نتایج جستجو برای: tetra arms

تعداد نتایج: 35748  

Journal: :hepatitis monthly 0
mohammad hashemi cellular and molecular research center, zahedan university of medical sciences, zahedan, ir iran; department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran; department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran. tel: +98-9173640366, fax: +98-5413414571 hamideh hanafi bojd department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran ebrahim eskandari nasab department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran ali bahari department of internal medicine, school of medicine, mashhad university of medical sciences, mashhad, ir iran noor allah hashemzehi department of internal medicine, school of medicine, zahedan university of medical sciences, zahedan, ir iran sara shafieipour department of internal medicine, school of medicine, kerman university of medical sciences, kerman, ir iran

patients and methods eighty-three patients with diagnosis of nafld, and 93 healthy subjects were included in the study. tetra arms-pcr was designed to detect single nucleotide polymorphisms. results a significant difference was found between nafld and control group regarding the rs266729 polymorphism (χ2 = 7.35, p = 0.025). the rs266729 polymorphism increased the risk of nafld in codominant (cc...

Journal: :gene, cell and tissue 0
zahra heidari infectious diseases and tropical medicine research center, zahedan university of medical sciences, zahedan, ir iran; department of histology, school of medicine, zahedan university of medical sciences, zahedan, ir iran hamidreza mahmoudzadeh sagheb infectious diseases and tropical medicine research center, zahedan university of medical sciences, zahedan, ir iran; department of histology, school of medicine, zahedan university of medical sciences, zahedan, ir iran nadia sheibak department of histology, school of medicine, zahedan university of medical sciences, zahedan, ir iran; department of histology, school of medicine, zahedan university of medical sciences, zahedan, ir iran. tel: +98-5433295794, fax: +98-5433295794

conclusions the results of the present study showed that tgf-β1 (-509) c/t is strongly associated with quantitative parameters of connective tissue constituents of interdental papilla in cp patients. results the volume density (vʋ) of epithelium, connective tissue, collagenous and non-collagenous matrix and blood vessels had statistically significant differences between the control and chronic ...

ژورنال: :مجله دانشگاه علوم پزشکی مازندران 0
فریدون مجتهدزاده f modjtahed zadeh متخصص کودکان و فوق تخصص ژنتیک، عضو هیئت علمی دانشگاه علوم پزشکی مازندران

سابقه و هدف : با توجه به شیوع بیماری بتاتالاسمی در مازندران، به منظور تعیین انواع موتاسیون های این بیماری این تحقیق در بیماران و خانواده های مراجعه کننده به درمانگاه تالاسمی بیمارستان بوعلی سینای ساری در سال 1373 انجام گرفت. مواد و روش ها : تحقیق به روش توصیفی روی 44 خانواده تالاسمیک انجام گرفت (در این تحقیق، هر خانواده تالاسمیک عبارت است ازیک فرزند بیمار به اضافه والدین آنها که حاملین ژن بیمار...

Journal: :iranian red crescent medical journal 0
milad gholami department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, ir iran hossein darvish behavioral sciences research center, shahid beheshti university of medical sciences, tehran, ir iran habib ahmadi department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, ir iran simin rahimi-aliabadi department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, ir iran babak emamalizadeh department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, ir iran mohammad reza eslami amirabadi behavioral sciences research center, shahid beheshti university of medical sciences, tehran, ir iran

background multiple sclerosis (ms) is an autoimmune disease that affects the central nervous system (cns). ms is one of the most common cause of neurological impairment at a young age with a complex etiology. the forkhead/winged helix (foxp3) gene encodes a transcription factor that plays an important role in the working and progress of regulatory t cells. loss of the foxp3 function impairs the...

