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H Bobby Gaspar

Showing results (41-50 of 115) with videos related to

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Clinical Immunology (Orlando, Fla.)|August 10, 2015
Spectrum of mutations in a cohort of UK patients with ADA deficient SCID: Segregation of genotypes with specific ethnicitiesStuart P Adams, Melanie Wilson, Elissar Harb, et al.
The Journal of Allergy and Clinical Immunology|September 9, 2018
Consensus approach for the management of severe combined immune deficiency caused by adenosine deaminase deficiencyDonald B Kohn, Michael S Hershfield, Jennifer M Puck, et al.
Blood|January 29, 2011
Neonatal diagnosis of severe combined immunodeficiency leads to significantly improved survival outcome: the case for newborn screeningLucinda Brown, Jinhua Xu-Bayford, Zoe Allwood, et al.
Blood|November 6, 2009
Functional characterization of alloreactive T cells identifies CD25 and CD71 as optimal targets for a clinically applicable allodepletion strategySujith Samarasinghe, Christoph Mancao, Martin Pule, et al.
Blood|September 16, 2004
Improved survival after unrelated donor bone marrow transplantation in children with primary immunodeficiency using a reduced-intensity conditioning regimenKanchan Rao, Persis J Amrolia, Alison Jones, et al.
British Journal of Haematology|April 9, 2005
Increased incidence of EBV-related disease following paediatric stem cell transplantation with reduced-intensity conditioningJonathan Cohen, Minal Gandhi, Paru Naik, et al.
Blood|April 26, 2007
Lentiviral vectors containing an enhancer-less ubiquitously acting chromatin opening element (UCOE) provide highly reproducible and stable transgene expression in hematopoietic cellsFang Zhang, Susannah I Thornhill, Steven J Howe, et al.
Molecular Therapy. Methods & Clinical Development|May 1, 2018
Preclinical Development of a Lentiviral Vector for Gene Therapy of X-Linked Severe Combined ImmunodeficiencyValentina Poletti, Sabine Charrier, Guillaume Corre, et al.
British Journal of Haematology|November 10, 2006
Capture and generation of adenovirus specific T cells for adoptive immunotherapyIlenia Chatziandreou, Kimberly C Gilmour, Anne-Marie McNicol, et al.
Scientific Reports|December 2, 2021
Metabolite and thymocyte development defects in ADA-SCID mice receiving enzyme replacement therapyFederico A Moretti, Giuliana Giardino, Teresa C H Attenborough, et al.
Pageof 12

Showing results (41-50 of 115) with videos related to

Sort By:
Pageof 12
Clinical Immunology (Orlando, Fla.)|August 10, 2015
Spectrum of mutations in a cohort of UK patients with ADA deficient SCID: Segregation of genotypes with specific ethnicitiesStuart P Adams, Melanie Wilson, Elissar Harb, et al.
The Journal of Allergy and Clinical Immunology|September 9, 2018
Consensus approach for the management of severe combined immune deficiency caused by adenosine deaminase deficiencyDonald B Kohn, Michael S Hershfield, Jennifer M Puck, et al.
Blood|January 29, 2011
Neonatal diagnosis of severe combined immunodeficiency leads to significantly improved survival outcome: the case for newborn screeningLucinda Brown, Jinhua Xu-Bayford, Zoe Allwood, et al.
Blood|November 6, 2009
Functional characterization of alloreactive T cells identifies CD25 and CD71 as optimal targets for a clinically applicable allodepletion strategySujith Samarasinghe, Christoph Mancao, Martin Pule, et al.
Blood|September 16, 2004
Improved survival after unrelated donor bone marrow transplantation in children with primary immunodeficiency using a reduced-intensity conditioning regimenKanchan Rao, Persis J Amrolia, Alison Jones, et al.
British Journal of Haematology|April 9, 2005
Increased incidence of EBV-related disease following paediatric stem cell transplantation with reduced-intensity conditioningJonathan Cohen, Minal Gandhi, Paru Naik, et al.
Blood|April 26, 2007
Lentiviral vectors containing an enhancer-less ubiquitously acting chromatin opening element (UCOE) provide highly reproducible and stable transgene expression in hematopoietic cellsFang Zhang, Susannah I Thornhill, Steven J Howe, et al.
Molecular Therapy. Methods & Clinical Development|May 1, 2018
Preclinical Development of a Lentiviral Vector for Gene Therapy of X-Linked Severe Combined ImmunodeficiencyValentina Poletti, Sabine Charrier, Guillaume Corre, et al.
British Journal of Haematology|November 10, 2006
Capture and generation of adenovirus specific T cells for adoptive immunotherapyIlenia Chatziandreou, Kimberly C Gilmour, Anne-Marie McNicol, et al.
Scientific Reports|December 2, 2021
Metabolite and thymocyte development defects in ADA-SCID mice receiving enzyme replacement therapyFederico A Moretti, Giuliana Giardino, Teresa C H Attenborough, et al.
Pageof 12