Hematopoietic stem cell transplantation (HSCT) is used to treat a wide range of hematologic and non-hematologic disorders. Recently, interest has grown in the potential of autologous HSCT coupled to gene therapy for the treatment of genetic blood disorders as a way of avoiding the severe immunologic reactions associated with allogeneic HSCT. However, the remaining risks in using myeloablative conditioning regimens to allow relatively small numbers of transplanted HSCs to be transplanted greatly limit the applicability of this approach. Nonmyeloablative regimens would be an appealing alternative but necessitate the generation of large numbers of genetically corrected HSCs to achieve therapeutic levels of chimerism. In this thesis I have expl...
Transplantation of genetically modified hematopoietic stem cells is a potential therapy for a variet...
Hematopoietic stem cell (HSC)–targeted gene transfer is an attractive approach for the treatment of ...
Hematopoietic stem cell (HSC) transplant with gene therapy has recently emerged as a successful clin...
Hematopoietic stem cell transplantation (HSCT) is used to treat a wide range of hematologic and non-...
Patients with severe sickle cell disease (SCD) are candidates for gene therapy using autologous hema...
AbstractGene therapy, the replacement of normal human beta- or gamma-globin genes into the hematopoi...
The development of strategies to extensively expand HSCs ex vivo could greatly improve the utility ...
Expansion of hematopoietic stem cells (HSCs) for therapeutic purposes has been a “holy grail&#...
Gene therapy for inherited diseases affecting the hematopoietic system requires transplantation and ...
Background Extensive efforts to develop hematopoietic stem cell (HSC) based gene therapy have been h...
Summary: Ex vivo gene therapy based on CD34+ hematopoietic stem cells (HSCs) has shown promising res...
Umbilical cord blood (UCB) is a well established alternative source of haematopoietic stem/progenito...
Successful gene therapy of -thalasse-mia will require replacement of the abnor-mal erythroid compart...
Thesis (Ph. D.)--Massachusetts Institute of Technology, Biological Engineering Division, 2006.Includ...
Hematopoietic stem and progenitor cells (HSC) have been widely used in allogeneic transplant procedu...
Transplantation of genetically modified hematopoietic stem cells is a potential therapy for a variet...
Hematopoietic stem cell (HSC)–targeted gene transfer is an attractive approach for the treatment of ...
Hematopoietic stem cell (HSC) transplant with gene therapy has recently emerged as a successful clin...
Hematopoietic stem cell transplantation (HSCT) is used to treat a wide range of hematologic and non-...
Patients with severe sickle cell disease (SCD) are candidates for gene therapy using autologous hema...
AbstractGene therapy, the replacement of normal human beta- or gamma-globin genes into the hematopoi...
The development of strategies to extensively expand HSCs ex vivo could greatly improve the utility ...
Expansion of hematopoietic stem cells (HSCs) for therapeutic purposes has been a “holy grail&#...
Gene therapy for inherited diseases affecting the hematopoietic system requires transplantation and ...
Background Extensive efforts to develop hematopoietic stem cell (HSC) based gene therapy have been h...
Summary: Ex vivo gene therapy based on CD34+ hematopoietic stem cells (HSCs) has shown promising res...
Umbilical cord blood (UCB) is a well established alternative source of haematopoietic stem/progenito...
Successful gene therapy of -thalasse-mia will require replacement of the abnor-mal erythroid compart...
Thesis (Ph. D.)--Massachusetts Institute of Technology, Biological Engineering Division, 2006.Includ...
Hematopoietic stem and progenitor cells (HSC) have been widely used in allogeneic transplant procedu...
Transplantation of genetically modified hematopoietic stem cells is a potential therapy for a variet...
Hematopoietic stem cell (HSC)–targeted gene transfer is an attractive approach for the treatment of ...
Hematopoietic stem cell (HSC) transplant with gene therapy has recently emerged as a successful clin...