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H Bobby Gaspar

Showing results (51-60 of 115) with videos related to

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Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|July 13, 2020
Busulfan Pharmacokinetics in Adenosine Deaminase-Deficient Severe Combined Immunodeficiency Gene TherapyKathryn L Bradford, Siyu Liu, Maja Krajinovic, et al.
Blood|May 27, 2006
Serial transplantation of mismatched donor hematopoietic cells between HLA-identical sibling pairs with congenital immunodeficiency: in vivo tolerance permits rapid immune reconstitution following T-replete transplantation without GVHD in the secondary recipientJonathan M Cohen, Valerie Rogers, H Bobby Gaspar, et al.
Blood|May 16, 2007
Successful treatment of lymphoproliferative disease complicating primary immunodeficiency/immunodysregulatory disorders with reduced-intensity allogeneic stem-cell transplantationJonathan M Cohen, Neil J Sebire, Julia Harvey, et al.
Cell Transplantation|August 25, 2017
Autologous Transplantation of Amniotic Fluid-Derived Mesenchymal Stem Cells into Sheep FetusesS W Steven Shaw, Sveva Bollini, Khalil Abi Nader, et al.
Blood|July 21, 2010
Impaired Epstein-Barr virus-specific CD8+ T-cell function in X-linked lymphoproliferative disease is restricted to SLAM family-positive B-cell targetsAndrew D Hislop, Umaimainthan Palendira, Alison M Leese, et al.
Journal of Clinical Immunology|April 28, 2007
Sequence analysis of TNFRSF13b, encoding TACI, in patients with systemic lupus erythematosusUlrich Salzer, Jennifer Birmelin, Chiara Bacchelli, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 9, 2008
Self-inactivating gammaretroviral vectors for gene therapy of X-linked severe combined immunodeficiencySusannah I Thornhill, Axel Schambach, Steven J Howe, et al.
British Journal of Haematology|October 24, 2006
CD34 stem cell top-ups without conditioning after initial haematopoietic stem cell transplantation for correction of incomplete haematopoietic and immunological recovery in severe congenital immunodeficienciesClaire Booth, Jean-Antoine Ribeil, Françoise Audat, et al.
Blood|April 25, 2019
Clinical and immunological features in a cohort of patients with partial DiGeorge syndrome followed at a single centerGiuliana Giardino, Nesrine Radwan, Patra Koletsi, et al.
Cell Transplantation|November 25, 2010
Autologous transplantation of amniotic fluid-derived mesenchymal stem cells into sheep fetusesS W Steven Shaw, Sveva Bollini, Khalil Abi Nader, et al.
Pageof 12

Showing results (51-60 of 115) with videos related to

Sort By:
Pageof 12
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|July 13, 2020
Busulfan Pharmacokinetics in Adenosine Deaminase-Deficient Severe Combined Immunodeficiency Gene TherapyKathryn L Bradford, Siyu Liu, Maja Krajinovic, et al.
Blood|May 27, 2006
Serial transplantation of mismatched donor hematopoietic cells between HLA-identical sibling pairs with congenital immunodeficiency: in vivo tolerance permits rapid immune reconstitution following T-replete transplantation without GVHD in the secondary recipientJonathan M Cohen, Valerie Rogers, H Bobby Gaspar, et al.
Blood|May 16, 2007
Successful treatment of lymphoproliferative disease complicating primary immunodeficiency/immunodysregulatory disorders with reduced-intensity allogeneic stem-cell transplantationJonathan M Cohen, Neil J Sebire, Julia Harvey, et al.
Cell Transplantation|August 25, 2017
Autologous Transplantation of Amniotic Fluid-Derived Mesenchymal Stem Cells into Sheep FetusesS W Steven Shaw, Sveva Bollini, Khalil Abi Nader, et al.
Blood|July 21, 2010
Impaired Epstein-Barr virus-specific CD8+ T-cell function in X-linked lymphoproliferative disease is restricted to SLAM family-positive B-cell targetsAndrew D Hislop, Umaimainthan Palendira, Alison M Leese, et al.
Journal of Clinical Immunology|April 28, 2007
Sequence analysis of TNFRSF13b, encoding TACI, in patients with systemic lupus erythematosusUlrich Salzer, Jennifer Birmelin, Chiara Bacchelli, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 9, 2008
Self-inactivating gammaretroviral vectors for gene therapy of X-linked severe combined immunodeficiencySusannah I Thornhill, Axel Schambach, Steven J Howe, et al.
British Journal of Haematology|October 24, 2006
CD34 stem cell top-ups without conditioning after initial haematopoietic stem cell transplantation for correction of incomplete haematopoietic and immunological recovery in severe congenital immunodeficienciesClaire Booth, Jean-Antoine Ribeil, Françoise Audat, et al.
Blood|April 25, 2019
Clinical and immunological features in a cohort of patients with partial DiGeorge syndrome followed at a single centerGiuliana Giardino, Nesrine Radwan, Patra Koletsi, et al.
Cell Transplantation|November 25, 2010
Autologous transplantation of amniotic fluid-derived mesenchymal stem cells into sheep fetusesS W Steven Shaw, Sveva Bollini, Khalil Abi Nader, et al.
Pageof 12