نتایج جستجو برای: slc29a3 gene mutation

تعداد نتایج: 1284717  

Journal: :international journal of fertility and sterility 0

background: ghezel sheep are highly prolific and one of the local sheep breeds in iran and turkey. growth differentiation factor-9 (gdf9) gene has been found to be essential for growth and differentiation of early ovarian follicles. novel mutations in gdf9 have been associated with increased ovulation rates and high litter sizes in heterozygous carriers. therefore, fecundity gene for gdf9 (fecg...

Majid Yavarian, Mehran Karimi, Mozhgan Shahian, Narges Rezaie,

Background: The frequency of pyruvate kinase (PK) deficiency, an autosomal recessive defect, is approximately 3 per 10,000 individuals in Shiraz and surrounding areas, and is increased due to high consanguinity marriage frequency. The purpose of this study is to obtain data on the frequency and spectrum of gene mutation of PK in newborns, from Shiraz and surrounding areas. Materials and Methods...

Ahmad Reza Bahrmand, Elham Safarpour, Mahnaz Saifi, Morteza Masoumi, Somayeh Bahrami,

  Tuberculosis is a serious global public health problem and its high prevalence is stron gly associated with the enhancement of drug resistance. In this study we demonstrate a multiplex allele-specific polymerase chain reaction (MAS)-PCR assay to simultaneously detect mutations in the first and third bases of the embB gene codon 306 ATG in ethambutol (EMB) resistant isolates of Mycobacterium t...

Journal: :journal of dentistry, tehran university of medical sciences 0
p motahhary assistant professor, dental research center of tehran university of medical sciences, tehran, iran. f baghaie s mamishi b pourakbari s mahmoudi p amini shakib

head and neck squamous cell carcinoma, including oral squamous cell carcinoma (oscc) is the sixth most common cancer in the human population. despite significant efforts committed in treatment of oscc the overall survival rate of oscc has not improved significantly. activating mutations in the fibroblast growth factor receptor 3 (fgfr3) genes are responsible for some human cancers, including bl...

Journal: :بینا 0
مهدی نیلی احمدآبادی m nili ahmadabadi تهران- میدان قزوین- بیمارستان فارابی- مرکز تحقیقات چشم فرهام حافظ خیابان f khiabani دانشگاه علوم پزشکی تهران رضا کارخانه r karkhaneh دانشگاه علوم پزشکی تهران محمد ریاضی اصفهانی m riazi esfehani مرکز پژوهش های مهندسی ژنتیک و بیوتکنولوژی محمدرضا منصوری mr mansouri دانشگاه علوم پزشکی تهران محمدعلی زارع ma zare دانشگاه علوم پزشکی تهران مسعود هوشمند

purpose: to determine the association between norrie disease (nd) gene mutations and advanced stages of retinopathy of prematurity (rop) in premature neonates who were referred to farabi eye hospital, tehran, iran during 2005-2007. methods: fifty infants including 28 male and 22 female subjects with rop stage 3 or worse were enrolled in this case series. all three exons of nd gene underwent pol...

Journal: :مجله دانشگاه علوم پزشکی شهید صدوقی یزد 0
منصور صالحی m salehi . [email protected] رسول صالحی r salehi بهرام نصر اصفهانی b nasr- esfahani

introduction: mucopolysaccharidosis i (mps-i) is an autosomal recessive lysosomal storage diseases, caused by α-l-iduronidase (idua) enzyme deficiency. the clinical manifestations of mps-i patients are variable ranging from severe to mild, and therefore prediction of disease severity is difficult. from when idua gene has been cloned more than 109 distinct mutations have been identified in it an...

Journal: :archives of clinical infectious diseases 0
maryam vaezjalali department of microbiology, faculty of medicine, shahid beheshti university of medical sciences, tehran, ir iran hanieh rezaee department of microbiology, faculty of medicine, shahid beheshti university of medical sciences, tehran, ir iran; urology and nephrology research center, shahid beheshti university of medical sciences, tehran, ir iran hosein goudarzi department of microbiology, faculty of medicine, shahid beheshti university of medical sciences, tehran, ir iran; department of microbiology, faculty of medicine, shahid beheshti university of medical sciences, tehran, ir iran. tel.:+98-2123872556, fax: +98-2122439964

conclusions: premature stop codon in the s gene was observed in all countries with evaluable hbv genome sequences. co-existence of detectable hepatitis b surface antigen (hbsag) and s gene premature stop codon was inconsistent with other studies. investigations on yield truncated hbsag are suggested to determine if they can affect elisa hbsag results. background: we have previously reported on ...

ژورنال: پژوهش در پزشکی 2005

Background : Most of the offending genes of diseases are quite big and complex with varieties of exons. Gene montage is a new technique for formation of a big linked DNA segment that could be easily detected by DNA sequencing or Denaturing High Performance Liquid Chromatography (DHPLC). Methods : Exons 2,20,23 and 24 of BRCA1 gene were linked and analyzed by DNA sequencing. Exons 2 and 20 are i...

ابهجی, مریم, اسمیت, ریچارد, بزاز زادگان, نیلوفر, جوان, محمد خلیل, خدایی, حسین, دهقانی, عاطفه, ریاض الحسینی, یاسر, سیفتی, مرتضی, مغنی باشی, مهدی, میراب, محمود, نجم آبادی, حسین, کهریزی, کیمیا,

Introduction: Hearing loss is the most common sensory neural defect in humans, affecting 1 in 1000 neonates, with over half of these cases predicted to be hereditary in nature. Most hereditary hearing loss is inherited in a recessive fashion, accounting for approximately 80 % of non-syndromic hearing loss (NSHL). Mutations in GJB2 gene are major cause of inherited deafness in the European an...

ژورنال: پیاورد سلامت 2008
توگه, غلام رضا, علی مقدم, کامران, عین اللهی, ناهید, غفاری, سید حمیداله, فردوسی, شیرین, قوام زاده, اردشیر, موسوی, سید اسد اله, نادعلی, فاطمه, چاردولی, بهرام,

Background and Aim : Myeloproliferative neoplasms are clonal and heterogeneous disorders of hematopoietic stem cells lead to increase of one or more cell lines in the blood. Recently, the acquired mutation JAK2 V617F has been described in the majority of patients with myeloproliferative neoplasms (MPNs).This mutation is characterized by a G to T transverse at nucleotide 1849 in exon 12 of the J...

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