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L D Notarangelo

Showing results (131-140 of 165) with videos related to

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Journal of Medical Genetics|September 22, 2001
Six novel mutations in the PRF1 gene in children with haemophagocytic lymphohistiocytosisR Clementi, U zur Stadt, G Savoldi, et al.
Immunology Letters|January 1, 1996
Ontogeny of CD40L [corrected] expression by activated peripheral blood lymphocytes in humansD Brugnoni, P Airò, D Graf, et al.
British Journal of Haematology|September 30, 1998
Molecular and biochemical characterization of JAK3 deficiency in a patient with severe combined immunodeficiency over 20 years after bone marrow transplantation: implications for treatmentF Bozzi, G Lefranc, A Villa, et al.
Immunobiology|September 19, 2000
Combined immunodeficiencies due to defects in signal transduction: defects of the gammac-JAK3 signaling pathway as a modelL D Notarangelo, S Giliani, P Mella, et al.
Prenatal Diagnosis|March 12, 1999
Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysisS Giliani, M Fiorini, P Mella, et al.
Bone Marrow Transplantation|April 30, 2002
B cell function after haploidentical in utero bone marrow transplantation in a patient with severe combined immunodeficiencyJ Bartolomé, F Porta, A Lafranchi, et al.
Clinical Immunology (Orlando, Fla.)|May 4, 2000
Development of autologous T lymphocytes in two males with X-linked severe combined immune deficiency: molecular and cellular characterizationP Mella, L Imberti, D Brugnoni, et al.
Immunology Today|October 1, 1995
BTKbase: a database of XLA-causing mutations. International Study GroupM Vihinen, M D Cooper, G de Saint Basile, et al.
Molecular and Cellular Biology|July 13, 2000
Mutations in conserved regions of the predicted RAG2 kelch repeats block initiation of V(D)J recombination and result in primary immunodeficienciesC A Gomez, L M Ptaszek, A Villa, et al.
The Journal of Experimental Medicine|August 10, 2000
X-linked lymphoproliferative disease. 2B4 molecules displaying inhibitory rather than activating function are responsible for the inability of natural killer cells to kill Epstein-Barr virus-infected cellsS Parolini, C Bottino, M Falco, et al.
Pageof 17

Showing results (131-140 of 165) with videos related to

Sort By:
Pageof 17
Journal of Medical Genetics|September 22, 2001
Six novel mutations in the PRF1 gene in children with haemophagocytic lymphohistiocytosisR Clementi, U zur Stadt, G Savoldi, et al.
Immunology Letters|January 1, 1996
Ontogeny of CD40L [corrected] expression by activated peripheral blood lymphocytes in humansD Brugnoni, P Airò, D Graf, et al.
British Journal of Haematology|September 30, 1998
Molecular and biochemical characterization of JAK3 deficiency in a patient with severe combined immunodeficiency over 20 years after bone marrow transplantation: implications for treatmentF Bozzi, G Lefranc, A Villa, et al.
Immunobiology|September 19, 2000
Combined immunodeficiencies due to defects in signal transduction: defects of the gammac-JAK3 signaling pathway as a modelL D Notarangelo, S Giliani, P Mella, et al.
Prenatal Diagnosis|March 12, 1999
Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysisS Giliani, M Fiorini, P Mella, et al.
Bone Marrow Transplantation|April 30, 2002
B cell function after haploidentical in utero bone marrow transplantation in a patient with severe combined immunodeficiencyJ Bartolomé, F Porta, A Lafranchi, et al.
Clinical Immunology (Orlando, Fla.)|May 4, 2000
Development of autologous T lymphocytes in two males with X-linked severe combined immune deficiency: molecular and cellular characterizationP Mella, L Imberti, D Brugnoni, et al.
Immunology Today|October 1, 1995
BTKbase: a database of XLA-causing mutations. International Study GroupM Vihinen, M D Cooper, G de Saint Basile, et al.
Molecular and Cellular Biology|July 13, 2000
Mutations in conserved regions of the predicted RAG2 kelch repeats block initiation of V(D)J recombination and result in primary immunodeficienciesC A Gomez, L M Ptaszek, A Villa, et al.
The Journal of Experimental Medicine|August 10, 2000
X-linked lymphoproliferative disease. 2B4 molecules displaying inhibitory rather than activating function are responsible for the inability of natural killer cells to kill Epstein-Barr virus-infected cellsS Parolini, C Bottino, M Falco, et al.
Pageof 17