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The Journal of Clinical Endocrinology and Metabolism
|
December 1, 1981
Genetic and hormonal characterization of cryptic 21-hydroxylase deficiency
L S Levine, B Dupont, F Lorenzen, et al.
Stem Cell Research & Therapy
|
July 30, 2013
Generation and characterization of transgene-free human induced pluripotent stem cells and conversion to putative clinical-grade status
Jason P Awe, Patrick C Lee, Cyril Ramathal, et al.
Nature Medicine
|
July 14, 1998
T lymphocytes with a normal ADA gene accumulate after transplantation of transduced autologous umbilical cord blood CD34+ cells in ADA-deficient SCID neonates
D B Kohn, M S Hershfield, D Carbonaro, et al.
Cell
|
December 28, 2006
Neuronal transcriptome of Aplysia: neuronal compartments and circuitry
Leonid L Moroz, John R Edwards, Sathyanarayanan V Puthanveettil, 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.
Genome Medicine
|
September 29, 2018
T cell dynamics and response of the microbiota after gene therapy to treat X-linked severe combined immunodeficiency
Erik L Clarke, A Jesse Connell, Emmanuelle Six, et al.
Iscience
|
May 31, 2022
High-level correction of the sickle mutation is amplified <i>in vivo</i> during erythroid differentiation
Wendy Magis, Mark A DeWitt, Stacia K Wyman, et al.
The Journal of Allergy and Clinical Immunology
|
December 1, 2022
The diagnosis of severe combined immunodeficiency (SCID): The Primary Immune Deficiency Treatment Consortium (PIDTC) 2022 Definitions
Christopher C Dvorak, Elie Haddad, Jennifer Heimall, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 5, 2014
T-cell immunotherapy: looking forward
Jacqueline Corrigan-Curay, Hans-Peter Kiem, David Baltimore, 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 52
Search research articles
Search
Showing results (441-450 of 516) with videos related to
Sort By:
Page
of 52
The Journal of Clinical Endocrinology and Metabolism
|
December 1, 1981
Genetic and hormonal characterization of cryptic 21-hydroxylase deficiency
L S Levine, B Dupont, F Lorenzen, et al.
Stem Cell Research & Therapy
|
July 30, 2013
Generation and characterization of transgene-free human induced pluripotent stem cells and conversion to putative clinical-grade status
Jason P Awe, Patrick C Lee, Cyril Ramathal, et al.
Nature Medicine
|
July 14, 1998
T lymphocytes with a normal ADA gene accumulate after transplantation of transduced autologous umbilical cord blood CD34+ cells in ADA-deficient SCID neonates
D B Kohn, M S Hershfield, D Carbonaro, et al.
Cell
|
December 28, 2006
Neuronal transcriptome of Aplysia: neuronal compartments and circuitry
Leonid L Moroz, John R Edwards, Sathyanarayanan V Puthanveettil, 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.
Genome Medicine
|
September 29, 2018
T cell dynamics and response of the microbiota after gene therapy to treat X-linked severe combined immunodeficiency
Erik L Clarke, A Jesse Connell, Emmanuelle Six, et al.
Iscience
|
May 31, 2022
High-level correction of the sickle mutation is amplified <i>in vivo</i> during erythroid differentiation
Wendy Magis, Mark A DeWitt, Stacia K Wyman, et al.
The Journal of Allergy and Clinical Immunology
|
December 1, 2022
The diagnosis of severe combined immunodeficiency (SCID): The Primary Immune Deficiency Treatment Consortium (PIDTC) 2022 Definitions
Christopher C Dvorak, Elie Haddad, Jennifer Heimall, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 5, 2014
T-cell immunotherapy: looking forward
Jacqueline Corrigan-Curay, Hans-Peter Kiem, David Baltimore, 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 52