Add to ORKGRetroviral gene transfer into human hematopoietic cells: an in vitro kinetic stud
Human hematopoiesis originates in a population of stem cells with transplantable lympho-myeloid rec...
Efficient gene delivery still represents a major hurdle for the realisation of hematopoietic stem ce...
The efficient introduction of exogenous genes into primary lymphocytes is potentially important both...
We have developed the experimental and logistical conditions for the clinical application of retrovi...
In order to improve the efficiency of gene transduction into human hematopoietic stem cells by retro...
In order to improve the efficiency of gene transduction into human hematopoietic stem cells by retro...
Retroviral vectors derived from the Moloney murine leukemia virus have been used in successful and p...
Gene therapy may open new perspectives in the treatment of numerous hematopoietic and metabolic diso...
Recombinant retroviruses (gammaretro-, lenti- and foamy-viral vectors) are used for gene therapy as ...
AbstractFor the past two decades, concerted efforts have been made to treat human disease by replaci...
Retroviral vector–mediated gene transfer into hematopoietic stem cells provides a potential-ly curat...
A novel lentiviral vector targets gene transfer into human hematopoietic stem cells in marrow from p...
We have generated a cell line, designated POAM-P1, shedding amphotropic recombinant retroviruses car...
Hematopoietic stem and progenitor cells (HSC) have been widely used in allogeneic transplant procedu...
Lentiviral vectors containing recombinant envelope proteins that target hematopoietic stem cells hav...
Human hematopoiesis originates in a population of stem cells with transplantable lympho-myeloid rec...
Efficient gene delivery still represents a major hurdle for the realisation of hematopoietic stem ce...
The efficient introduction of exogenous genes into primary lymphocytes is potentially important both...
We have developed the experimental and logistical conditions for the clinical application of retrovi...
In order to improve the efficiency of gene transduction into human hematopoietic stem cells by retro...
In order to improve the efficiency of gene transduction into human hematopoietic stem cells by retro...
Retroviral vectors derived from the Moloney murine leukemia virus have been used in successful and p...
Gene therapy may open new perspectives in the treatment of numerous hematopoietic and metabolic diso...
Recombinant retroviruses (gammaretro-, lenti- and foamy-viral vectors) are used for gene therapy as ...
AbstractFor the past two decades, concerted efforts have been made to treat human disease by replaci...
Retroviral vector–mediated gene transfer into hematopoietic stem cells provides a potential-ly curat...
A novel lentiviral vector targets gene transfer into human hematopoietic stem cells in marrow from p...
We have generated a cell line, designated POAM-P1, shedding amphotropic recombinant retroviruses car...
Hematopoietic stem and progenitor cells (HSC) have been widely used in allogeneic transplant procedu...
Lentiviral vectors containing recombinant envelope proteins that target hematopoietic stem cells hav...
Human hematopoiesis originates in a population of stem cells with transplantable lympho-myeloid rec...
Efficient gene delivery still represents a major hurdle for the realisation of hematopoietic stem ce...
The efficient introduction of exogenous genes into primary lymphocytes is potentially important both...