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S Nonoyama

Showing results (51-60 of 66) with videos related to

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The Journal of Clinical Investigation|January 1, 1995
Diminished expression of CD40 ligand by activated neonatal T cellsS Nonoyama, L A Penix, C P Edwards, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|September 17, 2010
Characteristics of paediatric patients with 2009 pandemic influenza A(H1N1) and severe, oxygen-requiring pneumonia in the Tokyo region, 1 September-31 October 2009M Nishiyama, Y Yoshida, M Sato, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1994
CD40 ligand expression is defective in a subset of patients with common variable immunodeficiencyM Farrington, L S Grosmaire, S Nonoyama, et al.
The Journal of Clinical Investigation|August 1, 1994
The random inactivation of the X chromosome carrying the defective gene responsible for X-linked hyper IgM syndrome (X-HIM) in female carriers of HIGM1D Hollenbaugh, L H Wu, H D Ochs, et al.
The Journal of Clinical Investigation|August 26, 1998
Absence of IgD-CD27(+) memory B cell population in X-linked hyper-IgM syndromeK Agematsu, H Nagumo, K Shinozaki, et al.
Clinical and Experimental Rheumatology|September 3, 2010
Hyper IgM syndrome and complement Clq deficiency in an individual with systemic lupus erythematosus-like diseaseI Tsuge, Y Kondo, Y Nakajima, et al.
Journal of Investigational Allergology & Clinical Immunology|October 16, 2010
Ataxia-telangiectasia in a patient presenting with hyper-immunoglobulin M syndromeA Aghamohammadi, K Imai, K Moazzami, et al.
Immunity|October 8, 1999
Ku in the cytoplasm associates with CD40 in human B cells and translocates into the nucleus following incubation with IL-4 and anti-CD40 mAbT Morio, S H Hanissian, L B Bacharier, et al.
Journal of Immunology (Baltimore, Md. : 1950)|September 21, 2001
Characterization of mutations, including a novel regulatory defect in the first intron, in Bruton's tyrosine kinase gene from seven Korean X-linked agammaglobulinemia familiesE K Jo, H Kanegane, S Nonoyama, et al.
Blood|March 9, 1999
Involvement of wiskott-aldrich syndrome protein in B-cell cytoplasmic tyrosine kinase pathwayY Baba, S Nonoyama, M Matsushita, et al.
Pageof 7

Showing results (51-60 of 66) with videos related to

Sort By:
Pageof 7
The Journal of Clinical Investigation|January 1, 1995
Diminished expression of CD40 ligand by activated neonatal T cellsS Nonoyama, L A Penix, C P Edwards, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|September 17, 2010
Characteristics of paediatric patients with 2009 pandemic influenza A(H1N1) and severe, oxygen-requiring pneumonia in the Tokyo region, 1 September-31 October 2009M Nishiyama, Y Yoshida, M Sato, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1994
CD40 ligand expression is defective in a subset of patients with common variable immunodeficiencyM Farrington, L S Grosmaire, S Nonoyama, et al.
The Journal of Clinical Investigation|August 1, 1994
The random inactivation of the X chromosome carrying the defective gene responsible for X-linked hyper IgM syndrome (X-HIM) in female carriers of HIGM1D Hollenbaugh, L H Wu, H D Ochs, et al.
The Journal of Clinical Investigation|August 26, 1998
Absence of IgD-CD27(+) memory B cell population in X-linked hyper-IgM syndromeK Agematsu, H Nagumo, K Shinozaki, et al.
Clinical and Experimental Rheumatology|September 3, 2010
Hyper IgM syndrome and complement Clq deficiency in an individual with systemic lupus erythematosus-like diseaseI Tsuge, Y Kondo, Y Nakajima, et al.
Journal of Investigational Allergology & Clinical Immunology|October 16, 2010
Ataxia-telangiectasia in a patient presenting with hyper-immunoglobulin M syndromeA Aghamohammadi, K Imai, K Moazzami, et al.
Immunity|October 8, 1999
Ku in the cytoplasm associates with CD40 in human B cells and translocates into the nucleus following incubation with IL-4 and anti-CD40 mAbT Morio, S H Hanissian, L B Bacharier, et al.
Journal of Immunology (Baltimore, Md. : 1950)|September 21, 2001
Characterization of mutations, including a novel regulatory defect in the first intron, in Bruton's tyrosine kinase gene from seven Korean X-linked agammaglobulinemia familiesE K Jo, H Kanegane, S Nonoyama, et al.
Blood|March 9, 1999
Involvement of wiskott-aldrich syndrome protein in B-cell cytoplasmic tyrosine kinase pathwayY Baba, S Nonoyama, M Matsushita, et al.
Pageof 7