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L D Notarangelo

Showing results (121-130 of 165) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|December 20, 1994
Structural basis for chromosome X-linked agammaglobulinemia: a tyrosine kinase diseaseM Vihinen, D Vetrie, H S Maniar, et al.
The Journal of Pathology|February 21, 2007
CEACAM1/VEGF cross-talk during neuroblastic tumour differentiationP L Poliani, S Mitola, M Ravanini, et al.
Nature|February 11, 1993
Defective expression of T-cell CD40 ligand causes X-linked immunodeficiency with hyper-IgMU Korthäuer, D Graf, H W Mages, et al.
Mucosal Immunology|May 18, 2017
Jak3 deficiency blocks innate lymphoid cell developmentM L Robinette, M Cella, J B Telliez, et al.
British Journal of Haematology|June 20, 1998
Mutation analysis by a non-radioactive single-strand conformation polymorphism assay in nine families with X-linked severe combined immunodeficiency (SCIDX1)G S Wengler, S Giliani, M Fiorini, et al.
Bone Marrow Transplantation|October 3, 2006
Stem cell transplantation for the Wiskott-Aldrich syndrome: a single-center experience confirms efficacy of matched unrelated donor transplantationS-Y Pai, D DeMartiis, C Forino, et al.
Genes and Immunity|October 8, 2010
PTX3 genetic variations affect the risk of Pseudomonas aeruginosa airway colonization in cystic fibrosis patientsM Chiarini, C Sabelli, P Melotti, et al.
Science (New York, N.Y.)|October 20, 1995
Gene therapy in peripheral blood lymphocytes and bone marrow for ADA- immunodeficient patientsC Bordignon, L D Notarangelo, N Nobili, et al.
Cell|June 18, 1998
Partial V(D)J recombination activity leads to Omenn syndromeA Villa, S Santagata, F Bozzi, et al.
Bone Marrow Transplantation|May 24, 2005
Hematopoietic stem cell transplantation in Omenn syndrome: a single-center experienceE Mazzolari, D Moshous, C Forino, et al.
Pageof 17

Showing results (121-130 of 165) with videos related to

Sort By:
Pageof 17
Proceedings of the National Academy of Sciences of the United States of America|December 20, 1994
Structural basis for chromosome X-linked agammaglobulinemia: a tyrosine kinase diseaseM Vihinen, D Vetrie, H S Maniar, et al.
The Journal of Pathology|February 21, 2007
CEACAM1/VEGF cross-talk during neuroblastic tumour differentiationP L Poliani, S Mitola, M Ravanini, et al.
Nature|February 11, 1993
Defective expression of T-cell CD40 ligand causes X-linked immunodeficiency with hyper-IgMU Korthäuer, D Graf, H W Mages, et al.
Mucosal Immunology|May 18, 2017
Jak3 deficiency blocks innate lymphoid cell developmentM L Robinette, M Cella, J B Telliez, et al.
British Journal of Haematology|June 20, 1998
Mutation analysis by a non-radioactive single-strand conformation polymorphism assay in nine families with X-linked severe combined immunodeficiency (SCIDX1)G S Wengler, S Giliani, M Fiorini, et al.
Bone Marrow Transplantation|October 3, 2006
Stem cell transplantation for the Wiskott-Aldrich syndrome: a single-center experience confirms efficacy of matched unrelated donor transplantationS-Y Pai, D DeMartiis, C Forino, et al.
Genes and Immunity|October 8, 2010
PTX3 genetic variations affect the risk of Pseudomonas aeruginosa airway colonization in cystic fibrosis patientsM Chiarini, C Sabelli, P Melotti, et al.
Science (New York, N.Y.)|October 20, 1995
Gene therapy in peripheral blood lymphocytes and bone marrow for ADA- immunodeficient patientsC Bordignon, L D Notarangelo, N Nobili, et al.
Cell|June 18, 1998
Partial V(D)J recombination activity leads to Omenn syndromeA Villa, S Santagata, F Bozzi, et al.
Bone Marrow Transplantation|May 24, 2005
Hematopoietic stem cell transplantation in Omenn syndrome: a single-center experienceE Mazzolari, D Moshous, C Forino, et al.
Pageof 17