ژورنال: :مجله دانشگاه علوم پزشکی گیلان 0
زیور صالحی z salehi department of biology, faculty of sciences, university of guilan, rasht, iranگروه زیست شناسی، دانشکده علوم پایه، دانشگاه گیلان، رشت، ایران سمانه محمددوست s mohammaddoust epartment of biology, faculty of sciences, university of guilan, rasht, iranگروه زیست شناسی، دانشکده علوم پایه، دانشگاه گیلان، رشت، ایران حمید سعیدی ساعدی h saeidi saedi department of radiation oncology, cs, rasht, iranﮔﺮوه رادﻳﻮﺗﺮاﭘﻲ و اﻧﻜﻮﻟﻮژی، داﻧﺸﻜﺪه ﭘﺰﺷﻜﻲ، داﻧﺸﮕﺎه ﻋﻠﻮم ﭘﺰ ﺷﻜﻲ ﮔﻴﻼن، رﺷﺖ، اﻳﺮان

مقدمه: تعدادی از گوناگونی ژنتیکی در ژن های کدکننده ی سلنوپروتئین ها نتایج کارکردی دارند.sep15 ویژگی آنتی اکسیدان دارد، بنابراین ممکن است در فرآیند سرطان زایی نیز دخیل باشد. شناخته شده ترین پلی مورفیسم این ژن، g1125a (rs5859)، در ناحیه ی 3'utr ژن واقع شده و دربردارنده جایگزینی g به a در موقعیت ۱۱۲۵ است. هدف: تعیین پیوستگی ژنتیکی پلی مورفیسم g1125aژن sep15با بدخیمی پستان. مواد و روش ها: این ...

Journal: :reports of biochemistry and molecular biology 0
reza mirfakhraie tel: +98 21 22427903; fax: +98 21 23872572 zeeba kamaliyan department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, iran. sara pouriamanesh department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, iran. mona amin-beidokhti department of medical genetics, school of medicine, shahid beheshti university of medical sciences, tehran, iran. amir rezagholizadeh biology department, islamic azad university, east tehran branch, tehran, iran.

background: the piwi-interacting rna (pirna) pathway has an essential role in transposon silencing, meiosis progression, spermatogenesis, and germline maintenance. hiwi genes are critical for pirna biogenesis and function. therefore, polymorphisms in hiwi genes contribute to spermatogenesis defects and can be considered as risk factors for male infertility. the aim of the present study was to i...

Journal: :international journal of reproductive biomedicine 0
shokoufeh fazelnia touraj farazmandfar seyed mohammad bagher hashemi-soteh

background: spontaneous abortion is considered as the most complex problem during pregnancy. thrombophilia is resumed as a cause of recurrent pregnancy loss (rpl). glycoprotein iiia (gpiiia) gene is involved in thrombosis and abortion. angiotensin converting enzyme (ace) converts angiotensin i to angiotensin ii and is involved in thrombosis. the most common polymorphism in this gene is the inse...

2017
Andreas Lemmerer Xolani Motlaung

Four mol-ecular salts made from hexa-methyl-ene-tetra-minium and 2-chloro-4-nitro-benzoate have been synthesized and are reported, namely ammonium hexa-methyl-ene-tetra-minium bis-(2-chloro-4-nitro-benzoate), NH4+·C6H13N4+·2C7H3ClNO4-, (I), hexa-methyl-ene-tetra-minium hydrogen bis-(2-chloro-4-nitro-benzoate), 0.5C6H13N4+·C7H3.50ClNO4-, (II), hexa-methyl-ene-tetra-minium 2-chloro-4-nitro-benzoa...

Majid Motovali-Bashi, Tayyebeh Ghasemi,

Background: &beta-thalassemia is the most common monogenic disorder in human. The (CT) polymorphism at -158 upstream region of the &gammaG-globin gene and pharmacological factors such as hydroxyurea have been reported to influence &gamma-globin gene expression and the severity of clinical symptoms of &beta-thalassemia. Methods: In the present study, 51 &beta-thalassemia intermediate patients w...

ژورنال: فیض 2016
نیمی هویدی, الهه, هاشمی, سیده سارا, کهن, لیلا,

سابقه و هدف: ناباروری یکی از مشکلات عمده در زندگی افراد است و یکی از دلایل مهم آن بیماری اندومتریوز است. اندومتریوز یکی از شایع‌ترین بیماری‌های سیستم تناسلی زنان است که به‌صورت رشد بافت اندومتر در خارج از رحم تعریف می‌شود. مطالعات اخیر نشان داده است کهmiRNA ­ها و mRNAهای هدف آن‌ها در اندومتریوز بیان متفاوتی دارند. هدف از این مطالعه بررسی ارتباط واریانت­ های ژنتیکی rs41291957 و rs4705342 ژن miR-...

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