نتایج جستجو برای: single nucleotide poly morphism

تعداد نتایج: 1025175  

Journal: :medical journal of islamic republic of iran 0
ali mohammad foroughmand dept of genetics, college of sciences, shahid chamran university, ahvaz,iranسازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university) maryam haidari dept of genetics, college of sciences, shahid chamran university, ahvaz,iran.سازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university) hamid galehdari dept of genetics, college of sciences, shahid chamran university, ahvaz-iranسازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university) atefeh pooryasin dept of genetics, college of sciences, shahid chamran university, ahvaz,iran.سازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university) seyed reza kazeminejad dept of genetics, college of sciences, shahid chamran university, ahvaz,iran.سازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university) shiva hosseini dept of genetics, college of sciences, shahid chamran university, ahvaz, iranسازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university)

abstract   background: the disrupted-in-schizophrenia 1 (disc1) gene, on the chromosome position 1q42, was initially identified at the breakpoint of a balanced translocation, t(1,11)(q42.1q14.3), which segregated with major mental disorders in a large scottish family.   methods: our samples included 200 unrelated patients diagnosed with schizophrenia on the basis of dsm-iv criteria and 200 norm...

Journal: :hepatitis monthly 0
imran tipu institute of biochemistry and biotechnology, university of the punjab, lahore, pakistan; manchester institute of biotechnology, university of manchester, manchester, uk; institute of biochemistry and biotechnology, university of the punjab, lahore, pakistan. tel: +92-3214029804 fiona marriage manchester institute of biotechnology, university of manchester, manchester, uk; centre for integrated genomic medical research, university of manchester, manchester, uk zia-ur-rahman farooqi manchester institute of biotechnology, university of manchester, manchester, uk; national university of science and technology, islamabad, pakistan hazel platt centre for integrated genomic medical research, university of manchester, manchester, uk muhammad amin athar institute of biochemistry and biotechnology, university of the punjab, lahore, pakistan philip john day manchester institute of biotechnology, university of manchester, manchester, uk; centre for integrated genomic medical research, university of manchester, manchester, uk

background polymorphisms in the interferon λ (inf λ) genes on chromosome 19 have been associated with clearance of hepatitis c virus (hcv) induced by interferon and ribavirin therapy however there is no such data available for pakistani patients with hcv infection. objectives in this study, the effects of single nucleotide polymorphisms (snps) have been investigated in response to treatment wit...

Journal: :thrita 0
zahra salehi department of medical biotechnology, school of allied medicine, iran university of medical sciences, tehran, ir iran arshad hosseini department of medical biotechnology, school of allied medicine, iran university of medical sciences, tehran, ir iran; department of medical biotechnology, school of allied medicine, iran university of medical sciences, tehran, ir iran. tel: +98-2186704604, fax: +98-2188622533 mohammad najafi department of biochemistry, school of medicine, iran university of medical sciences, tehran, ir iran hussain ahmad department of medical biotechnology, school of advanced technologies in medicine, international campus, tehran university of medical sciences, tehran, ir iran mohammad reza fayazi department of medical biotechnology, school of advanced technologies in medicine, tehran university of medical sciences, tehran, ir iran

results no significant correlation was seen in rs3743527 and rs129081 polymorphism’s allelic and genotypic frequencies between the patient group and control individuals (p value > 0.05). the average frequencies of rs129081 g and c alleles was 40 (58%) and 29 (42%), respectively. in our sample the average frequencies of rs3743527 c and t alleles, were 41 (61%) and 28 (39%), respectively. the res...

Journal: :international journal of molecular and cellular medicine 0
behnam alipoor department of biochemistry, faculty of medicine, tehran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences) hamid ghaedi department of medical genetics, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) mir davood omrani department of medical genetics, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) milad bastami department of medical genetics, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences) reza meshkani department of biochemistry, faculty of medicine, tehran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences) taghi golmohammadi department of biochemistry, faculty of medicine, tehran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences)

it has been suggested that single nucleotide polymorphisms (snps) in genes involved in toll-like receptors (tlrs) pathway may exhibit broad effects on function of this network and might contribute to a range of human diseases. however, the extent to which these variations affect tlr signaling is not well understood. in this study, we adopted a bioinformatics approach to predict the consequences...

