نتایج جستجو برای: molecular screening

تعداد نتایج: 847376  

Urmia Lake is the largest lake in the Iranian plateau and the second largest Salt Lake in the world. This study was conducted to identify hypersaline bacteria in the lake through the screening with molecular markers. For the molecular study of the bacterial microbiome of the lake, samples were collected from water, sludge and soil of the different parts of the lake during different seasons of 2...

آتشی, امیر, ابراهیمی, علیرضا, صراف‌نژاد, عبدالفتاح, قوامی عادل, مهستی, نظری, فهیمه, نیکنامی, زهره,

Hemoglobinopathies are most common inherited disorders in the world; approximately 7 percent of the worldwide population and 5-6 percent of population of Iran are carriers. The hemoglobin disorders inherit as autosomal recessive and are very common in the Mediterranean area and much of the Asia and Africa. The control of this inherited disorders need to genetic counseling and accurate screening...

A set of Xanthohumol derivatives were selected and molecular docking studies of these ‎compounds on thioredoxin reductase were conducted. Based on new structural patterns using in ‎silico-screening study, new potent lead compounds were designed. The results due to validated ‎docking protocols lead to find that Thr58, Gly57, Gly21, Asp334, Glu163, Ala130, IIe332, ‎Val44 and Gly132 are the main a...

Journal: :DARU Journal of Pharmaceutical Sciences 2014

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تربیت مدرس - دانشکده پزشکی 1391

به دلیل عوارض غیر قابل جبران توکسوپلاسموزیس در افراد دچار نقص سیستم ایمنی و نوزادان متولد شده از مادران آلوده، نیاز مبرم به تکنیک های سریع، حساس و دقیق برای شناسایی توکسوپلاسما گوندی احساس می شود. روش های مولکولی به عنوان روش های حساس تر و اختصاصی-تر از رو ش های سرولوژیک در تشخیص توکسوپلاسموزیس مطرح هستند. در این مطالعه، استفاده از روش real-time nasba برای سنجش کمی بار انگلی در خون ر ت های آلو...

Ali Bazi , Ebrahim Miri-Moghaddam ,

Abstract β-thalassemia major (β –TM) is the most common thalassemia severe phenotype among Iranians. In recent years, molecular understanding of pathogenesis of β –TM has provided a great opportunity regarding diagnostic issues. Creating comprehensive molecular databases provides highly sensitive diagnostic tools for β –TM and effective prenatal diagno...

Journal: :Bioorganic & Medicinal Chemistry Letters 2007

Journal: :Gastroenterology Research and Practice 2012

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