نتایج جستجو برای: g145r mutation

تعداد نتایج: 291423  

Journal: :acta medica iranica 0
p. fard-esfahani p. mohammadi-torbati s. khatami s. zeinali m. taghikhani m. allahyari

familial defective apolipoprotein (apo) b 100 (fdb) causes early-onset coronary heart diseases (chd). it is produced by r3500q mutation of the apob gene resulting in decreased binding of ldl to ldl receptor. we screened the apo b gene for r3500q mutation in 130 hypercholesterolemic patients, among whom 30 patients met criteria of familial hypercholesterolemia (fh). the prevalence of r3500q alle...

Journal: :international journal of hematology-oncology and stem cell research 0
mehrdad payande medical biology research center, kermanshah university of medical sciences, kermanshah, iran mohammad erfan zare medical biology research center, kermanshah university of medical sciences, kermanshah, iran; student saber ghanbari haji shure student of medical lab sciences in research committee, kermanshah university of medical sciences, kermanshah, iran farhad shaveisi zadeh medical genetics department, faculty of medicine, shahid beheshti university of medical sciences and

myeloproliferative neoplasms (mpns) such as polycythemia vera, essential thrombocythemia, primary myelofibrosis and chronic myeloid leukemia have too similar and accurate way to differentiate their is study of genetic disorders in these patients. philadelphia chromosome is a sure way to definitively diagnose cml. recently, jak2v617f mutation introduced as a diagnostic marker for other myeloprol...

ژورنال: :gene, cell and tissue 0
farah talebi department of genetic, faculty of sciences, shahid chamran university of ahvaz, ahvaz, ir iran farideh ghanbari department of genetic, faculty of sciences, shahid chamran university of ahvaz, ahvaz, ir iran; department of genetic, faculty of sciences, shahid chamran university of ahvaz, ahvaz, ir iran. tel/fax: +98-6136233884 javad mohammadi asl department of medical genetics, faculty of medicine, ahvaz jundishapur university of medical sciences, ahvaz, ir iran

conclusions bioinformatics analyses using sift, mutation taster and polyphen-2 indicated that p.ile563val was predicted to be damaging, disease causing, and probably damaging to and causing ldb3 dysfunction. as such, this mutation produces novel protein coding transcripts, which might explain the mfm phenotype in the patient. introduction myofibrillar myopathy (mfm) is a rare human disease, cha...

Journal: :مجله بین المللی زیست و زیست پزشکی 0
haleh akhavan-niaki genetic laboratory of amirkola children's hospital, babol university of medical sciences, babol, iran reza youssefi kamangari genetic laboratory of amirkola children's hospital, babol university of medical sciences, babol, iran ali banihashemi genetic laboratory of amirkola children's hospital, babol university of medical sciences, babol, iran mandana azizi genetic laboratory of amirkola children's hospital, babol university of medical sciences, babol, iran

beta thalassemia is the  most common autosomal recessive disorder. the present study reports a rare β globin gene mutation, hbb: c.180g>a: codon 59 (aag/aaa), in a patient from gilan province, northern iran. nucleotide sequencing of amplified dna belonging to a 35 years old man presenting mild hypochromia revealed a synonymous mutation due to a g>a conversion at the third position of codon 59 o...

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)...

خاتمی, مهری, قانعی یخدان, زهرا,

Introduction: The Brugada syndrome (BrS) belongs to cardiac arrhythmia disorders that is seen on the echocardiogram bands and is a significant cause of sudden death in young adults. At the molecular level, mechanisms that contribute to BrS are mutations in genes that encode for ion channels. It has been reported that the activity of ion channels in cardiomyocytes is sensitive to ATP level. This...

Abdolvahab Moradi Alijan Tabarraei, Amir Ghaemi, Masoud Bazouri Naeme Javid, Sareh Zhand

Objective(s): It has been reported that the mutation of the pre-core (PC) and basal-core promoter (BCP) may play an important role in the development of HBV-related hepatocellular carcinoma (HCC). In this study the PC and BCP mutations were investigated in chronic HBV patients. Materials and Methods:In this study, 120 chronic HBV patients from Golestan, Northeast of Iran who were not vaccinated...

ژورنال: پیاورد سلامت 2009
بهار, بابک, توگه, غلام رضا, درگاهی, حسین, علی مقدم, کامران, غفاری, حمیداله, قوام زاده, اردشیر, نادعلی, فاطمه, چهاردولی, بهرام, کریم زاده, پریسا,

Background and Aim: The JAK2 is an acquired mutation that is observed in majority of patients with classical Philadelphia-negative Myeloproliferative neoplasms that include polycythemia vera (PV), essential thrombocythemia (ET), primary myelofibrosis (PMF). This acquired mutation is characterized by a G to T transversion at nucleotide 1849 in exon 12 of the JAK2 gene, leading to a substitution ...

  Objective(s): The major antibiotic efflux pump of Esherichia coli is AcrAB-TolC. The first part of the pump, AcrAB, is encoded by acrAB operon. The expression of this operon can be kept elevated by overexpression of an activator, MarA following inactivation of MarR and AcrR repressors due to mutation in encoding genes, marR and acrR, respectively. The aims of this research were to us...

ژورنال: پژوهش در پزشکی 2004
طاهره غازیانی, , حسین سندی, , محمد رضا آگاه, , محمد رضا زالی, , مریم جزایری, , پیمان ادیبی, ,

Background : Finding an association between HFE mutations and hepatitis C especially in those with iron overload is the focus of recent researches. We examined the frequency of these mutations and ferritin level in a group of patients with different stages of hepatitis B and healthy individuals.  Materials and methods : A total of 75 (18 carrier, 57 chronic) cases of HBsAg positive patients and...

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