; 8(10):1274-6. PubMed ID: 17001625
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Gene therapy for primary immunodeficiencies.
    Fischer A; Hacein-Bey Abina S; Touzot F; Cavazzana M
    Clin Genet; 2015 Dec; 88(6):507-15. PubMed ID: 25708106
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Gene therapy for severe combined immunodeficiency].
    Petersen LB; Jensen TG
    Ugeskr Laeger; 2010 Jun; 172(23):1756-8. PubMed ID: 20534204
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Drug evaluation: ADA-transduced hematopoietic stem cell therapy for ADA-SCID.
    Taupin P
    IDrugs; 2006 Jun; 9(6):423-30. PubMed ID: 16752313
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The leukemogenic risk of integrating retroviral vectors in hematopoietic stem cell gene therapy applications.
    Kang EM; Tisdale JF
    Curr Hematol Rep; 2004 Jul; 3(4):274-81. PubMed ID: 15217557
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A new direction for gene therapy: intrathymic T cell-specific lentiviral gene transfer.
    Seggewiss R; Dunbar CE
    J Clin Invest; 2005 Aug; 115(8):2064-7. PubMed ID: 16075048
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Retroviral vectors: new applications for an old tool.
    Barquinero J; Eixarch H; PĂ©rez-Melgosa M
    Gene Ther; 2004 Oct; 11 Suppl 1():S3-9. PubMed ID: 15454951
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Gene therapy. Panel urges limits on X-SCID trials.
    Kaiser J
    Science; 2005 Mar; 307(5715):1544-5. PubMed ID: 15761128
    [No Abstract]   [Full Text] [Related]  

  • 38. Successes and risks of gene therapy in primary immunodeficiencies.
    Chinen J; Puck JM
    J Allergy Clin Immunol; 2004 Apr; 113(4):595-603; quiz 604. PubMed ID: 15100660
    [TBL] [Abstract][Full Text] [Related]  

  • 39. In vivo transduction by intravenous injection of a lentiviral vector expressing human ADA into neonatal ADA gene knockout mice: a novel form of enzyme replacement therapy for ADA deficiency.
    Carbonaro DA; Jin X; Petersen D; Wang X; Dorey F; Kil KS; Aldrich M; Blackburn MR; Kellems RE; Kohn DB
    Mol Ther; 2006 Jun; 13(6):1110-20. PubMed ID: 16651028
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Adenosine deaminase deficiency: clinical expression, molecular basis, and therapy.
    Hershfield MS
    Semin Hematol; 1998 Oct; 35(4):291-8. PubMed ID: 9801258
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.