Journal: :iranian journal of veterinary research 2014
s. choudhary n. gupta g. jethra

prions are unprecedented infectious pathogens that cause a group of invariably fatal neurodegenerative disease by an entirely novel mechanism. the conformational change in prion proteins results in a change from a predominantly α-helical protein to a β-sheet form, which causes scrapie in sheep and goat. the present study was carried out to identify polymorphisms of the prion protein gene (prp) ...

Journal: :Journal of virology 2009
Dina Uzri Lee Gehrke

Cytoplasmic viral RNAs with 5' triphosphates (5'ppp) are detected by the RNA helicase RIG-I, initiating downstream signaling and alpha/beta interferon (IFN-alpha/beta) expression that establish an antiviral state. We demonstrate here that the hepatitis C virus (HCV) 3' untranslated region (UTR) RNA has greater activity as an immune stimulator than several flavivirus UTR RNAs. We confirmed that ...

Journal: :acta medica iranica 0
seyed hamid jamaldini department of genetics, genetic research center, university of social welfare and rehabilitation sciences, tehran, iran. mojgan babanejad department of genetics, genetic research center, university of social welfare and rehabilitation sciences, tehran, iran. reza mozaffari department of genetics, cardiogenetic research center, tehran, iran-department of genetics, shahid rajaie cardiovascular medical & research center, tehran, iran. nooshin nikzat department of genetics, genetic research center, university of social welfare and rehabilitation sciences, tehran, iran. khadijeh jalalvand department of genetics, genetic research center, university of social welfare and rehabilitation sciences, tehran, iran. azadeh badiei department of genetics, genetic research center, university of social welfare and rehabilitation sciences, tehran, iran.

coronary artery disease (cad) is the leading cause of mortality in many parts of the world. genome-wide association studies (gwas) have identified several genetic variants associated with cad in low-density lipoprotein receptor (ldlr) locus. this study was evaluated the possible association of genetic markers at ldlr locus with cad irrespective to lipid profile and as well as the association of...

Journal: :anesthesiology and pain medicine 0
mahsa motavaf department of molecular medicine, rezvan medical research institute, iran saeid safari department of molecular medicine, rezvan medical research institute, iran; department of anesthesiology, rasoul akram medical center, iran university of medical sciences (iums), iran seyed moayed alavian department of molecular medicine, rezvan medical research institute, iran; baqiyatallah research center for gastroenterology and liver diseases, baqiyatallah university of medical sciences, iran +98-2188945186, [email protected]; baqiyatallah research center for gastroenterology and liver diseases, baqiyatallah university of medical sciences, iran +98-2188945186, [email protected]

Journal: :iranian journal of allergy, asthma and immunology 0
somayeh ahmadlou department of medical genetics, school of medicine, tehran university of medical sciences, tehran, iran mohsen akhiani department of rheumatology, alborz hospital, karaj, iran ahmad salimzadeh rheumatology research center, sina hospital, tehran university of medical sciences, tehran, iran mohammad keramatipour department of medical genetics, school of medicine, tehran university of medical sciences, tehran, iran

the association of rs10818488 snp located in traf1/c5 region with rheumatoid arthritis (ra), has been picked up by genome-wide association studies. independent studies in different populations revealed inconsistent results. the aim of this study was to investigate the possible association of this snp with ra in iranian population. a total of 362 cases and 422 healthy controls were recruited in ...

Journal: :مجله دانشگاه علوم پزشکی کرمانشاه 0
seddigheh heidarian farzaneh sabahi seyed reza mohebbi mohammad reza zali

introduction: hepatitis b is a potentially life-threatening infection that causes acute infection and chronic hepatitis with progression to cirrhosis and hepatocellular carcinoma (hcc). interleukin-12 (il12) is responsible for activation of th1 immune responses, leading to possible clearance of hbv infection from the host’s body. the host’s immune-genetic background plays an important role in t...

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