نتایج جستجو برای: کمپلکس iga – α1at
تعداد نتایج: 30614 فیلتر نتایج به سال:
چکید ه سابقه و هدف آرتریت روماتوئید یک بیماری مزمن التهابی شدید می باشد. در بیماری های التهابی از جمله آرتریت روماتوئید میزان iga در سرم افزایش می یابد که به دنبال آن iga اضافی می تواند بابرخی از پروتئین های موجود درسرم از جمله آلفا-1-آنتی تریپسین ( a 1 at ) میانکنش داشته و تشکیل کمپلکس غیرایمنی بدهد. آزمایش های سرولوژی رایج تشخیصی برای آرتریت روماتوئید از جمله rf ، esr وcrp در مواردی پاسخ من...
چکید ه سابقه و هدف آرتریت روماتوئید یک بیماری مزمن التهابی شدید میباشد. در بیماریهای التهابی از جمله آرتریت روماتوئید میزان IgA در سرم افزایش مییابد که بهدنبال آن IgA اضافی میتواند بابرخی از پروتئینهای موجود درسرم از جمله آلفا-1-آنتی تریپسین ( a 1 AT ) میانکنش داشته و تشکیل کمپلکس غیرایمنی بدهد. آزمایشهای سرولوژی رایج تشخیصی برای آرتریت روماتوئید از جمله RF ، ESR وCRP در مواردی پاس...
Association between reduced serum alpha-1 antitrypsin (α1AT) concentration and HIV infection has been reported. The possible role of α1AT in a subset of people living with HIV who achieved control over HIV-1 disease progression without treatment has not been substantiated. We thus hypothesized that increased serum concentrations of α1AT would be associated with control of HIV disease progressio...
α1-Antitrypsin (α1AT) deficiency, the most common serpinopathy, results in both emphysema and liver disease. Over 90% of all clinical cases of α1AT deficiency are caused by the Z variant in which Glu342, located at the top of s5A, is replaced by a Lys which results in polymerization both in vivo and in vitro. The Glu342Lys mutation removes a salt bridge and a hydrogen bond but does not effect t...
Polymerization of the Z variant alpha-1-antitrypsin (Z-α1AT) results in the most common and severe form of α1AT deficiency (α1ATD), a debilitating genetic disorder whose clinical manifestations range from asymptomatic to fatal liver and/or lung disease. As the altered conformation of Z-α1AT and its attendant aggregation are responsible for pathogenesis, the polymerization process per se has bec...
UNLABELLED Point mutants of alpha1 -antitrypsin (α1AT) form ordered polymers that are retained as inclusions within the endoplasmic reticulum (ER) of hepatocytes in association with neonatal hepatitis, cirrhosis, and hepatocellular carcinoma. These inclusions cause cell damage and predispose to ER stress in the absence of the classical unfolded protein response (UPR). The pathophysiology underl...
Emphysema and liver cirrhosis can be caused by the Z mutation (Glu342Lys) in the serine protease inhibitor α1-antitrypsin (α1AT), which is found in more than 4% of the Northern European population. Homozygotes experience deficiency in the lung concomitantly with a massive accumulation of polymers within hepatocytes, causing their destruction. Recently, it was proposed that Z-α1AT polymerizes by...
α(1)-Antitrypsin (α1AT) deficiency is a disease with multiple manifestations, including cirrhosis and emphysema, caused by the accumulation of stable polymers of mutant protein in the endoplasmic reticulum of hepatocytes. However, the molecular basis of misfolding and polymerization remain unknown. We produced and crystallized a trimeric form of α1AT that is recognized by an antibody specific f...
BACKGROUND Alpha 1-antitrypsin (α1AT) belongs to the superfamily of serpins and inhibits different proteases. α1AT protects the lung from cellular inflammatory enzymes. In the absence of α1AT, the degradation of lung tissue results to pulmonary complications. The pulmonary route is a potent noninvasive route for systemic and local delivery. The aerosolized α1AT not only affects locally its main...
C-reactive protein (CRP), serum amyloid A (SAA), interleukin-6 (IL-6), α1-antitrypsin (α1AT), α1-acid glycoprotein (α1AG) and ceruloplasmin (CP) are acute inflammatory biomarkers that increase in various conditions including infection, inflammation, malignancy and tissue disturbance. In contrast, α2-macroglobulin (α2M) is involved in inflammation through its function as a carrier protein of IL-...
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