نتایج جستجو برای: gene polymorphisms

تعداد نتایج: 1168765  

اسماعیلی, رسول, برخورداری, عسگر, حسن‌زاده, تقی, سعیدی جم, مسعود, پائولی, مکس,

Background: Hypercholesterolemia is considered a major risk factor for pancreatitis, atherosclerosis and coronary heart disease. Cholesteryl ester transfer protein gene polymorphisms are known to be associated with changes in lipid levels. We investigated the association between a polymorphism in the CETP gene (D442G) with plasma lipid levels and CETP activity in patients with hypercholesterole...

Alireza Irani, Amin Reza Nikpoor, Fazel Gorjipour, Hajar Aryan, Hossein Nazari, Kazem Mousavizadeh, Khalil Ghasemi Falavarjani, Mohammad Askari, Mohammad Hosein Sanati, Mohsen Mazidi,

Background: Half of the cases of vision loss in people under 60 years of age have been attributed to age-related macular degeneration (AMD). This is a multifactorial disease with late onset. It has been demonstrated that many different genetic loci are implicated in the risk of developing AMD in different populations. In the current study, we investigated the association of high-temperature &lr...

Background and Objectives: Varicocele is one of the most common causes of male infertility. Varicocele is an abnormal dilatation and tortuosity of veins of the pampiniform plexus, which drain the testis. Studies have shown that elevated level of oxidative stress markers, such as nitric oxide (NO) in the dilated veins of patients with varicocele impair testicular function. The aim of this study,...

Journal: :journal of advanced medical sciences and applied technologies 0
farzane arianfar department of medical genetics, shiraz university of medical sciences, shiraz, iran hassan dastsooz department of medical genetics, shiraz university of medical sciences, shiraz, iran nazanin vahedi department of medical genetics, shiraz university of medical sciences, shiraz, iran zeinab fadaei department of medical genetics, shiraz university of medical sciences, shiraz, iran mohammad hadi imanieh shiraz transplant research center, gastroenterohepatology research center, namazi teaching hospital, shiraz university of medical sciences, shiraz, iran seyed mohsen dehghani

background: wilson disease (wd) is caused by numerous pathogenic mutations of the atp7b gene. there are several mutation screening methods that can be used for the diagnosis and carrier detection of wd, however such methods are costly and time-consuming. therefore, other diagnostic methods should be used for urgent situations such as prenatal diagnosis. objective: to report common polymorphisms...

ژورنال: پژوهش در پزشکی 2006
دکتر حسین سندی, , دکتر محمدرضا آگاه, , دکتر محمدرضا زالی, , دکتر مریم ظفرقندی, , لیلا علیدوست, ,

Abstract: Background: Autoimmune hepatitis (AIH) is a chronic inflammatory liver disorder of unknown etiology. The search for gene polymorphisms has suggested that Glutathion-s-transferase (GST), enzymes that metabolize carcinogens, drug, and foreign compounds, may play a role in susceptibility to autoimmune liver disease and its severity. The objective of this study was to investigate for a r...

Journal: :jundishapur journal of microbiology 0
anvar soleimani department of clinical biochemistry, school of medicine, mashhad university of medical sciences, mashhad, ir iran houshang rafatpanah inflammation and inflammatory diseases research centre, mashhad university of medical sciences, mashhad, ir iran amin reza nikpoor department of immunogenetic and cell culture, immunology research center, school of medicine, mashhad university of medical sciences, mashhad, ir iran mehrdad kargari department of basic medical science, neyshabur university of medical sciences, neyshabur, ir iran daryoush hamidi alamdari biochemistry and nutrition research center, department of clinical biochemistry, school of medicine, mashhad university of medical sciences, mashhad, ir iran; biochemistry and nutrition research center, department of clinical biochemistry, school of medicine, mashhad university of medical sciences, mashhad, ir iran. tel: +98-9151017650, fax: +98-5118828574

conclusions according to our result, 1525g/a and 1595c/t were in strong linkage disequilibrium and the polymorphisms of the trail gene in the 3’ utr region were not associated with the outcome of hbv infection. results our data showed that genotypes 1525g/a and 1595c/t were in complete linkage disequilibrium and the genotype frequencies at the two positions were the same. no significant differe...

Journal: :hepatitis monthly 0
bita behnava iran hepatitis network, tehran, ir iran; baqiyatallah research center for gastroenterology and liver diseases, baqiyatallah university of medical sciences, tehran, ir iran; middle east liver diseases (meld) center, tehran, ir iran heidar sharafi iran hepatitis network, tehran, ir iran; baqiyatallah research center for gastroenterology and liver diseases, baqiyatallah university of medical sciences, tehran, ir iran; middle east liver diseases (meld) center, tehran, ir iran; armin pathobiology laboratory, tehran, ir iran maryam keshvari iran hepatitis network, tehran, ir iran; blood transfusion research center, high institute for research and education in transfusion medicine, tehran, ir iran ali pouryasin iran hepatitis network, tehran, ir iran; armin pathobiology laboratory, tehran, ir iran; department of biology, arsanjan branch, islamic azad university, arsanjan, ir iran leila mehrnoush iran hepatitis network, tehran, ir iran; middle east liver diseases (meld) center, tehran, ir iran shima salimi iran hepatitis network, tehran, ir iran; middle east liver diseases (meld) center, tehran, ir iran

patients and methods this cross - sectional study was conducted on 143 thalassemic patients with chronic hepatitis c, who were treated with a combination of peg-ifn and rbv regimen. the rs12979860 and rs8099917 polymorphisms were assessed as the most common polymorphisms near the il28b gene by the polymerase chain reaction-restriction fragment length polymorphism (pcr-rflp) method. objectives w...

بیرانوند, الهام , جیواد, فرشته , حسن نیا, هادی , رفیعی, علیرضا , عابدیان کناری, سعید , غفاری, جواد , یزدانی, جمشید ,

Background and purpose: Âllergic rhinitis is one symptomatic nasal disorders induced after contact with allergen in atopic individuals. Ït leads to ÏgË-mediated inflammation of the membranes lining the nose. Ïn addition to environmental factors, genetic predispositions play an important part in susceptibility to this disease. The aim of the present study was to determine the association betwe...

Journal: :journal of research in medical sciences 0
asghar ebadifar nazila ameli hamid reza khorramkhorshid koorosh kamali mehdi salehizeinabadi

background: we studied the role of maternal folic acid supplementation in modifying the effects of  methylenetetrahydrofolate reductase (mthfr c677t and a1298c) gene polymorphisms in iranian children with oral clefts. materials and methods: forty?seven newborn infants with orofacial cleft and their mothers were selected randomly. mothers were matched regarding dietary folate intake.the genotypi...

Bahram Mohammad Soltani, Feyzollah Hashemi-Gorji, Javad Mowla, Mahdis Ekrami, Maryam Torabi, Mohammad Miryounesi, Soudeh Ghafouri-Fard, Zahra Mohebbi,

Background: Familial hypercholesterolemia (FH) is a frequent autosomal dominant disorder of lipoprotein metabolism. This disorder is generally caused by mutations in low-density lipoprotein receptor (LDLR), apolipoprotein B 100 (APOB), and proprotein convertase subtilisin/kexin type 9 (PCSK9) genes. In the present study, we aimed at identifying the common LDLR and APOB gene mutations in an Iran...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید