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The Journal of Clinical Investigation
|
November 3, 2006
Gene therapy of metachromatic leukodystrophy reverses neurological damage and deficits in mice
Alessandra Biffi, Alessia Capotondo, Stefania Fasano, et al.
Human Gene Therapy
|
March 17, 2004
Mobilized blood CD34+ cells transduced and selected with a clinically applicable protocol reconstitute lymphopoiesis in SCID-Hu mice
Sara Deola, Samantha Scaramuzza, Roberto Sciarretta Birolo, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
November 27, 2004
IL-3 or IL-7 increases ex vivo gene transfer efficiency in ADA-SCID BM CD34+ cells while maintaining in vivo lymphoid potential
Francesca Ficara, Daniela B Superchi, Raisa Jofra Hernández, et al.
Nature Medicine
|
May 2, 2002
Immune reconstitution in ADA-SCID after PBL gene therapy and discontinuation of enzyme replacement
Alessandro Aiuti, Sergio Vai, Alessandra Mortellaro, et al.
Blood
|
November 19, 2005
Suicide gene therapy of graft-versus-host disease induced by central memory human T lymphocytes
Attilio Bondanza, Veronica Valtolina, Zulma Magnani, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 25, 2006
Retroviral vector integration deregulates gene expression but has no consequence on the biology and function of transplanted T cells
Alessandra Recchia, Chiara Bonini, Zulma Magnani, et al.
Blood
|
December 17, 2008
Peripheral blood lymphocytes genetically modified to express the self/tumor antigen MAGE-A3 induce antitumor immune responses in cancer patients
Raffaella Fontana, Marco Bregni, Arcadi Cipponi, et al.
Nature Medicine
|
May 30, 2018
Monocyte-derived IL-1 and IL-6 are differentially required for cytokine-release syndrome and neurotoxicity due to CAR T cells
Margherita Norelli, Barbara Camisa, Giulia Barbiera, et al.
Blood
|
November 20, 2012
IL-7 and IL-15 instruct the generation of human memory stem T cells from naive precursors
Nicoletta Cieri, Barbara Camisa, Fabienne Cocchiarella, et al.
Blood
|
July 13, 2006
Ex vivo gene therapy with lentiviral vectors rescues adenosine deaminase (ADA)-deficient mice and corrects their immune and metabolic defects
Alessandra Mortellaro, Raisa Jofra Hernandez, Matteo M Guerrini, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 96) with videos related to
Sort By:
Page
of 10
The Journal of Clinical Investigation
|
November 3, 2006
Gene therapy of metachromatic leukodystrophy reverses neurological damage and deficits in mice
Alessandra Biffi, Alessia Capotondo, Stefania Fasano, et al.
Human Gene Therapy
|
March 17, 2004
Mobilized blood CD34+ cells transduced and selected with a clinically applicable protocol reconstitute lymphopoiesis in SCID-Hu mice
Sara Deola, Samantha Scaramuzza, Roberto Sciarretta Birolo, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
November 27, 2004
IL-3 or IL-7 increases ex vivo gene transfer efficiency in ADA-SCID BM CD34+ cells while maintaining in vivo lymphoid potential
Francesca Ficara, Daniela B Superchi, Raisa Jofra Hernández, et al.
Nature Medicine
|
May 2, 2002
Immune reconstitution in ADA-SCID after PBL gene therapy and discontinuation of enzyme replacement
Alessandro Aiuti, Sergio Vai, Alessandra Mortellaro, et al.
Blood
|
November 19, 2005
Suicide gene therapy of graft-versus-host disease induced by central memory human T lymphocytes
Attilio Bondanza, Veronica Valtolina, Zulma Magnani, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 25, 2006
Retroviral vector integration deregulates gene expression but has no consequence on the biology and function of transplanted T cells
Alessandra Recchia, Chiara Bonini, Zulma Magnani, et al.
Blood
|
December 17, 2008
Peripheral blood lymphocytes genetically modified to express the self/tumor antigen MAGE-A3 induce antitumor immune responses in cancer patients
Raffaella Fontana, Marco Bregni, Arcadi Cipponi, et al.
Nature Medicine
|
May 30, 2018
Monocyte-derived IL-1 and IL-6 are differentially required for cytokine-release syndrome and neurotoxicity due to CAR T cells
Margherita Norelli, Barbara Camisa, Giulia Barbiera, et al.
Blood
|
November 20, 2012
IL-7 and IL-15 instruct the generation of human memory stem T cells from naive precursors
Nicoletta Cieri, Barbara Camisa, Fabienne Cocchiarella, et al.
Blood
|
July 13, 2006
Ex vivo gene therapy with lentiviral vectors rescues adenosine deaminase (ADA)-deficient mice and corrects their immune and metabolic defects
Alessandra Mortellaro, Raisa Jofra Hernandez, Matteo M Guerrini, et al.
Page
of 10