نتایج جستجو برای: hyper immunoglobulin e syndrome

تعداد نتایج: 1675937  

Journal: :iranian journal of allergy, asthma and immunology 0
j. majidi a. zavaran ilosseini zm. hassan mh. alimohamadian

immunoglobulin e is one of the five classes of immonoglobulins that plays an important role in allergic diseases. production of monoclonal antibodies by a single clonotype against different epitopes of immunoglobulin e has high priority in development of diagnostic kits. in this study, an attempt was made to produce monoclonal antibodies against human immunoglobulin e. balb/c mice were immunize...

Journal: :Microbial pathogenesis 1999
L Wang H Curd P R Reeves

Shiga toxin-producing Escherichia coli strains of serogroup O111 are the most frequently isolated non-O157 strains causing outbreaks of gastroenteritis with haemolytic uraemic syndrome (HUS). O antigen is a major antigen in Gram-negative bacteria, and it has been shown that O111 is a protective antigen. Attenuated Salmonella enterica sv Typhimurium aroA strain STM-1 was used as a live carrier t...

Journal: :medical journal of islamic republic of iran 0
shohreh movahedi fellowship in infertility, department of infertility of shariati hospital, tehran university of medical sciences, tehran, iran. leili safdarian fellowship in infertility, department of infertility, tehran university of medical sciences, tehran, iran. marzieh agahoseini department of infertility of shariati hospital, tehran university of medical sciences, tehran, iran. ashraf aleyasin department of infertility of shariati hospital, tehran university of medical sciences, tehran, iran. sepideh khodaverdi endometriosis research center, iran university of medical sciences, tehran, iran. sara asadollah endometriosis research center, iran university of medical sciences, tehran, iran.

background: release of vascular endothelial growth factor (vegf) by ovaries in response to hcg administration is one of the main mechanisms of ovarian hyper stimulation syndrome. since dopamine/dopamine receptor2 (dp-r2) pathway activity -mediated by vegf/ vascular endothelial growth factor receptor 2 (vegfr-2) signaling-, is associated with angiogenic events, dopamine agonists were used for th...

Journal: :iranian journal of allergy, asthma and immunology 0
mojgan safari nima rezaei mehrdad hajilooi asghar aghamohammadi qiang pan-hammarstrom lennart hammarstrom

immunoglobulin class switch recombination deficiencies (ig csr deficiencies) or hyper igm syndromes (higm) are a group of primary immunodeficiency diseases, characterized by defective cd40 signaling of b cells resulting into a csr and a somatic hypermutation. the affected patients are characterized with reduced serum levels of igg and iga, and normal or elevated level of igm, which lead to incr...

Setareh Abdoli, Simin Almasi,

Background: Sjögren’s syndrome is the second most common systemic autoimmune disease after rheumatoid arthritis, RA, with a prevalence of about 0.5% in the general population. It occurs primarily in perimenopausal women (at a ratio of women to men of 9: 1) Sjögren’s syndrome is characterized by lymphocytic infiltration to exocrine glands. The specific autoantibodies of this syndrome are against...

Journal: :The Journal of Experimental Medicine 1985
L Mayer D N Posnett H G Kunkel

Evidence is presented for the existence of a "switch" T cell derived from a patient with mycosis fungoides/Sezary's syndrome. The serum immunoglobulin profile in this patient revealed high IgG and IgA but no detectable IgM. Peripheral blood mononuclear cells from this patient secreted only IgG and IgA in the presence of pokeweed mitogen. T cells (Trac) co-cultured with normal allogeneic non-T c...

Journal: :Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi 2004
Chen-Tong Hsu Yu-Tsan Lin Yao-Hsu Yang Bor-Luen Chiang

Hyperimmunoglobulin E syndrome is a primary immunodeficiency disease characterized by markedly high titers of serum immunoglobulin E (IgE), chronic eczema, recurrent staphylococcal infections, pneumatoceles, reduced neutrophil chemotaxis, and variable impaired T cell function. There are no clinical tools for diagnosis and definitive laboratory investigation. Variability of presentation makes it...

2015
Mattia Capulli Antonio Maurizi Luca Ventura Nadia Rucci Anna Teti

In about 70% of patients affected by autosomal dominant osteopetrosis type 2 (ADO2), osteoclast activity is reduced by heterozygous mutations of the CLCN7 gene, encoding the ClC-7 chloride/hydrogen antiporter. CLCN7(G215R)-, CLCN7(R767W)-, and CLCN7(R286W)-specific siRNAs silenced transfected mutant mRNA/EGFP in HEK293 cells, in RAW264.7 cells and in human osteoclasts, with no change of CLCN7(W...

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