نتایج جستجو برای: mutation analysis

تعداد نتایج: 3045422  

Journal: :Information and Software Technology 2018

Journal: :The Journal of Molecular Diagnostics 2013

Journal: :Japanese Journal of Cancer Research 1998

Objective(s): Jervell and Lange–Nielsen syndrome is an autosomal recessive disorder caused by mutations in KCNQ1 or KCNE1 genes. The disease is characterized by sensorineural hearing loss and long QT syndrome. Methods: Here we present a 3.5-year-old female patient, an offspring of consanguineous marriage, who had a history of recurrent syncope and congenital sensorineural deafness. The patient ...

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...

پایان نامه :وزارت بهداشت، درمان و آموزش پزشکی - دانشگاه علوم پزشکی و خدمات بهداشتی درمانی استان کرمان 1389

چکیده ندارد.

Journal: :journal of kermanshah university of medical sciences 0
nasibe karimi ali bidmeshkipour keyghobad ghadiri reza alibakhshi

introduction: cystic fibrosis (cf) is a common genetic disorder in white populations with an autosomal recessive pattern, caused by mutations in the cftr gene. the frequency of more than 1950 various mutations reported in the cftr gene significantly varies in different populations. ∆f508 is a common mutation in exon 10, which is first addressed in the molecular analysis of the disease. other ex...

Journal: :international journal of molecular and cellular medicine 0
somayeh reiisi medical genetics department, national institute of genetic engineering and biotechnology (nigeb).سازمان اصلی تایید شده: پژوهشگاه ملی مهندسی ژنتیک و زیست فناوری mohammad hosein sanati medical genetics department, national institute of genetic engineering and biotechnology (nigeb).سازمان اصلی تایید شده: پژوهشگاه ملی مهندسی ژنتیک و زیست فناوری mohammad amin tabatabaiefar medical genetics department, ahvaz jundishapur university of medical sciences, ahvaz, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی جندی شاپور اهواز (ahvaz jundishapur university of medical sciences) shahla ahmadian cellular and molecular research center, shahrekord university of medical sciences, shahrekord, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهرکرد (shahr kord university of medical sciences) salimeh reiisi biochemistry department, maleke-ashtar university of technology, tehran iran. shahrbanoo parchami cellular and molecular research center, shahrekord university of medical sciences, shahrekord, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهرکرد (shahr kord university of medical sciences)

sensorineural non-syndromic hearing loss is the most common disorder which affects 1 in 500 newborns. hearing loss is an extremely heterogeneous defect with more than 100 loci identified to date. according to the studies, mutations in gjb2 are estimated to be involved in 50- 80% of autosomal recessive non-syndromic hearing loss cases, but contribution of other loci in this disorder is yet ambig...

Journal: :iranian rehabilitation journal 0
reihaneh alikhani genetic research center, university of social welfare and rehabilitation sciences, tehran, iran. fatemeh ostaresh genetic research center, university of social welfare and rehabilitation sciences, tehran, iran. mojgan babanejad genetic research center, university of social welfare and rehabilitation sciences, tehran, iran. nilofar bazazzadegan genetic research center, university of social welfare and rehabilitation sciences, tehran, iran. hossein najmabadi genetic research center, university of social welfare and rehabilitation sciences, tehran, iran. kimia kahrizi genetic research center, university of social welfare and rehabilitation sciences, tehran, iran.

objectives: hearing loss (hl) is the most common sensory disorder, and affects 1 in 1000 newborns. about 50% of hl is due to genetics and 70% of them are non-syndromic with a recessive pattern of inheritance. up to now, more than 50 genes have been detected which are responsible for autosomal recessive non-syndromic hearing loss, (arnshl). in  iran, hl is one of the most common disabilities due...

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