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Molecular Therapy : the Journal of the American Society of Gene Therapy
|
October 20, 2019
Improved Titer and Gene Transfer by Lentiviral Vectors Using Novel, Small β-Globin Locus Control Region Elements
Richard A Morgan, Mildred J Unti, Bamidele Aleshe, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 14, 2016
CRISPR/Cas9-Mediated Correction of the Sickle Mutation in Human CD34+ cells
Megan D Hoban, Dianne Lumaquin, Caroline Y Kuo, et al.
Blood Advances
|
April 20, 2026
Clinical Outcomes of Lentiviral Vector Gene Therapy for Sickle Cell Disease
Chattip Prueksapraopong, Augustine Fernandes, Beatriz Campo Fernandez, et al.
Journal for Immunotherapy of Cancer
|
August 2, 2020
Human CLEC9A antibodies deliver NY-ESO-1 antigen to CD141<sup>+</sup> dendritic cells to activate naïve and memory NY-ESO-1-specific CD8<sup>+</sup> T cells
Kelly-Anne Masterman, Oscar L Haigh, Kirsteen M Tullett, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 11, 2019
Editing the Sickle Cell Disease Mutation in Human Hematopoietic Stem Cells: Comparison of Endonucleases and Homologous Donor Templates
Zulema Romero, Anastasia Lomova, Suzanne Said, et al.
Transplantation Proceedings
|
June 24, 1998
Retransplantation for recurrent hepatitis C following tacrolimus or cyclosporine immunosuppression
R M Ghobrial, S Colquhoun, H Rosen, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
November 22, 2013
Preclinical demonstration of lentiviral vector-mediated correction of immunological and metabolic abnormalities in models of adenosine deaminase deficiency
Denise A Carbonaro, Lin Zhang, Xiangyang Jin, et al.
The Journal of Clinical Investigation
|
July 19, 2013
β-globin gene transfer to human bone marrow for sickle cell disease
Zulema Romero, Fabrizia Urbinati, Sabine Geiger, et al.
Blood
|
March 4, 2015
Correction of the sickle cell disease mutation in human hematopoietic stem/progenitor cells
Megan D Hoban, Gregory J Cost, Matthew C Mendel, et al.
Blood
|
May 11, 2021
Long-term outcomes after gene therapy for adenosine deaminase severe combined immune deficiency
Bryanna Reinhardt, Omar Habib, Kit L Shaw, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 103) with videos related to
Sort By:
Page
of 11
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
October 20, 2019
Improved Titer and Gene Transfer by Lentiviral Vectors Using Novel, Small β-Globin Locus Control Region Elements
Richard A Morgan, Mildred J Unti, Bamidele Aleshe, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 14, 2016
CRISPR/Cas9-Mediated Correction of the Sickle Mutation in Human CD34+ cells
Megan D Hoban, Dianne Lumaquin, Caroline Y Kuo, et al.
Blood Advances
|
April 20, 2026
Clinical Outcomes of Lentiviral Vector Gene Therapy for Sickle Cell Disease
Chattip Prueksapraopong, Augustine Fernandes, Beatriz Campo Fernandez, et al.
Journal for Immunotherapy of Cancer
|
August 2, 2020
Human CLEC9A antibodies deliver NY-ESO-1 antigen to CD141<sup>+</sup> dendritic cells to activate naïve and memory NY-ESO-1-specific CD8<sup>+</sup> T cells
Kelly-Anne Masterman, Oscar L Haigh, Kirsteen M Tullett, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 11, 2019
Editing the Sickle Cell Disease Mutation in Human Hematopoietic Stem Cells: Comparison of Endonucleases and Homologous Donor Templates
Zulema Romero, Anastasia Lomova, Suzanne Said, et al.
Transplantation Proceedings
|
June 24, 1998
Retransplantation for recurrent hepatitis C following tacrolimus or cyclosporine immunosuppression
R M Ghobrial, S Colquhoun, H Rosen, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
November 22, 2013
Preclinical demonstration of lentiviral vector-mediated correction of immunological and metabolic abnormalities in models of adenosine deaminase deficiency
Denise A Carbonaro, Lin Zhang, Xiangyang Jin, et al.
The Journal of Clinical Investigation
|
July 19, 2013
β-globin gene transfer to human bone marrow for sickle cell disease
Zulema Romero, Fabrizia Urbinati, Sabine Geiger, et al.
Blood
|
March 4, 2015
Correction of the sickle cell disease mutation in human hematopoietic stem/progenitor cells
Megan D Hoban, Gregory J Cost, Matthew C Mendel, et al.
Blood
|
May 11, 2021
Long-term outcomes after gene therapy for adenosine deaminase severe combined immune deficiency
Bryanna Reinhardt, Omar Habib, Kit L Shaw, et al.
Page
of 11