نتایج جستجو برای: single nucleotide

تعداد نتایج: 949916  

Journal: :iranian journal of radiation research 0
h. v. goutham department of radiation biology & toxicology, school of life sciences, manipal university, manipal, karnataka, india k. d. mumbrekar department of radiation biology & toxicology, school of life sciences, manipal university, manipal, karnataka, india n. hitendra department of biotechnology, school of life sciences, manipal university, manipal, karnataka india. b. m. vadhiraja department of radiation oncology, manipal hospital, bangalore, karnataka, india d. j. manipal university department of radiotherapy & oncology, shiridi saibaba cancer hospital and research centre, kasturba hospital, manipal, karnataka, india b. s. shiridi saibaba cancer hospital and research centre department of radiation biology & toxicology, school of life sciences, manipal university, manipal, karnataka, india

background: normal tissue toxicity continues to remain as a major challenge for radiation oncologists for delivering the total dose to the tumour cells in cancer patients. cellular, molecular and plasma based early biomarkers to predict the overreactions and non-overreactions of normal tissue toxicity before the initiation of radiotherapy can be valuable for personalised treatment. the aim of t...

Journal: :international journal of molecular and cellular medicine 0
maryam mafi golchin department of genetics, faculty of medicine, babol university of medical sciences, babol, iran. sayyed mohammad hossein ghaderian department of medical genetics, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran. haleh akhavan-niaki department of genetics, faculty of medicine, babol university of medical sciences, babol, iran. rozita jalalian cardiovascular research center, mazandaran university of medical sciences, sari, iran. laleh hedari department of medical genetics, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran. ali reza salami department of biotechnology, university of tehran, tehran, iran.

coronary artery disease (cad) including myocardial infarction (mi) as its complication, is one of the most common heart diseases worldwide and also in iran, with extremely elevated mortality. cad is a multifactorial disorder. twin and family studies at different loci have demonstrated that genetic factors have an important role in the progression of cad. many studies have reported a significant...

Journal: :iranian biomedical journal 0
حمیدرضا خرم خورشید hamid reza khorram khorshid raymond dalgleish

background: several methods have been developed for detection of sequence variation in genes and each has its advantages and disadvantages. a disadvantage of them is that the simpler, cost-effective methods are commonly perceived as being less sensitive in their detection of sequence variation, whereas those with proven sensitivity have a requirement for complex or expensive laboratory equipmen...

Journal: :caspian journal of internal medicine 0
mozhgan moazami-goudarzi stem cell research center, tabriz university of medical science, tabriz, iran majid farshdousti-hagh hematology and oncology research center, tabriz university of medical science, tabriz, iran abbasali hoseinpour-feizi hematology and oncology research center, tabriz university of medical science, tabriz, iran mehdi talebi hematology and oncology research center, tabriz university of medical science, tabriz, iran ali-akbar movassaghpour-akbari hematology and oncology research center, tabriz university of medical science, tabriz, iran karim shams-asanjan hematology and oncology research center, tabriz university of medical science, tabriz, iran

background: bcl-2 is the most important anti-apoptotic regulator and bax is a pro-apoptotic protein. the status of these parameters or the ration of bcl-2 to bax is important in malignant cell fate as well as normal cells. methods: sixty-two all patients and 62 healthy sex-and age-matched controls were studied. after genotyping, the promoter region of the bax and bcl-2 genes by rflp-pcr method ...

خیام نکوئی, سید محتبی, بابائیان جلودار, نادعلی , خادمیان, راحله , مردی, محسن , ناخدا, بابک,

There is a lot of information about genes sequence but their functions are still unknown. So, to fill the gap between structure and function of these sequences many reverse genetic researches have been done. Current experiment studying, how to design gene-specific primers, that can determine single nucleotide diversity and its impact on gene function.This research was condacted at International...

Journal: :hepatitis monthly 0
sayyad khanizadeh department of virology, faculty of medical sciences, tarbiat modares university, p.o. box: 14115-331, ir iran +98-2182883836, [email protected] mehrdad ravanshad department of virology, faculty of medical sciences, tarbiat modares university, p.o. box: 14115-331, ir iran +98-2182883836, [email protected]; department of virology, faculty of medical sciences, tarbiat modares university, p.o. box: 14115-331, ir iran +98-2182883836, [email protected] seyed reza reza mohebbi research center for gastroenterology and liver disease, shaheed beheshti university of medical sciences, p.o. box: 14115-331, ir iran +98-2122432515, [email protected]; research center for gastroenterology and liver disease, shaheed beheshti university of medical sciences, p.o. box: 14115-331, ir iran +98-2122432515, [email protected] hamed naghoosi research center for gastroenterology and liver disease, shaheed beheshti university of medical sciences, p.o. box: 14115-331, ir iran +98-2122432515, [email protected] mohamad ebrahim abrahim tahaei research center for gastroenterology and liver disease, shaheed beheshti university of medical sciences, p.o. box: 14115-331, ir iran +98-2122432515, [email protected] seyed dawood dawood mousavi nasab department of virology, faculty of medical sciences, tarbiat modares university, p.o. box: 14115-331, ir iran +98-2182883836, [email protected]

