نتایج جستجو برای: c3 polymorphism

تعداد نتایج: 123520  

2017
Shyamal K. Talukder Malay C. Saha

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...

Journal: :Haematologica 2014
Tommaso Rondelli Antonio M Risitano Régis Peffault de Latour Michela Sica Benedetta Peruzzi Patrizia Ricci Wilma Barcellini Anna Paola Iori Carla Boschetti Veronica Valle Veronique Frémeaux-Bacchi Maria De Angioletti Gerard Socie Lucio Luzzatto Rosario Notaro

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...

Journal: :The New England journal of medicine 2007
John R W Yates Tiina Sepp Baljinder K Matharu Jane C Khan Deborah A Thurlby Humma Shahid David G Clayton Caroline Hayward Joanne Morgan Alan F Wright Ana Maria Armbrecht Baljean Dhillon Ian J Deary Elizabeth Redmond Alan C Bird Anthony T Moore

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 ...

Journal: :Journal of the American Society of Nephrology : JASN 2015
Li Zhu Ya-Ling Zhai Feng-Mei Wang Ping Hou Ji-Cheng Lv Da-Min Xu Su-Fang Shi Li-Jun Liu Feng Yu Ming-Hui Zhao Jan Novak Ali G Gharavi Hong Zhang

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...

2017
A. Inkeri Lokki Tea Kaartokallio Ville Holmberg Päivi Onkamo Lotta L. E. Koskinen Päivi Saavalainen Seppo Heinonen Eero Kajantie Juha Kere Katja Kivinen Anneli Pouta Pia M. Villa Leena Hiltunen Hannele Laivuori Seppo Meri

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 ...

Journal: :History Studies International Journal of History 2018

Journal: :International Journal of Current Science Research and Review 2022

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...

2012
Gergely Losonczy Attila Vajas Lili Takács Erika Dzsudzsák Ágnes Fekete Éva Márhoffer László Kardos Éva Ajzner Begoña Hurtado Pablo Garcia de Frutos András Berta István Balogh

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 ...

ژورنال: :مجله دانشکده پزشکی دانشگاه علوم پزشکی مشهد 0
مرتضی مرتضی بنیادی mortaza bonyadi associate professor in molecular medical genetics- animal biology dept. faculty of natural sciences, university of tabriz.tabriz-دانشیار ژنتیک پزشکی مولکولی، گروه علوم جانوری، دانشکده علوم طبیعی ، دانشگاه تبریز، تبریز، ایران ساناز ساناز رنجبر راد sanaz ranjbar rad msc in genetics, biology dept. faculty of natural sciences, islamic azad university of ahar. aharدانشجوی ارشد ژنتیک ، گروه زیست شناسی ، دانشکده علوم طبیعی ، دانشگاه آزاد اسلامی اهر ، اهر ایران محمد حسین محمد حسین جبارپور بنیادی mohammad hossein jabbarpour bonyadi md in ophthalmology, ophthalmologist, eye section, faculty of medicine, gonabad university of medical sciences, gonabad.متخصص چشم پزشکی، دانشگاه علوم پزشکی گناباد،گناباد، ایران حمید حمید احمدیه hamid ahmadieh professor in retina. ophthalmic research center, shahid beheshty university of medical sciences. tehranاستاد شبکیه، مرکز تحقیقات چشم، دانشگاه علوم پزشکی شهید بهشتی، تهران، ایران

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 ...

Journal: :iranian journal of public health 0
ah keyhani mr nowroozi

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...

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