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Long-term expression of human adenosine deaminase in mice transplanted with retrovirus-infected hematopoietic stem cells.
Long-term in vivo expression of a murine adenosine deaminase gene in rhesus monkey hematopoietic cells of multiple lineages after retroviral mediated gene transfer into CD34+ bone marrow cells.
Retrovirus-mediated gene transfer of human adenosine deaminase: expression of functional enzyme in murine hematopoietic stem cells in vivo.
Retrovirus-mediated transfer of human adenosine deaminase gene sequences into cells in culture and into murine hematopoietic cells in vivo.
Transfer and expression of human ADA in murine hematopoietic stem cells.
Retroviral gene transfer of human adenosine deaminase in murine hematopoietic cells: effect of selectable marker sequences on long-term expression.
ADHESION AND STEM CELL SURVIVAL AND ENGRAFTMENT
GENETIC MODIFICATION/ALTERNATIVE SOURCES OF STEM CELL
Evolving Gene Therapy in Primary Immunodeficiency.
Gene therapy advances but struggles to interpret safety data in small animal models.
Progress in genetic therapy for severe combined immunodeficiency associated with adenosine deaminase deficiency.