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B Kohn

Showing results (361-370 of 516) with videos related to

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Human Gene Therapy|January 11, 2021
Safe and Effective <i>In Vivo</i> Targeting and Gene Editing in Hematopoietic Stem Cells: Strategies for Accelerating DevelopmentPaula Cannon, Aravind Asokan, Agnieszka Czechowicz, et al.
Gene Therapy|August 11, 2023
Biodistribution of lentiviral transduced adipose-derived stem cells for "ex-vivo" regional gene therapy for bone repairJennifer A Bell, Kevin Collon, Cory Mayfield, et al.
Journal of Clinical Immunology|June 29, 2021
Normal IgH Repertoire Diversity in an Infant with ADA Deficiency After Gene TherapyCarolyn H Baloh, Samiksha A Borkar, Kai-Fen Chang, et al.
Blood|October 24, 2002
Gene therapy of RAG-2-/- mice: sustained correction of the immunodeficiencyFrank Yates, Michèle Malassis-Séris, Daniel Stockholm, et al.
Nature Medicine|October 1, 1995
Engraftment of gene-modified umbilical cord blood cells in neonates with adenosine deaminase deficiencyD B Kohn, K I Weinberg, J A Nolta, et al.
Ciba Foundation Symposium|January 1, 1987
Gene therapy: efforts at developing large animal models for autologous bone marrow transplant and gene transfer with retroviral vectorsM A Eglitis, P W Kantoff, J R McLachlin, et al.
The Journal of Allergy and Clinical Immunology|June 6, 2016
Primary Immune Deficiency Treatment Consortium (PIDTC) updateLinda M Griffith, Morton J Cowan, Luigi D Notarangelo, et al.
Molecular Therapy. Nucleic Acids|January 30, 2017
Reactivating Fetal Hemoglobin Expression in Human Adult Erythroblasts Through BCL11A Knockdown Using Targeted EndonucleasesCarmen F Bjurström, Michelle Mojadidi, John Phillips, et al.
The Journal of Experimental Medicine|July 1, 1987
Expression of human adenosine deaminase in nonhuman primates after retrovirus-mediated gene transferP W Kantoff, A P Gillio, J R McLachlin, et al.
Experimental Hematology|February 15, 2015
Potentially therapeutic levels of anti-sickling globin gene expression following lentivirus-mediated gene transfer in sickle cell disease bone marrow CD34+ cellsFabrizia Urbinati, Phillip W Hargrove, Sabine Geiger, et al.
Pageof 52

Showing results (361-370 of 516) with videos related to

Sort By:
Pageof 52
Human Gene Therapy|January 11, 2021
Safe and Effective <i>In Vivo</i> Targeting and Gene Editing in Hematopoietic Stem Cells: Strategies for Accelerating DevelopmentPaula Cannon, Aravind Asokan, Agnieszka Czechowicz, et al.
Gene Therapy|August 11, 2023
Biodistribution of lentiviral transduced adipose-derived stem cells for "ex-vivo" regional gene therapy for bone repairJennifer A Bell, Kevin Collon, Cory Mayfield, et al.
Journal of Clinical Immunology|June 29, 2021
Normal IgH Repertoire Diversity in an Infant with ADA Deficiency After Gene TherapyCarolyn H Baloh, Samiksha A Borkar, Kai-Fen Chang, et al.
Blood|October 24, 2002
Gene therapy of RAG-2-/- mice: sustained correction of the immunodeficiencyFrank Yates, Michèle Malassis-Séris, Daniel Stockholm, et al.
Nature Medicine|October 1, 1995
Engraftment of gene-modified umbilical cord blood cells in neonates with adenosine deaminase deficiencyD B Kohn, K I Weinberg, J A Nolta, et al.
Ciba Foundation Symposium|January 1, 1987
Gene therapy: efforts at developing large animal models for autologous bone marrow transplant and gene transfer with retroviral vectorsM A Eglitis, P W Kantoff, J R McLachlin, et al.
The Journal of Allergy and Clinical Immunology|June 6, 2016
Primary Immune Deficiency Treatment Consortium (PIDTC) updateLinda M Griffith, Morton J Cowan, Luigi D Notarangelo, et al.
Molecular Therapy. Nucleic Acids|January 30, 2017
Reactivating Fetal Hemoglobin Expression in Human Adult Erythroblasts Through BCL11A Knockdown Using Targeted EndonucleasesCarmen F Bjurström, Michelle Mojadidi, John Phillips, et al.
The Journal of Experimental Medicine|July 1, 1987
Expression of human adenosine deaminase in nonhuman primates after retrovirus-mediated gene transferP W Kantoff, A P Gillio, J R McLachlin, et al.
Experimental Hematology|February 15, 2015
Potentially therapeutic levels of anti-sickling globin gene expression following lentivirus-mediated gene transfer in sickle cell disease bone marrow CD34+ cellsFabrizia Urbinati, Phillip W Hargrove, Sabine Geiger, et al.
Pageof 52