نتایج جستجو برای: gene frequency

تعداد نتایج: 1580534  

امیرغفران, زهرا, کمالی, اسکندر, افلاکی, الهام, عبد نیک‌فرجام, بهاره,

  Backhground & Aim: Several lines of evidence have indicated that NO might be important in the pathogenesis of RA. NO could be synthesized by an enzyme called inducible nitric oxide synthase (iNOS). iNOS is expressed in the synovium, cartilage and lymphomononuclear cells of synovial fluid and lymphocytes and monocytes of peripheral blood of RA patients. Several studies have shown that iNOS gen...

Journal: :hepatitis monthly 0
jamal sarvari department of bacteriology and virology, school of medicine, shiraz university of medical sciences, shiraz, ir iran hossin norozian department of bacteriology and virology, school of medicine, shiraz university of medical sciences, shiraz, ir iran mohamad reza fattahi gastroenterohepatology research center, shiraz university of medical sciences, shiraz, ir iran neda pirbonyeh department of bacteriology and virology, school of medicine, shiraz university of medical sciences, shiraz, ir iran afagh moattari department of bacteriology and virology, school of medicine, shiraz university of medical sciences, shiraz, ir iran; department of bacteriology and virology, shiraz university of medical sciences, shiraz, ir iran. tel/fax: +98-7112304356

conclusions our findings indicate that heterogeneity at +2109 locus of ifn-γ gene but not at +874 locus could interfere with successful therapy in patients infected with hcv genotype 1. results of 158 patients, 110 (69.5%) subjects achieved svr and 48 (30.5%) subjects did not respond to therapy. the frequency of aa genotype (p = 0.001; or: 11.2; ci: 2.26-63.21) and a allele (p = 0.01; or: 3.23;...

Introduction: Hemophilia B is an X-linked recessive genetic disease caused by mutations in the coagulation Factor IX gene. Mutations in the Factor IX gene result in dysfunction or deficiency of coagulation factor of IX. Direct mutation analysis involves the ideal method for molecular diagnosis of the disease. However, due to the high number of identified mutations in the gen, the lack of a comm...

Journal: :archives of breast cancer 0
mahin ahangar oskouee department of microbiology &virology, faculty of medicine , tabriz university of medical sciences, tabriz, iran shohreh shahmahmoudi department of virology, school of public health, tehran university of medical sciences, tehran, iran rakhshandeh nategh department of virology, school of public health, tehran university of medical sciences, tehran, iran heidar-ali esmaeili department of pathobiology, tabriz university of medical sciences, tabriz, iran firozeh safaeyan department of microbiology &virology, faculty of medicine , tabriz university of medical sciences, tabriz, iran maryam zareinghalame moghaddam department of microbiology, international branch of shahid beheshti medical university , tehran, iran

background: the tp53 gene is the most important tumor suppressor gene in humans. the aim of our study was to determine the genotype frequency of three common tp53 polymorphisms (codon 72 bstui and intron 6 mspi, as well as the intron 3) in a group of iranian women with and without breast cancer. methods: paraffin-embedded specimens of 65 malignant breast cancer cases and 65 cases with benign br...

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 ...

Journal: :iranian journal of public health 0
d.d.farhud p.amirshahi sh.hedayat

the distribution of haptoglobin types of iranian living in bandaranbas (n=1246) is reported. hp1 gene frequencies reported in the literature for different populations in iran are given. comparison of the know hp1 distribution patterns show that the present hp1 frequency (0.266) is similar to other populations in iran.

Journal: :iranian journal of immunology 0
abdol rahim nikzamir department of medical biochemistry, faculty of medicine, tehran university of medical sciences, tehran, iran taghi golmohammadi department of medical biochemistry, faculty of medicine, tehran university of medical sciences, tehran, iran manouchehr nakhjavani department of endocrinology and metabolism, faculty of medicine, tehran university of medical sciences, tehran, iran mahine zahraei department of medical biochemistry, faculty of medicine, tehran university of medical sciences, tehran, iran ali akbar amirzargar immunogenetic laboratory, department of immunology, faculty of medicine, tehran university of medical sciences, tehran, iran

background: angiotensin i converting enzyme (ace) is a zinc metalloproteinase, converts ang-i to ang- ii, a pro-inflammatory agent which may contribute to pathophysiology of some diseases like type 2 diabetes. objective: to investigate the relationship between ace i/d polymorphism and type 2 diabetes in 261 iranian casecontrol pairs. methods: 170 patients (85 type 2 diabetics with nephropathy a...

Journal: :gene, cell and tissue 0
milad mohammadoo khorasani student scientific research center, zahedan university of medical sciences, zahedan, ir iran; department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran saeedeh salimi department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran; cellular and molecular research center, zahedan university of medical sciences, zahedan, ir iran; cellular and molecular research center, zahedan university of medical sciences, zahedan, ir iran and department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran. tel: +98-.5413414563, fax: +985413414563 azam hajizade student scientific research center, zahedan university of medical sciences, zahedan, ir iran; department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran maryam moossavi department of biology, university of sistan and baluchestan, zahedan, ir iran ehsan tabatabai student scientific research center, zahedan university of medical sciences, zahedan, ir iran; department of clinical biochemistry, school of medicine, zahedan university of medical sciences, zahedan, ir iran minoo yaghmaei department of obstetrics and gynecology, school of medicine, zahedan university of medical sciences, zahedan, ir iran

background uterine leiomyoma (uls) is the most common gynecological tumor and a significant health concern for many women .the interleukin-1 receptor antagonist (il-1ra) is a naturally occurring cytokine inhibiting interleukin- 1 (il-1) activity by binding to the il-1 receptors without signal transduction. objectives the aim of this study was to investigate the association between interleukin-1...

Journal: :jundishapur journal of microbiology 0
roghayeh ghazalsofala inflammation and inflammatory diseases research center, mashhad university of medical sciences, mashhad, ir iran seyed abdolrahim rezaee inflammation and inflammatory diseases research center, mashhad university of medical sciences, mashhad, ir iran houshang rafatpanah rheumatic diseases research center, mashhad university of medical sciences, mashhad, ir iran rosita vakili inflammation and inflammatory diseases research center, mashhad university of medical sciences, mashhad, ir iran kiarash ghazvini antimicrobial resistance research center, mashhad university of medical sciences, mashhad, ir iran fatemeh heidarnejad inflammation and inflammatory diseases research center, mashhad university of medical sciences, mashhad, ir iran

patients and methods in this cross-sectional study, peripheral mononuclear cells (pbmcs) were isolated from peripheral blood of 29 patients with newly diagnosed pulmonary tb and 19 patients with positive tuberculin skin test. the pbmcs were activated with ppd for 72 hours. activated cells were harvested, rna was extracted and cdna was synthesized. a real-time taqman method was designed and opti...

ژورنال: ارمغان دانش 2019

Tyrosinemia is a rare autosomal recessive genetic disease caused by fumarylacetoacetate hydrolase deficiency. 40 different mutation have been recognized related to Tyrosinemia that could be found in all extend of the gene with higher frequency from exon 8 to 14. Because of the size of FAH gene it's impossible to Sequence whole length of the gene by one round of sequencing reaction. Aim of this ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید