نتایج جستجو برای: hyper igm

تعداد نتایج: 40595  

2016
Nobuko Matsushita Midori Suzuki Emi Ikebe Shun Nagashima Ryoko Inatome Kenichi Asano Masato Tanaka Masayuki Matsushita Eisaku Kondo Hidekatsu Iha Shigeru Yanagi

Tax1-binding protein 1 (TAX1BP1) is a ubiquitin-binding protein that restricts nuclear factor-κB (NF-κB) activation and facilitates the termination of aberrant inflammation. However, its roles in B-cell activation and differentiation are poorly understood. To evaluate the function of TAX1BP1 in B cells, we established TAX1BP1-deficient DT40 B cells that are hyper-responsive to CD40-induced extr...

Journal: :Cell 2000
Masamichi Muramatsu Kazuo Kinoshita Sidonia Fagarasan Shuichi Yamada Yoichi Shinkai Tasuku Honjo

Induced overexpression of AID in CH12F3-2 B lymphoma cells augmented class switching from IgM to IgA without cytokine stimulation. AID deficiency caused a complete defect in class switching and showed a hyper-IgM phenotype with enlarged germinal centers containing strongly activated B cells before or after immunization. AID-/- spleen cells stimulated in vitro with LPS and cytokines failed to un...

2010
Beatriz Rodríguez-Bayona Ana Ramos-Amaya José J Pérez-Venegas Carmen Rodríguez José A Brieva

INTRODUCTION Systemic lupus erythematosus (SLE) is characterized by B cell hyper-activation and auto-reactivity resulting in pathogenic auto-antibody generation. The phenotypic analysis of blood B cell subsets can be used to understand these alterations. METHODS The combined detection of CD19, CD27 and IgD (or IgM) by flow cytometry (FC) analysis delineates five well-defined blood B cell-subs...

Journal: :Journal of Korean Medical Science 2002
Eun Kyeong Jo Hyung Seok Kim Min Young Lee Motohiro Iseki Jae Ho Lee Chang Hwa Song Jeong Kyu Park Tai Ju Hwang Hoon Kook

X-linked hyper-IgM syndrome (XHIM) is a rare primary immunodeficiency disorder, caused by mutations of the gene encoding CD40 ligand (CD40L; CD154). We report the clinical manifestations and mutational analysis of the CD40L gene observed in a male patient from a XHIM family. Having hypogammaglobulinemia and elevated IgM, the 3-yr-old boy exhibited the characteristic clinical features of XHIM. T...

Journal: :Journal of investigational allergology & clinical immunology 2009
S Kashef M Mehdi Ghaedian N Rezaei Z Karamizadeh A Aghamohammadi A Durandy Q Pan-Hammarstrom L Hammarstrom

Growth hormone deficiency (GHD) may be associated with a number of immunodeficiency diseases, but its association with immunoglobulin class switch recombination (Ig CSR) deficiencies is very rare. We report the case of a patient with a history of recurrent diarrhea and respiratory infections diagnosed with hyper IgM syndrome on the basis of immunological findings (low serum levels of IgG and Ig...

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