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Blood
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February 3, 1998
Development of autologous, oligoclonal, poorly functioning T lymphocytes in a patient with autosomal recessive severe combined immunodeficiency caused by defects of the Jak3 tyrosine kinase
D Brugnoni, L D Notarangelo, A Sottini, et al.
Blood
|
March 15, 1997
Mutation analysis of IL2RG in human X-linked severe combined immunodeficiency
J M Puck, A E Pepper, P S Henthorn, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
April 26, 2001
Comparison of five retrovirus vectors containing the human IL-2 receptor gamma chain gene for their ability to restore T and B lymphocytes in the X-linked severe combined immunodeficiency mouse model
G J Avilés Mendoza, N E Seidel, M Otsu, 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.
Immunity
|
December 1, 1996
Signaling via IL-2 and IL-4 in JAK3-deficient severe combined immunodeficiency lymphocytes: JAK3-dependent and independent pathways
S A Oakes, F Candotti, J A Johnston, et al.
Molecular Cell
|
December 14, 2001
Unexpected effects of FERM domain mutations on catalytic activity of Jak3: structural implication for Janus kinases
Y J Zhou, M Chen, N A Cusack, et al.
Blood
|
November 14, 1997
Structural and functional basis for JAK3-deficient severe combined immunodeficiency
F Candotti, S A Oakes, J A Johnston, et al.
Genes and Immunity
|
January 10, 2002
Unexpected and variable phenotypes in a family with JAK3 deficiency
D M Frucht, M Gadina, G J Jagadeesh, et al.
The New England Journal of Medicine
|
July 17, 2014
Activated STING in a vascular and pulmonary syndrome
Y Liu, A A Jesus, B Marrero, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 49) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 49 results.
Blood
|
February 3, 1998
Development of autologous, oligoclonal, poorly functioning T lymphocytes in a patient with autosomal recessive severe combined immunodeficiency caused by defects of the Jak3 tyrosine kinase
D Brugnoni, L D Notarangelo, A Sottini, et al.
Blood
|
March 15, 1997
Mutation analysis of IL2RG in human X-linked severe combined immunodeficiency
J M Puck, A E Pepper, P S Henthorn, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
April 26, 2001
Comparison of five retrovirus vectors containing the human IL-2 receptor gamma chain gene for their ability to restore T and B lymphocytes in the X-linked severe combined immunodeficiency mouse model
G J Avilés Mendoza, N E Seidel, M Otsu, 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.
Immunity
|
December 1, 1996
Signaling via IL-2 and IL-4 in JAK3-deficient severe combined immunodeficiency lymphocytes: JAK3-dependent and independent pathways
S A Oakes, F Candotti, J A Johnston, et al.
Molecular Cell
|
December 14, 2001
Unexpected effects of FERM domain mutations on catalytic activity of Jak3: structural implication for Janus kinases
Y J Zhou, M Chen, N A Cusack, et al.
Blood
|
November 14, 1997
Structural and functional basis for JAK3-deficient severe combined immunodeficiency
F Candotti, S A Oakes, J A Johnston, et al.
Genes and Immunity
|
January 10, 2002
Unexpected and variable phenotypes in a family with JAK3 deficiency
D M Frucht, M Gadina, G J Jagadeesh, et al.
The New England Journal of Medicine
|
July 17, 2014
Activated STING in a vascular and pulmonary syndrome
Y Liu, A A Jesus, B Marrero, et al.
Page
of 5