نتایج جستجو برای: c3 polymorphism
تعداد نتایج: 123520 فیلتر نتایج به سال:
Most important food and feed crops in the world belong to the C3 grass family. The future of food security is highly reliant on achieving genetic gains of those grasses. Conventional breeding methods have already reached a plateau for improving major crops. Genomics tools and resources have opened an avenue to explore genome-wide variability and make use of the variation for enhancing genetic g...
Complement blockade by eculizumab is clinically effective in hemolytic paroxysmal nocturnal hemoglobinuria. However, the response is variable and some patients remain dependent on red blood cell transfusions. In 72 patients with hemolytic paroxysmal nocturnal hemoglobinuria on eculizumab we tested the hypothesis that response may depend on genetic polymorphisms of complement-related genes. We f...
BACKGROUND Age-related macular degeneration is the most common cause of blindness in Western populations. Susceptibility is influenced by age and by genetic and environmental factors. Complement activation is implicated in the pathogenesis. METHODS We tested for an association between age-related macular degeneration and 13 single-nucleotide polymorphisms (SNPs) spanning the complement genes ...
Complement activation is common in patients with IgA nephropathy (IgAN) and associated with disease severity. Our recent genome-wide association study of IgAN identified susceptibility loci on 1q32 containing the complement regulatory protein-encoding genes CFH and CFHR1-5, with rs6677604 in CFH as the top single-nucleotide polymorphism and CFHR3-1 deletion (CFHR3-1∆) as the top signal for copy...
Preeclampsia (PE) is a common vascular disease of pregnancy with genetic predisposition. Dysregulation of the complement system has been implicated, but molecular mechanisms are incompletely understood. In this study, we determined the potential linkage of severe PE to the most central complement gene, C3. Three cohorts of Finnish patients and controls were recruited for a genetic case-control ...
Chronic venous diseases (CVD), including varicose veins, are among the most common in developed countries Europe and United States affect one third to half of population, especially women. Among many achievements knowledge pathogenesis achievements, it should be noted identification role matrix metalloproteinases (MMPs) as important mediators degenerative process associated with onset progressi...
Age-related macular degeneration (AMD) is the leading cause of blindness in the elderly in the developed world. Numerous genetic factors contribute to the development of the multifactorial disease. We performed a case-control study to assess the risk conferred by known and candidate genetic polymorphisms on the development of AMD. We searched for genetic interactions and for differences in dry ...
مقدمه تخریب وابسته به سن ماکولا (amd) شایعترین علت نابینایی برگشت ناپذیر در افراد مسن سراسر جهان محسوب می شود. در کنار عوامل محیطی از جمله سن و مصرف سیگار، واریانتهای ژنتیکی از لوکوس های ژنی متعدد با این بیماری ارتباط دارد. پلی مورفیسم های متعددی در بروز این بیماری دخیل می باشند که یکی از آنها پلی مورفیسم rs2230199 ژن c3 است که مهمترین پروتئین سیستم کمپلمان را کد میکند. در این مطالعه ما به ...
background: the serum levels of c 3 , c4, and the total hemolytic activity of complement system (ch50) of patients exposed to mustard gas (mg) in the battlefield were measured in this study. methods: c3 and c4 were measured by single radial immunodifusion and ch50 was evaluated according to total hemolytic activity of the serum. results: the serum levels of c 3 showed a significant increase...
نمودار تعداد نتایج جستجو در هر سال
با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید