نتایج جستجو برای: t arms pcr
تعداد نتایج: 884808 فیلتر نتایج به سال:
Background: Recurrent pregnancy loss (RPL) is a common problem among couples, and acquired thrombophilia is the well-known etiology of RPL. The aim of this study was to establish the association between inherited thrombophilic gene polymorphisms and RPL. Methods: This case-control study was conducted on 50 women with unexplained RPL and 50 parous women with no history of miscarriage (age range...
The aim of the study is to obtain an optimal arm section for the structures like pulleys, gears, flywheels etc. considering variation of rim thickness with pulley radius. Presently, the design of arm pulley with thin rim is being carried out with an assumption that the bending moment (BM) is shared by half the number of arms, whereas in case of arm gear or V-Belt pulley the assumption is made t...
Vitiligo is brought on by functional melanocyte loss and manifests as white maculae that may cover the whole body's skin. There a genetic background in pathogenesis of vitiligo. Polymorphisms different parts catalase gene affect disease activity result less catalase, thus, accumulation hydrogen peroxide, one oxidative factors damage melanocytes. We evaluated CAT 262 polymorphism vitiligo patien...
PURPOSE To evaluate mutations in the visual system homeobox gene 1 (VSX1) and superoxide dismutase 1 (SOD1) genes with keratoconus (KTCN), direct sequencing was performed in an Iranian population. METHODS One hundred and twelve autosomal dominant KTCN patients and fifty-two unaffected individuals from twenty-six Iranian families, as well as one hundred healthy people as controls were enrolled...
سرطان پستان، فراوان ترین سرطان در بین زنان می باشد. علت سرطان پستان مجموعه ای از عوامل ژنتیکی، محیطی و سبک زندگی می باشد. مطالعات همراهی کل ژنوم، پلی مورفیسم هایی در ژن fgfr2 را شناسایی کردند که با سرطان پستان همراهی نشان می دهند. ژن گیرنده فاکتور رشد فیبروبلاستی 2 (fgfr2) یکی از اعضای خانواده گیرنده های تیروزین کیناز بوده که پروتئین گیرنده فاکتور رشد فیبروبلاستی را کد می کند. fgfr2 نقش اساسی د...
ERCC5 plays crucial role in excision repair DNA damage induced by UV in NER pathway. Single neuleotide polymorphism in ERCC5 were responsible for different cancers.Therefore, current study evaluated the relationship between ERCC5 (rs1047768 T>C) polymorphism and the risk of breast cancer in Pakistani population. The rs1047768 polymorphism was screened among 175 female...
Background: The bovine AGPAT6 gene is one of the potential candidate genes governing milk fat synthesis.Objectives: Identification of single nucleotide polymorphisms (SNP) in the targeted region of AGPAT6 gene and their effect on expected breeding values (EBV) of first lactation milk production traits viz. fat %, fat yield and 305 days milk yield in Karan Fries (KF) breeding bulls were so...
Introduction: Multiple Sclerosis (MS) is a disease of central nervous system that mainly causes lesions or plaques in the spinal cord and brain. The purpose of this study was to analyze the relation between c.-813C>T (rs2070744) and c.894G>T (rs1799983) polymorphisms of NOS3 gene and MS in Iranian patients. Methods: A total of 78 patients with MS and 80 healthy controls were screened for NOS3 ...
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