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Journal of Veterinary Internal Medicine
|
August 27, 2010
Pulmonary abnormalities in dogs with leptospirosis
B Kohn, K Steinicke, G Arndt, et al.
The Journal of Experimental Medicine
|
November 1, 1996
Reconstitution of T cell receptor signaling in ZAP-70-deficient cells by retroviral transduction of the ZAP-70 gene
N Taylor, K B Bacon, S Smith, et al.
Biorxiv : the Preprint Server for Biology
|
November 24, 2025
TriLeukeVax: A CD80/IL-15/IL-15Rα Expressing Autologous AML Cell Vaccine Elicits Robust Anti-Leukemic Cytolytic Activity
Jacob Du, Uthpala N Wijayaratna, Xinyue Wang, et al.
Pediatric Transplantation
|
September 30, 2008
Clinical and genetic heterogeneity in Omenn syndrome and severe combined immune deficiency
Tanja A Gruber, Ami J Shah, Michelle Hernandez, et al.
Blood
|
August 15, 2000
Lentiviral vectors for efficient delivery of CD80 and granulocyte-macrophage- colony-stimulating factor in human acute lymphoblastic leukemia and acute myeloid leukemia cells to induce antileukemic immune responses
R Stripecke, A A Cardoso, K A Pepper, et al.
Stem Cell Reports
|
November 13, 2020
β-Globin Lentiviral Vectors Have Reduced Titers due to Incomplete Vector RNA Genomes and Lowered Virion Production
Jiaying Han, Kevin Tam, Feiyang Ma, et al.
Molecular Therapy. Methods & Clinical Development
|
May 15, 2024
A novel high-titer, bifunctional lentiviral vector for autologous hematopoietic stem cell gene therapy of sickle cell disease
Kevyn L Hart, Boya Liu, Devin Brown, et al.
Nature Medicine
|
March 18, 2003
Clonality analysis after retroviral-mediated gene transfer to CD34+ cells from the cord blood of ADA-deficient SCID neonates
Manfred Schmidt, Denise A Carbonaro, Carsten Speckmann, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 1, 1982
Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia
B Kohn, L S Levine, M S Pollack, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
May 3, 2006
In vivo transduction by intravenous injection of a lentiviral vector expressing human ADA into neonatal ADA gene knockout mice: a novel form of enzyme replacement therapy for ADA deficiency
Denise A Carbonaro, Xiangyang Jin, Denise Petersen, et al.
Page
of 52
Search research articles
Search
Showing results (321-330 of 516) with videos related to
Sort By:
Page
of 52
Journal of Veterinary Internal Medicine
|
August 27, 2010
Pulmonary abnormalities in dogs with leptospirosis
B Kohn, K Steinicke, G Arndt, et al.
The Journal of Experimental Medicine
|
November 1, 1996
Reconstitution of T cell receptor signaling in ZAP-70-deficient cells by retroviral transduction of the ZAP-70 gene
N Taylor, K B Bacon, S Smith, et al.
Biorxiv : the Preprint Server for Biology
|
November 24, 2025
TriLeukeVax: A CD80/IL-15/IL-15Rα Expressing Autologous AML Cell Vaccine Elicits Robust Anti-Leukemic Cytolytic Activity
Jacob Du, Uthpala N Wijayaratna, Xinyue Wang, et al.
Pediatric Transplantation
|
September 30, 2008
Clinical and genetic heterogeneity in Omenn syndrome and severe combined immune deficiency
Tanja A Gruber, Ami J Shah, Michelle Hernandez, et al.
Blood
|
August 15, 2000
Lentiviral vectors for efficient delivery of CD80 and granulocyte-macrophage- colony-stimulating factor in human acute lymphoblastic leukemia and acute myeloid leukemia cells to induce antileukemic immune responses
R Stripecke, A A Cardoso, K A Pepper, et al.
Stem Cell Reports
|
November 13, 2020
β-Globin Lentiviral Vectors Have Reduced Titers due to Incomplete Vector RNA Genomes and Lowered Virion Production
Jiaying Han, Kevin Tam, Feiyang Ma, et al.
Molecular Therapy. Methods & Clinical Development
|
May 15, 2024
A novel high-titer, bifunctional lentiviral vector for autologous hematopoietic stem cell gene therapy of sickle cell disease
Kevyn L Hart, Boya Liu, Devin Brown, et al.
Nature Medicine
|
March 18, 2003
Clonality analysis after retroviral-mediated gene transfer to CD34+ cells from the cord blood of ADA-deficient SCID neonates
Manfred Schmidt, Denise A Carbonaro, Carsten Speckmann, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 1, 1982
Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia
B Kohn, L S Levine, M S Pollack, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
May 3, 2006
In vivo transduction by intravenous injection of a lentiviral vector expressing human ADA into neonatal ADA gene knockout mice: a novel form of enzyme replacement therapy for ADA deficiency
Denise A Carbonaro, Xiangyang Jin, Denise Petersen, et al.
Page
of 52