نتایج جستجو برای: restriction fragment length polymorphisms

تعداد نتایج: 472754  

Journal: :Nucleic acids research 1990
R Herzog K Holzmann N Blin

A. Zahedmehr, M. Lak R. Sharifian S. Delmaghani S. Zeinali

Background: Hemophilia B is an X-linked recessive coagulation disorder caused by factor IX deficiency.  Analysis of factor IX gene polymorphisms is considered the best approach for prenatal diagnosis and carrier detection of hemophilia B where the identification of gene mutation is not easily possible. Objective: To study the frequency of three factor IX-linked restriction fragment length polym...

Akbari MT Asgari N Babamohammadi GH Zare Sh

Background: The role of apolipoprotien E polymorphisms do not diagnostic correctly in recurrent pregnancy loss etiology but Apo E has been shown to play an important role in lipid metabolism in pregnancy. We evaluated these polymorphisms in Iranian women with unexplained recurrent pregnancy loss. Materials and Methods: 5 ml Blood were sampling from 81 women with a history of two or more consecu...

احمدی شادمهری, اشرف, احمدی شادمهری, اعظم, امیرزرگر, علی‌اکبر, سریال, شیلا, شکرگزار, محمدعلی, فرهادی, الهام, محمودی, مهدی, مرادی, بتول, نیکنام, محمد حسین,

Background: Multiple sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system with presumed autoimmune origin. T cells are considered to play a pivotal role in orchestrating the self-reactive immune responses in multiple sclerosis (MS). This study was performed to investigate the role of polymorphisms of the programmed cell death 1 (PD-1) gene on susceptibili...

Hamid Bakshi Nasaruddin Khaja Radhey Sham Sharma Roya Rozati, Satyanarayana Reddy B Simha Baludu Giragalla Srikanth Doddmaneni

Background Endometriosis is one of the most commonly encountered benign problems in gynaecology. It is frequently associated with chronic pelvic pain, dysmenorrhoea, menorrhagia and dyspareunia, which lead to infertility. We determined the possible association between CYP1A1 MspI and GSTM1 null polymorphism in the pathogenesis of endometriosis. MaterialsAndMethods Ninety seven cases of endometr...

Journal: :cell journal 0

uterine leiomyoma (ul) is the most common benign smooth muscle cell tumor with as yet unknown etiology and pathogenesis. this study was carried out to investigate the association of esr1-351 a>g, esr1 -397 t>c and cyp1a1 (ile462val) polymorphisms with ul in female patients of iranian origin. in this case-control study, 276 patients with ul and 156 healthy women were recruited. the genetic polym...

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