نتایج جستجو برای: rs1799983

تعداد نتایج: 76  

2015
Sinem Yalcintepe Ozturk Ozdemir Servet Ozden Hacivelioglu Cisem Akurut Evrim Koc Ahmet Uludag Emine Cosar Fatma Silan

The aim of this study was to investigate the possible role of multiple inherited thrombophilic gene variations in women with unexplained spontaneous abortions. For this purpose, the Factor V Leiden (FVL) (rs6025), Prothrombin G20210A (rs1799963), MTHFR C677T (rs1801133), PAI-1 4G/5G (rs1799889), ACE I/D (rs1799752), eNOS E298D (rs1799983), and Apo E E2/E3/E4 (rs429358) polymorphisms were genoty...

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پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه شهید چمران اهواز - دانشکده علوم 1391
پروانه دیناروند, سعید رضا خاتمی, علی محمد فروغمند, سعید یزدان خواه,

بروز آترواسکلروزیس در شریانهای کرونری را بیماری شریان کرونری (coronery artery disease) می نامند cad .شایعترین بیماری قلبی است که با تجمع غیر طبیعی لیپید ، مواد چربی در جدار عروق مشخص می شود و باعث انسداد ، تنگی رگها و کاهش جریان خون به عضله میوکارد می گردد این تجمع مواد را آتروما یا پلاک می گویند. در کشورمان و دیگر نقاط دنیا سالانه تعداد زیادی ازافراد بدلیل این بیماری و پیامد ناشی از آن سکته قل...

Journal: :Cardiovascular Diabetology 2018

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Journal: :international journal of molecular and cellular medicine 0
sinem yalcintepe department of medical genetics, faculty of medicine, canakkale onsekiz mart university, canakkale, turkey. ozturk ozdemir department of medical genetics, faculty of medicine, canakkale onsekiz mart university, canakkale, turkey. servet ozden hacivelioglu department of gynecology and obstetrics, school of medicine, canakkale onsekiz mart university, canakkale, turkey. cisem akurut department of medical genetics, faculty of medicine, canakkale onsekiz mart university, canakkale, turkey. evrim koc department of gynecology and obstetrics, school of medicine, canakkale onsekiz mart university, canakkale, turkey. ahmet uludag department of medical genetics, faculty of medicine, canakkale onsekiz mart university, canakkale, turkey.

the aim of this study was to investigate the possible role of multiple inherited thrombophilic gene variations in women with unexplained spontaneous abortions. for this purpose, the factor v leiden (fvl) (rs6025), prothrombin g20210a (rs1799963), mthfr c677t (rs1801133), pai-1 4g/5g (rs1799889), ace i/d (rs1799752), enos e298d (rs1799983), and apo e e2/e3/e4 (rs429358) polymorphisms were genoty...

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Journal: :Endocrine, metabolic & immune disorders drug targets 2010
Aldi T Kraja Michael A Province Robert J Straka Jose M Ordovas Ingrid B Borecki Donna K Arnett

The fibric acid derivative, fenofibrate (FF) has been used in the US since 1998 to manage patients with dyslipidemia. Typical changes in serum lipids as result a of FF treatment include clinically important mean reductions of serum triglycerides (TG) by a mean change of -93.7 mg/dL (-39.3%), increases of high density lipoprotein cholesterol (HDLC) by +5.5 mg/dL (+12.4%), and reductions in low d...

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2013
Santosh Dahgam

Background Polymorphisms in nitric oxide synthasegenes (NOS1, NOS2, and NOS3) have been suggestedto have a major impact on fraction of exhaled nitric oxide(FENO), a biomarker of airway inflammation. However,the genetic contribution of NOS polymorphisms to FENOis not fully understood. The aim of this study was toinvestigate comprehensively the association betweens...

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