67. Correction of Anemia in β-Thalassemia Mice with a Lentiviral Vector Encoding a Human β-Globin Gene Is Dependent on Polyclonal Reconstitution with a Majority of Stem Cells with Integrations Supporting Pancellular Expresssion

67. Correction of Anemia in β-Thalassemia Mice with a Lentiviral Vector Encoding a Human β-Globin Gene Is Dependent on Polyclonal Reconstitution with a Majority of Stem Cells with Integrations Supporting Pancellular Expresssion

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65. A Genetic T racking Approach T o Studying In V ivo Tracking To Vivo Hematopoiesis and Response to Cytokines in NonHuman Primates Ken Kuramoto,1 Brian Agricola,1 Mark Metzger,1 Robert Donahue,1 Christof von Kalle,2 Cynthia Dunbar.1 1 Molecular Hematopoiesis Section, Hematology Branch, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland, United States; 2Dept. of Internal Medicine, and Institue for Molecular Medicine and Cell Research, University of Freiburg, Germany. 4              

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66. Highly Efficient Gene T ransfer into Macaque Transfer Repopulating Cells Using Concentrated RD1 14RD114Pseudotype V ector Vector Peter A. Horn,1 Julia C. Morris,1 Laura J. Peterson,1 Bobbie M. Thomasson,1 Peter Kurre,1,2 Hans-Peter Kiem.1,3 1 Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States; 2Department of Pediatrics, University of Washington, Seattle, WA, United States; 3 Department of Medicine, University of Washington, Seattle, WA, United States.     @$886"           

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67. Correction of Anemia in β-Thalassemia Mice with a Lentiviral V ector Encoding a Human β-Globin Gene Is Vector Dependent on Polyclonal Reconstitution with a Majority of Stem Cells with Integrations Supporting Pancellular Expresssion Suzan Imren,1 Robert Pawliuk,2 Benjamin Cavilla,1 Connie J. Eaves,1 Louis D. Wadsworth,3 Margaret Hale,1 Ronald L. Nagel,4 Mary E. Fabry,4 Philippe Leboulch,2,5,6 R. Keith Humphries.1 1 Terry Fox Laboratory, BC Cancer Agency, Vancouver, BC, Canada; 2Genetix Pharmaceutical Ltd, Cambridge, MA, United States; 3Department of Pathology and Laboratory Medicine, Childrens and Women′s Health Centre of BC, Vancouver, BC, Canada; 4Albert Einstein College of Medicine, Bronx, NY, United States; 5Massachusetts Institute of Technology, Cambridge, MA, United States; 6Harvard Medical School and Brigham and Womens Hospital, Boston, MA, United States. (           β"    

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68. Detection of Pluripotent Hematopoietic Cells in SCID-X1 Gene Therapy Manfred Schmidt,1 Salima Hacein-Bey,2 Francoise LeDeist,2 Nina Lemke,1 Manuela Wissler,1 Alain Fischer,2 Marina CavazzanaCalvo,2 Christof von Kalle.1,3 1 Internal Medicine I, University of Freiburg, Freiburg, Germany; 2 Unite d′Immunologie et d′Hematologie Pediuatriques, Hopital Necker, Paris, France; 3Molecular Medicine and Cell Research, University of Freiburg, Freiburg, Germany.          

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69. Efficient Selective Enrichment of Hematopoietic Stem Cells T ransduced with MFGS Retrovirus Encoding Transduced Benzyl Guanine Resistant Methylguanine Methyltransferase Linked to Marker Genes or to Therapeutic Chronic Granulomatous Disease Genes Uimook Choi,1 Jordana M. De Leon,1 Harry L. Malech.1 1 Laboratory of Host Defenses, NIAID, National Institutes of Health, Bethesda, MD, United States.                   -C(/ 1    

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