نتایج جستجو برای: amplification refractory mutation system

تعداد نتایج: 2569291  

A Ghasemi, A Ghotaslou, B Chahardouli, F Nadali, S Abbasian, S Rostami,

Background Myeloproliferative disorders are a group of diseases characterized by increased proliferation of myeloid lineage. In addition to JAK2V617F mutation, several mutations in the c-MPL gene were described in patients with Philadelphia-negative chronic myeloproliferative disorders that could be important in the pathogenesis of diseases. The aim of present study was to investigate the fre...

ژورنال: پژوهش در پزشکی 2004
اکرم نریمانی, , , Derakhshan F, سروین پیمان, , سید جواد میرحسنی مقدم, , فرامرز درخشان, , فرناز تقی زاده, , محمدرضا زالی, , نسترن نوروزی, ,

Background : Familial Mediterranean fever (FMF) is an autosomal recessive disease, which is characterized by recurrent short episodes of inflammation in serous membranes. It is most prevalent in Western Mediterranean population. MEFV is the only gene currently known to be associated with this disease. Previous studies revealed that 6% of Iranian Jewish residents in Israel were carriers of MEFV ...

Background and purpose: Beta-thalassemia is an autosomal recessive disease characterized by reduction or complete absence of beta-globin gene expression. This study aimed to find out and determine the spectrum of beta-globin gene mutations and especially rare mutation in beta-carrier couple in Babolsar, north region of Iran. This is very important in perinatal diagnosis of thalassemia. Materia...

Journal: :hepatitis monthly 0
hassan dastsooz department of medical genetics, shiraz university of medical sciences, shiraz, ir iran; department of molecular medicine, shiraz university of medical sciences, shiraz, ir iran mohammad hadi imanieh shiraz transplant research center, gastroenterohepatology research center, namazi teaching hospital, shiraz university of medical sciences, shiraz, ir iran seyed mohsen dehghani shiraz transplant research center, gastroenterohepatology research center, namazi teaching hospital, shiraz university of medical sciences, shiraz, ir iran mahmood haghighat shiraz transplant research center, gastroenterohepatology research center, namazi teaching hospital, shiraz university of medical sciences, shiraz, ir iran maryam moini department of internal medicine, gastroenterology and hepatology research center, shiraz university of medical sciences, shiraz, ir iran majid fardaei department of medical genetics, shiraz university of medical sciences, shiraz, ir iran; department of molecular medicine, shiraz university of medical sciences, shiraz, ir iran; stem cell and transgenic technology research center, shiraz university of medical sciences, shiraz, ir iran; department of medical genetics, shiraz university of medical sciences, 7134853185, shiraz, ir iran. tel: +98-7112349610, fax: +98-7112349610

results using these two sets, we identified h1069q mutation in four patients, c.2335t > g mutation in three, c.3061-1g > a splice site mutation in five, c.3305t > c mutation in one, and c.3809a > g mutation in two patients. conclusions the multiplex arms assay used in this study can be an efficient, reliable, and cost effective method as a primary screen for patients with wilson disease. patien...

2014
Zhiyuan Wu Yunqing Zhang Xinju Zhang Xiao Xu Zhihua Kang Shibao Li Chen Zhang Bing Su Ming Guan

A multiplex snapback primer system was developed for the simultaneous detection of JAK2 V617F and MPL W515L/K mutations in Philadelphia chromosome- (Ph-) negative myeloproliferative neoplasms (MPNs). The multiplex system comprises two snapback versus limiting primer sets for JAK2 and MPL mutation enrichment and detection, respectively. Linear-After exponential (LATE) PCR strategy was employed f...

Beta-thalassemia is one of the most common autosomal recessive disorders in the world population resulting from over 200 different mutations of HBB gene. Beta-thalassemias are caused by point mutations or, more rarely, deletions in the HBB gene leading to reduced (beta+) or absent (beta0) synthesis of the beta chains of hemoglobin (Hb). High-resolution melting of polymerase chain reaction (PCR)...

Journal: :Journal of clinical pathology 1993
P Patel Y M Lo J I Bell J S Wainscoat

AIMS To detect HLA susceptibility and protective alleles associated with insulin dependent diabetes mellitus (IDDM) using a multiplex amplification refractory mutation system (ARMS). These include DR3 and DR4 alleles at the DRB1 locus, presence or absence of aspartic acid at position 57 (Asp-57) of the DQB1 locus, and presence or absence of arginine at position 52 (Arg-52) of the DQA1 locus. ...

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...

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