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S Giliani

Showing results (11-20 of 44) with videos related to

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Prenatal Diagnosis|July 27, 1999
Prenatal diagnosis of JAK3 deficient SCIDR F Schumacher, P Mella, F Lalatta, et al.
Bone Marrow Transplantation|May 16, 2007
First report of successful stem cell transplantation in a child with CD40 deficiencyE Mazzolari, G Lanzi, C Forino, et al.
Mutation Research|March 1, 1994
Molecular analysis of the XP-D gene in Italian families with patients affected by trichothiodystrophy and xeroderma pigmentosum group DC Mondello, T Nardo, S Giliani, et al.
Immunodeficiency|January 1, 1993
Analysis of X-chromosome inactivation in bone marrow precursors from carriers of Wiskott-Aldrich syndrome and X-linked severe combined immunodeficiency: evidence that the Wiskott-Aldrich gene is expressed prior to granulocyte-macrophage colony-forming-unitE Mantuano, F Candotti, S Giliani, et al.
Carcinogenesis|June 1, 1993
Genetic heterogeneity of the excision repair defect associated with trichothiodystrophyM Stefanini, P Lagomarsini, S Giliani, et al.
American Journal of Human Genetics|April 1, 1995
Characterization of nine novel mutations in the CD40 ligand gene in patients with X-linked hyper IgM syndrome of various ancestryP Macchi, A Villa, D Strina, et al.
The Journal of Pathology|August 26, 1998
Defective actin polymerization in EBV-transformed B-cell lines from patients with the Wiskott-Aldrich syndromeF Facchetti, L Blanzuoli, W Vermi, et al.
European Journal of Immunology|August 1, 1994
Ineffective expression of CD40 ligand on cord blood T cells may contribute to poor immunoglobulin production in the newbornD Brugnoni, P Airò, D Graf, et al.
Human Mutation|January 1, 1994
C to T mutation causing premature termination of CD40 ligand at amino acid 221 in a patient affected by hyper IgM syndromeA Villa, D Strina, P Macchi, et al.
Immunodeficiency|January 1, 1993
Molecular analysis of X-linked immunodeficiency with hyper-IgM and X-linked lymphoproliferative syndromeL D Notarangelo, E Mantuano, S Bione, et al.
Pageof 5

Showing results (11-20 of 44) with videos related to

Sort By:
Pageof 5
Prenatal Diagnosis|July 27, 1999
Prenatal diagnosis of JAK3 deficient SCIDR F Schumacher, P Mella, F Lalatta, et al.
Bone Marrow Transplantation|May 16, 2007
First report of successful stem cell transplantation in a child with CD40 deficiencyE Mazzolari, G Lanzi, C Forino, et al.
Mutation Research|March 1, 1994
Molecular analysis of the XP-D gene in Italian families with patients affected by trichothiodystrophy and xeroderma pigmentosum group DC Mondello, T Nardo, S Giliani, et al.
Immunodeficiency|January 1, 1993
Analysis of X-chromosome inactivation in bone marrow precursors from carriers of Wiskott-Aldrich syndrome and X-linked severe combined immunodeficiency: evidence that the Wiskott-Aldrich gene is expressed prior to granulocyte-macrophage colony-forming-unitE Mantuano, F Candotti, S Giliani, et al.
Carcinogenesis|June 1, 1993
Genetic heterogeneity of the excision repair defect associated with trichothiodystrophyM Stefanini, P Lagomarsini, S Giliani, et al.
American Journal of Human Genetics|April 1, 1995
Characterization of nine novel mutations in the CD40 ligand gene in patients with X-linked hyper IgM syndrome of various ancestryP Macchi, A Villa, D Strina, et al.
The Journal of Pathology|August 26, 1998
Defective actin polymerization in EBV-transformed B-cell lines from patients with the Wiskott-Aldrich syndromeF Facchetti, L Blanzuoli, W Vermi, et al.
European Journal of Immunology|August 1, 1994
Ineffective expression of CD40 ligand on cord blood T cells may contribute to poor immunoglobulin production in the newbornD Brugnoni, P Airò, D Graf, et al.
Human Mutation|January 1, 1994
C to T mutation causing premature termination of CD40 ligand at amino acid 221 in a patient affected by hyper IgM syndromeA Villa, D Strina, P Macchi, et al.
Immunodeficiency|January 1, 1993
Molecular analysis of X-linked immunodeficiency with hyper-IgM and X-linked lymphoproliferative syndromeL D Notarangelo, E Mantuano, S Bione, et al.
Pageof 5