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Human Gene Therapy
|
September 10, 2016
Lentivirus Mediated Correction of Artemis-Deficient Severe Combined Immunodeficiency
Divya Punwani, Misako Kawahara, Jason Yu, et al.
Nature Communications
|
November 21, 2013
Platelet-targeted gene therapy with human factor VIII establishes haemostasis in dogs with haemophilia A
Lily M Du, Paquita Nurden, Alan T Nurden, et al.
Blood
|
March 14, 2007
Cytokine-independent growth and clonal expansion of a primary human CD8+ T-cell clone following retroviral transduction with the IL-15 gene
Cary Hsu, Stephanie A Jones, Cyrille J Cohen, 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.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
March 26, 2015
[(18)F]FHBG PET/CT Imaging of CD34-TK75 Transduced Donor T Cells in Relapsed Allogeneic Stem Cell Transplant Patients: Safety and Feasibility
Linda G Eissenberg, Michael P Rettig, Julie K Ritchey, et al.
Molecular Therapy. Methods & Clinical Development
|
May 28, 2015
Preclinical safety and efficacy of an anti-HIV-1 lentiviral vector containing a short hairpin RNA to CCR5 and the C46 fusion inhibitor
Orit Wolstein, Maureen Boyd, Michelle Millington, et al.
Molecular Therapy. Methods & Clinical Development
|
September 14, 2018
Screening Clinical Cell Products for Replication Competent Retrovirus: The National Gene Vector Biorepository Experience
Kenneth Cornetta, Lisa Duffy, Steven A Feldman, et al.
Science Translational Medicine
|
May 8, 2024
The translational gap for gene therapies in low- and middle-income countries
Kevin W Doxzen, Jennifer E Adair, Yris Maria Fonseca Bazzo, 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.
Human Gene Therapy
|
March 23, 2013
Gene therapy for rare diseases: summary of a National Institutes of Health workshop, September 13, 2012
Marina O'Reilly, Donald B Kohn, Jeffrey Bartlett, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 88) with videos related to
Sort By:
Page
of 9
Human Gene Therapy
|
September 10, 2016
Lentivirus Mediated Correction of Artemis-Deficient Severe Combined Immunodeficiency
Divya Punwani, Misako Kawahara, Jason Yu, et al.
Nature Communications
|
November 21, 2013
Platelet-targeted gene therapy with human factor VIII establishes haemostasis in dogs with haemophilia A
Lily M Du, Paquita Nurden, Alan T Nurden, et al.
Blood
|
March 14, 2007
Cytokine-independent growth and clonal expansion of a primary human CD8+ T-cell clone following retroviral transduction with the IL-15 gene
Cary Hsu, Stephanie A Jones, Cyrille J Cohen, 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.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
March 26, 2015
[(18)F]FHBG PET/CT Imaging of CD34-TK75 Transduced Donor T Cells in Relapsed Allogeneic Stem Cell Transplant Patients: Safety and Feasibility
Linda G Eissenberg, Michael P Rettig, Julie K Ritchey, et al.
Molecular Therapy. Methods & Clinical Development
|
May 28, 2015
Preclinical safety and efficacy of an anti-HIV-1 lentiviral vector containing a short hairpin RNA to CCR5 and the C46 fusion inhibitor
Orit Wolstein, Maureen Boyd, Michelle Millington, et al.
Molecular Therapy. Methods & Clinical Development
|
September 14, 2018
Screening Clinical Cell Products for Replication Competent Retrovirus: The National Gene Vector Biorepository Experience
Kenneth Cornetta, Lisa Duffy, Steven A Feldman, et al.
Science Translational Medicine
|
May 8, 2024
The translational gap for gene therapies in low- and middle-income countries
Kevin W Doxzen, Jennifer E Adair, Yris Maria Fonseca Bazzo, 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.
Human Gene Therapy
|
March 23, 2013
Gene therapy for rare diseases: summary of a National Institutes of Health workshop, September 13, 2012
Marina O'Reilly, Donald B Kohn, Jeffrey Bartlett, et al.
Page
of 9