background chronic hepatitis b virus (hbv) infection is a multifactorial disease that can result in serious clinical complications. host genetic background especially the genes that encode immunologic factors like inf-γ and its receptor (ifn-γ r) are critical in the pathogenesis of infection. materials and methods genomic dna from peripheral blood samples of 200 chronically hbv infected patient...

Journal: :iranian journal of basic medical sciences 0
motahar heidari-beni department of community nutrition, school of nutrition and food sciences, isfahan university of medical sciences, isfahan, iran roya kelishadi child growth and development research center, research institute for primordial prevention of non-communicable disease, isfahan university of medical sciences, isfahan, iran marjan mansourian department of biostatistics and epidemiology, school of health, isfahan university of medical sciences, isfahan, iran gholamreza askari department of community nutrition, school of nutrition and food sciences, isfahan university of medical sciences, isfahan, iran

objective(s): this study aims to investigate joint association between cholesterol ester transfer protein (cetp) polymorphisms and body mass index (bmi) or birth weight with the risk of dyslipidemia in iranian children and adolescents. materials and methods:this study was conducted as a sub-study of the “school-based nationwide health survey” (caspian-iii). we randomly selected 750 samples from...

Journal: :iranian journal of basic medical sciences 0
jia-yuan pu department of respiratory, the first hospital, lanzhou university, lanzhou 730000, china wei dong department of immunology, west china school of preclinical and forensic medicine, sichuan university, chengdu 610041, china lin zhang department of forensic biology, west china school of preclinical and forensic medicine, sichuan university, chengdu 610041, china wei-bo liang department of forensic biology, west china school of preclinical and forensic medicine, sichuan university, chengdu 610041, china yan yang department of obstetrics and gynecology, west china second university hospital, sichuan university, chengdu 610041, china mei-li lv department of immunology, west china school of preclinical and forensic medicine, sichuan university, chengdu 610041, china

objective(s): accumulating evidence has demonstrated that mirnas contribute to various genetic and epigenetic modifications in the pathogenesis of gastric cancer (gc). recent studies focused on the four single nucleotide polymorphisms (snps) of pre-mirnas including rs11614913, rs3746444, rs2910164, and rs2292832. it was suggested that these four snps were significantly associated with the risk ...

Journal: :international journal of endocrinology and metabolism 0
hamid ghalandari department of clinical nutrition and dietetics, faculty of nutrition sciences and food technology, shahid beheshti university of medical sciences, tehran, ir iran firoozeh hosseini-esfahani nutrition and endocrine research center, obesity research center, research institute for endocrine sciences, shahid beheshti university of medical sciences, tehran, ir iran parvin mirmiran nutrition and endocrine research center, obesity research center, research institute for endocrine sciences, shahid beheshti university of medical sciences, tehran, ir iran; department of clinical nutrition and dietetics, national nutrition and food technology research institute, faculty of nutrition sciences and food technology, shahid beheshti university of medical sciences, tehran, ir iran; nutrition and endocrine research center,obesity research center, research institute for endocrine sciences, shahid beheshti university of medical sciences,tehran, ir iran. tel: +98-2122402463, fax: +98-2122432500

conclusions in general, our study suggests that the association between lep/lepr and ghrl/ghsr with overweight/obesity and the related metabolic disturbances is inconclusive. these results may be due to unidentified gene-environment interactions. more investigations are needed to further clarify this association. results the most prevalent leptin/leptin receptor genes (lep/lepr) and ghrelin/ghr...

Uncovering DNA sequence variations that correlate with phenotypic changes, e.g., diseases, is the aim of sequence variation studies. Common types sequence variations are Single nucleotide polymorphism (SNP, pronounced snip).SNPs are the third-generation molecular marker. SNP represents a DNA sequence variant of a single base pair with the minor allele occurring in more than 1% of a given popula...

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