نتایج جستجو برای: slc29a3 gene mutation

تعداد نتایج: 1284717  

Journal: :jundishapur journal of microbiology 0
chiman karami department of virology, ahvaz jundishapur university of medical sciences, ahvaz, iran ahmad h adli department of virology, golestan university of medical sciences, gorgan, iran sareh zhand department of biotechology, golestan university of medical sciences, gorgan, iran alijan tabarraei department of microbiology, golestan university of medical sciences, gorgan, iran reza talei department of microbiology, lorestan university of medical sciences, khorramabad, iran mohsen saeidi stem cell research center, golestan university of medical sciences, gorgan, iran

background co-infection with human immunodeficiency virus (hiv) and hepatitis b virus (hbv) is common due to shared routes of transmission, as reported approximately 10% of 33 million hiv-infected patients worldwide are chronically infected with hbv. mutations of hbsag especially within the “a” determinant could alter the antigenicity of the protein, causing failure of hbsag neutralization and ...

A. Karami, A. Khalilpoor F. Biramijamal M. Eshraghi M. Ghanei S. Arjmand

Objective Mustard gas (MG) is a poisoning chemical, mutagenic and carcinogenic alkylating agent. It is used during World War I and also Iran-Iraq conflict. The p53 tumor suppressor gene is involved in the pathogenesis of malignant disease. The aim of this study is to determine possible mutation in p53 gene of lung sample from mustard gas exposed patients. Material and Methods Twelve lung bio...

Farhud, Daryoush, Pourkalhor , Hanieh ,

Neurofibromatosis is a genetic disorder that causes tumors in nerve tissue. These tumors can grow in any part of the nervous system, including the brain, spinal cord and nerves. The disease gene can be passed from a parent to a child through marked autosomal dominant inheritance or it can happen due to a spontaneous mutation of a gene. A parent with neurofibromatosis has a 50% chance of passing...

Journal: :مجله دانشگاه علوم پزشکی کرمانشاه 0
rahim golmohamadi department of anatomical medicine, sabzevar university of medical sciences mehdi nikbakht department of anatomical medicine, isfahan university of medical sciences

introduction: colorectal cancer (crc) is one of the most prevalent cancers in the world. genetic disorders and dietary habits play a part in crc. the most important cancer suppressor gene is p53. different mutations rates in 7th exon of p53 gene are reported in different areas  which may have a relationship with prognosis of crc. this study examines the relationship between mutation in 7th exon...

Journal: :iranian journal of child neurology 0
mohammad mehdi heidari* 1. department of biology, school of sciences, yazd university, yazd, iran mehri khatami 1. department of biology, school of sciences, yazd university, yazd, iran jafar pourakrami 2. department of biology, faculty of sciences, science and research branch of the islamic azad university, tehran, iran.

how to cite this article: heidari mm , khatami m, pourakrami j. novel point mutations in frataxin gene in iranian patients with friedreich’s ataxia. iran j child neurol. 2014 winter; 8(1):32-36.   objective friedreich’s ataxia is the most common form of hereditary ataxia with autosomal recessive pattern. more than 96% of patients are homozygous for gaa repeat extension on both alleles in the fi...

Journal: :international journal of reproductive biomedicine 0
mir davood omrani agneta nordenskhold

background: for screening sequence variations in genes, rapid turnover time is of fundamental importance. while, many of the current methods are unfortunately time consuming and technically difficult to implement. denaturing high-performance liquid chromatography (dhplc) method had been shown to be a high-throughput, time saving, and economical tool for mutation screening. objective: in the pre...

Journal: :iranian journal of basic medical sciences 0
a. karami research center of molecular biology, baqiyatallah medical sciences university tehran, iran f. biramijamal national institute of genetic engineering and biotechnology, tehran, iran m. ghanei research center of chemical injuries, baqiyatallah medical science university, tehran, iran 5- manitoba institute of cell biology, cancer care manitoba, winnipeg, mb, canada s. arjmand research center of molecular biology, baqiyatallah medical sciences university tehran, iran m. eshraghi research center of molecular biology, baqiyatallah medical sciences university tehran, iran a. khalilpoor research center of molecular biology, baqiyatallah medical sciences university tehran, iran

objective mustard gas (mg) is a poisoning chemical, mutagenic and carcinogenic alkylating agent. it is used during world war i and also iran-iraq conflict. the p53 tumor suppressor gene is involved in the pathogenesis of malignant disease. the aim of this study is to determine possible mutation in p53 gene of lung sample from mustard gas exposed patients. material and methods twelve lung biopsy...

Journal: :iranian journal of child neurology 0
zahra pirzadeh assistant professor of pediatric neurology, qazvin medical university of medical sciences, qazvin, iran

objectiveglutaric aciduria type 1 (gal 1) is a cerebral organic academia, which manifests as encephalopathy with long-term neurological handicap. in this study, clinical presentation, neuroimaging, molecular finding of cgdh mutation of our patients were reviewed.materials and methodsthis was a descriptive and cross-sectional study. patients in whom gla1 were suspected by clinical manifestation,...

Journal: :acta medica iranica 0
sanambar sadighi department of medical oncology, cancer research center, cancer institute of iran, tehran university of medical sciences, tehran, iran. mahsa ghaffari-moghaddam department of medical genetics, cancer research center, cancer institute of iran, tehran university of medical sciences, tehran, iran. mojtaba saffari department of medical genetics, cancer research center, cancer institute of iran, tehran university of medical sciences, tehran, iran. and departement of medical genetics, school of medicine, tehran university of medical genetics, tehran, iran. mohammad ali mohagheghi department of surgical oncology, cancer research center, cancer institute of iran, tehran university of medical sciences, tehran, iran. reza shirkoohi department of medical genetics, cancer research center, cancer institute of iran, tehran university of medical sciences, tehran, iran

desmoids tumors, characterized by monoclonal proliferation of myofibroblasts, could occur in 5-10% of patients with familial adenomatous polyposis (fap) as an extra-colonic manifestation of the disease. fap can develop when there is a germ-line mutation in the adenomatous polyposis coli gene. although mild or attenuated fap may follow mutations in 5΄ extreme of the gene, it is more likely that ...

Journal: :iranian biomedical journal 0
علی رمضانی ali ramazani کیمیا کهریزی kimia kahrizi مریم رزاقی آذر maryam razaghiazar نجات مهدیه nejat mahdieh paul koppens

background: congenital adrenal hyperplasia (cah, the inherited inability to synthesize cortisol) is one of the most common (1 in 10000 to 1 in 15000) autosomal recessive disorders. more than 95% of cases of cah are caused by 21-hydroxylase deficiency (21-ohd). females with severe, classic 21-ohd are exposed to excess androgens prenatally and are born with virilized external genitalia. most pati...

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