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Cell
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June 18, 1998
Partial V(D)J recombination activity leads to Omenn syndrome
A Villa, S Santagata, F Bozzi, et al.
Immunobiology
|
September 19, 2000
Combined immunodeficiencies due to defects in signal transduction: defects of the gammac-JAK3 signaling pathway as a model
L D Notarangelo, S Giliani, P Mella, et al.
Prenatal Diagnosis
|
March 12, 1999
Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysis
S Giliani, M Fiorini, P Mella, 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 characterization
P Mella, L Imberti, D Brugnoni, 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 cells
S Parolini, C Bottino, M Falco, et al.
Nature Genetics
|
July 11, 2000
Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis
A Frattini, P J Orchard, C Sobacchi, et al.
Autoimmunity Reviews
|
September 4, 2012
Aicardi-Goutieres syndrome, a rare neurological disease in children: a new autoimmune disorder?
Elisa Fazzi, Marco Cattalini, Simona Orcesi, et al.
Immunological Reviews
|
February 24, 2001
Of genes and phenotypes: the immunological and molecular spectrum of combined immune deficiency. Defects of the gamma(c)-JAK3 signaling pathway as a model
L D Notarangelo, S Giliani, C Mazza, et al.
Lancet (London, England)
|
November 30, 1996
In-utero transplantation of parental CD34 haematopoietic progenitor cells in a patient with X-linked severe combined immunodeficiency (SCIDXI)
G S Wengler, A Lanfranchi, T Frusca, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 25, 2001
Mutations of CD40 gene cause an autosomal recessive form of immunodeficiency with hyper IgM
S Ferrari, S Giliani, A Insalaco, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 44) with videos related to
Sort By:
Page
of 5
Cell
|
June 18, 1998
Partial V(D)J recombination activity leads to Omenn syndrome
A Villa, S Santagata, F Bozzi, et al.
Immunobiology
|
September 19, 2000
Combined immunodeficiencies due to defects in signal transduction: defects of the gammac-JAK3 signaling pathway as a model
L D Notarangelo, S Giliani, P Mella, et al.
Prenatal Diagnosis
|
March 12, 1999
Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysis
S Giliani, M Fiorini, P Mella, 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 characterization
P Mella, L Imberti, D Brugnoni, 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 cells
S Parolini, C Bottino, M Falco, et al.
Nature Genetics
|
July 11, 2000
Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis
A Frattini, P J Orchard, C Sobacchi, et al.
Autoimmunity Reviews
|
September 4, 2012
Aicardi-Goutieres syndrome, a rare neurological disease in children: a new autoimmune disorder?
Elisa Fazzi, Marco Cattalini, Simona Orcesi, et al.
Immunological Reviews
|
February 24, 2001
Of genes and phenotypes: the immunological and molecular spectrum of combined immune deficiency. Defects of the gamma(c)-JAK3 signaling pathway as a model
L D Notarangelo, S Giliani, C Mazza, et al.
Lancet (London, England)
|
November 30, 1996
In-utero transplantation of parental CD34 haematopoietic progenitor cells in a patient with X-linked severe combined immunodeficiency (SCIDXI)
G S Wengler, A Lanfranchi, T Frusca, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 25, 2001
Mutations of CD40 gene cause an autosomal recessive form of immunodeficiency with hyper IgM
S Ferrari, S Giliani, A Insalaco, et al.
Page
of 5