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H Bobby Gaspar

Showing results (61-70 of 115) with videos related to

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Human Gene Therapy|June 19, 2008
Abnormal expression of only the CD34 part of a transgenic CD34/herpes simplex virus-thymidine kinase fusion protein is associated with ganciclovir resistanceEmad Bennour, Christophe Ferrand, Jean-Paul Rémy-Martin, et al.
Blood|July 23, 2008
Cognitive and behavioral abnormalities in children after hematopoietic stem cell transplantation for severe congenital immunodeficienciesPenny Titman, Elizabeth Pink, Emily Skucek, et al.
Science Translational Medicine|August 26, 2011
Long-term persistence of a polyclonal T cell repertoire after gene therapy for X-linked severe combined immunodeficiencyH Bobby Gaspar, Samantha Cooray, Kimberly C Gilmour, et al.
Nature Communications|March 13, 2021
Long-term lymphoid progenitors independently sustain naïve T and NK cell production in humansNatalia Izotova, Christine Rivat, Cristina Baricordi, et al.
Journal of Clinical Immunology|February 10, 2015
Variable phenotype of severe immunodeficiencies associated with RMRP gene mutationsWinnie Ip, H Bobby Gaspar, Robert Kleta, et al.
The Journal of Allergy and Clinical Immunology|January 23, 2018
T-cell gene therapy for perforin deficiency corrects cytotoxicity defects and prevents hemophagocytic lymphohistiocytosis manifestationsSujal Ghosh, Marlene Carmo, Miguel Calero-Garcia, et al.
The Journal of Allergy and Clinical Immunology|August 15, 2016
Mutations in linker for activation of T cells (LAT) lead to a novel form of severe combined immunodeficiencyChiara Bacchelli, Federico A Moretti, Marlene Carmo, et al.
Nature|September 22, 2006
Gene therapy: X-SCID transgene leukaemogenicityAdrian J Thrasher, H Bobby Gaspar, Christopher Baum, et al.
Mechanisms of Ageing and Development|July 5, 2005
The impact of telomere erosion on memory CD8+ T cells in patients with X-linked lymphoproliferative syndromeFiona J Plunkett, Ornella Franzese, Lavina L Belaramani, et al.
Molecular Therapy. Methods & Clinical Development|May 3, 2019
Pre-clinical Safety and Efficacy of Lentiviral Vector-Mediated <i>Ex Vivo</i> Stem Cell Gene Therapy for the Treatment of Mucopolysaccharidosis IIIAStuart M Ellison, Aiyin Liao, Shaun Wood, et al.
Pageof 12

Showing results (61-70 of 115) with videos related to

Sort By:
Pageof 12
Human Gene Therapy|June 19, 2008
Abnormal expression of only the CD34 part of a transgenic CD34/herpes simplex virus-thymidine kinase fusion protein is associated with ganciclovir resistanceEmad Bennour, Christophe Ferrand, Jean-Paul Rémy-Martin, et al.
Blood|July 23, 2008
Cognitive and behavioral abnormalities in children after hematopoietic stem cell transplantation for severe congenital immunodeficienciesPenny Titman, Elizabeth Pink, Emily Skucek, et al.
Science Translational Medicine|August 26, 2011
Long-term persistence of a polyclonal T cell repertoire after gene therapy for X-linked severe combined immunodeficiencyH Bobby Gaspar, Samantha Cooray, Kimberly C Gilmour, et al.
Nature Communications|March 13, 2021
Long-term lymphoid progenitors independently sustain naïve T and NK cell production in humansNatalia Izotova, Christine Rivat, Cristina Baricordi, et al.
Journal of Clinical Immunology|February 10, 2015
Variable phenotype of severe immunodeficiencies associated with RMRP gene mutationsWinnie Ip, H Bobby Gaspar, Robert Kleta, et al.
The Journal of Allergy and Clinical Immunology|January 23, 2018
T-cell gene therapy for perforin deficiency corrects cytotoxicity defects and prevents hemophagocytic lymphohistiocytosis manifestationsSujal Ghosh, Marlene Carmo, Miguel Calero-Garcia, et al.
The Journal of Allergy and Clinical Immunology|August 15, 2016
Mutations in linker for activation of T cells (LAT) lead to a novel form of severe combined immunodeficiencyChiara Bacchelli, Federico A Moretti, Marlene Carmo, et al.
Nature|September 22, 2006
Gene therapy: X-SCID transgene leukaemogenicityAdrian J Thrasher, H Bobby Gaspar, Christopher Baum, et al.
Mechanisms of Ageing and Development|July 5, 2005
The impact of telomere erosion on memory CD8+ T cells in patients with X-linked lymphoproliferative syndromeFiona J Plunkett, Ornella Franzese, Lavina L Belaramani, et al.
Molecular Therapy. Methods & Clinical Development|May 3, 2019
Pre-clinical Safety and Efficacy of Lentiviral Vector-Mediated <i>Ex Vivo</i> Stem Cell Gene Therapy for the Treatment of Mucopolysaccharidosis IIIAStuart M Ellison, Aiyin Liao, Shaun Wood, et al.
Pageof 12